TW200532010A - Systems, methods, and catalysts for producing a crude product - Google Patents

Systems, methods, and catalysts for producing a crude product Download PDF

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TW200532010A
TW200532010A TW093139061A TW93139061A TW200532010A TW 200532010 A TW200532010 A TW 200532010A TW 093139061 A TW093139061 A TW 093139061A TW 93139061 A TW93139061 A TW 93139061A TW 200532010 A TW200532010 A TW 200532010A
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Taiwan
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crude oil
catalyst
product
content
feed
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TW093139061A
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Chinese (zh)
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Opinder Kishan Bhan
Scott Lee Wellington
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Shell Int Research
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G45/00Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/20Vanadium, niobium or tantalum
    • B01J23/22Vanadium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/24Chromium, molybdenum or tungsten
    • B01J23/28Molybdenum
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/60Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G29/00Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
    • C10G29/04Metals, or metals deposited on a carrier
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G45/00Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
    • C10G45/02Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
    • C10G45/04Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/04Liquid carbonaceous fuels essentially based on blends of hydrocarbons
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/60Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J35/64Pore diameter
    • B01J35/6472-50 nm
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/60Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J35/66Pore distribution
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/0009Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/0201Impregnation
    • B01J37/0203Impregnation the impregnation liquid containing organic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/20Characteristics of the feedstock or the products
    • C10G2300/201Impurities
    • C10G2300/202Heteroatoms content, i.e. S, N, O, P
    • C10G2300/203Naphthenic acids, TAN
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/20Characteristics of the feedstock or the products
    • C10G2300/201Impurities
    • C10G2300/205Metal content

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Catalysts (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Lubricants (AREA)
  • Manufacture Of Alloys Or Alloy Compounds (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Contact of a crude feed with one or more catalysts produces a total product that include a crude product. The crude product is a liquid mixture at 25 DEG C and 0.101 Mpa. One or more other properties of the crude product may be changed by at least 10% relative to the respective properties of the crude feed.

Description

200532010 九、發明說明: 【發明所屬之技術領域】 本發明大體上係有關處理原油進料之系統、方法和觸 媒亚且有關旎使用這類系統、方法和觸媒生產的組成物。 更洋σ之,本文中所述的特定具體實例係有關用以將原油 進料轉化成總產物之系統、方法和觸媒,纟中此總產物含 有原/由產物,其在25°C和〇·101 MPa下為液態混合物而且 與原油進料的個別性質相比具有一或多種已改變的性質。 【先前技術】 e m刖运,驭使⑺莨夭口孜儒加工 、:、:種不適當性質之原油通常稱為“劣質原油' 酸性I二原’甴可此包含造成原油進料之總酸值(“TAN,,)的 -夂性成刀。具有相當高τ 加工& κ Ν的< 貝原油在輪送期間及/或 刀工此4質原油期間可能合 W ^ ^ rb ^ 成孟屬兀件的腐蝕。移除劣 貝原油中的酸性成分匕 们Ή 分。或者+ 此涉及用各種鹼化學中和酸性成 用耐蝕全、s ^止 、叹備及/或加工設備中。使 ]蚀至屬通常涉及可觀的費 ^ 耐蝕金屬y e i 、 現行設備中使用 萄了月匕不疋吾人所期望的。 可能涉及在於〜β /々上 ρ制腐餘的另一種方法 夂在輪廷及/或加工劣質 到劣質原油。使用腐蝕#ρ Μ ” 'j將腐蝕抑制劑添加 及/或由;^ 抑制劑可能對加工原油所用的設備 戈由,製造之產物的品質有負面影響/用的-備 力貝原油通常包含相去旦 物會有使用習 里、?遠物。這類大量殘留 用白知5又備難以輪送及/或 向。 τ成本貴的傾 200532010 原子(例如硫、氧,和 下對觸媒有不利的影 劣質原油通常包含有機結合的雜 氮)。有機結合的雜原子於若干情況 響。 劣質原油可能包含相當大量的金屬污染物,例如鎳、 叙,及/或鐵。在加工這類原油期間,金屬污染物及/或金 :污染物的化合物可能會沈積在觸媒表面上或觸媒的孔隙 體積中。這類沈積物可能會導致觸媒活性的下降。 、 在加工劣質原油期間焦炭可能會急劇地形成及/或沈積 在觸媒表面上。使受到焦炭污染的觸媒之催化活性再生的 成本可能是昂貴的。再生期間所使用的高溫也可能使觸媒 的活性降低及/或導致觸媒劣化。 劣質原油可能包含有機酸金屬鹽形態的金屬(例如鈣、 鉀二及/或鈉)。有機酸金屬鹽形態的金屬典型而言無法藉 由白矣方法’例如脫鹽及/或酸洗從劣質原油中分離。 β當存在有機酸金屬鹽形態的金屬_,f知方法常遇到 題”典型沈積在觸媒之外表面附近的錄和鈒相比,有 機酸金屬鹽形態的金屬可能會優先沈積在觸媒粒子間的孔 隙體積中,牲兄,丨β ^ /疋在觸媒床的頂部。污染物,例如有機酸 =一悲'的金屬沈積在觸媒床頂部通常會導致通過觸婵 μ壓降增⑽且實際±㈣㈣觸職。再者 金屬鹽=態的金屬可能會導致觸媒的快速減活性。 每克劣::油可此包含有機氧化合物。加工具有含氧量為 f貝原油中至少含〇·〇〇2克的氧之劣質原油的處理設 工期間可能會遇到問題。有機氧化合物在加工期間 200532010 又熱衿可此會生成鬲級氧化物(例如酮及/或由醇的氧化生 成馱及/或由醚的氧化生成酸),其難以從處理過的原油 中移除及/或在加工期間可能會腐蝕/污染設備並且 送管線堵塞。 ^ /質原油可能包含不飽和烴。當加工不飽和烴時,特 別疋如果會產生由裂解法而來的不飽和片#,則氫的均量 通常必須增加。加工期間的氫化,其典型而言涉及活性氣 化觸媒的使用,可能啦 匕而要抑制不飽和片段形成焦炭。氫的 生產成本昂貴及/或輸送到處理設備成本昂貴。 劣貝原油在以習知設備加工期間也會傾向於表現出不 :定性。原油不穩定性會有導致在加工期間成分相分離及/ :生成非理想副產物(例如硫化氯、纟,和二氧化碳)的傾 向 〇 、 習知方法通常缺乏改傲少所広, 之改k名質原油之選定性質,而不合 ”、、、者改變劣質原油之其他性質的能力。舉例而言,習知 =常缺乏顯著降低劣質原油中的TAN而同時僅以期望量 能:劣質原油中特定成分(例如硫或金屬污染物)之含量的 若干用以改善原油口所ϋ ^ 口口貝勺方法包括將稀釋劑添加至劣 :原油以降低造成不利性質之成分的重量百分率。狭而, :、、加稀釋劑通常會因為稀釋劑的成本及/或 二 .^ 彡貝原油的成本。稀釋劑添加至劣質 原油於若干情況下可能會降低此《油的穩定性。 頒予S^akar等人的美國專利案號6,547,957;頒予 200532010200532010 IX. Description of the invention: [Technical field to which the invention belongs] The present invention relates generally to systems, methods, and catalysts for processing crude oil feeds, and to the use of such systems, methods, and catalysts to produce compositions. More specifically, the specific examples described herein relate to systems, methods, and catalysts used to convert crude oil feeds to total products, where the total product contains raw / free products at 25 ° C and It is a liquid mixture at 0.1 MPa and has one or more changed properties compared to the individual properties of the crude feed. [Prior technology] em 刖 transportation, processing, and processing of crude oil of inappropriate quality are commonly referred to as "inferior crude oils" acid I two raw materials ", which may include the total acidity of the crude oil feed The value of "(TAN ,,)" is a knife. The relatively high τ processing & κN < < " > shell crude oil may cause W ^^^ rb ^ corrosion during the rotation and / or during the cutting of this grade 4 crude oil. Remove the acidic components from the crude oil. Or + This involves the neutralization of acidic compounds with various alkali chemistry, corrosion resistance, chemical resistance, and / or processing equipment. Corrosion usually involves a considerable amount of expense ^ Corrosion resistant metal y e i, which is used in current equipment is not what we expect. May involve another method for making rotten residues on ~ β / 々 夂 in round and / or processing inferior to inferior crude oil. The use of corrosion # ρ Μ ″ to add corrosion inhibitors and / or; ^ inhibitors may have a negative impact on the equipment used to process crude oil, the quality of the products manufactured / used-Bei Libei crude oil usually contains phase depletion Once the material is used, it will be far away. Such large amounts of residues are difficult to be rotated and / or directed. Τ expensive 200532010 atoms (such as sulfur, oxygen, and other harmful to the catalyst) Inferior crude oils often contain organically bound heteronitrogens. Organically bound heteroatoms can react in a number of situations. Inferior crudes may contain a significant amount of metal contaminants such as nickel, Syria, and / or iron. During processing of such crudes Metal pollutants and / or gold: Compounds of pollutants may be deposited on the catalyst surface or in the catalyst's pore volume. Such deposits may cause a decrease in catalyst activity. Coke may be processed during the processing of inferior crude oil Will form and / or deposit sharply on the catalyst surface. The cost of regenerating the catalytic activity of a catalyst contaminated with coke may be expensive. The high temperature used during regeneration may also cause the catalyst Reduced activity and / or cause catalyst degradation. Inferior crude oils may contain metals in the form of metal salts of organic acids (such as calcium, potassium di and / or sodium). Metals in the form of metal salts of organic acids typically cannot be treated by the method 'Such as desalination and / or pickling is separated from inferior crude oil. Β When organic metals in the form of metal salts of organic acids are present, the method often encounters the question "Compared with the conventional deposition of the catalyst near the surface of the catalyst, The metal in the form of an organic acid metal salt may be preferentially deposited in the pore volume between the catalyst particles, and the man, β ^ / 疋 is on the top of the catalyst bed. Contaminants, such as organic acids = a tragic 'metal deposit on the top of the catalyst bed will usually result in an increase in the μ pressure drop through contact and actual contact. Furthermore, metals in the metal salt state may cause rapid deactivation of the catalyst. Per gram inferior :: The oil may contain organic oxygen compounds. Problems may be encountered during processing facilities for processing inferior crude oils having an oxygen content of at least 0.002 grams of oxygen in crude oil with an oxygen content of f. During the processing of the organic oxygen compound in 200532010, it will be hot again. This will generate high-grade oxides (such as ketone and / or alcohol from alcohol and / or ether from acid), which is difficult to remove from processed crude oil. Remove and / or may corrode / contaminate equipment and block pipelines during processing. ^ / Mass crude oil may contain unsaturated hydrocarbons. When processing unsaturated hydrocarbons, in particular, if unsaturated flakes # produced by the cracking method are produced, the average amount of hydrogen must generally be increased. Hydrogenation during processing, which typically involves the use of active gasification catalysts, may inhibit the formation of coke by unsaturated fragments. Hydrogen is expensive to produce and / or expensive to transfer to processing equipment. Inferior crude oil also tends to show instability during processing with conventional equipment: qualitative. Crude oil instability tends to cause component phase separation and / or the formation of non-ideal by-products (such as chlorine sulfide, tritium, and carbon dioxide) during processing. Conventional methods are often lacking. The selected properties of high-quality crude oils, but not the ability to change other properties of low-quality crude oils. For example, it is often known that there is often a lack of significant reduction of TAN in low-quality crude oils while at the same time only the desired amount of energy: Several of the contents of ingredients (such as sulfur or metal contaminants) are used to improve the mouth of the crude oil. Mouth spoon method includes adding a diluent to the inferior: crude oil to reduce the weight percentage of the ingredients that cause adverse properties. Narrow: Adding a diluent is usually due to the cost of the diluent and / or the cost of the crude oil. The addition of diluent to inferior crude oil may reduce the stability of this oil under certain circumstances. Awarded to S ^ akar et al U.S. Patent No. 6,547,957; granted 200532010

Meyers等人的6,277,269;頒予如油等人的6加⑽ 頒予Bearden等人的5,928,5〇2,·頒予仏訂如等人 頒予⑽⑽等人# 5,897,769;頒予Trachte 寺人的5,871,636,·及料Tanaka#人的5,85i,38i係叙述 加工原油的各種方法、系統及觸媒。然而,這些專利中所 =的方法、系統及觸媒因為以上提出的許多技 有受限的適用性。 /、 間5之,劣質原油通常具有非理想性質(例如相當高的 TAN,在處理期間變得 魏相合士 ο 的傾向’及/或在處理期間消 曰里風的傾向)。其他非理想性質包括相當大量的非 :想成分(例如殘留物、有機結合雜原子、金屬污染物、有 機酸金屬鹽形態之金屬’及/或有機氧化合物)。這類性質 會傾向於導致習知輪祥β / 4、 、 彳义白知輸达及/或處理設備方面的問題,包括在6,277,269 by Meyers et al .; 6 plus 颁 by Ruyou et al. 5,928,502 by Bearden et al., 仏 by Ruding et al. By ⑽⑽ et al. # 5,897,769; by Trachte 5,871,636, and materials Tanaka # 5,85i, 38i describe various methods, systems and catalysts for processing crude oil. However, the methods, systems, and catalysts described in these patents have limited applicability due to many of the techniques proposed above. / 、 Among other things, inferior crude oil usually has non-ideal properties (for example, a relatively high TAN, a tendency to become Wei Xianghe ο during processing ′ and / or a tendency to eliminate leprosy during processing). Other non-ideal properties include a considerable amount of non-ideal components (such as residues, organically bound heteroatoms, metal contaminants, metals in the form of metal salts of organic acids' and / or organic oxygen compounds). This type of property tends to lead to problems with the knowledge of Lianxiang β / 4, Lianyi Baizhi's delivery and / or processing equipment, including

处理期間腐I虫增加,觸草I 9 觸媒π0)7減紐,製程堵塞,及/或氫使 ^增加。因此’對於使劣質原油轉化成具有更多理想性質 原油產物的改U統、方法,及/或觸媒仍有顯著經濟上 口 =上的需求。同樣對於能改變劣質原油之選定性質而 觸^ 名貝原油之其他性質的系、統、方法,及/或 蜀媒也有顯著經濟上和技術上的需求。 【發明内容】 產本I月大""上係有關用以將原油進料轉化成含有原油 :物而在若干具體實例中含有非可凝氣體的總產物之系 法和觸媒。本發明大體上亦有關含有其中成分之新 '、、'且&的組成物。這類組成物能使用本文中所述的系統和 200532010 方法來獲得。 本發明係提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油 / 其中該原油產物在下為液態混=該 原:由進料具有至少〇.3 # TAN,該至少—種觸媒具有中位 孔位在9G A至18G A之範圍内的孔徑分佈’該孔徑分佈中 至少咖的總孔數具有在45A之中位孔徑範圍内的孔徑, 其中孔徑分佈係藉由ASTM&剛2測定;及控制接觸條 件以便使該原油產物具有TAN最多為9〇%之該原油進料的 TAN ’其中TAN係藉由ASTM法D664測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在饥和〇.⑻Mpa下為液態混合物,該 原油進料具有至少G 3 @ TAN,該至少―種觸媒具有中位 孔徑至少為9〇A的孔徑分佈,其藉由ASTM&D428^^j定, 該觸媒在每克觸媒中’以翻的重量計,含有〇侧i克至0.08 克的鉑、-或多種紹化合物,或其混合物;及控制接觸條 件以便使該原油產物具有TAN最多為9〇%之該原油進料的 TAN ’其中TAN係藉由ASTM法D664測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物\ 其中該原油產物在况和〇1〇1 Mpa下為液態混合物,該 原油進料具有至少〇.3的TAN,其藉由astmd664測定,z 該至少-種觸媒具有中位孔徑至少為18qA的孔徑分佈, 200532010 其藉由ASTM4 D4282測定,該觸媒具有包含週期表 爛的一或多種金屬,週期表第6搁之一或多種金屬的 多種化合物’或其混合物的孔徑分佈;及控制接觸條件以 便使該原油產物具有TAN最多4 9〇%之該原油進 TAN,其中TAN係藉由ASTM法D664測定。 、本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物: 其中該原油產物在饥和G.1G1 Mpa下為液態混合物,今 ^由進料具有至少〇·3的TAN,其藉由ASTM法D664測 二次至v種觸媒包含:⑷週期表第6欄的一或多種 ^屬二週期表第6攔之—或多種金屬的—或多種化合物, :、、口物’及(b)週期表第丨〇攔的一或多種金屬,週 ^表第1G攔之—或多種金屬的—或多種化合物,或其混 口物’其中第10欄金屬總量與第6攔金屬總量的莫耳比 f…。的範圍内,·及控制接觸條件以便使該原油產物 :有則最多為9〇%之該原油進料的⑽,其中tan係 猎由ASTM法D664測定。 本發明亦提供生產原油產物之方法,其包括··使原油 =料與一或多種觸媒接觸以生產含有原油產物的總產物, =該原油產物在25t和0.101MPa下為液態混合物,該 ^由進科具有至少〇.3的TAN’該一或多種觸媒包含⑷第 :種觸媒’其係於每克第一種觸媒中,以金屬重量計,含 a 1至〇·06克之週期表第6攔的-或多種金屬,週 第6攔之-或多種金屬的一或多種化合物,或其混合 10 200532010 物;及(b)第二種觸媒,該第二 稷觸媒在母克弟二種觸媒 中’以至屬重量計,含有至少〇 夕〇·02克之週期表第ό欄的一 或多種金屬’週期表第6攔之—或多種金屬的-或多種化 合物,或其混合物;及控制接觸條件以便使該原油產物呈 有丁AN最多為90%之該原油進料 、 沒卞十的TAN,其中ΤΛΝ係藉 由ASTM法D664測定。 本發明亦提供觸媒組成物,其包括:⑷週期表第5 欄的-或多種金屬,週期表帛5攔之一或多種金屬的一或 多種化合物’或其混合物;⑻载體,其具㈣氧化紹含量 為母克載體中至少(M克的θ氧化紹,其藉由χ射線繞射測 定:其中該觸媒具有中位孔徑至少為2越的孔徑分佈, 其藉由ASTM法D4282測定。 本發明亦提供觸媒組成物,其包括:⑷週期表第6 ,的或多種金屬’週期表第6攔之—或多種金屬的一或 多種化合物’或其混合物;⑻載體,其具有Θ氧化鋁含量 為每克載體中至少^克的θ氧化|g,其藉由χ射線繞射測 定丄其中該觸媒具有中位孔徑至少為23〇Α的孔徑分佈, 其藉由ASTM法D4282測定。 本發明亦提供觸媒組成物,其包括:(a)週期表第5 攔的-或多種金屬,週期表帛5攔之―或多種金屬的一或 多種化合物,週期表第6攔的一或多種金屬,週期表第6 摘之或夕種金屬的一或多種化合物,或其混合物;(b)載 ^其具有0氧化鋁含量為每克載體中至少0.1克的Θ氧化 鋁,其藉由x射線繞射測定;其中該觸媒具有中位孔徑至 200532010 少為2 3 0 A的孔經分蚀 ^ ^ 布’其精由ASTM法D4282測定。 1本發明亦提供生產觸媒之方法,其包括:使载體與— 或多種金屬結合以形成載體 '、 θ氧化铭,而一或多種=“&物,其中該載體包含 八戸、 /夕種金屬包括週期表第5攔的一或多種 孟屬,週期表第5攔之一 < 多^ & . Α夕種金屬的一或多種化合物, 或”混合物;於至少4〇〇 〇c的㈤痄 3入 的/皿度τ熱處理θ氧化銘載體/ &物;及形成觸媒,其㈣觸媒具有中位孔徑至少 為230Α的孔徑分佈,其藉由astm法〇4282測定。 本發明亦提供生產觸媒之方法,其包括:使载體與一 或多種金屬結合以形成載體/金屬混合物,其中該載體包含 Θ乳化紹,而一或多種金屬包括週期表第6攔的一或多種 金屬,,週期表第6攔之_或多種金屬的_❹種化合物, 或”匕口物,灰至少_ C的溫度下熱處理Θ氧化|g載體/ 金屬混合物’·及形成觸媒,其中該觸媒具有中位孔徑至少 為230人的孔徑分佈,其藉由ASTM法〇4282測定。During the treatment, the number of rot insects increased, and the number of catalysts I9 and catalyst π0) 7 decreased, the process was blocked, and / or hydrogen increased ^. Therefore, there is still a significant economic need for reforming systems, methods, and / or catalysts to convert inferior crude oil into crude products with more desirable properties. There is also a significant economic and technical need for systems, systems, methods, and / or media that can change the selected properties of inferior crude oils and touch other properties of Mingbei crude oil. [Summary of the Invention] The production system of this month is related to a system and a catalyst for converting a crude oil feed into a crude product containing crude oil and in some specific examples a non-condensable gas. The present invention is also generally directed to compositions containing novel ',,' and & Such compositions can be obtained using the system described in this article and the 200532010 method. The present invention provides a method for producing a crude oil product, which comprises: contacting a crude oil feed with one or more catalysts to produce a crude oil-containing product / wherein the crude oil product is in a liquid state below = the original: the feed has at least 0.3 # TAN, the at least one catalyst has a pore size distribution with a median pore position in the range of 9G A to 18G A 'The total number of pores in the pore size distribution has a pore size in the 45A median pore size range, where The distribution is determined by ASTM &2; and the contact conditions are controlled so that the crude oil product has a TAN of the crude oil feed with a TAN of up to 90%, where TAN is determined by ASTM method D664. The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture under the condition of 0.1 Mpa and the crude oil; The feed has at least G 3 @ TAN, and the at least one catalyst has a pore size distribution with a median pore size of at least 90A, which is determined by ASTM & D428 ^^ j. It contains 0.1 to 0.08 grams of platinum,-or more compounds, or mixtures thereof; and controls the contact conditions so that the crude oil product has a TAN of TAN of up to 90% of the crude oil feed. Among them, TAN is measured by ASTM method D664. The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at a temperature of 0,001 Mpa, The crude feed has a TAN of at least 0.3, as measured by asmd664, and the at least one catalyst has a pore size distribution with a median pore size of at least 18qA. 200532010 It is measured by ASTM4 D4282, and the catalyst has a cycle containing Table 1 shows the pore size distribution of one or more metals, 6 or more compounds of one or more metals of the Periodic Table, or a mixture thereof; and controls the contact conditions so that the crude oil product has a TAN of up to 4 90% of the crude oil into the TAN. , Where TAN is determined by ASTM method D664. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product: wherein the crude oil product is a liquid mixture under the conditions of G.1G1 Mpa, Now the feed has a TAN of at least 0.3, which is measured by ASTM method D664 twice to v. The catalyst contains: ⑷ one or more of the sixth column of the periodic table ^ belongs to the sixth column of the second periodic table—or Multi-metal—or multiple compounds,: ,,,,,,, and (b) one or more metals listed in Table 1 of the periodic table, one or more metals in Table 1—or multiple compounds, or a mixture thereof Mouthpieces, in which the molar ratio f of the total amount of metal in column 10 to the total amount of metal in column 6 f ... Within the range of, and control the contact conditions so that the crude oil product: there is at most 90% of the plutonium of the crude oil feed, wherein the tan series is determined by ASTM method D664. The invention also provides a method for producing a crude oil product, which comprises: contacting crude oil with one or more catalysts to produce a total product containing the crude oil product, = the crude oil product is a liquid mixture at 25 t and 0.101 MPa, and ^ Jinke has a TAN of at least 0.3. The one or more catalysts include: the first catalyst, which is contained in the first catalyst per gram, based on the weight of the metal, and contains 1 to 0.06 grams of The sixth or more metals of the periodic table, the sixth or more of the week, or one or more compounds of the metals, or a mixture thereof 10 200532010; and (b) the second catalyst, the second catalyst Among the two catalysts of the mother gram, 'the one or more metals containing at least 0,02 grams of column one of the periodic table', based on the weight of the catalyst, in the sixth column of the periodic table-or more metals-or more compounds, or Its mixture; and controlling the contact conditions so that the crude oil product exhibits a maximum of 90% of the crude oil feed, TAN of the crude oil, wherein TΛN is determined by ASTM method D664. The present invention also provides a catalyst composition comprising: (i) one or more metals in column 5 of the periodic table, one or more compounds of one or more metals in the periodic table, or a mixture thereof; (ii) a carrier, which has The content of osmium oxide is at least (M grams of θ oxide in the mother gram carrier, which is determined by X-ray diffraction: where the catalyst has a pore size distribution with a median pore size of at least 2%, and it is measured by ASTM method D4282 The present invention also provides a catalyst composition, which includes: (6) of the periodic table or more of the metal 'or 6 or more compounds of the periodic table' or a mixture of one or more of the metals' or a mixture thereof; The alumina content is at least ^ grams of θ oxidation | g per gram of carrier, which is determined by X-ray diffraction, where the catalyst has a pore size distribution with a median pore size of at least 23 ° A, which is determined by ASTM method D4282 The present invention also provides a catalyst composition, which includes: (a) the fifth or more metals of the periodic table, the five or more of the periodic table-one or more compounds of the plurality of metals, one of the six or more compounds of the periodic table Or more metals, gold of the sixth periodic table One or more compounds, or mixtures thereof; (b) containing Θ alumina having an alumina content of at least 0.1 g per gram of support, as determined by x-ray diffraction; wherein the catalyst has a median The pores with a pore diameter of up to 200532010 are less than 2 3 0 A. The fineness is determined by ASTM method D4282. 1 The present invention also provides a method for producing a catalyst, which includes: combining a carrier with—or a plurality of metals to Form a carrier ', θ oxidation, and one or more = "& substances, wherein the carrier contains ytterbium, / metal species including one or more mongolia of the fifth table of the periodic table, one of the fifth table of the periodic table < ^ &Amp;. One or more compounds, or "mixtures" of A metal species; heat treatment at least 4,000 ° C / degree τ heat treatment θ oxidation of the carrier / amp; and the formation of catalysts The catalyst has a pore size distribution with a median pore size of at least 230A, which is determined by the astm method 04282. The present invention also provides a method for producing a catalyst, which comprises: combining a carrier with one or more metals to form a carrier / Metal mixture, wherein the carrier contains Θ emulsified, and one or Kinds of metal include one or more metals in the sixth table of the periodic table, _ compounds of _ or more metals in the sixth table of the periodic table, or "daggers, ash heat treatment at a temperature of at least _C Θ oxidation | g support / Metal mixture 'and forming a catalyst, wherein the catalyst has a pore size distribution with a median pore size of at least 230 people, which is determined by the ASTM method 04282.

本發明亦提供生產原油產物之方法,其包括:使原油 違料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25。(:和G.1G1购下為液態混合物,該 原油進料具有至少0.3 @ TAN,該至少一種觸媒具有中位 孔仫至v為180A的孔徑分佈,其藉由法BUM測 疋’該觸媒具有包含Θ氧化紹和週期表第6攔的一或多種 金屬,週期表第6欄之一或多種金屬的一或多種化合物, 或其混合物的孔徑分佈;及控制接觸條件以便使該原油產 物具有TAN最多為90%之該原油進料的TAN,其中TAN 12 200532010 知猎由A S T Μ法D 6 6 4測定。 ❿ 本發明亦提供生產原油產物之方法,其包括:於氫源 存在下,使原油進料與一或多種觸媒接觸以生產含有原油 產物的總產物’其中該原油產物在25t和〇 i〇i Mpa下為 液態混合物,該原油進料具有至少〇3白々tan,該原油進 料具有含氧量為每克原油進料至少有〇〇〇〇1克的氧,該至 少-種觸媒具有中位孔徑至少為9GA的孔徑分佈,其藉\ ASTM法D4282測^ ;及控制接觸條件使ΤΑΝ減少以便使 該原油產物具有ΤΑΝ最多為90%之該原油進料的ΤΑΝ, 亚且減少含有機氧化合物的含量以便使該原油產物具有含 氧量最多為90%之該原油進料的含氧量,其中ταν係藉由 AS™法D664測定,而含氧量係藉由ASTM法趵85測曰定。 、本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在说和〇·1〇1 Mpa下為液態混合物,該 原油進料具有至少(Μ @ TAN,該至少—種觸媒在每克觸 媒中,以金屬重量計,含有至少〇.〇〇1克之週期表第㈠闌 的一或多種金屬’週期表第6攔之一或多種金屬的一或多 種化合物’或其混合物;及控制接觸條件以便使接觸區中 的液體空間速度㈣10h…並且使該原油產物具有TAN 取多為90%之該原油進料的ΤΑΝ,其中ταν係藉由Mm 法D664測定。 本發明亦提供生產原油產物之方法’其包括:於氯源 子下,使原油進料與一或多種觸媒接觸以生產含有原油 13 200532010 產物的總產私γ# A ^ ^ 物其中該原油產物在25。〇和0.101 MPa下為 、:。“勿’遺原油進料具有至少〇. 1白勺TAN,該原油進 八有各爪里為每克原油進料至少有〇.⑻〇1克的硫,該至 某匕3週期表第6欄的一或多種金屬,週期表第 欄之或多種金屬的一或多種化合物,或其混合物;及 控㈣觸條件以便使該原油進料於接觸期間在選定率下吸 刀子氫以抑制該原油進料在接觸期間的相分離,使 多個接觸區中的液體空間速度超^lOh-1,使該原油產物 具有TAN最多為9G%之該原油進料的TAN,並且使該原 產物具有含硫量為7〇至13〇%之該原油進料的含硫量, a、t 丁謂切由ASTM法D664測定,而含硫量係藉由 ASTM 法 D4294 測定。 卜本發明亦提供生產原油產物之方法,其包括:於氣態 氫源存在下’使原油進料與一或多種觸媒接觸以生產含有 原油產$的總產物’其中該原油產物纟25°C和G.HH MPa 下為液態混合物;及控制接觸條件以便使該原油進料於接 觸期間在選定率下吸取氫以抑制該原油進料在接觸期間的 ♦本發明亦提供生產原油產物之方法,其包括··於一或 多種觸媒存在了,使原油進料與氫接觸以生產 ,1〇] …把合物;及控制接觸條件以便使該原油進料於第—I吸 取條件下及接著於第二氫吸取條件下與氫接觸,第^吸 取條件與第二氫吸取條件不同,控制第一氫吸取條件=氫 14 200532010 的淨吸取以防止原油進料/總產物混 二 值減至1.5以 下’該原油產物的一或多種性質與該原油進夕 個別性質相比最多冑90%的改變。 、$夕種 本發明亦提供生產原油產物之方法,其包括 〜 溫度下,使原油進料與一或多種觸媒接觸,接著於第:溫 度下接觸以生產含有原油產物的總產物, ^ -fr . π 1Λ1 八Τ 5亥原油產物 在25 c和0.101 Mpa下為液態 少0 ταμ 观巧原油進料具有至 ·的ΤΑΝ,及控制接觸條件使第一接觸㈤ 第二接觸溫度“接m少低於 使忒原油產物與該原油進料The present invention also provides a method for producing a crude oil product, comprising: contacting crude oil with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is at 25. (: And G.1G1 are purchased as a liquid mixture, the crude oil feed has at least 0.3 @ TAN, the at least one catalyst has a pore size distribution from median pores to v of 180A, which is measured by the method BUM The medium has a pore size distribution containing Θ oxide and one or more metals of the sixth table of the periodic table, one or more compounds of one or more metals of column 6 of the periodic table, or a mixture thereof; and controlling the contact conditions so that the crude oil product TAN with a maximum of 90% of the crude oil feed, of which TAN 12 200532010 is determined by ASTM method D 6 64. ❿ The present invention also provides a method for producing crude oil products, which includes: in the presence of a hydrogen source, A crude oil feed is contacted with one or more catalysts to produce a total product containing a crude oil product 'wherein the crude oil product is a liquid mixture at 25 t and 100 Mpa, the crude oil feed has at least 03 Baitan, the crude oil The feed has an oxygen content of at least 0.001 g of oxygen per gram of crude feed, and the at least one catalyst has a pore size distribution with a median pore size of at least 9GA, which is measured by the ASTM method D4282 ^; and Controlling exposure conditions reduces TAN The crude oil product is made to have a TAN of the crude oil feed having a TAN of up to 90%, and the content of organic oxygen compounds is reduced so that the crude oil product has an oxygen content of the crude oil feed having an oxygen content of up to 90% Among them, ταν is determined by AS ™ method D664, and oxygen content is determined by ASTM method 趵 85. The present invention also provides a method for producing crude oil products, which includes: contacting crude oil with-or more Medium to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at said and 0.11 Mpa, and the crude oil feed has at least (M @ TAN, the at least one catalyst per gram of catalyst In the medium, one or more metals containing one or more metals of the sixth table of the Periodic Table or one or more compounds thereof, or a mixture thereof, containing at least 0.001 g of the appendix of the Periodic Table, based on the weight of the metal; and controlled contact; and The conditions are such that the liquid space velocity in the contact zone is ㈣10h ... and that the crude oil product has a TAN of 90% of the crude oil feed, where ταν is determined by Mm method D664. The present invention also provides a crude oil product Method 'which includes: contacting a crude oil feed with one or more catalysts under a chlorine source to produce a total production γ # A ^ ^ containing a product of crude oil 13 200532010 wherein the crude oil product is at 25.0 and 0.101 MPa The following is: "." 'The crude oil feed has at least 0.1 TAN, the crude oil is fed into each claw, and at least 0.01 g of sulfur per gram of crude oil is fed. 3 One or more metals in column 6 of the periodic table, one or more compounds of metals or columns in the periodic table, or a mixture thereof; and controlling the contact conditions so that the crude oil feed sucks a knife at a selected rate during the contact period Hydrogen is used to suppress the phase separation of the crude oil feed during the contact, to make the liquid space velocity in multiple contact zones exceed ^ Oh-1, so that the crude oil product has a TAN of the crude oil feed with a TAN of 9G% at most, and The original product has a sulfur content of 70 to 130% of the crude oil feed. The a and t dice cuts are determined by ASTM method D664, and the sulfur content is measured by ASTM method D4294. The present invention also provides a method for producing a crude oil product, which includes: 'contacting a crude oil feed with one or more catalysts to produce a total product containing crude oil production in the presence of a gaseous hydrogen source' wherein the crude oil product is 纟 25 ° C And G.HH MPa is a liquid mixture; and controlling the contact conditions so that the crude oil feed absorbs hydrogen at a selected rate during the contact period to inhibit the crude oil feed during the contact period. The present invention also provides a method for producing a crude oil product, This includes: when one or more catalysts are present, contacting the crude oil feed with hydrogen to produce, 10] ... the compound; and controlling the contact conditions so that the crude oil feed is under the first -I absorption conditions and then It is in contact with hydrogen under the second hydrogen absorption condition. The third absorption condition is different from the second hydrogen absorption condition. Control the first hydrogen absorption condition = hydrogen 14 200532010 to prevent the crude oil feed / total product mixed value from being reduced to 1.5. Below, one or more properties of the crude oil product are changed by up to 90% compared to the individual properties of the crude oil. The present invention also provides a method for producing a crude oil product, which comprises contacting a crude oil feed with one or more catalysts at a temperature, followed by contacting at a temperature of: to produce a total product containing a crude oil product, ^- fr. π 1Λ1 Eight T 5 Hai crude oil product is less liquid at 25 c and 0.101 Mpa 0 ταμ Guan Qiao crude oil feed has a TAN of ·, and control the contact conditions so that the first contact 接触 second contact temperature "then m less Below the feed of the crude oil product with the crude oil

相比,具有最多為90%的TAN, NIn comparison, with a maximum of 90% TAN, N

法D664測定。 TAN係藉由ASTM 本發明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸草 ’、 夕種觸媒接觸以生產含有原油產物的總產物, 其中该原油產物在2 S η ί γμ λ >τ π 初在25 c和0.101 MPa下為液態混合物,誃 — ^ Ο.3的丁AN,該原油進料具有含硫量 每克原油進料至少有〇 〇〇n j古 ”'、 十主/有0.0001克的硫’該至少一種觸媒包含 週期表第6攔的—或多種金屬,週期表第6搁之一或多種 金屬的一或多種化合物’或其混合物;及控制接觸條件以 便使該原油產物具# TAN最多$ 9〇%之該原油進料的 TAN’並且使該原油產物具有含硫量為7〇至應之該原 油進㈣含硫量,其中TAN係藉由ASTM法D664測定, 而含硫量係藉由ASTM法D4294測定。 本毛明亦提供生產原油產物之方法,其包括··使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 15 200532010 其中該原油產物在25t;和0.101 MPaT為液態混合物,該 =油進料具有至少〇.丨的TAN,該原油進料具有殘留物含 量為每克原油進料至少有Ο」克的殘留物,該至少一種觸 媒包含週期表第6櫊的一或多種金屬,週期表第6攔之一 或多種金屬的-或多種化合物,或其混合物;及控制接觸 條件以便使該原油產物具有ΤΑΝ最多為9〇%之該原油進料 勺TAN,使s亥原油產物具有殘留物含量為至工之該 原油進料的殘留物含量,其中TAN係藉由ASTM法叫料 測定,而殘留物含量係藉由ASTM法D5307測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物’, 其中該原油產物在2rc和0.101 MPa下為液態混合物,該 :油進料具有至少ο」& TAN,該原油進料具有vg〇含 夏為每克原油進料至少冑0」克的VG〇,該至少一種觸媒 ^含週期表第6攔的一或多種金屬,週期表第6欄之一或 :種金屬的一或多種化合物,或其混合物;及控制接觸條 以便使該原油產物具有TAN最多為9〇%之該原油進料的 、AN ’使該原油產物具有VG〇含量為7〇至之該原油 =的VGO含量’其中VG〇含量係藉由A—法 本發明亦提供生產原油產物之方法,其包括:使原油 :料與-或多種觸媒接觸以生產含有原油產物的總產物, 二中該原油產物在25t和〇.1〇1 Mpa下為液態混合物,該Assay D664. TAN is also provided by ASTM. The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is at 2 S η γ μ λ > τ π is a liquid mixture initially at 25 c and 0.101 MPa, 誃 — ^ 0.25. Butan AN, the crude oil feed has a sulfur content of at least 0.0000nj per gram of crude oil feed "Ancient", ten masters / 0.0001 grams of sulfur, "the at least one catalyst contains the sixth or more metals of the periodic table, one or more compounds of one or more metals of the periodic table," or a mixture thereof; And control the contact conditions so that the crude oil product has #TAN of at most $ 90% of the TAN of the crude oil feed and the crude oil product has a sulfur content of 70 to the corresponding sulfur content of the crude oil feed, where TAN It is measured by ASTM method D664, and the sulfur content is measured by ASTM method D4294. Ben Maoming also provides a method for producing crude oil products, which includes: contacting a crude oil feed with-or various catalysts to produce crude oil containing Total product of products, 15 200532010 The product is a liquid mixture at 25t; and 0.101 MPaT is a liquid mixture, the = oil feed has a TAN of at least 0.1, the crude feed has a residue content of at least 0 "grams of residue per gram of crude feed, the at least one The catalyst contains one or more metals of the sixth table of the Periodic Table, one or more of the metals of the periodic table-or more compounds, or a mixture thereof; and controlling the contact conditions so that the crude oil product has a TAN of up to 90% The crude oil feed spoon TAN, so that the crude oil product has a residue content of the crude oil feed to the process, where TAN is determined by the ASTM method and the residue content is determined by the ASTM method. D5307 determination. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with one or more catalysts to produce a total product containing the crude oil product, wherein the crude oil product is a liquid mixture at 2rc and 0.101 MPa, which: The oil feed has at least o " TAN, the crude oil feed has vg0 containing at least 」0" grams of VG per gram of crude oil feed, and the at least one catalyst ^ contains one or A plurality of metals, one of column 6 of the periodic table or one or more compounds of a metal, or a mixture thereof; and an AN 'that controls the contact strips so that the crude oil product has a TAN of up to 90% of the crude oil feed. The crude oil product has a VG0 content of 70 to the crude VGO content of the crude oil = wherein the VG0 content is by A method. The present invention also provides a method for producing a crude oil product, including: The catalyst is contacted to produce a total product containing a crude oil product, which is a liquid mixture at 25t and 0.11 Mpa.

原油進料具有至少〇 3的TAN 1 1AN该至少一種觸媒可藉由下 16 200532010 使載體與週期表第6欄的-或多種金屬,週期表 二 = 之一或多種金屬的一或多種化合物,或其混合物結 °產生觸媒刖驅物;於一或多種含硫化合物存在下在The crude oil feed has a TAN 1 1AN of at least 0. The at least one catalyst can be used by the following 16 200532010 to make the carrier and the column 6 of the periodic table-or more metals, the periodic table two = one or more compounds of one or more metals. , Or a mixture thereof to produce a catalyst driver; in the presence of one or more sulfur compounds

::::的溫度下加熱此觸媒前㈣ 妾知餘件以便使該原油產物具有TAN 進料的TAN。 夕為90%之該原油 本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 〆、中該原油產物在25t和〇.1()1 MPa下為液態混合物,該 原油進料在37_rc(10(rF)下具有至少1〇cSt的黏度,該原 :由進:具有至少10的API比重,該至少—種觸媒包含週 期表第6攔的-或多種金屬,週期表第6攔之—或多種金 屬的—或多種化合物’或其混合物;及控制接觸條件以便 使該原油產物具有纟37.rc下的黏度最多為9〇%之該原油 進料在37.8。(:下的黏度,並且使該原油產物具有剔比重 為7〇至130%之該原油進料的Αρι比重,其中Αρι比重係 藉由ASTM法D6822測定,而黏度係藉由astm法的669 測定。 、本發明亦提供生產原油產物之方法,其包括:使原油 、料人或夕種觸媒接觸以生產含有原油產物的總產物, 其中该原油產物在25°C和0.101 MPa下為液態混合物,該 原油進料具有至少〇1的TAN,該一或多種觸媒包含:一 或夕種含有釩,一或多種釩化合物,或其混合物的觸媒; 只附加觸媒,其中該附加觸媒包含一或多種第6攔金屬, 17 200532010 或多種第6攔金屬的一或多種化合物,或其組合;及控 · 制接觸备、件以便使該原油產物具有TAN最多為9〇%之該原 油進料的丁AN,其中TAN係藉由八8頂法d664測定。 广本發明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25它和〇·1〇1 MPa下為液態混合物,該 原油進料具有至少〇.〗的TAN;在接觸期間產生氫;及控 制接觸條件以便使該原油產物具有TAN最多為90%之該原 油進料的TAN,其中TAN係藉由八31^法加以測定。 ❿ 、本發明亦提供生產原油產物之方法,其包括:使原油 、料人或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在坑和MPaT為液態混合物,該 原:由,料具有至少〇1❸TAN,該至少一種觸媒包含釩, 或夕種釩化合物,或其混合物;及控制接觸條件以便使 接觸*度至少為200°C,使該原油產物具有丁AN最多為90% 之忒原油進料的TAN,其中TAN係藉由astm法DM#測 定 ° · 、本發明亦提供生產原油產物之方法,其包括··使原油 進料14 一或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25t和〇·1〇1 MPa下為液態混合物,該 原^進料具有至少〇1的TAN,該至少一種觸媒包含釩, 、或夕種釩化合物,或其混合物;在接觸期間供應含有氫 勺氣奴源’該氣流係以原油進料流動相反的方向供應;及 控制接觸條件以便使該原油產物具有TAN最多為90%之該 18 200532010 原油進料的TAN ’其中TAN係藉由ASTM法D664測定。 本毛明亦提供生產原油產物之方法,其包括·使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中忒原油產物在251和0.1〇1 MPa下為液態混合物,該 原油進料在每克原油進料中具有至少0.00002克的總 Ni/V/Fe合$,該至少一種觸媒包含釩,一或多種釩化合 物,或其混合物,該釩觸媒具有中位孔徑至少為i8〇A的 孔徑分佈’·及控制接觸條件以便使該原油產物具有總 Νϊ/V/Fe含量最多為90%之該原油進料的Ni/V/Fe含量,其 中Ni/V/Fe含量係藉由ASTM法D57〇8測定。 本毛月亦提供生產原油產物之方法,#包括:使原油 進料舁或夕種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25t和〇·1〇1 MPa下為液態混合物,該 至少-種觸媒包含釩,一或多種釩化合物,或其混合物, 該原油進料包含—或多種有機酸的-或多種驗金屬鹽,一 或多種有機酸的-或多種鹼土金屬鹽,或其混合物,該原 油進料在每克原油進料中具有至少、〇〇〇〇〇1克之有機酸金 屬鹽形態的驗金屬和驗土金屬總含量;及控制接觸條件以 便使該原油產物具有有機酸金屬鹽形態之驗金屬和驗土金 屬總含量最"90%之該原油進料中有機酸金屬鹽形能的 驗金屬和驗土金屬含量’其中有機酸金屬鹽形態的驗金屬 和鹼土金屬含量係藉由ASTM法D丨3丨8測定。 本發明亦提供生產原油產物之方法,其包括:使原、、由 進料與-或多種觸媒接觸.以生產含有原油產物的總產物; 19 200532010Before heating this catalyst at a temperature of ::::, know the remainder so that the crude oil product has a TAN feed TAN. The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product; .1 () is a liquid mixture at 1 MPa, the crude oil feed has a viscosity of at least 10 cSt at 37_rc (10 (rF), the source: from the feed: has an API specific gravity of at least 10, the at least one catalyst Containing the sixth or more metals of the periodic table, the sixth or more metals of the periodic table—or multiple compounds' or mixtures thereof; and controlling the contact conditions so that the crude oil product has the highest viscosity at 纟 37.rc 90% of the crude oil feed is at a viscosity of 37.8. (:, And the crude product has an Aρ specific gravity of 70 to 130% of the crude feed, wherein the Aρ specific gravity is determined by ASTM method D6822 The viscosity is measured by the ASTM method of 669. The present invention also provides a method for producing a crude oil product, which comprises: contacting crude oil, a raw material or a catalyst to produce a total product containing a crude oil product, wherein the crude oil Product at 25 ° C and 0.101 MPa It is a liquid mixture. The crude oil feed has a TAN of at least 0. The one or more catalysts include: one or more catalysts containing vanadium, one or more vanadium compounds, or mixtures thereof; only additional catalysts, wherein the The additional catalyst contains one or more 6th metal, 17 200532010 or one or more compounds of the 6th metal, or a combination thereof; and control of contact equipment so that the crude oil product has a TAN of up to 90% The Ding AN of the crude oil feed, of which TAN is determined by the 8-8 method d664. The present invention also provides a method for producing a crude oil product, which includes: contacting the crude oil feed with one or more catalysts to produce crude oil containing The total product of the product, wherein the crude oil product is a liquid mixture at 25 MPa and 0.11 MPa, the crude oil feed has a TAN of at least 0.01; hydrogen is produced during the contact; and the contact conditions are controlled so that the crude oil The product has a TAN of up to 90% of the TAN of the crude oil feed, wherein the TAN is determined by the method 八. The invention also provides a method of producing a crude oil product, which includes: Match To produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture in the pit and MPaT, the source: the material has at least 0❸ TAN, the at least one catalyst contains vanadium, or a vanadium compound, or a mixture And control the contact conditions so that the contact degree is at least 200 ° C, so that the crude oil product has a TAN of at least 90% of the TAN crude oil feed, where TAN is determined by the astm method DM # °, the present invention A method of producing a crude product is also provided, which includes contacting the crude feed 14 with one or more catalysts to produce a total product containing a crude product, wherein the crude product is a liquid mixture at 25t and 0.11 MPa, The raw feed has a TAN of at least 0, the at least one catalyst contains vanadium, or a vanadium compound, or a mixture thereof; and a hydrogen-containing gas source is supplied during the contact. The gas stream flows as a crude oil feed. Supply in the opposite direction; and control the contact conditions so that the crude oil product has a TAN of the 18 200532010 crude oil feed with a TAN of 90% at most, where TAN is determined by ASTM method D664. Ben Maoming also provides a method for producing crude oil products, which includes: contacting a crude oil feed with one or more catalysts to produce a total product containing crude oil products, wherein the crude oil product is a liquid mixture at 251 and 0.10 MPa, The crude feed has at least 0.00002 grams of total Ni / V / Fe combined per gram of crude feed, the at least one catalyst comprises vanadium, one or more vanadium compounds, or a mixture thereof, and the vanadium catalyst has a median The pore size distribution of at least i80A 'and the contact conditions are controlled so that the crude oil product has a Ni / V / Fe content of the crude oil feed with a total Nϊ / V / Fe content of up to 90%, where Ni / V / Fe content is measured by ASTM method D57708. This gross month also provides a method for producing crude oil products, including: contacting crude oil feedstocks or catalysts to produce a total product containing crude oil products, wherein the crude oil product is liquid at 25t and 0.11 MPa A mixture, the at least one catalyst comprising vanadium, one or more vanadium compounds, or a mixture thereof, the crude feed comprising-or more organic acids-or more metal test salts, one or more organic acids-or alkaline earth metals Salt, or a mixture thereof, the crude oil feed has a total metal and earth metal content in the form of an organic acid metal salt of at least 10,000 grams per gram of crude oil feed; and controlling the contact conditions so that the crude oil The product has the organic acid metal salt form and the total metal content and soil test metal content is "90% of the organic acid metal salt form energy and metal content in the crude oil feed." Metal and alkaline earth metal contents were determined by ASTM method D 3, 8 8. The present invention also provides a method for producing a crude oil product, comprising: contacting a raw material, a feedstock, and-or a plurality of catalysts to produce a total product containing a crude oil product; 19 200532010

其中邊原油產物在2 5 C和〇 · 1 0 1 Μ P a下為液態混合物,該 原油進料包含一或多種有機酸的一或多種驗金屬鹽,一或 多種有機酸的一或多種鹼土金屬鹽,或其混合物,該原油 進料在每克原油進料中具有至少0·00001克之有機酸金屬 鹽形態的驗金屬和驗土金屬總含量,該至少一種觸媒具有 中位孔控在90人至1 80 Α之範圍内的孔徑分佈,該孔徑分 佈中至少60%的總孔數具有在45 A之中位孔徑範圍内的 孔徑,其中孔徑分佈係藉由ASTM法D4282測定;及控制 接觸條件以便使該原油產物具有有機酸金屬鹽形態之鹼金 屬和鹼土金屬總含量最多為90%之該原油進料的有機酸金 屬鹽形恶的鹼金屬和鹼土金屬含量,其中有機酸金屬鹽形 態的鹼金屬和鹼土金屬含量係藉由ASTM法Dl318測定。Wherein the crude oil product is a liquid mixture at 25 C and 0.11 MPa, and the crude oil feed contains one or more metal salts of one or more organic acids, and one or more alkaline earths of one or more organic acids. Metal salt, or a mixture thereof, the crude oil feed has a total metal and soil test metal content in the form of an organic acid metal salt per gram of crude feed, the at least one catalyst having a median pore control in Pore size distribution in the range of 90 to 1 80 Α, at least 60% of the total number of pores in the pore size distribution has a pore size in the 45 A median pore size range, wherein the pore size distribution is determined by ASTM method D4282; and control Contact conditions so that the crude oil product has a total alkali metal and alkaline earth metal content of up to 90% of the organic acid metal salt form. The organic acid metal salt of the crude oil feed forms an evil alkali metal and alkaline earth metal content, of which the organic acid metal salt The form of alkali metal and alkaline earth metal content was measured by ASTM method D318.

本务明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25t:和O.HH MPa下為液態混合物,該 原油進料在每克原油進料中具有至少〇•⑽〇〇2克的總 Ni/V/Fe含量,該至少一種觸媒具有中位孔徑在刈人至 A之範圍内的孔徑分佈,該孔徑分佈中至少、㈣的總孔數 具有在45 A之中位孔徑範圍内的孔徑,其中孔徑分佈係藉 由ASTM法D4282測定;及控制接觸條件以便使該原油產 物具有總而V/Fe含量最多為9〇%之該原油進料的似職 含量,其巾Nl/V/Fe含量係藉由ASTM法D5708測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與種觸媒接觸以生產含有原油產物的總產物, 20 200532010 其中該原油產物在25。 ,^ ± C和MPaT為液態混合物,該 原油進料在母克原油進 科中具有至少0.00001克之有機酸 金屬鹽形態的鹼金屬和 双上至屬總含$,該至少一種觸媒 具有中位孔徑至少為! t …、〇A的孔徑分佈,其藉由ASTM法 D42 82測定,該觸拔θ ^人 ”一有包含週期表第6攔的一或多種金 屬,週期表第6欄之—斗、夕# α庙 、 或夕種金屬的一或多種化合物,或 其混合物的孔徑分佑· R “ f ^ ’及彳工制接觸條件以便使該原油產物The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at 25t: and O.HH MPa The crude oil feed has a total Ni / V / Fe content of at least 0.002 g per gram of crude oil feed, and the at least one catalyst has a pore size distribution with a median pore diameter ranging from 刈 to A In the pore size distribution, at least the total number of pores in the pore size has a pore size in the 45 A median pore size range, wherein the pore size distribution is determined by ASTM method D4282; and the contact conditions are controlled so that the crude oil product has a total V / The similar content of the crude oil feed with an Fe content of up to 90%, and its Nl / V / Fe content was determined by ASTM method D5708. The invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with a catalyst to produce a total product containing a crude oil product, wherein the crude oil product is at 25. ^ ± C and MPaT are liquid mixtures. The crude oil feed has at least 0.00001 grams of alkali metal and alkali metals in the form of organic acid metal salts in the parent crude oil. The at least one catalyst has a median The aperture is at least! The pore size distribution of t, 〇A, which is measured by ASTM method D42 82, the contacting θ ^ person "has one or more metals containing the sixth block of the periodic table, the sixth column of the periodic table-Dou, Xi # The pore diameters of α, α, or one or more compounds of metals, or mixtures thereof, can be divided into R'f 'and contact conditions in order to make the crude oil product

具有有機酸金屬鹽形能夕从a M 心之鹼金屬和鹼土金屬總含量最多為The organic acid metal salt can form a total content of alkali metals and alkaline earth metals from a

90%之該原油進料中有櫓醅 金屬孤形怨的驗金屬和驗土金 屬含量,其中有機酸金屬_你能 ^ i屬鹽形恶的鹼金屬和鹼土金屬含量 係藉由A S T Μ法D1 3 1 8測定。 、本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物,90% of the crude oil feed has metal and soil metal content, and the content of organic acid metal _ you can be alkali metal and alkaline earth metal in salt form is determined by AST M method D1 3 1 8 determination. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product,

其中該原油產物在2代和〇·_ Mpa下為液態混合物,該 原油進料包含一或多種有機酸的一或多種鹼金屬鹽,一或 多種有機酸的-或多種鹼土金屬鹽,或其混合@,該原油 進料在每克原油進料中具有至少〇.〇〇〇〇1克之有機酸金屬 鹽形態的鹼金屬和鹼土金屬總含量,該至少一種觸媒具有 中位孔徑至少為230A的孔徑分佈,其藉由ASTM法D4282 ’貝J疋,该觸媒具有包含週期表第6欄的一或多種金屬,週 -月表第6欄之一或多種金屬的一或多種化合物,或其混合 物的孔徑分佈;及控制接觸條件以便使該原油產物具有有 枝S文金屬鹽形恶之驗金屬和驗土金屬總含量最多為9 〇 %之 該原油進料中有機酸金屬鹽形態的驗金屬和鹼土金屬含 21 200532010 量,其中有機酸金屬鹽形態的鹼金屬和鹼土金屬含量係藉 由ASTM法D1318測定。 本發明亦提供生產原油產物之方法,其包括··使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25°C和〇·ΐ〇ι MPa下為液態混合物,該 原油進料具有總Ni/V/Fe含量為每克原油進料中至少有 0.00002克的Ni/V/Fe,該至少一種觸媒具有中位孔徑至少 為230A的孔徑分佈,其藉由ASTM法〇4282測定,該觸 媒具有包含週期表第6欄的一或多種金屬,週期表第“闌馨 之一或多種金屬的一或多種化合物,或其混合物的孔徑分 佈;及控制接觸條件以便使該原油產物具有總Ni/v/Fe含 量最多為90%之該原油進料的Ni/V/Fe含量,其中Νί/ν/]^ 含量係藉由ASTM法D5708測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25t和㈣1 MPa下為液態混合物該 原油進料包含-或多種有機酸的一或多種驗金屬鹽,一《 # 多種有機酸的-或多種驗土金屬鹽,或其混合物,該原油 進料在每克原油進料中具有至少0 00001克之有機酸金屬 鹽形態的鹼金屬和鹼土金屬總含量,該至少一種觸媒具有 中位孔徑至少為9GA的孔徑分佈,其藉由ASTM法D4282 測定,該觸媒在每克觸媒中,以翻的重量計,具有總含鉬 量為0.0001克至〇 3古沾相 斗、々 凡 W克的鉑、一或多種翻化合物,或其混 合物;及控制接觸條# # # # ”牛便使忒原油產物具有有機酸金屬 22 200532010 鹽形態之驗金屬和驗土金屬總含量最多為9q%之該原油進 料中有機酸金屬鹽形態的鹼金屬和鹼土金屬含量,其中 機酸金屬鹽形態的驗金屬和鹼土金屬含量係藉由饥 D 1 3 1 8測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在饥和0.101 MPa下為液態混合物,兮 原油進料具有至少〇.3#tan且該原油進料在每克原油進 料中具有至少為0.00002克的總Ni/V/Fe含量,該至少一 種觸媒具有中位孔徑至少A A 一 仅芏夕马90A的孔徑分佈,其藉由astm 法D4282測定,該觸媒在每克觸媒中,以翻的重量計,且 有總含翻量為0.0001克至〇·3克的銘、一或多種翻化合物, 或其混合物;及控制接觸條件以便使該原油產物且有TAN 最多為慨之該原油進料的ΤΑΝ且該原油產物具有總 Nl/WFe含量最多為90%之該原油進料的Ni/V/Fe含量,JL :而V/Fe含量係藉由ASTM^57〇8測定,而I·係 藉由ASTM法D664測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與—或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25〇Γ夺 C # 0.101 MPa下為液態混合物,該 原油進料包含一或多種有機酸的一或多種驗金屬鹽,-或 多種有機酸的-或多種驗土金屬鹽,或其混合物,該原油 =在每克原'油進料中具有至少0 00001克之有機酸金屬 鹽形態的驗金屬和驗土金屬總含量,該至少包 23 200532010 ::⑷週期表第6攔的一或多種金屬’週期表第6攔之 一或多^種金屬的-或多種化合物,或其混合物;及⑻週 :表第10攔的一或多種金屬’週期表第1〇欄之一或多種 金屬的-或多種化合物’或其混合物,其中第10攔金屬 總量與第6欄金屬總量的莫耳比在i i 1G的範圍内;及 控制接觸條件以便使該原油產物具有有機酸金屬鹽形態之 鹼金屬和鹼土金屬總含量最多為9〇%之該原油進料中:機 酸金屬鹽形態的鹼金屬和鹼土金屬含量,#中有機酸金屬 ^形態的鹼金屬和鹼土金屬含量係藉由ASTm法DUU測 定。 本發明亦提供生產原油產物之方法’其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25°C和0·101 MPaT為液態混合物,該 原油進料具有總Ni/V/Fe含量為每克原油進料中至少有 ^•00002克的Ni/V/Fe,該至少—種觸媒包含:⑷週期表 f 6攔的一或多種金屬,週期表第6搁之一或多種金屬^ 二或多種化合物’或其混合物;A (b)週期表第ι〇攔的 一或多種金屬,週期表第1〇攔之一或多種金屬的一或多 種化合物,或其混合物,其中第1〇櫊金屬總量與第6欄 金屬總量的莫耳比纟i至1G的範_ ;及控制接觸條件 以便使該原油產物具有總Ni/V/Fe含量最多為9〇%之該原 油進料的Ni/V/Fe含量,其中NL/V/Fe含量係藉由astm 法D5708測定。 本發明亦提供生產原油產物之方法,其包括:使原油 24 200532010 進料與一或多種觸媒接觸以生產 座3有原油產物的總產物, 其中該原油產物在25°C和0.101 MPa τ y ^ λ MPa下為液癌混合物,該 原油進料包含-或多種有機酸的—或多種驗金屬鹽,一或 多種有機酸的—或多種驗土_,或其混合物,該原油 進料在每克原油進料中具有至少〇 〇_…有機酸金屬 鹽形態的驗金屬和鹼土金屬總含量,言玄一或多種觸媒包 含:⑷第-種觸媒,該第—種觸媒在每克第一種觸媒中, 以金屬重量計,含有0 〇〇〇1至〇 ’、 頁·刪1 i 〇·06克之週期表第6攔的Wherein the crude oil product is a liquid mixture at 2nd generation and 0 · Mpa, the crude oil feed comprises one or more alkali metal salts of one or more organic acids, one or more alkaline earth metal salts of one or more organic acids, or Mix @, the crude oil feed has a total alkali metal and alkaline earth metal content in the form of an organic acid metal salt per gram of crude oil feed, the at least one catalyst has a median pore size of at least 230A Pore size distribution by ASTM method D4282 'Beijing J 疋, the catalyst has one or more compounds containing one or more metals in column 6 of the periodic table, one or more compounds in column 6 of the week-monthly table, or The pore size distribution of its mixture; and controlling the contact conditions so that the crude oil product has a branched metal salt-shaped metal and soil metal content of up to 90% of the organic acid metal salt form in the crude oil feed The test metal and alkaline earth metal contained 21 200532010, among which the content of alkali metal and alkaline earth metal in the form of metal salt of organic acid was determined by ASTM method D1318. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is at 25 ° C and 0. MPa Is a liquid mixture, the crude feed has a total Ni / V / Fe content of at least 0.00002 grams of Ni / V / Fe per gram of crude feed, the at least one catalyst has a pore size distribution with a median pore size of at least 230A, It is measured by ASTM method 04282, and the catalyst has a pore size distribution comprising one or more metals in column 6 of the periodic table, one or more compounds of one or more metals in the periodic table, or a mixture thereof; and The contact conditions were controlled so that the crude product had a Ni / V / Fe content of the crude feed with a total Ni / v / Fe content of up to 90%, where the Νί / ν /] ^ content was determined by ASTM method D5708. The invention also provides a method of producing a crude oil product, comprising: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at 25t and ㈣1 MPa. The crude oil feed contains -Or more organic acids One or more metal test salts, one or more organic acid- or multiple soil test metal salts, or mixtures thereof, the crude oil feed has at least 0 0 0001 grams of alkali metal in the form of an organic acid metal salt per gram of crude oil feed And alkaline earth metal content, the at least one catalyst has a pore size distribution with a median pore size of at least 9GA, as determined by ASTM method D4282. The catalyst has a total molybdenum content per gram of catalyst based on the weight of the catalyst. The amount is between 0.0001 grams and 0.33 grams of ancient dipsticks, 10,000 grams of platinum, one or more compounds, or mixtures thereof; and control contact strips # # # # ”The cow ’s crude oil products have organic acid metals 22 200532010 Alkali and alkaline earth metal content of organic acid metal salt in the crude oil feed with a total content of 9q% of metal and soil metal in salt form. The metal and alkaline earth metal content of organic acid metal salt form is determined by Hunger D 1 3 1 8 was determined. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at 0.101 MPa, Material has at least 0.3 # tan and the crude oil feed has a total Ni / V / Fe content of at least 0.00002 grams per gram of crude oil feed, the at least one catalyst has a median pore size of at least AA The pore size distribution of 90A is determined by the astm method D4282. The catalyst is based on the weight of the catalyst per gram of catalyst, and has a total content of 0.0001 to 0.3 grams, one or more types of catalyst. A compound, or a mixture thereof; and controlling the contact conditions so that the crude oil product has a TAN of the crude oil feed with a maximum TAN and the crude oil product has a total Ni / WFe content of up to 90% of the Ni / V / Fe content, JL: The V / Fe content was measured by ASTM ^ 57〇8, and I · was measured by ASTM method D664. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with—or a plurality of catalysts—to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at 25 ° C # 0.101 MPa The crude oil feed contains one or more metal test salts of one or more organic acids,-or multiple organic test salts-or metal test salts, or mixtures thereof. The crude oil = has At least 0 00001 grams of total metal and soil metal content in organic acid metal salt form, the package contains at least 23 200532010 :: one or more metals in the sixth column of the periodic table 'one or more of the six metals in the periodic table -Or more compounds, or mixtures thereof; and weekly: one or more metals of one or more metals of column 10 of the Periodic Table, or mixtures thereof, of the tenth metal The molar ratio of the total amount to the total amount of the metal in column 6 is within the range of ii 1G; and the contact conditions are controlled so that the crude oil product has the total content of alkali metals and alkaline earth metals in the form of metal salts of organic acids. Crude oil feed : Alkali metal and alkaline earth metal content of organic acid metal salt form, the organic acid metal ^ # alkali and alkaline earth metal content ASTm method aspect of the system by DUU measured. The present invention also provides a method of producing a crude oil product, which includes: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at 25 ° C and 0 · 101 MPaT, The crude oil feed has a total Ni / V / Fe content of at least ^ • 00002 grams of Ni / V / Fe per gram of crude oil feed, and the at least one catalyst includes: one or more of ⑷ periodic table f 6 Metal, one or more metals of the sixth table of the periodic table ^ two or more compounds' or mixtures thereof; A (b) one or more metals of the first table of the periodic table, one or more of the metal of the tenth table of the periodic table One or more compounds, or mixtures thereof, in which the molar ratios of the total metal of the 10th metal and the total metal of the 6th column range from 1 to 1G; and controlling the contact conditions so that the crude oil product has a total Ni / V The Ni / V / Fe content of the crude oil feed with a maximum / Fe content of 90%, wherein the NL / V / Fe content is determined by the astm method D5708. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil 24 200532010 feed with one or more catalysts to produce a total product of crude oil products in Block 3, wherein the crude oil product is at 25 ° C and 0.101 MPa τ y ^ It is a liquid cancer mixture at λ MPa. The crude oil feed contains-or more organic acids-or more metal test salts, one or more organic acid-or more soil tests, or a mixture thereof. Gram crude oil feed has a total content of test metal and alkaline earth metal in the form of organic acid metal salt, at least one or more catalysts include: the first catalyst, the first catalyst per gram In the first catalyst, based on the weight of the metal, it contains 0.006 to 0 ′, page 6 of the periodic table of the table.

一或多種金屬,週_ 6攔之-或多種金屬的一或多種 化:物’或其混合物;A (b)第二種觸媒,該第二種觸媒 在每克第二種觸媒中’以金屬重量計,含有至少〇〇2克之 週期表第6攔的一或多種金屬,週期表第6欄之一或多種 金屬的-或多種化合物,或其混合物;及控制接觸條件以 便使該原油產物具有有機酸金屬鹽形態之驗金屬和驗土金 屬總含量最多4 90%之該原油進料中有機酸金屬鹽形態的 鹼金屬和鹼土金屬含量’其中有機酸金屬鹽形態的鹼金屬One or more metals, weekly 6 or more-one or more species of metals: substances' or mixtures thereof; A (b) a second catalyst, the second catalyst at a gram of the second catalyst Medium ', based on the weight of the metal, contains at least 002 grams of one or more metals in Period 6 of the Periodic Table, one or more metals in column 6 of the Periodic Table-or more compounds, or mixtures thereof; and controlling the contact conditions so that The crude oil product has a total metal test and soil test metal content of organic acid metal salt form of up to 4 90% of the alkali metal and alkaline earth metal content of the organic acid metal salt form in the crude oil feed, of which the alkali metal in the form of the organic acid metal salt

和驗土金屬含量係藉由ASTM法D1318測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25。(:和G.1G1 MPa下為液態混合物,該 原/由進料包δ或多種有機酸的一或多種驗金屬鹽,一或 多種有機酸的一或多種鹼土金屬鹽,或其混合物,該原油 進料在每克原油進料中具有至少〇〇〇〇〇ι克之有機酸金屬 i形恶的鹼金屬和鹼土金屬總含量,該至少一種觸媒在每 25 200532010 克觸媒中,以金屬重量計,含有至少〇 〇〇1克之週期表第 ‘ 6、欄的一或多種金屬,週期表第6攔之一或多種金屬的一 或多種化合物,或其混合物;及控制接觸條件以便使接觸 區中的液體空間速度超過101rl,並且使該原油產物具有 有機S义孟屬鹽形態之驗金屬和驗土金屬總含量最多為 之該原油進料中有機酸金屬鹽形態的鹼金屬和鹼土金屬含 里,其中有機酸金屬鹽形態的鹼金屬和鹼土金屬含量係藉 由ASTM法;〇 1 3 1 8測定。 本發明亦提供生產原油產物之方法,其包括··使原油 籲 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中该原油產物在25°C和0.101 MPa下為液態混合物,該 原油進料在母克原油進料中具有至少0.00002克的總 /FC έ i,该至少一種觸媒在每克觸媒中,以金屬重 $計,含有至少0.001克之週期表第6欄的一或多種金屬, 週期表第6欄之-或多種金屬的一或多種化合物,或其混 合物;及控制接觸條件以便使接觸區中的液體空間速度超 過1 0 h ,並且使該原油產物具有總含量最多為列% φ 之該原油進料的Nl/V/Fe含量,其中Ni/V/Fe含量係藉由 ASTM 法 D5708 測定。 本發明亦提供生產原油產物之方法,其包括··使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 一中4原油產物在25 C和0· 1 0 1 MPa下為液態混合物,該 原油進料在每克原油進料中具有含氧量至少為〇〇〇〇1克的 氧3 ‘里至少為0.0001克的硫,該至少一種觸媒包含週 26 200532010 期表第6攔的一或多種金屬,週期表第6搁之一或多種金 屬的一或多種化合物,或其混合物;及控制接觸條件以便 使°玄原’由產物具有含氧量最多為90%之該原油進料的含氧 置,亚且使該原油產物具有含硫量為7〇至13〇%之該原油 進料的含硫量,其中含氧量係藉由ASTM法E385測定, 而含硫量係藉由ASTM法D4294測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料人或夕種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25t:和G1G1他下為液態混合物,該 原油進料在每克原油進料中具有至少〇 〇〇〇〇2克的總 N:i/V/Fe含量,含硫量至少為〇 〇〇〇1克的硫,該至少一種 觸媒包含週期表第6橱的一或多種金屬,週期表第6攔之 一或多種金屬的一或多種化合物,或其混合物;及控制接 觸條件以便使該原油產物具有總Ni/V/Fe含量最多為9〇% 之該原油進料的Ni斤/Fe含量,並且使該原油產物具有含 石”l里為70至1 3 0 %之遠原油進料的含硫量,其中ni/v/fe 含量係藉由ASTM法D5708測定,而含硫量係藉由astm 法D4294測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25°C和0.101 MPa下為液態混合物,該 原油進料包含一或多種有機酸的一或多種鹼金屬鹽,一或 多種有機酸的一或多種驗土金屬鹽,或其混合物,該原油 進料在每克原油進料中具有至少0.00001克之有機酸金屬 27 200532010 鹽形態的鹼金屬和鹼土金屬總含量,殘留物含量至少為〇1 克的绞邊物,該至少一種觸媒包含週期表第6欄的一或多 種至屬,週期表第6欄之一或多種金屬的一或多種化合物, 或其此合物,及控制接觸條件以便使該原油產物具有有機 酉义至屬鹽形態之鹼金屬和鹼土金屬總含量最多為之該 原油進料中有機酸金屬鹽形態的鹼金屬和鹼土金屬含量, 並且使該原油產物具有殘留物含量為7〇至13〇%之該原油 進=的殘留物含量,其中有機酸金屬鹽形態的驗金屬和驗 j金屬含量係藉由ASTM法Dm8測定,而殘留物含量係 藉由AST1V[法D5307測定。 、本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25t;和0.101 MPa下為液態混合物,該 原油進料在每克原油進料中具有殘留物含量至少為〇.丨克 的殘邊物,至少0.00002克的總Ni/V/Fe含量,該至少一 種觸媒,含週期表帛6攔的—或多種金屬,週期表第6搁 之或多種金屬的一或多種化合物’或其混合物;及控制 接觸in件以便使該原油產物具有總Ni/v/Fe含量最多為9〇% ,該^進㈣Nl/V/Fe含量,並且使該原油產物具有殘° 留物含量為7〇至13〇%之該原油進料的殘留物 苴The test soil metal content was determined by ASTM method D1318. The present invention also provides a method of producing a crude oil product, comprising: contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is at 25. (: And G.1G1 MPa is a liquid mixture, the original / by the feed bag δ or more organic acid one or more metal test salts, one or more organic acid one or more alkaline earth metal salts, or a mixture thereof, the The crude oil feed has a total alkali metal and alkaline earth metal content of at least 10,000 grams of organic acid metal i-formaldehyde per gram of crude oil feed. By weight, containing at least 0.001 g of one or more metals of column '6 of the periodic table, one or more compounds of one or more metals of the periodic table, or mixtures thereof; and controlling the contact conditions so that the contact The space velocity of the liquid in the zone exceeds 101rl, and the crude oil product has the total content of metal and earth metal in the form of organic S, and is the alkali metal and alkaline earth metal in the form of organic acid metal salt in the crude oil feed. The content of alkali metal and alkaline earth metal in the form of organic acid metal salt is determined by ASTM method; 013 1 18. The present invention also provides a method for producing a crude oil product, which includes: The crude oil product is contacted with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at 25 ° C and 0.101 MPa, and the crude oil feed has at least 0.00002 grams of total crude oil feed. / FC i i, the at least one catalyst in metal per gram of catalyst contains at least 0.001 grams of one or more metals in column 6 of the periodic table, one or more metals in column 6 of the periodic table Or more compounds, or mixtures thereof; and controlling the contact conditions such that the liquid space velocity in the contact zone exceeds 10 h and the crude oil product has a total content of Nl / V / Fe of the crude oil feed of up to column% φ Content, wherein the Ni / V / Fe content is determined by ASTM method D5708. The present invention also provides a method for producing a crude oil product, which includes: contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product The crude oil product of Yizhong 4 is a liquid mixture at 25 C and 0.1 10 MPa, and the crude oil feed has at least 0.0001 grams of oxygen 3 'per gram of crude oil feed. For 0.0001 grams of sulfur, this at least The catalyst includes one or more metals of the 26th period of the 200532010 table, one or more compounds of one or more metals of the 6th table of the periodic table, or a mixture thereof; and controlling the contact conditions so that The oxygen content of the crude oil feed having an oxygen content of at most 90%, and the crude oil product having a sulfur content of 70 to 13% of the crude oil feed, wherein the oxygen content is It is measured by ASTM method E385, and the sulfur content is measured by ASTM method D4294. The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil supplier or a catalyst to produce a total product containing crude oil. Product, where the crude product is a liquid mixture at 25t: and G1G1, and the crude feed has a total N: i / V / Fe content of at least 20,000 grams per gram of crude feed, containing sulfur An amount of at least 0.001 g of sulfur, the at least one catalyst comprising one or more metals of cabinet 6 of the periodic table, one or more compounds of one or more metals of periodic table 6, or a mixture thereof; and The contact conditions are controlled so that the crude oil product has a total Ni / V / The Fe content is at most 90% of the Ni kg / Fe content of the crude oil feed, and the crude oil product has a sulphur content of 70 to 130% of the crude oil feed, including ni / The v / fe content is determined by ASTM method D5708, and the sulfur content is determined by astm method D4294. The invention also provides a method for producing a crude product, comprising: contacting a crude feed with one or more catalysts to produce a total product containing a crude product, wherein the crude product is a liquid mixture at 25 ° C and 0.101 MPa, the The crude oil feed contains one or more alkali metal salts of one or more organic acids, one or more earth test metal salts of one or more organic acids, or a mixture thereof. The crude oil feed has at least 0.00001 grams per gram of crude oil feed. Organic acid metal 27 200532010 The total content of alkali and alkaline earth metals in salt form and a residue of at least 0.01 g of edging. The at least one catalyst contains one or more of the subordinates in column 6 of the periodic table. One or more compounds of one or more metals in column 6, or a combination thereof, and controlling the contact conditions so that the crude oil product has an organic meaning to a salt form, and the total content of alkali metals and alkaline earth metals is at most for the crude oil. The content of alkali metals and alkaline earth metals in the form of metal salts of organic acids in the feed, and the crude oil product has a residue content of 70 to 130% of the crude oil content The metal content and metal content of the organic acid metal salt are determined by ASTM method Dm8, and the residue content is measured by AST1V [method D5307. The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product, wherein the crude oil product is at 25t; and a liquid mixture at 0.101 MPa, the The crude oil feed has a residual content of at least 0.1 g per gram of crude oil feed, a total Ni / V / Fe content of at least 0.00002 g, and the at least one catalyst, including —Or more than one metal, one or more compounds of the more than one metal ”or a mixture thereof; and controlling the contact pieces so that the crude oil product has a total Ni / v / Fe content of up to 90%, the ^ The Nl / V / Fe content is fed, and the crude oil product is made to have a residue content of 70 to 13% of the residue of the crude oil feed.

Ni/V/Fe ^ λ ^ τ 里係猎由ASTM & D57〇8㈣定,而殘留物 仏猎由ASTMS D53〇7測定。 進料亦提供生產原油產物之方法’其包括:使原油 心、-或多種觸媒接觸以生產含有原油產物的總產物, 28 200532010 其中該原油產物古9 ς。 座物在25C和0·101 MPa下為液態混合物, 原油進料包令_ 少% 1 夕 S 或夕種有機酸的一或多種鹼金屬鹽,一或 夕種有機I的一或多種鹼土金屬冑,或其混合物,該原油 進枓在母克原油進料中具有至少〇.1 i的減壓瓦斯油 (“VGO”)含 |,π ηΑΛ1 ^ 入 〇·0001克之有機酸金屬鹽形態的鹼金屬和 •、至屬、、、心3里,該至少一種觸媒包含週期表第6攔的一Ni / V / Fe ^ λ ^ τ is determined by ASTM & D57〇8, and residue hunting is determined by ASTM D53〇7. The feedstock also provides a method of producing a crude oil product 'which comprises: contacting a crude oil core,-or a plurality of catalysts to produce a total product containing a crude oil product, 28 200532010 wherein the crude oil product is ancient 9 ς. The substrate is a liquid mixture at 25C and 0 · 101 MPa. The crude oil feed order is less than 1% S or one or more alkali metal salts of organic acids, or one or more alkaline earth metals of organic I.胄, or a mixture thereof, the crude oil feed has at least 0.1 i vacuum gas oil ("VGO") in the mother gram crude feed containing |, π ηΑΛ1 ^ in the form of a metal salt of organic acid of 0.0001 g Alkali metals and •, genus ,,, and 3, the at least one catalyst includes one of the sixth block of the periodic table

=多種金屬’週期表第6欄之—或多種金屬的—或多種化 合物’或其混合物;及控制接觸條件以便使該原油產物具 有。有機酸金屬鹽形態之鹼金屬和鹼土金屬總含量最多為 9〇2之该原油進料中有機酸金屬鹽形態的鹼金屬和鹼土金 屬含量,並且使該原油產物具有VG〇含量為7〇至13〇% 之該原油進料的VG0含量,其中VGO含量係藉由AStm 法D5307測定,而有機酸金屬鹽形態的鹼金屬和鹼土金屬 含量係藉由ASTM法D1318測定。= Multiple metals '-column 6 of the periodic table-or multiple metals-or multiple compounds' or mixtures thereof; and controlling the contact conditions so that the crude oil product possesses it. The total content of alkali metal and alkaline earth metal in the form of organic acid metal salt is at most 920, and the content of alkali metal and alkaline earth metal in the form of organic acid metal salt in the crude oil feed, and the crude product has a VG content of 70 to The VG0 content of this crude oil feed was 130%, where the VGO content was determined by AStm method D5307, and the alkali metal and alkaline earth metal content in the form of metal salts of organic acids were determined by ASTM method D1318.

本發明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在乃^和〇1〇1 Mpa下為液態混合物,該 原油進料在每克原油進料中具有至少〇 〇〇〇〇2克的總 •/V/Fe § i,至少〇· 1克的vg〇含量,該至少一種觸媒 包含週期表第6攔的一或多種金屬,週期表第6欄之一或 多種金屬的一或多種化合物,或其混合物;及控制接觸條 件以便使该原油產物具有總Ni/V/Fe含量最多為9〇%之該 原油進料的Ni/V/Fe含量,並且使該原油產物具有VG〇含 里為70至130%之该原油進料的vg〇含量,其中VGO含 29 200532010 量係藉由ASTM法D5307測定,而Ni/V/Fe含量係藉由 ASTM法D5708測定。 曰 本發明亦提供生產原油產物之方法,其包括··使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25。。和0.101 MPa下為液態混合物,該 原油進料包含一或多種有機酸的一或多種鹼金屬鹽,一或 夕種有機酸的一或多種鹼土金屬鹽,或其混合物,該原油 進料在每克原油進料中具有至少〇〇〇〇〇1克之有機酸金屬 鹽形態的鹼金屬和鹼土金屬總含量,該至少一種觸媒可藉 由下列獲得··使載體與週期表第6欄的一或多種金屬,週 期表第6欄之一或多種金屬的一或多種化合物,或其混合 物結合以產生觸媒前驅物,於一或多種含硫化合物存在 下在低於400 C的溫度下加熱此觸媒前驅物形成觸媒; 及控制接觸條件以便使該原油產物具有有機酸金屬鹽形態 之鹼金屬和鹼土金屬總含量最多為9〇%之該原油進料中有 機酸金屬鹽形態的鹼金屬和鹼土金屬含量,其中有機酸金 屬鹽形您的鹼金屬和鹼土金屬含量係藉由ASTM法 測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料人或夕種觸媒接觸以生產含有原油產物的總產物, 其中忒原油產物在25°C和〇_ 1〇1 MPa下為液態混合物,該 原油進料在每克原油進料中具有至少〇 〇〇〇〇2克的總 Ni/V/Fe含量,該至少一種觸媒可藉由下列獲得:使載體 與週期表第6攔的一或多種金屬,週期表第6欄之一或多 30 200532010 種金屬的-或多種化合物’或其混合物結合以產生觸媒前 驅物;於一或多種含硫化合物存在下,在低於4〇〇t的溫 度下加熱此觸媒前驅物形成觸媒;及控制接觸條件以便使 該原油產物具有總Nl/V/Fe含量最多為9〇%之該原油進料 的Ni/V/Fe含$,其中Ni/V/Fe含量係藉由astm法⑽ 測定。 本發明亦提供在每克原油組成物中含有下列者的原油 組成物·至少0.001克之沸程分佈在〇1〇1 MPa下介於95 °C和26(TC之間的烴;至少〇.〇〇1克之沸程分佈在〇· ι〇ι他 下介於26GC和320°C之間的烴;至少〇·⑻!克之沸程分佈 在〇·101 MPa下介於320。(:和65GX:之間的烴;以及在每克 原油產物中含有大於〇克,但小於〇〇1克的一或多種觸媒。 本發明亦提供在每克原油組成物中含有下列者的原油 組成物·至少〇.〇1克的硫,其藉由astm法D4294測定; 至少〇·2克的殘留物,其藉由ASTM法D5307測定,該組 成物具有至少1.5之MCR含量與c5瀝青質含量的重量比, 其中MCR含量係藉由ASTM法〇453〇測定,q瀝青質含 昼係藉由ASTM法D2007測定。 本發明亦提供生產原油產物之方法,其包括:使原油 進料與一或多種觸媒接觸以生產含有原油產物的總產物, “中4原油產物在2 5 C和0.1 0 1 Μ P a下可冷凝,該原油進 料在每克原油進料中具有至少〇 〇〇1克的MCR含量,該至 少一種觸媒可藉由下列獲得:使載體與週期表第6攔的一 或多種金屬,週期表第6攔之一或多種金屬的一或多種化 31 200532010 合物’或其混合物結合以產生觸媒前驅物 硫化合物存在下,在低☆ 5GGt的溫 或夕種含 AL· ^ Λ> gn …、此觸媒前驅 物犧媒;及控制接觸條件以便使該原油產 含量最多4 90%之該原油進料的MCR含量,其中' _含 1係藉由ASTM法D4530測定。 巧The present invention also provides a method for producing a crude oil product, comprising: contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is a liquid mixture at a temperature of 0.001 and 0.001 Mpa The crude oil feed has a total • / V / Fe §i of at least 0.0002 grams per gram of crude oil feed, a vg0 content of at least 0.1 grams, and the at least one catalyst comprises the first One or more metals, one or more compounds of one or more metals in column 6 of the periodic table, or a mixture thereof; and controlling the contact conditions so that the crude oil product has a total Ni / V / Fe content of up to 90% The Ni / V / Fe content of the crude oil feed, and the crude oil product has a vg0 content of the crude oil feed with a VG0 content of 70 to 130%, of which the VGO content is 29 200532010 by the ASTM method D5307 The Ni / V / Fe content was measured by ASTM method D5708. The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil product is at 25 ° C. . And a liquid mixture at 0.101 MPa, the crude oil feed comprises one or more alkali metal salts of one or more organic acids, one or more alkaline earth metal salts of one or more organic acids, or a mixture thereof. A gram of crude oil feed has a total alkali metal and alkaline earth metal content in the form of a metal salt of an organic acid of at least 10,000 g. The at least one catalyst can be obtained by using a carrier and one in column 6 of the periodic table. One or more metals, one or more compounds of one or more metals in column 6 of the periodic table, or a mixture thereof to produce a catalyst precursor, which is heated at a temperature below 400 C in the presence of one or more sulfur-containing compounds A catalyst precursor to form a catalyst; and controlling the contact conditions so that the crude oil product has an alkali metal and alkaline earth metal content in the form of organic acid metal salt in a total amount of 90% of the alkali metal in the form of organic acid metal salt in the crude feed And alkaline earth metal content, where the organic acid metal salt forms your alkali metal and alkaline earth metal content are determined by the ASTM method. The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil feed person or a catalyst to produce a total product containing a crude oil product, wherein the crude oil product at 25 ° C and 0-10.1 MPa is Liquid mixture, the crude feed having a total Ni / V / Fe content of at least 200000 grams per gram of crude feed, the at least one catalyst can be obtained by: One or more metals that are blocked, one or more of the 30th column of the Periodic Table of the 2005 20052010 metal or compounds or mixtures thereof to produce a catalyst precursor; in the presence of one or more sulfur-containing compounds, at less than The catalyst precursor is heated at a temperature of 400 t to form a catalyst; and the contact conditions are controlled so that the crude oil product has a total Nl / V / Fe content of 90% Ni / V / Fe of the crude oil feed Contains $, where Ni / V / Fe content is determined by the astm method⑽. The present invention also provides a crude oil composition containing the following in each gram of crude oil composition. At least 0.001 grams of a hydrocarbon having a boiling range distribution between 95 ° C and 26 ° C at 0,001 MPa; at least 0.00. 〇1 gram boiling range distribution of hydrocarbons between 26GC and 320 ° C under 〇ιιιο; at least 〇! ⑻! Gram boiling range distribution between 320. MPa at 0. 101 MPa. (: And 65GX: Hydrocarbons; and one or more catalysts containing more than 0 g, but less than 0.01 g per gram of crude oil product. The present invention also provides a crude oil composition containing at least one of the following per gram of crude oil composition. 0.001 g of sulfur, determined by astm method D4294; at least 0.2 g of residue, measured by ASTM method D5307, the composition has a weight ratio of MCR content to c5 asphaltene content of at least 1.5 The MCR content is determined by ASTM method 0453〇, and the q asphaltene content is determined by ASTM method D2007. The present invention also provides a method for producing a crude oil product, which includes: crude oil feed and one or more catalysts Contact to produce a total product containing crude oil products, "Medium 4 crude oil products at 2 5 C and 0.1 0 1 Condensable at MPa, the crude feed has an MCR content of at least 0.001 grams per gram of crude feed, and the at least one catalyst can be obtained by: Or more than one metal, one or more compounds of one or more metals in the sixth table of the Periodic Table 31 200532010 compound 'or a mixture thereof to produce a catalyst precursor sulfur compound in the presence of low ☆ 5GGt warm or evening species containing AL ^ Λ > gn…, the catalyst precursor sacrificial catalyst; and the contact conditions to control the MCR content of the crude oil feed with a crude oil content of up to 4 90%, where '_containing 1 is determined by ASTM method D4530 Qiao

本發明亦提供生產原油產物之方法,其包括:使原油 進料與-或多種觸媒接觸以生產含有原油產物的總產物, 其中該原油產物在25 t和〇·1〇1购下可冷凝,該原油 進料在每克原油進料中具有至少〇 〇〇1克的Mcr含量,該 至少一種觸媒具有中位孔徑在7〇人至18〇人之範圍内的孔 徑分佈,該孔徑分佈中至少6〇%的總孔數具有在45人之 中位孔徑範圍内的孔徑,其中孔徑分佈係藉由astm法 D4282測定;及控制接觸條件以便使該原油產物具有mcr 最多為90%之該原油進料的MCR,其中MCR係藉由α§τμ 法D45 30測定。 本發明亦提供在每克組成物中含有下列者的原油組成 物·最多0.004克的氧,其藉由ASTM法E385測定;最 修 多0.003克的硫,其藉由ASTM法D4294測定;及至少0 3 克的殘留物,其藉由AST1V[法D5307測定。 本發明亦提供在每克組成物中含有下列者的原油組成 物:最多0.004克的氧,其藉由ASTM法Ε385測定;最 多0.003克的硫,其藉由ASTM法D4294測定;最多〇.〇4 克的驗性氮,其藉由ASTM法D2896測定;至少0.2克的 殘留物,其藉由ASTM法D5307測定;及該組成物具有最 32 200532010 多為〇·5的TAN,其藉由ASTM法D664測定。 、 本發明亦提供在每克組成物中含有下列者的原油組成 物:至少0.001克的硫,其藉由ASTm法D4294測定;至 少0.2克的殘留物,其藉由ASTM法D5307測定;該組成 物具有至;1.5之MCR含量與c5瀝青質含量的重量比, 及該組成物具有最多為〇·5的TAN,其中TAN係藉由ASTM 法D664測定,MCR的重量係藉由ASTM法D4530測定, 而I瀝青質的重量係藉由ASTM法D2007測定。 於若干具體實例中,本發明與結合本發明之一或多種 _ 方法或組成物者亦提供下列原油進料··(a)尚未於精煉廠 中處理,蒸館及/或分餾者;含有碳數大於4之成分者, 該原油進料在每克原油進料中含有至少〇·5克的這類進 料;(c)包含烴,其部分具有:在〇 1〇i MPa下低於10〇t 的沸程分佈,在0.101 MPa下介於l〇〇°C和200。〇之間的沸 程分佈,在0.101 MPa下介於200°C和3 00°C之間的沸程分 佈,在0.101 MPa下介於300°C和400°C之間的沸程分佈, 以及在0.101 MPa下介於400°C和650°C之間的沸程分佈; 春 (d)在每克原油進料中含有至少·· 0·001克之具有沸程分佈 在0.101 MPa下低於1〇〇。〇的烴,0.001克之具有沸程分佈 在0.101 MPa下介於i〇〇°c和200°C之間的烴,〇_〇〇1克之 具有沸程分佈在0.101 MPa下介於200°C和300°C之間的 烴,0.001克之具有沸程分佈在0.101 MPa下介於300°c和 4 〇 0 C之間的煙’及0 · 〇 0 1克之具有沸程分佈在〇. 1 〇 1 μ p a 下介於400°C和650°C之間的烴;(e)具有至少為〇」,至 33 200532010 少為0.3,或是在〇·3至20’ 0.4至10,或〇.5至$之範圍 内的TAN ; (f)具有在〇·1〇1 MPa下至少為2〇〇〇c的起始 ’弗點,(g)包含錄、飢和鐵,(h)在每克原油進料中含有 至少0.00002克的總N"V/Fe ;⑴包含硫;⑴在每克原 油進料中含有至少0.0001克或0.05克的硫;(k)在每克原 油進料中含有至少0.001克的VGO; (1)在每克原油進料 中含有至少0.1克的殘留物;(m)包含含氧烴;(n) 一或 多種有機酸的一或多種鹼金屬鹽,一或多種有機酸的一或 多種鹼土金屬鹽,或其混合物;(〇)包含有機酸的至少一 種辞鹽;及/或(p)包含有機酸的至少一種石申鹽。 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦k供可措由移除原油中的石腦油及比石 腦油更具揮發性之化合物而得到的原油進料。 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦&供使原油進料與一或多種觸媒接觸以 生產含有原油產物之總產物的方法,其中該原油進料和原 油產物兩者都具有C5瀝青質含量和MCR含量,且· r、 • 原 油進料之C:5遞青質含量和原油進料之MCR含量的和為s, 原油產物之C5瀝青質含量和原油產物之MCR含量的和為 S’,控制接觸條件以便使S’最多為99%的S ;及/或(b)押 制接觸條件以便使原油產物之]Vi C R含量與原油產物之^ 遞青質含量的重量比在1·2至2.0,或1.3至1.9的範圍内5 於若干具體實例中,本發明與結合本發明之一 取多種 方法或組成物者亦提供氫源,其中該氫源為:(a)氣能·(Μ 34 200532010 氫氣;(C)曱烷;(d)輕烴;(e)惰性氣體;及/或⑴其 混合物。 於若干具體實例中,本發明與結合本發明之—或多種 方法或組成物者亦提供使原油進料與一或多種觸媒接觸以 生產含有原油產物之總產物的方法,#中該原油進料在位 於或連接到近海設備的接觸區中進行接觸。 於若干具體實命j巾,本發明與結合本發明之_或多種 方法或組成物者亦提供一種方法,其包含於氣體及/或氯源 存在下,使原油進料與一或多種觸媒接觸及控制接觸條件 以便使·(a)氣恶氫源與原油進料的比在與一或多種觸媒 接觸之每立方米的原油進料中為5至8〇〇標準立方米之氣 態氫源的範圍内;(b)藉由改變氫源分壓以控制氬的選定 淨吸取率;(c)氫的吸取率使原油產物具有小於〇·3的 了 AN,但氫的吸取係小於在接觸期間會導致原油進料和總 產物之間貫質上相分離的氫吸取量;(d)氫的選定吸取率 在每立方米的原油進料中為1至30或1至80標準立方米 之氫源的範圍内;(e)氣體及/或氫源的液體空間速度至少 為11 ^,至少為15 h·】,或最多為2〇 ^ ;⑴在接觸期 間控制氣體及/或氫源之分壓;(g)接觸溫度在50至5001 的範圍内,氣體及/或氫源的總液體空間速度在〇·1至3〇 h_ 】的範圍内,氣體及/或氫源的總壓力在1〇至2〇 Mpa的範 圍内,(h)氣體及/或氫源的流動係朝著與原油進料流動相 反的方向;(i)該原油產物具有H/C為70至130%之該原 油進料的H/C ; (j)由該原油進料吸取的氫在每立方米的 35 200532010 原油進料中最多為80及/或i至8〇或i至5〇標準立方米 之氫的範圍内;(k)該原油產物具有總Ni/V/Fe含量最多 為90%,最多為50%’或最多為10%之該原油進料的Ni~/Fe 含量;(!)該原油產物具有硫含量為7〇至13〇%或8〇至The present invention also provides a method for producing a crude oil product, which comprises: contacting a crude oil feed with-or a plurality of catalysts to produce a total product containing a crude oil product, wherein the crude oil product is condensable at 25 t and 0.11 purchase The crude feed has an Mcr content of at least 0.001 grams per gram of crude feed, the at least one catalyst has a pore size distribution with a median pore size ranging from 70 to 180 people, and the pore size distribution At least 60% of the total number of pores has a pore size in the median pore size range of 45 people, where the pore size distribution is determined by the astm method D4282; and the contact conditions are controlled so that the crude product has an mcr of 90% at most The MCR of the crude feed, where MCR is determined by the α§τμ method D45 30. The present invention also provides a crude oil composition containing the following in each gram of composition: up to 0.004 grams of oxygen, as measured by ASTM method E385; up to 0.003 grams of sulfur, as measured by ASTM method D4294; and at least 0.3 g of residue as determined by AST1V [Method D5307. The present invention also provides a crude oil composition containing the following in each gram of composition: up to 0.004 g of oxygen, as measured by ASTM method E385; up to 0.003 g of sulfur, as measured by ASTM method D4294; up to 0.00. 4 grams of experimental nitrogen, determined by ASTM method D2896; at least 0.2 grams of residue, measured by ASTM method D5307; and the composition has a maximum of 32 200532010 TAN, which is more than 0.5 Assay D664. The present invention also provides a crude oil composition containing the following in each gram of composition: at least 0.001 grams of sulfur, measured by ASTM method D4294; at least 0.2 grams of residue, measured by ASTM method D5307; the composition The weight ratio of MCR content to c5 asphaltene content of 1.5, and the composition has a TAN of up to 0.5, where TAN is measured by ASTM method D664, and the weight of MCR is measured by ASTM method D4530 The weight of I asphaltene was measured by ASTM method D2007. In several specific examples, the present invention and one or more of the methods or compositions of the present invention also provide the following crude oil feeds ... (a) those that have not been processed in a refinery, steamed and / or fractionated; contain carbon For components with a number greater than 4, the crude oil feed contains at least 0.5 grams of this type of feed in each gram of crude oil feed; (c) contains hydrocarbons, some of which have: less than 10 at 0.1 MPa The boiling range distribution of 〇t is between 100 ° C and 200 at 0.101 MPa. A boiling range distribution between 〇, a boiling range distribution between 200 ° C and 300 ° C at 0.101 MPa, a boiling range distribution between 300 ° C and 400 ° C at 0.101 MPa, and Boiling range distribution between 400 ° C and 650 ° C at 0.101 MPa; spring (d) contains at least · 0 · 001 grams per gram of crude oil feed with a boiling range distribution below 0.101 MPa 〇〇. 〇hydrocarbons, 0.001 grams of hydrocarbons with a boiling range distribution between 0.1 ° C and 200 ° C at 0.101 MPa, 〇_〇〇01 grams of hydrocarbons with a boiling range distribution at 0.101 MPa and 200 ° C and Hydrocarbons between 300 ° C, 0.001 grams of fumes with a boiling range distribution between 0.1 ° C and 300 ° C at 0.101 MPa, and 0 · 〇0 1 grams of fumes with a boiling range distribution of 0.1 1 〇1 Hydrocarbons between 400 ° C and 650 ° C at μ pa; (e) have at least 0 ″, less than 33 200532010, or 0.3, or 0.3 to 20 ′ 0.4 to 10, or 0.5 TAN in the range of $; (f) has a starting point of at least 2000c at 0.11 MPa, (g) contains iron, hunger, and iron, (h) per gram Crude feed contains at least 0.00002 grams of total N " V / Fe; ⑴ contains sulfur; ⑴ contains at least 0.0001 grams or 0.05 grams of sulfur per gram of crude feed; (k) contains at least 0.001 grams of sulfur per gram of crude feed 0.001 grams of VGO; (1) contains at least 0.1 grams of residue per gram of crude feed; (m) contains oxygenated hydrocarbons; (n) one or more alkali metal salts of one or more organic acids, one or more One or more alkaline earth metal salts of organic acids Or mixtures thereof; (square) comprising at least one organic acid salts speech; and / or (p) comprising at least one organic acid salt Shi Shen. In several specific examples, the present invention and those combining one or more methods or compositions of the present invention also provide crude oils that can be obtained by removing naphtha from crude oil and compounds more volatile than naphtha. Feed. In several specific examples, the present invention and a combination of one or more methods or compositions of the present invention are also & a method for contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, wherein the crude oil Both the feed and crude product have C5 asphaltene content and MCR content, and · r, • The sum of the C: 5 cyanide content of crude oil feed and the MCR content of crude oil feed is s, and the C5 pitch of crude oil product is The sum of the mass content and the MCR content of the crude oil product is S ′, and the contact conditions are controlled so that S ′ is at most 99% of S; and / or (b) the contact conditions are restrained so that the CR CR content of the crude product and the crude product ^ The weight ratio of the cyanine content is in the range of 1.2 to 2.0, or 1.3 to 1.9. 5 In some specific examples, the present invention and a combination of one of the present invention to take a variety of methods or compositions also provide a hydrogen source, The hydrogen source is: (a) gas energy (M 34 200532010 hydrogen; (C) pinane; (d) light hydrocarbons; (e) inert gas; and / or tritium mixtures thereof.) In several specific examples, the present Inventions and combinations of the invention—or methods or compositions are also mentioned A method of contacting a crude oil feed with one or more catalysts to produce a total product containing a crude oil product, where the crude oil feed is contacted in a contact zone located or connected to an offshore facility. In a number of specific lifelines, The present invention and those combining one or more methods or compositions of the present invention also provide a method comprising contacting a crude oil feed with one or more catalysts in the presence of a gas and / or chlorine source and controlling the contact conditions in order to make · (A) The ratio of gaseous hydrogen source to crude oil feed is in the range of 5 to 800 standard cubic meters of gaseous hydrogen source per cubic meter of crude oil feed in contact with one or more catalysts; (b) The selected net uptake of argon is controlled by changing the partial pressure of the hydrogen source; (c) The uptake of hydrogen makes the crude oil product have an AN less than 0.3, but the uptake of hydrogen is less than that during the contact will cause crude oil feed and The amount of hydrogen uptake through the phase separation between the total products; (d) The selected hydrogen uptake rate is within the range of 1 to 30 or 1 to 80 standard cubic meters of hydrogen source per cubic meter of crude oil feed; e) The liquid space velocity of the gas and / or hydrogen source is at least 11 ^ At least 15 h ·], or at most 2 0 ^; 控制 control the partial pressure of the gas and / or hydrogen source during the contact; (g) the contact temperature is in the range of 50 to 5001, the total of the gas and / or hydrogen source The space velocity of the liquid is in the range of 0.1 to 30 h_], and the total pressure of the gas and / or hydrogen source is in the range of 10 to 20 MPa. (H) The flow of the gas and / or hydrogen source is toward The direction opposite to the flow of the crude oil feed; (i) the crude oil product has an H / C of 70 to 130% of the H / C of the crude oil feed; (j) the hydrogen absorbed by the crude oil feed per cubic meter of 35 200532010 The crude oil feed has a range of up to 80 and / or i to 80 or i to 50 standard cubic meters of hydrogen; (k) the crude product has a total Ni / V / Fe content of up to 90% and up to The Ni ~ / Fe content of the crude oil feed is 50% 'or up to 10%; (!) The crude oil product has a sulfur content of 70 to 130% or 80 to

之該原油進料的硫含量;(m)該原油產物具有vg〇含量 為70至130%或90至110%之該原油至13〇%或9進料的 VGO含量;(n)該原油產物具有殘留物含量為至】Μ% 之該原油進料的殘留物含量;(〇)該原油產物具有氧含量 ,多為90%,最多為70%,最多為5〇%,最多為4〇%,或 最多為10〇/。之該原油進料的氧含量;(p)該原油產物且有 有。機酸金屬鹽形態的鹼金屬和鹼土金屬總含量最多為 最夕為5 0 /〇,或最多$ ! 〇%之該原油進料的有機酸The sulfur content of the crude feed; (m) the crude product has a VGO content of 70 to 130% or 90 to 110% of the crude to a 13% or 9 feed VGO content; (n) the crude product Has a residue content of the crude oil feed of up to M%; (0) the crude oil product has an oxygen content, mostly 90%, up to 70%, up to 50%, up to 40% , Or up to 10〇 /. The oxygen content of the crude feed; (p) the crude product and yes. The total content of alkali metals and alkaline earth metals in the form of organic acid metal salts is at most 50 / 〇, or at most $! 〇% of the organic acid of the crude oil feed

金屬鹽形態的鹼金屬和鹼土金屬含量;(q)在接觸期間, 該原油進料的P值至少為以;⑴該原油產物具有在378 C下的黏度最多為9G%,最多為观,或最多& 1〇%之該 原油進料在37.代下的黏度;⑷該原油產物具有AM比 重為70至130%之該原油進料的Αρι比重;及/或⑴咳 =產物具有TAN最多為90%,最多為5〇%,最多為應, 取夕為20%,或最多為1〇%之該原油進料的 0,1至。一至。.2,或。.…的範圍内。 於若干具體實例中,本發明與結合本發明之一或多種 =或組成物者亦提供—種方法,其包含使原油進料與一 二種觸媒接觸及控制接觸條件以減少含有機氧化合物的 ’、中.(a) ’咸少選疋有機氧化合物的含量以便使該 36 200532010 原油產f具有含氧量最多㈣%之該原油進料的含氧量;⑻ ::機乳化“勿的至少—種化合物包含羧酸之金屬鹽;⑷ έ有機氧化合物的至少— 種化6物包έ羧酸之鹼金屬鹽;(d) έ有機氧化合物的至少_ ν種化合物包含羧酸之鹼土金屬 ⑷含有機氧化合物的至少—種化合物包含㈣之金 胃包括週期表第12攔的—或多種金屬;⑴ 该原油產物具有含非羧酸有機化合物含量最多為90%之該 原油進料中的含非幾酸有機化合物含量;及/或⑻該原 油進枓中的至少一種含氧化合物係產自含環烷酸或非羧酸 的有機氧化合物。 、於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦提供_種方法,其包含使原油進料與一 ^種觸媒接觸,其中··⑷於第-溫度下,使該原油進 舁至;-種觸媒接觸,接著於第二溫度下接觸,控制接 、1卞:二便使第—接觸溫度至少低於第二接觸溫度30°c ; (b)方;弟-風吸取條件下然後在第二氯吸取條件下,使该 原油進料與氫接觸,第一吸取條件的溫度係至少低於第二 吸取條件的溫度㈣,·(〇於第一溫度下,使該原油進料 ”至^種觸媒接觸’接著於第二溫度下接觸,控制接觸Contents of alkali metals and alkaline earth metals in the form of metal salts; (q) during the contact, the crude oil feed has a P value of at least ⑴; ⑴ the crude oil product has a viscosity of up to 9G% at 378 C, or Up to 10% of the viscosity of the crude oil feed at 37. generation; ⑷ the crude oil product has an Aρι specific gravity of 70 to 130% of the crude oil feed; and / or cough = the product has the most TAN It is 90%, maximum 50%, maximum response, 20%, or 10% of the crude oil feed. One to one. .2, or. .…In the range. In several specific examples, the present invention and a combination of one or more of the present invention or a composition also provide a method comprising contacting a crude oil feed with one or two catalysts and controlling the contact conditions to reduce organic oxygen compounds (A) 'Select the content of 疋 organic oxygen compounds so that the 36 200532010 crude oil production has the oxygen content of the crude oil feed with the maximum oxygen content of ㈣%; At least one of the compounds contains a metal salt of a carboxylic acid; at least one of the organic oxygen compounds includes an alkali metal salt of a carboxylic acid; (d) at least one of the organic oxygen compounds includes a carboxylic acid Alkaline earth metal ⑷ At least one compound containing organic oxygen compounds ㈣ Gold stomach including ㈣ of the periodic table-or more metals; ⑴ The crude oil product has a crude oil feed containing a non-carboxylic acid organic compound content of up to 90% Content of non-acidic acid-containing organic compounds; and / or at least one oxygen-containing compound in the crude oil is produced from naphthenic or non-carboxylic acid-containing organic oxygen compounds. In several specific examples, the present invention versus A method is also provided in combination with one or more methods or compositions of the present invention, which comprises contacting a crude oil feed with a catalyst, wherein the crude oil is fed to the-at the-temperature;- This kind of catalyst is contacted, and then contacted at the second temperature, the control contact, 1 卞: Second, the first contact temperature is at least 30 ° c lower than the second contact temperature; (b) Fang; under the conditions of wind absorption Under the second chlorine absorption condition, the crude oil feed is brought into contact with hydrogen, and the temperature of the first absorption condition is at least lower than the temperature of the second absorption condition ㈣, (the crude oil is fed at the first temperature "to ^ Catalyst contact 'followed by contact at a second temperature to control contact

条件X便使第_接觸溫度最多低於第二接觸溫度綱。C 在接觸期間產斗_ g ^ 屋生風乳,(e)在接觸期間產生氫氣,並且押 制接觸條件以便使該原油進料吸取至少―部分的生成氯 m由進料與第一和第二種觸媒接觸,該原油進料盘第 一種觸媒的接觸生成初原油產物,其中此初原油產物具有 37 200532010 TAN最多為9〇%之該原油進料的μ 器中進行接觸;(h)方弗塍广“ (g)方;堆豐床反應 該原油進料在盥一 €吝 妾觸,(1)使 該一或多種觸錤A如細* 、力觸媒接觸,(j) 觸媒為釩觸媒,使該原油進 觸之後,於_、、届六+ 十在每该叙觸媒接 後方、風源存在下與附加觸媒接 方米原油進料1至? Λ神.住 )風心以母立 士冰 軚準立方米之範圍内的速幸產4 · m 在接觸期間產生氳,於气雕# ^丨 〇逑革產生,(I) 下,使嗜H 、*肢 父一部分生成氫的存在 使θ原,由進料與附加 便使氣體流動朝著盘原料’ ”且控制接觸條件以 向;W使該^㈣ 動和生成氨流動相反的方 於第二=油進料於第-溫度下與鈒觸媒接觸,隨後 溫度至少低於第_、ι接觸’控制接觸條件以便使第一 使該原油進料愈附…广⑻在接觸期間產生氫氣, 加觸媒吸取至少—部 ^接觸條件以便使該附 度下使該;f,成虱,及/或(〇)隨後於第二溫 第二溫度至少為l8〇t。 “觸’控制接觸條件以便使 於若干具體實例 方法明與結合本發明之—或多種 成次、、且成物者亦提供一 或多種觸媒接觸,其中·…山使原油進料與- 含氧化鋁、氧化石々^ a '亥觸媒為受載觸媒而載體包 化鎂,^ # 氧化矽—氧化鋁、氧化鈦、氧化鈔、氧The condition X makes the first contact temperature lower than the second contact temperature. C. The bucket is produced during the contact period. G ^ The raw wind milk, (e) Hydrogen is generated during the contact period, and the contact conditions are restrained so that the crude oil feed absorbs at least a part of the generated chlorine m from the feed and the first and the first. Two kinds of catalysts are contacted. The contact of the first catalyst of the crude oil feed tray generates an initial crude oil product, wherein the initial crude oil product has 37 200532010 TAN with a maximum of 90% of the crude oil feed in the μ device; h) Fang Fang's "(g) Fang; the reactor bed reflects the contact of the crude oil feed in the toilet, (1) the one or more contacts A such as fine *, force catalyst contact, (j ) The catalyst is a vanadium catalyst. After the crude oil is brought into contact, at _ ,, and 6 + 10, after each contact with the catalyst, and with the presence of a wind source, it will contact the additional catalyst with a square meter of crude oil feed 1 to? Λ Divine. Live) Fengxin produces 4 · m within a range of quasi-cubic cubic meters of the mother's ice moraine, and produces 氲 during the contact period, which is produced in the air carving # ^ 丨 〇 逑 leather, (I) The existence of hydrogen generated by a part of the limb father makes θ the original, and feeds and attaches to make the gas flow toward the disk material '"and control the contact conditions to; The second step is to make the reaction and the ammonia flow opposite. The second is that the oil feed is in contact with the catalyst at the first temperature, and then the temperature is at least lower than the first contact. The crude feed became more attached ... Guangxi produced hydrogen during the contact, and the catalyst absorbed at least-part of the contact conditions in order to make the attachment under the condition; f, lice, and / or (〇) subsequently at a second temperature The second temperature is at least 180t. "Touch 'to control the contact conditions so that a number of specific examples and methods can be used in conjunction with the present invention-or multiple times, and the creator also provides one or more catalyst contacts, where ... Shanshan crude oil feed and-containing Alumina, oxidized stone 亥 a 'Hai catalyst is a loaded catalyst and the carrier encapsulates magnesium, ^ # silica-alumina, titanium oxide, banknote oxide, oxygen

化鎮,或其混合物 半鲒羊L 性;(c)此方本 ^觸媒為受載觸媒而載體為多孔 處理過的附加觸媒;(d)在;^别已在高於·c之溫度下 年;及心)豸至少—:二種觸媒的壽命至少為°.5 種觸媒係於固定床中或懸浮於原 38 200532010 油進料中。 於右干具體實例中,本發明與結合本發明之夕 方法或組成物者亦接^ 或多種 几知供—種方法,其包含使原油 或多種觸媒接觸,駐少—種㈣為受_媒或塊狀二屬 觸媒’該受載觸媒或塊狀金屬觸媒:⑷&含週期表第屬5 至10攔的-或多種金屬,週期表第5至1〇欄之—或多種 金屬的-或多種化合物,或其混合物;(b)在每克觸媒中 含有至少〇.〇〇〇1克,0.0001至0.6克,或〇〇〇1至〇3克 之:週期表第5至10欄的一或多種金屬,週期表第5至⑺ 攔之-或多種金屬的一或多種化合物,或其混合物;⑷包 含週期^ 6至1G欄的—或多種金屬,週期表第6至10 或多種金屬的一或多種化合物,或其混合物;⑷包 k功表第7至1〇欄的一或多種金屬,週期表第7至⑺ 搁之—或多種金屬的一或多種化合物,或其混合物;⑷在 :克觸媒中含有〇.〇〇〇1至〇·6克或〇〇〇1至〇3克之:週 j : : 7至1〇攔的一或多種金屬,週期表第7至欄之 或夕種金屬的-或多種化合物,或其混合物The chemical properties of Huazhen, or its mixture of semi-goat sheep; (c) this square catalyst is a loaded catalyst and the carrier is a porous treated additional catalyst; (d) at; ^ not already higher than · c The temperature is below the year; and the heart) : at least-: the life of the two catalysts is at least °. 5 catalysts are in a fixed bed or suspended in the original 38 200532010 oil feed. In the specific example of the right stem, the present invention and the method or composition combining the present invention are also provided with one or more methods, which include contacting crude oil or a variety of catalysts. Medium or massive two-type catalyst 'The loaded catalyst or massive metal catalyst: ⑷ & Contains metals 5 to 10 of the periodic table-or more metals, columns 5 to 10 of the periodic table-or more Metallic- or multiple compounds, or mixtures thereof; (b) containing at least 0.0001 g, 0.0001 to 0.6 g, or 0.0001 to 0.3 g per gram of catalyst: 5 to 6 of the periodic table One or more metals in column 10, 5 to 周期 of the periodic table-one or more compounds of metals, or mixtures thereof; ⑷ containing columns ^ 6 to 1G-or more of metals in periodic table 6 to 10 One or more compounds of one or more metals, or mixtures thereof; one or more metals including columns 7 to 10 of the work table, 7 to 8 of the periodic table—or one or more compounds of multiple metals, or Mixture; ⑷ in: gram catalyst contains 0.0001 to 0.6 g or 0.001 to 03 g: week j: 7 1〇 bar one or more metals of the Periodic Table of the column 7 to metals or evening - or more compounds, or mixtures thereof,

週期矣# C 一 ^ : 至6攔的一或多種金屬,週期表第5至6攔之 、周:多種金屬的—或多種化合物,或其混合物;⑻包含 =表第5攔的—或多種金屬,週期表第5欄之—或多種 八^的3戈多種化合物,或其混合物;⑻在每克觸媒中 :至少 〇·〇〇(Η 克,〇._ 至 0.6 克,〇 〇〇1 至 〇 3 克,〇 〇〇5 八^克,或〇·01至〇·08克之:週期表第5欄的一或多種 孟-’週期表f 5欄之-或多種金屬的—或多種化合物, 39 200532010 或其物;⑴包含週期表第6攔的— 期表弟6攔之—或多種金屬的—或多種化 金屬,週 物;⑴在每克觸媒中含有〇〇〇〇ι至〇 ° ,或其混合 克,0.005 至(M 克,〇 〇 •克’ 0.001 至 0.3 里υ·υ8克之週期妾 或多種金屬,週期表第6櫊之—或多 弟6攔的一 合物,或其混合物;㈨包、*屬的-或多種化 屬、闲如主啓 週期表弟W欄的一嗖夕鍤八 屬’週期表弟1〇㈣之-或多種金屬的一或多種:夕心 至03克之.中有〇.0001至〇·6克或_ 克之.週期表弟1〇攔的-或多種金屬,週期表第1〇 ^ 次夕種化合物,或其混合物;(m)包 含釩,一或多種釩化合物, 次八化合物;(η)包含鎳,一 或夕種錄化合物,或其混合物;⑷包含鈷,-或多種銘 化合物’或其混合物;(Ρ)包含钥,-或多種鉬化合物, 或其混合物;⑷在每克觸媒中含有0 001至03克或0 005 至0·1克的:鉬,一或多種鉬化合物,或其混合物;(Γ)包 3鎢’ -或多種鶴化合物,或其混合物;⑷在每克觸媒 3有0.001至0.3克的:鎢,一或多種鎢化合物’或其 混合物;⑴&含週期表帛Η闌的一或多種金屬和週期表 攔的—或多種金屬,其中第1G攔金屬與第6欄金屬 的莫耳比為1纟5 ’⑷包含週期表第^ 5棚的一或多種元 素,週期表第丨5欄之一或多種元素的一或多種化合物, 或其混合物;⑺在每克觸媒中含有〇 〇〇〇〇1至〇 〇6克之: 種元素的一或 週/月表第15棚的一或多種元素,週期表第15欄之一或多 多種化合物,或其混合物;(w)磷,一或多 40 200532010 種磷化合物,或其混合物;A> 初(X)在母克觸媒中含有最多〇 克的(X氧化鋁;及/或(y)在各古奋活上甘山人 在母克觸媒中含有至少〇·5的 氧化鋁。 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦提供形成觸媒之方法,#包括使載體與 或夕種金屬結合以形成都轉/么厘 〜风戰體/金屬混合物,其中該載體包 含Θ氧化|呂,於至少4〇〇 ή6、、西疮πτ私士扣η ρ L的μ度下熱處理0氧化鋁載體/金 屬混合物,而且尚包括··⑷使載體/金屬混合物與水社入 以,成糊狀物,擠逐此糊狀物;(b)於至少8〇〇t的溫: 下藉由熱處理氧化鋁而得到θ氧化叙· , . ,. ^ 付乳化銘,及/或(c)使該觸媒 硫化。 於若干具體實例中,本發明與結合本發明之一或多種 去或、、且成物者亦提供一種方法,其包含使原油進料與一 或多種觸媒接觸,其中該—或多種觸媒的孔徑分佈具有⑷ 至少為60Α,至少為9〇α,至少為18〇α,至少為2〇〇α, 至少為230 Α,至少為300 Α,最多為23〇α,最多為5〇〇α, 或是在 90 至 180 A,100 至 140 A,120 至 130 A,230 至 250 A,180 至 500 A,23〇 至 5〇〇 A ;或 6〇 至 3〇〇 A 之範 圍内的中位孔梭;(b)至少60%的總孔數具有在45A、35A, 或25入之中位孔徑範圍内的孔徑;(c)至少為60 m2/g,至 )為90 m2/g,至少為100 m2/g,至少為120 m2/g,至少為 5〇 m /g ’至少為20〇 m2/g,或至少為220 m2/g的表面積; 及/或(d)至少為0·3 cm3/g,至少為〇·4 cm3/g,至少為〇.5 11 /g ’或至少為〇·7 cm3/g之所有孔徑的總體積。 41 200532010 於若干具體實例中,本發明與結合本發明之-或多種 :法或組成物者亦提供-種方法,其包含使原油進料與一 或多種受載觸媒接觸,苴中 儿 八甲3戟月豆·(a)包含氧化鋁、氧 化石夕、氧化石夕-氧化 虱匕鋁乳化鈦、氧化鍅、氧化鎂,或其混 合物,及/或沸石;(b)白八以儿, 々 、 包3 丫虱化鋁及/或δ氧化鋁;(c)在 人士載"中3有至彡〇·5克的γ氧化鋁;⑷在每克載體中 3有至少0.3克或至彡〇 5克的㊀氧化紹;⑷&含以氧化 銘、γ氧化鋁、δ氣化鈕、^ 鋁θ虱化鋁,或其混合物;(f)在每Period 矣 # C ^: One or more metals from 6 to 6, and from week 5 to 6 of the periodic table: multiple metals—or multiple compounds, or mixtures thereof; ⑻ contains = Table 5—or more Metals, column 5 of the periodic table—or more than three compounds, or mixtures thereof; ⑻ per gram of catalyst: at least 〇〇〇〇 (Η g, 〇._ to 0.6 g, 〇〇〇〇 1 to 0.03 grams, 0.005 grams, or 0.01 to 0.08 grams: one or more Meng in column 5 of the periodic table-'f 5 in column-or more metals-or more Compound, 39 200532010 or something thereof; ⑴ contains the sixth block of the periodic table-the cousin of the period 6-or more of the metal-or a variety of metal, the weekly matter; 含有 per gram of the catalyst contains 〇00〇ι To 〇 °, or its mixed gram, 0.005 to (M gram, 〇 •• '0.001 to 0.3 ri · υ8 gram cycle 妾 or more metals, the sixth table of the periodic table-or a combination of 6 , Or a mixture of them; bag, * genus-or a variety of genus, leisurely as the main column of the periodic table brother W column of the eight genus' periodic cousin 10 ㈣- One or more of a variety of metals: from the heart to 03 grams. There are 0.0001 to 0.6 grams or _ grams of the-or more metals of the Periodic Table, 10th, the compound of the 10th order of the periodic table, Or a mixture thereof; (m) containing vanadium, one or more vanadium compounds, sub-eight compounds; (η) containing nickel, one or more compounds, or mixtures thereof; ⑷ containing cobalt,-or multiple compounds, or mixtures thereof (P) contains molybdenum,-or more molybdenum compounds, or mixtures thereof; (i) contains 0.001 to 03 grams or 0 005 to 0.1 grams per gram of catalyst: molybdenum, one or more molybdenum compounds, or Mixtures; (Γ) containing 3 tungsten '-or more crane compounds, or mixtures thereof; rhenium at 0.001 to 0.3 g per gram of catalyst 3: tungsten, one or more tungsten compounds' or mixtures thereof; ⑴ & with periodic table The one or more metals of the diaphragm and the metal of the periodic table—or more than one metal, in which the molar ratio of metal 1G to metal in column 6 is 1 纟 5 '⑷ contains one or more elements of the fifth shed of the periodic table , One or more compounds of one or more elements in column 5 of the periodic table, or a mixture thereof; Each gram of the catalyst contains 0.001 to 006 grams of: one or more elements of one or more week / monthly table of one element, one or more compounds of column 15 of the periodic table, or Mixtures; (w) phosphorus, one or more 40 200532010 phosphorus compounds, or mixtures thereof; A > Primary (X) contains up to 0 g of (X alumina) in the master gram catalyst and / or (y) in each The ancient Fenhuo Shangshan people contain at least 0.5 alumina in the mother catalyst. In some specific examples, the present invention and a combination of one or more methods or compositions of the present invention also provide a method for forming a catalyst. , # Including the carrier combined with or a metal to form Du Zhuan / Mo Li ~ Feng war body / metal mixture, wherein the carrier contains Θ oxidation | Lu, at least 400, 6, sore πτPrivate buckle η ρ L is heat-treated at a degree of 0 ° alumina support / metal mixture, and it also includes ⑷ to make the support / metal mixture and water company into a paste, squeeze this paste; (b) at least 8 〇〇t's temperature: θ oxidized by heat treatment of alumina,... ^ Fu emulsion Ming, and / or (c ) The catalyst is vulcanized. In several specific examples, the present invention and one or more of the present inventions are combined with one another, and the creator also provides a method comprising contacting a crude oil feed with one or more catalysts, wherein the-or more catalysts Has a pore size distribution of at least 60A, at least 90A, at least 18Oa, at least 200A, at least 230A, at least 300A, at most 23A, and at most 500A , Or in the range of 90 to 180 A, 100 to 140 A, 120 to 130 A, 230 to 250 A, 180 to 500 A, 230 to 500 A; or 60 to 300 A Position hole shuttle; (b) at least 60% of the total number of holes has a pore size in the range of 45A, 35A, or 25 in the median pore size; (c) at least 60 m2 / g, to) 90 m2 / g, A surface area of at least 100 m2 / g, at least 120 m2 / g, at least 50 m / g 'at least 200 m2 / g, or at least 220 m2 / g; and / or (d) at least 0 · The total volume of all pore sizes of 3 cm3 / g, at least 0.4 cm3 / g, at least 0.5 11 / g 'or at least 0.7 cm3 / g. 41 200532010 In several specific examples, the present invention and the combination of the present invention-or multiple methods or compositions also provide a method comprising contacting a crude oil feed with one or more supported catalysts, A3 halberd beans · (a) contains aluminum oxide, stone oxide, stone oxide-aluminum oxide, titanium oxide, hafnium oxide, magnesium oxide, or a mixture thereof, and / or zeolite; (b) Bai Yaoer 々, package 3 yaluminum alumina and / or δ alumina; (c) 3 to 彡 0.5 g of γ alumina in a person's load; ⑷ 3 at least 0.3 g per gram of carrier or Up to 205 grams of yttrium oxide; y < containing oxide, γ alumina, δ gasification button, ^ aluminum θ aluminum oxide, or mixtures thereof; (f) in each

克载體中含有最多0·1克的α氧化鋁。 、、於若干具體實例中,本發明與結合本發明之一或多種 I去或組成物者亦提供一種釩觸媒:⑷具有中位孔徑至 為60Α的孔從分佈;(b)包含載體,此載體包含㊀氧化 、呂’而核觸媒具有中位孔徑至少為6GA的孔徑分佈;⑷ ^含週期表第6攔的—或多種金屬,週期表第6欄之-或 :種金屬的一或多種化合物,或其混合物;及/或⑷在 每克觸媒中含有至少0·001克之:週期表第6搁的一或多The gram carrier contains up to 0.1 grams of alpha alumina. In some specific examples, the present invention and a combination of one or more of the present invention also provide a vanadium catalyst: ⑷ pore distribution from a median pore size to 60A; This carrier contains tritium oxide and Lu ', and the nuclear catalyst has a pore size distribution with a median pore size of at least 6GA; Or more compounds, or mixtures thereof; and / or rhenium containing at least 0.001 g per gram of catalyst: one or more of the 6th table

種孟屬’週期表第6攔之—或多種金屬的—或多種化合物, 或其混合物。 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦提供一種原油產物,其具有··㈠)最多 1 0.001 至 〇_5 ’ 0.01 至 0.2 ;或 〇 05 至 〇J 的 TAN ; 少…在每克原油產物中最多為〇 〇〇〇〇〇9克之有機酸金屬鹽 形態的鹼金屬和鹼土金屬;(c)在每克原油產物中最多為 •00002克之Ni/V/Fe ;及/或(d)在每克原油產物中大於 42 200532010 0克,但小於〇.〇1克的至少一種觸媒。 於若干具體實例中,本發明 七月與結合本發明之一或多種 方法或組成物者亦提供一,多 4夕種有機酸的一或多種鹼金屬 鹽,一或多種有機酸的一或容 • 或文]次夕種鹼土金屬鹽,或其混合物, 其中·(a)該至少一種驗全屬兔 屬為鍾、鈉,或鉀;及/或(b)該 至少一種鹼土金屬為鎂或鈣。 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦提供—種方法,其包含使原油進料與一 或多種觸媒接觸以生產含有肩、、山 有原油產物的總產物,此方法尚 包括:⑷使該原油產物與該原油進料相同或不同的原油 結合以形成適用於運輸的摻合你 ^ 句’(b)使該原油產物與該 原油進料相同或不同的;^、、山έ士人 Ν扪原油結合以形成適用於處理設備的 摻合物;(c)分餾該原油產物· 、 田座物,及/或(d)使該原油產物 分I留成為一或多種餾分,並且由守 且五由5亥至少一種餾分生產運輸 用燃料。 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦提供一種受載觸媒組成物,其:(a)在 母克載體中含有至少0.3克或至少〇5克的θ氧化鋁丨⑼在 載體中包含δ氧化鋁;⑷在每克載體中含有最多〇1克的 α氧化紹;⑷具有中位孔徑至少為⑽人的孔徑分佈;⑷ 具有該孔徑分佈之孔至少為G.3 em3/g或至少為^ 的孔體㈣具有至少60m2/g或至少9〇m2/g的表面積; ω包含週期表第7至10攔的一或多種金屬,週期表第7 至10欄之-或多種金屬的一或多種化合物,或其混合物; 43 200532010 (\、二3週期表第5攔的一或多種金屬,週期表第5欄之 或多種金屬的一或多種化合物,或其混合物;⑴在每 克觸媒中含有〇βΛΓη 夕 ’ ϋ·0001至〇·6克或0.001至0.3克之:一或 夕種$ 5攔金屬,-或多種第5欄金屬化合物,或其混合 (j)包3週期表第6攔的一或多種金屬,週期表第6 攔之一或多種今属& 孟屬的一或多種化合物,或其混合物;(k)在 每克觸媒中含有〇 〇〇〇Ί s 兩ϋ.0001至〇·6克或0.001至0.3克之:一 :夕種第6欄金屬,-或多種第6欄金屬化合物,或其混Species # 6 of the Periodic Table—or multiple metals—or multiple compounds, or mixtures thereof. In some specific examples, the present invention and those who combine one or more methods or compositions of the present invention also provide a crude oil product, which has a maximum of 1 0.001 to 0.005 '0.01 to 0.2; or 0.05 to 0.2. TAN of J; Less ... Alkali metals and alkaline earth metals in the form of organic acid metal salts of up to 9000 g per gram of crude oil product; (c) Up to • 0002 g of Ni / g per gram of crude oil product V / Fe; and / or (d) at least one catalyst greater than 42 200532010 0 g, but less than 0.01 g per gram of crude product. In some specific examples, the present invention and one or more methods or compositions combining the present invention also provide one or more alkali metal salts of one or more organic acids, one or more organic acids • or]] Alkaline earth metal salts, or mixtures thereof, of which: (a) the at least one species is a bell, sodium, or potassium; and / or (b) the at least one alkaline earth metal is magnesium or calcium. In several specific examples, the present invention and those combining one or more methods or compositions of the present invention also provide a method comprising contacting a crude oil feed with one or more catalysts to produce a crude oil product containing The total product of this method further includes: (i) combining the crude oil product with the same or different crude oil feed to form a blend suitable for transportation; (b) making the crude oil product the same as the crude oil feed Or different; ^, combined with Shantou NH 扪 crude oil to form a blend suitable for processing equipment; (c) fractionating the crude product, field products, and / or (d) fractionating the crude product I remains as one or more distillates, and at least one distillate is used to produce transportation fuel from Mori. In some specific examples, the present invention and those who combine one or more methods or compositions of the present invention also provide a supported catalyst composition, which: (a) contains at least 0.3 g or at least 0.05 g in a mother gram carrier Θ alumina 丨 ⑼ contains δ alumina in the carrier; 含有 contains a maximum of 0.01 g of α oxide per gram of the carrier; ⑷ has a pore size distribution with a median pore size of at least ⑽; pores with the pore size distribution Porous bodies of at least G.3 em3 / g or at least ^ have a surface area of at least 60 m2 / g or at least 90 m2 / g; ω contains one or more metals in the seventh to tenth of the periodic table, and seventh in the periodic table To one or more compounds of columns 10 to 10 or more, or mixtures thereof; 43 200532010 (\, two or three metals of the third periodic table, one or more compounds of column five or more of the periodic table , Or a mixture thereof; 含有 in each gram of catalyst 〇βΛΓη xi 'ϋ · 0001 to 0.6 g or 0.001 to 0.3 g: one or five kinds of metal,-or more than the fifth column metal compound, or Its mixture (j) consists of one or more metals in Block 6 of the Periodic Table, Block 6 in the Periodic Table One or more compounds of the genus & Mon, or mixtures thereof; (k) 0.00000 s per gram of catalyst, 0.001 to 0.6 g or 0.001 to 0.3 g per gram of catalyst: 1: Column 6 metal,-or multiple Column 6 metal compounds, or mixtures thereof

。物’⑴包含1凡,一或多種飢化合物,或其混合物;㈣包 含鉬,-或多種鉬化合物,或其混合物;⑻&含鎢,一 或多種鎢化合物,吱苴、、曰人l ^人 ^吧合物;包含鈷,一或多種鈷 化合物,或盆混入你· ’、σ ,及/或(Ρ)包含鎳,一或多種鎳化 合物,或其混合物。 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦提供—種原油組成物,#:⑷且有最 多=1,最多為0.5,最多為〇.3,或最多為〇.^ταν;⑻. The substance '⑴ contains one or more compounds, or mixtures thereof; ㈣ contains molybdenum,-or more molybdenum compounds, or mixtures thereof; ⑻ & contains tungsten, one or more tungsten compounds, 苴, 人, ^ Human body compound; contains cobalt, one or more cobalt compounds, or is mixed in with one's, σ, and / or (P) contains nickel, one or more nickel compounds, or a mixture thereof. In some specific examples, the present invention and those combining one or more methods or compositions of the present invention also provide a kind of crude oil composition, #: ⑷ and there is at most = 1, at most 0.5, at most 0.3, or at most 0. ^ ταν; ⑻

在每克組成物中含有至少〇⑽ υ.001克之沸私分佈在〇.1〇1 MPa 下介於价和·。c之間的煙;顧1,至少〇〇〇5Each gram of composition contains at least 〇. Υ. 001 grams of boiling private distribution between valence and · at 0.101 MPa. Smoke between c; Gu 1, at least 005

克或至/ 0.01克之彿程分佈在〇1〇1 Mpa下介於鳩。C 和320°C之間的烴;及至少〇 001 / ϋ·00ΐ克之沸程分佈在0·101 MPa 下介於320〇C和650〇C之間的炉· . — 士 2 u们/工,(c)在母克組成物中含有 至少0.0005克的鹼性氮;产益六△丄 从,(d)在母克組成物中含有至少 〇·〇〇ι克或至少θ·οι克的總氮量·及/ ^ a里,及/或0)在每克組成 物中含有最多0.00005克的總鎳和釩量。 44 200532010 於若干具體實例中,本發明與結合本發明之一或多種 方法或組成物者亦提供一種原油組成物,其包含一或多種 觸媒’該至少一種觸媒·( 3 )具有中位孔徑至少為1 8 〇人, 束夕為500 “ /入丨一 .....工A,^The dharma distribution of gram or to /0.01 gram is between dove at 010 MPa. Hydrocarbons between C and 320 ° C; and furnaces with a boiling range distribution of at least 0.001 / ϋ · 00ΐg at 0 · 101 MPa and between 320 ° C and 6500 ° C , (C) contains at least 0.0005 grams of basic nitrogen in the mother gram composition; Yili Liu △ 丄, (d) contains at least 0.0000 grams or at least θ · οι grams of the mother gram composition Total nitrogen content and / or a, and / or 0) contains up to 0.00005 grams of total nickel and vanadium per gram of composition. 44 200532010 In some specific examples, the present invention and those who combine one or more methods or compositions of the present invention also provide a crude oil composition comprising one or more catalysts' The at least one catalyst · (3) has a median The aperture is at least 180 people, and the beam is 500 "/in...........A, ^

至130 Λ的孔徑分佈;(b)具有至少90 A的中位孔徑,M 孔徑分佈中有超過60%的總孔數具有在45 A、35 A,哎25 j 之中位孔徑範圍内的孔徑;(c)具有至少1〇〇 ,至少 120 m2/g,或至少22〇 m2/g的表面積;(d)包含載體;録Pore size distribution to 130 Λ; (b) has a median pore size of at least 90 A, more than 60% of the total pore numbers in the M pore size distribution have pore sizes in the range of 45 A, 35 A, and 25 j median pore size (C) has a surface area of at least 100, at least 120 m2 / g, or at least 22 m2 / g; (d) includes a carrier;

載體包含氧化鋁、氧化矽、氧化矽_氧化鋁、氧化鈦、氧介 鍅、氧化鎂,沸石,及/或其混合物;(e)包含週期表第 至10欄的一或多種金屬,週期表第5至1〇攔之_^多福 金屬的-或多種化合物,或其混合物;(f) &含週期表第 攔的-或多種金屬,週期表第5攔之一或多種金屬的、一或 多種化合物,或其混合物;(g"每克觸媒中含有至少 0.0001克之:一或多種第5欄全 屬 或多種第5攔金屬 化合物,或其混合物;(h)包含 、,屬The support includes alumina, silica, silica-alumina, titania, oxonium oxide, magnesia, zeolite, and / or mixtures thereof; (e) one or more metals containing columns 10 to 10 of the periodic table, the periodic table 5th to 10th _ ^ Dover metal-or more compounds, or mixtures thereof; (f) & containing the first or more metals of the periodic table, one or more of the five metals of the periodic table, One or more compounds, or mixtures thereof; (g " containing at least 0.0001 grams per gram of catalyst: one or more of the fifth column of all or more of the fifth metal compounds, or mixtures thereof; (h) containing ,,

金屬’週_6欄之一或 次夕種 ^里孟屬的一或多種化人 或其混合物;⑴在每克觸 口 或多種第6攔金屬…或多種^有至少⑴咖克之:一 夕種弟6攔金屬化人物, 合物;(J)包含週期表第1〇攔的一 〇 、或八混 1 〇欄之-或多種全㉟P ”種金屬,週期表第 /或㈨包含週期表第15搁的—或 物;及 攔之一或多種元素的-或多種化合物,二、、:Γ期表第15 在進一步的具體實例中,本發明之特物/ 、疋具體實例的特 45 200532010 徵可和本發明之其他具體實例的特徵結合。例如,本發明 之一具體實例的特徵可和其他具體實例之特徵結合。 在進一步的具體實例中,原油產物可藉由本文中所述 的任一種方法和系統獲得。 在進一步的具體實例中,附加特徵可加入本文中所述 的特定具體實例。 【實施方式】 在此更詳細地敘述本發明的特定具體實例。本文中所 用的術語定義如下。 ASTM”係指美國材料試驗標準。 API比重’’係指在15 5。〇 (6〇τ)下的Αρι比重。絕 比重係藉由ASTM法D6822測定。 原油進料與原油產物的原子氫百分率和原子碳百分率 係藉由ASTM法D5291測定。 除另有況明外,原油進料、總產物,及/或原油產物的 沸程分佈係藉由ASTM》D5307測定。 C5瀝青質”係指不溶於戊烷的瀝青質。C5瀝青質含量 係藉由ASTM法D2007測定。 弟X攔金屬,,係指週期表第χ攔的一或多種金屬2 5、m第χ欄之—或多種金屬的-或多種化合物,其 (丁、對應方;週期表的攔數(例如1至12)。舉例而言,“第 攔,:或多種金屬的-或多種化合物。 弟X攔凡素係指週期表帛X才闌的一或多種元素, 46 200532010 /或义:表第x攔之一或多種元素的一或多種化人 中X係對應於週期表的欄數: 口勿’其 1 s姻;I〜 J主18)。舉例而言,“穿 攔凡素係指週期表第15搁的_或多種元 乐 表第1 5攔之—啖多锸 $及/或週期 次夕種兀素的一或多種化合物。 在本申請㈣範◎,週期表 金屬化合物重量,週期表的元素重量,期表的 合物重量係以金屬重量或元素重量計算:;=元素化 ί克觸媒使用❹.1克…3,則該觸媒中錮金屬二::: Ϊ為每克觸媒〇.〇67克。 、^重 “含量”係指以基質總重量計表示成重 分率之基質(例如原油逸枓 里百 分重量。“wtppm”係指以重量計的百萬分率。)中的成 ‘‘原油進料/總產物混合物,,待 的混合物。 “在處理期間與觸媒接觸 館分係指沸程分佈在〇 . 1 〇 1 。 MPa 下介於 204。(: (400 F )和343 C (650°F )之間的烴。鶴分八曰一 關刀含I係藉由ASTM法 D5307測定。 “雜原子”係指煙分子結構中所含的氧、氮,及/或硫。 雜原子含量係藉由ASTM法對於氧的Ε3δ5,對於總氣的 D5762及狀硫的D4294測定。“驗性氮總量”係指具有_ 小於40的氮化合物。驗性麵μ 酿f玍鼠(bn,)係藉由ASTM法D2896 測定。 氫原、係私氫及/或化合物及/或當原油進料和觸媒 存在下會反應而對原油進料中的化合物提供氫的化合物。 47 200532010 估 '括,但不限於烴(例如Clic4的烴,如甲户 1丙烧、丁幻、水,或其混合物。可進行;、乙 計對原油進料中的化合物所提供的淨氮量。衡以 “平板抗碎強度’’係指麼碎觸媒所需的壓縮力 碎強度係藉由ASTM法以丨乃測定。 反私 LHSV係指體積液體進料速率/觸媒總體積, J k (hi )表不。觸媒總體積係藉由總和接觸區右 媒體積來計算,如本文中所述者。 w有觸One of the metal 'week_6 columns or the next day species or one or more of the genus Limonis or their mixtures; ⑴ at the mouth of each gram of contact or multiple 6th metal ... or more ^ with at least ⑴: Species 6 metallized characters, compounds; (J) Contains 10 or eight mixed columns of the periodic table-10 or more full ㉟P "metals, the periodic table contains the periodic table The 15th -or matter; and the compound or compounds of one or more elements, the second and the fifth stage of the table 15 In a further specific example, the special feature of the present invention /, and the special feature of the special example 45 200532010 The characteristics may be combined with the characteristics of other specific examples of the present invention. For example, the characteristics of one specific example of the present invention may be combined with the characteristics of other specific examples. In a further specific example, the crude oil product may be obtained by the Obtained by any method and system. In further specific examples, additional features can be added to the specific specific examples described herein. [Embodiment] The specific specific examples of the present invention are described in more detail here. Definitions of terms used herein as follows. "ASTM" means the American Standard for Testing Materials. API specific gravity '' means at 15 5. Aρι specific gravity at 〇 (6〇τ). The absolute specific gravity was measured by ASTM method D6822. The atomic hydrogen percentage and atomic carbon percentage of crude oil feeds and crude products are determined by ASTM method D5291. Unless otherwise stated, the boiling range distributions of crude oil feeds, total products, and / or crude oil products are determined by ASTM "D5307. "C5 asphaltene" refers to asphaltenes that are insoluble in pentane. The content of C5 asphaltenes is determined by ASTM method D2007. The term "X metal" refers to one or more metals in the χ table of the periodic table. Column of—or more than one metal—or more than one compound, which (D, corresponding party; number of the periodic table (for example, 1 to 12). For example, “the first, or more than one metal—or more than one compound. Brother X Xanfansu refers to one or more elements of the periodic table 帛 X only, 46 200532010 / or meaning: One or more elements of one or more elements of the Xth table in the X series corresponds to the number of columns in the periodic table: Mouth not 'its 1 s marriage; I ~ J master 18). For example, "Panfanfansu" refers to one or more compounds in the 15th of the periodic table or one or more of the 15th Yuanle table— 啖 多 啖 $ and / or the cyclic species. Apply for the standard ◎, the weight of the metal compound of the periodic table, the weight of the elements of the periodic table, the weight of the compound of the periodic table is calculated based on the weight of the metal or element:;锢 Medium II in the catalyst ::: Ϊ is 0.067 grams per gram of catalyst. ^ Weight "content" refers to the matrix expressed as a weight fraction based on the total weight of the matrix (for example, the percentage weight of crude oil Yili "Wtppm" refers to the parts per million by weight.) Into the "crude oil feed / total product mixture, the mixture to be obtained." "Contact with the catalyst during processing means that the boiling range is distributed at 〇. 1 〇1. At 204 MPa. (: Hydrocarbons between (400 F) and 343 C (650 ° F). Hefenbayiyiguandao contains I is determined by ASTM method D5307. "Heteroatom" refers to the oxygen contained in the molecular structure of smoke , Nitrogen, and / or sulfur. Heteroatom content is determined by ASTM method for E3δ5 of oxygen, D5762 of total gas, and D4294 of sulfur-like sulfur. "Total nitrogen test" refers to nitrogen compounds with _ less than 40. Test surface μ fermented mole (bn,) is determined by ASTM method D2896. Hydrogen, hydrogen and / or compounds and / or react in the presence of crude oil feed and catalyst in crude oil feed Compounds that provide hydrogen. 47 200532010 Estimates include, but are not limited to, hydrocarbons (for example, Clic4 hydrocarbons, such as Kobe 1 propane, Ding Huan, water, or mixtures thereof. May be performed; The amount of net nitrogen provided by the compound. "Basic crush strength" refers to the compressive force required to crush the catalyst. The crush strength is determined by ASTM method. Anti-private LHSV refers to the volume of liquid feed. Rate / total volume of catalyst, J k (hi) represents. The total volume of catalyst is calculated by summing the right media volume of the contact area. Those mentioned in the text.

液u物,,係指包含在標準溫度和壓力(re,〇 MPa,後文稱為“STP”)下為液態之-或多種化合物…且成 物’或是包含s STP下為液態的—或多種化合物與在up 下為固態的-或多種化合物之組合的組成物。 週期表’係指2003年11月由國際純粹與應用化學聯 合會(IUPAC)所規定的週期表。 “有機酸金屬鹽形態的金屬,,係指鹼金屬、鹼土金屬、"Liquid material" refers to-or more compounds that are liquid at standard temperature and pressure (re, 0 MPa, hereinafter referred to as "STP") ... and the product is "or liquid containing STP"- A composition of one or more compounds in combination with a solid state or more compounds under up. The Periodic Table 'refers to the periodic table specified by the International Union of Pure and Applied Chemistry (IUPAC) in November 2003. "Metals in the form of metal salts of organic acids refer to alkali metals, alkaline earth metals,

鋅、砷、鉻,或其組合。有機酸金屬鹽形態的金屬含量係 藉由A S TM法D 1 3 1 8測定。 ‘‘微殘留碳’’(“MCR”)含量係指在蒸發和熱解基質後留 下的殘留炭量。MCR含量係藉由ASTM法D4530測定。 石腦油係指沸程分佈在〇· 1 〇 1 MPa下介於38 °C (1〇〇 F )和200 C (3 92 °F )之間的烴成分。石腦油含量係藉由 ASTM 法 D5307 測定。Zinc, arsenic, chromium, or a combination thereof. The metal content in the form of a metal salt of an organic acid was measured by the AS TM method D 1 3 1 8. The '' Micro Residual Carbon '("MCR") content refers to the amount of residual carbon left after the substrate is evaporated and pyrolyzed. The MCR content is measured by ASTM method D4530. Naphtha means a hydrocarbon component with a boiling range distribution between 38 ° C (100 F) and 200 C (3 92 ° F) at 0.1 MPa. The naphtha content is determined by ASTM method D5307.

Ni/V/Fe係指錄、飢、鐵,或其組合。 “Ni/V/Fe含量’’係指鎳、釩、鐵,或其組合的含量。 48 200532010 似術含量係藉由AS™法D5708測定。 “―,係指每立方米原油進料中的標準立 體。 “含非羧酸有機氧化合物,,係指不含羧基(-co2-)的有機 氧化合物。含非緩酸有機氧化合物包&,但不限於喊、環 醚、醇、芳族醇、_、醛’或其組合,其不含減。 不可政氣體”係指在STP下A氣態的成分及/或此等成 分之混合物。 P (办/合)值或‘p值”係指表示原油進料中瀝青質絮凝 _ 傾向的數值。p值的測定係由j· j· Heithaus見述於川π⑽/ <Ni / V / Fe refers to recording, starvation, iron, or a combination thereof. "Ni / V / Fe content" refers to the content of nickel, vanadium, iron, or a combination thereof. 48 200532010 The mimic content is determined by the AS ™ method D5708. "―, Means the amount per cubic meter of crude oil feed. Standard stereo. "Non-carboxylic acid-containing organic oxygen compounds refer to organic oxygen compounds that do not contain a carboxyl group (-co2-). Non-slow-acid organic oxygen compounds include & _, Aldehyde 'or a combination thereof, which does not contain minus. Uncontrollable gas "means an A gaseous component and / or a mixture of these components under STP. The P (off / on) value or 'p value' refers to a value indicating the tendency of asphaltenes to flocculate in crude oil feed. The measurement of the p value is described by J.J. Heithaus in Chuan π⑽ / <

Institute of Petroleum^ V〇l. 48? Number 458, February 19625 pp. 45-33 的 Measurement and Significance of AsphalteneMeasurement and Significance of Asphaltene by Institute of Petroleum ^ V〇l. 48? Number 458, February 19625 pp. 45-33

Peptization’、 “孔徑’’、“中位孔徑,,和“孔體積,,係指藉由aSTM法 D4284 (成140之接觸角的水銀孔率法)所測定的孔徑、中 位孔徑和孔體積。micromeritics® A9220 儀器(Micromeritics Inc·,Norcross Georgia,U_S.A_)可用來測定這些值。 ❿ “殘留物’’係指具有沸程分佈高於538 °C (1000 T)的 成分,如ASTM法D5307所測定者。 SCFB”係指每桶原油進料中的氣體標準立方吸。 觸媒的“表面積,,係藉由ASTM法D3663測定。 “TAN”係指總酸值,以每克(“g”)樣品中的〖OH毫克 數(“mg”)表示。TAN係藉由ASTM法D664測定。 “VGO”係指沸程分佈在0.101 MPa下介於343 °C (650 49 200532010 卞)和538 t (1〇〇〇 τ)之間的烴。VG〇含量係藉由astm 法D5307測定。 “黏度,,係指在37.8 t (100下的動黏度。黏度係 利用ASTM法D445測定。 在本申請案的情況下,應瞭解如果已試驗基質之性質 所得到的數值在試驗方法的限制範圍外時,則可修正及/或 重新权準此試驗方法以測試這類性質。 原油可生產及/或乾餾自含有構造物的烴接著使其穩定 化。原油可包含原油。原油通常為固體、半固體,及::液 體。穩定化可包括,但不限於移除原油中的不可凝氣體、 =、鹽’或其組合以形成穩定原油。這類穩定化通常可能 發生在,或鄰近於生產及/或乾餾場所。 穩定原油典型而言尚未在處 備中療餾及/或分餾以 、有特定彿程分佈(例如石腦油、餾分、VG0,及/或 潤滑油)的多成分。菽鶴包括 " 奸… 田匕括但不限於常壓蒸餾法及/或 減壓療餾法。未蒸餾及/或未分 不刀保的穩疋原油在每克原油Φ 可能包含數量至少為〇.5 Μ以… 兄原油中 ^ 9成刀之石厌數大於4的忐八 穩定原油的實例包括全原油、菹 刀 ^ ^ t “、、餘原油、脫鹽原油、脫Bg 瘵餘原油,或其組合。“茱餘 脱1 已私除至少一部分具有彿點在0101 匕 1 atm下為95卞)的成分。典型 ' C (在 原油中具有含量最多為 ° :备餘原油在每克蒸餘 。-克的這類成分。.〜為°·。5克’或最多為 干L疋原油具有可容許穩定原油藉由輪送載具(例如 50 200532010 管線、卡車,或船舶)輪送至習知處理設備的性質。其他原 油具有一或多個使它們不利的不適當性質。 ’、 … 、 貝 $貝原〉由對於 輸送載具及/或處理設備而言可能是不能接受 、 、 — 饮又的,因此會賦Peptization ', "pore size", "median pore size," and "pore volume" refer to the pore size, median pore size, and pore volume determined by the aSTM method D4284 (mercury porosity method with a contact angle of 140). A micromeritics® A9220 instrument (Micromeritics Inc., Norcross Georgia, U_S.A_) can be used to determine these values. ❿ "Residue" means a component with a boiling range distribution above 538 ° C (1000 T), such as the ASTM method Tested by D5307. "SCFB" refers to the standard cubic absorption of gas in the crude oil feed per barrel. The "surface area of the catalyst" is determined by ASTM method D3663. "TAN" means the total acid value, expressed as milligrams of OH ("mg") per gram ("g") of the sample. TAN is measured by ASTM method D664. "VGO" refers to hydrocarbons with a boiling range distribution between 343 ° C (650 49 200532010 卞) and 538 t (1000 τ) at 0.101 MPa. The VG0 content was measured by the astm method D5307. "Viscosity, refers to the dynamic viscosity at 37.8 t (100. Viscosity is measured using ASTM method D445. In the case of this application, it should be understood that if the properties of the tested substrate are obtained within the limits of the test method In addition, this test method can be modified and / or re-authorized to test such properties. Crude oil can be produced and / or carbonized from hydrocarbons containing structures and then stabilized. Crude oil can include crude oil. Crude oil is usually solid, Semi-solid, and :: liquid. Stabilization may include, but is not limited to, the removal of non-condensable gases, =, salts', or combinations thereof in crude oil to form stable crude oil. Such stabilization may typically occur at or near production And / or retorting sites. Stable crude oils are typically not prepared for multi-component distillation and / or fractionation, and have a multi-component distribution (such as naphtha, distillates, VG0, and / or lubricating oil). Including "… ... Tian Dizhu, but not limited to atmospheric distillation and / or reduced pressure distillation. Undistilled and / or unsecured stable crude oil may contain at least 0. per gram of crude oil Φ. 5 Μ to ... Brother crude oil Examples of 忐 9 stable knives with a stone anoresis number greater than 4 include all crude oils, knives ^ ^ t ", Yu crude oil, desalted crude oil, de-Bg Yu surplus crude oil, or a combination thereof." 朱 余 脱1 At least part of the ingredients with Buddha's point at 0101 and 1 atm at 95 卞 have been privately removed. Typical 'C (with a maximum content of ° in crude oil: the remaining crude oil is distilled per gram.-Gram of this type of ingredient .. ~ °°. 5 grams' or at most dry L 疋 crude oil has the property of allowing stable crude oil to be transported to conventional processing equipment by means of a shipping vehicle (eg 50 200532010 pipeline, truck, or ship). Others the crude oil so that they have one or more undesirable properties inappropriate ', ..., $ shell Kaibara> for the purposes of the delivery vehicle and / or the processing device may not be acceptable,, -. a drink and, therefore Fu

予劣貝原油低的經濟價值。此經濟價值可能就像亨、為八 劣質原油之谷态的生產、輸送及/或處理成本太昂貴=_ 劣質原油的性質可包括,但不限於:a)至少〇 1 少0.3的TAN;b)至少10cSt的黏度;c)最多為^的 比重,· d)總Nl/V/Fe含量為每克原油中至少有〇 〇〇〇〇2克 或至少有0·000!克的Ni/V/Fe; e)雜原子總含量為每克原 油中至少有0.005克的雜原子;f)殘留物含量為每克原油 中至少有0.01克的殘留物;g) Cs瀝青質含量為每克原油 中至少有0.04克的I瀝青質;h) MCR含量為每克原油中 至少有0.002克的MCR ; i)有機酸金屬鹽形態的金屬含量 為每克原油中至少有0.00001克的金屬;或]·)其組合。2 若干具體實例中,劣質原油在每克劣質原油中可包含至少 0·2克的殘留物,至少〇.3克的殘留物,至少〇·5克的殘= 物,或至少0.9克的殘留物。於若干具體實例中,劣質原 〉'由可能具有在0.1或0.3至20,〇·3或〇·5至1〇,或〇·4或 0·5至5之範圍内的TAN。於特定具體實例中,劣質原油 在每克劣質原油中可能具有至少〇·〇〇5克,至少〇.〇1克, 或至少0·02克的硫含量。 於若干具體實例中,劣質原油具有包括,但不限於下 列的性質:a)至少〇·5的TAN; b)含氧量為每克原油進 料至少有0.005克的氧;c) Cs瀝青質含量為每克原油進料 51 200532010 中至少有〇·〇4克的C5瀝青質 於具有API比重至少為10的砰:::望黏度(例如對 尔〆由進料而吕> 10 cSt) * 有機酸金屬鹽形態的金屬含量為各 ’ 馮母克原油中至少有0.00001 克的金屬;或f)其組合。 劣質原油在每克劣質原油中可白会· τ j a 3 ·至少 0 001 克, 至少0.005克,或至少〇·01克之沸 凡I哪牙王刀佈在0.101 MPa下Low economic value of crude oil. This economic value may be as expensive as the production, transportation, and / or treatment of the valley state of eight inferior crude oils. The nature of inferior crude oils may include, but is not limited to: a) a TAN of at least 0 and less than 0.3; b ) A viscosity of at least 10 cSt; c) a specific gravity of at most ^, d) a total Nl / V / Fe content of at least 20000 g or at least 0.00 000 g of Ni / V per gram of crude oil / Fe; e) total heteroatom content is at least 0.005 grams of heteroatoms per gram of crude oil; f) residue content is at least 0.01 grams of residues per gram of crude oil; g) Cs asphaltene content is per gram of crude oil At least 0.04 grams of I asphaltene; h) an MCR content of at least 0.002 grams of MCR per gram of crude oil; i) an organic acid metal salt in the form of a metal content of at least 0.00001 grams of metal per gram of crude oil; or] ·) Its combination. 2 In several specific examples, inferior crude oil may contain at least 0.2 grams of residues, at least 0.3 grams of residues, at least 0.5 grams of residues, or at least 0.9 grams of residues per gram of inferior crude oil. Thing. In some specific examples, the inferior element may have a TAN in the range of 0.1 or 0.3 to 20, 0.3 or 0.5 to 10, or 0.4 or 0.5 to 5. In certain specific examples, inferior crude oil may have a sulfur content of at least 0.0005 grams, at least 0.001 grams, or at least 0.02 grams per gram of inferior crude oil. In several specific examples, inferior crude oil has properties including, but not limited to: a) a TAN of at least 0.5; b) an oxygen content of at least 0.005 grams of oxygen per gram of crude oil feed; c) Cs asphaltenes The content is at least 0.04 grams of C5 asphaltene per gram of crude oil feed 51 200532010 with a API with a specific gravity of at least 10 ::: viscosity (e.g., the feed is from the feed to> 10 cSt) * The metal content in the form of a metal salt of an organic acid is at least 0.00001 g of metal in each of the von mother grams of crude oil; or f) a combination thereof. Inferior crude oil can be inferred per gram of inferior crude oil. Τ j a 3 · At least 0 001 grams, at least 0.005 grams, or at least 0.01 grams of boiling. Where I Niyawang knife cloth at 0.101 MPa

介於90 C和200°C之間的烴;至少〇 〇1克,至少〇 〇〇5克, 或至少〇·〇〇1克之沸程分佈在〇.101MPa下介於2〇〇。〇和3〇〇 °C之間的烴;至少0.001克,至少〇 〇〇5克,或至少〇 〇1 克之沸程分佈在0.101 MPa下介於300°C和40(TC之間的 烴;及至少0.001克,至少0.005克,或至少〇 〇1克之沸 程分佈在0.101 MPa下介於400°C和650°C之間的烴。 劣質原油在每克劣質原油中可包含··至少0.001克, 至少0.005克,或至少0.01克之沸程分佈在o.ioi MPa下Hydrocarbons between 90 C and 200 ° C; a boiling range distribution of at least 0.001 g, at least 0.05 g, or at least 0.001 g between 2000 and 0.0001 MPa. Hydrocarbons between 0 ° C and 300 ° C; hydrocarbons with a boiling range distribution of at least 0.001 g, at least 0.05 g, or at least 0.001 g between 300 ° C and 40 ° C at 0.101 MPa; And at least 0.001 grams, at least 0.005 grams, or at least 0.001 grams of hydrocarbons with a boiling range distribution between 0.1 ° C and 650 ° C at 0.101 MPa. Inferior crude oil may contain at least 0.001 per gram of inferior crude oil Grams, at least 0.005 grams, or at least 0.01 grams of boiling range distribution at o.ioi MPa

最多為100°C的烴;至少0.001克,至少0.005克,或至少 〇·〇1克之沸程分佈在〇·1〇1 MPa下介於100°C和200°C之間 的烴;至少0.001克,至少〇·〇〇5克,或至少〇·〇1克之沸 程分佈在0.101 MPa下介於200°C和300°C之間的烴;至少 0·001克,至少0.005克,或至少0·01克之沸程分佈在0·101 MPa下介於30(TC和400°C之間的烴;及至少0·0〇1克,至 少0.005克,或至少〇·〇1克之沸程分佈在0·101 MPa下介 於400°C和650°C之間的烴。 除了較高沸點的成分之外,若干劣質原油在每克劣質 原油中可包含至少〇·〇〇1克,至少0·005克,或至少0·01 52 200532010 克之沸程分佈在0.101 MPa下最多為100°c的烴。典型而 言,劣質原油在每克劣質原油中具有最多為0.2克或最多 為〇. 1克的這類烴含量。 若干劣質原油在每克劣質原油中可包含至少0.001 克,至少0.005克,或至少0.01克之沸程分佈在0.101 MPa 下至少為2 0 0 °C的煙。 若干劣質原油在每克劣質原油中可包含至少0.001 克’至少0.005克,或至少0.01克之沸程分佈至少為650 °c的烴。 可使用本文中所述方法處理的劣質原油實例包括,但 不限於來自世界下列地區的原油·· U.S. Gulf Coast和 southern California、Canada Tar sands、Brazilian Santos and Campos basins、Egyptian Gulf of Suez、Chad、United Kingdom North Sea、Angola Offshore、Chinese Bohai Bay、 Venezuelan Zulia、Malaysia 及 Indonesia Sumatra。 處理劣質原油可增進劣質原油的性質以便使該原油可 為輸送及/或處理所接受。 本文中欲處理的原油及/或劣質原油稱為‘‘原油進料,,。 此原油進料可如本文中所述的蒸餘原油。如本文中所述之 由處理原油進料所得的原油產物通常適用於输送及/或處 理。如本文中所述生產的原油產物性質比原油進料更接近 西德州中級原油的對應性質,或是比原油進料更接近布倫 特(Brent)原油的對應性質,藉此提高原油進料的經濟價 值。這類原油產物可用較少或不用預處理精煉,藉此提高 53 200532010 $予員處理可包括脫硫、脫金屬及/或常壓蒸餾以 除雜質。 '根據本明處理原油進料可包括在接觸區及/或結合兩 個或更多個接觸區中使原油進料與觸媒接觸。在接觸區 中,,油進料的至少一種性質與該原油進料的同樣性質相 比可錯亥原油進料與一或多種觸媒的接觸而改變。於若 干^只例中,在氫源存在下進行接觸。於若干具體實例 中,虱源為在特定接觸條件下反應而對原油 物提供相當少量氫的-或多種烴。 ° 圖1為接觸系統1〇〇的簡圖,其包含接觸區1〇2。原 油進料經由導管104進入接觸區102。接觸區可為反雇哭、 反f器之一部分、反應器之多個部分,或其組合。接觸區 白:员例包括堆疊床反應器、固定床反應器、㈣床反應器、 ㈣授拌槽式反應器⑺咖”卜流化床反應^喷霧反應 Z ’及液/液接觸器。於特定具體實例中,接觸系統係位於 或連接到近海設備。在接觸系統100中’原油進料與觸媒 的接觸可為連續或分批法。 此接觸區可包含一或多種觸媒(例如兩種觸媒)。於若 干具體貫例中,原油進料與兩種觸媒之第一種觸媒的接觸 可減少該原油進㈣TAN。已減少TAN的原油進料與第 —種觸媒的後續接觸係減少雜原子含量並增加API比重。 在其他具體實射,在原油料與—或多種觸媒接觸之 後,原油進料之TAN、黏度、Nl/V/Fe含量、雜原子含量、 殘留物含量、API比重,或是這些性質的組合與該原油進 54 200532010 料的同樣性質相比會改變至少1〇%。 ,特定具體實例中,接觸(I中的觸媒體積在10至60 月丑積/〇 ’ 2G至50體積%,或3()至4Q體積%之接觸區中原 油進料總體積的範圍内。於若干具體實例巾,觸媒和原油 進料的漿液在接觸區的每1〇〇克原油進料中可包含〇顧 克〇·005至5克,或〇.〇1至3克的觸媒。 尸接觸區中的接觸條件可包括,但不限於溫度、壓力、 氫源流動、原油進料流動’或其組合。控制若干具體實例 中的接觸條件以生產具有特性的原油產物。接 度可分佈在50至職,6〇至赠,7〇至_,或8〇 至42〇C的範圍。接觸區中的壓力可分佈在(M至20MPa’ ;二咖’4至1〇心或6至8略的範圍。原油進 枓,的LHSV通常分佈在0.1至3〇11-1,〇.5至2511-1’1至20 中,LHSV 15广、’或2至10 h 1的範圍。於若干具體實例 中LHSV至少為5 h-1,至少為! j 1,$丨 至少為2〇h' 至^為旧,至少為15h·、或 在氫源以氣體(例如氫氣)供應的具體實例中,氣能氫 =原:5進料的比率典型而言分佈在。.…二 N二广°,_ _,1 至 8,_ Nm、3, 2 至譯 , 至 3,000 NmVm3 ’或 10 至 800 Nm3/m3 斑觸媒 並It':氫源於若干具體實例中係與載送氣體結合 且==過接觸區。載送氣體可例如為氮、氣,及/或 飞載达乳體可促進接觸區中的原油進料流動 動。載送氣體亦可增進接觸區中的 5 瓜 1下用。於若干具體 55 200532010 二例中,氬源(例如氫、甲烷或乙烷)可用來作為載送氣體 並且再循環通過接觸區。 ^虱源可與導管104中的原油進料並流或經由導管106 分別進入接觸區102。於接觸區10”,原油進料與觸媒 的接觸係產生含有原油產物,而在若干具體實例中含有氣 體的總產物。於若干具體實例中,載送氣體係與原油進料 或在V s 1 06中與氫源結合。總產物可離開接觸區1 經由導管110進入分離區108。Hydrocarbons up to 100 ° C; at least 0.001 grams, at least 0.005 grams, or at least 0.001 grams of hydrocarbons with a boiling range distribution between 0.1 ° C and 200 ° C at 0.11 MPa; at least 0.001 Grams, at least 0.005 grams, or at least 0.001 grams of hydrocarbons with a boiling range distribution between 200 ° C and 300 ° C at 0.101 MPa; at least 0.001 grams, at least 0.005 grams, or at least 0.01 grams boiling range distribution of hydrocarbons between 30 ° C and 400 ° C at 0.101 MPa; and at least 0.001 grams, at least 0.005 grams, or at least 0.001 grams boiling range distribution Hydrocarbons between 400 ° C and 650 ° C at 0 · 101 MPa. In addition to the higher boiling point components, several inferior crudes may contain at least 0.001 g, at least 0 per gram of inferior crude. · 005 grams, or at least 0. 01 52 200532010 grams of hydrocarbons with a boiling range distribution of up to 100 ° C at 0.101 MPa. Typically, inferior crude oil has a maximum of 0.2 grams or a maximum of 0.1 per gram of inferior crude oil. The content of such hydrocarbons in grams. Several inferior crude oils may contain at least 0.001 grams, at least 0.005 grams, or at least 0.01 grams of boiling range distribution below 0.101 MPa per gram of inferior crude oil. Smoke at 200 ° C. Several inferior crude oils may contain at least 0.001 grams of at least 0.005 grams per gram of inferior crude oil, or at least 0.01 grams of hydrocarbons having a boiling range distribution of at least 650 ° C. The methods described herein may be used Examples of inferior crudes processed include, but are not limited to, crudes from the following regions of the world: US Gulf Coast and southern California, Canada Tar sands, Brazilian Santos and Campos basins, Egyptian Gulf of Suez, Chad, United Kingdom North Sea, Angola Offshore, Chinese Bohai Bay, Venezuelan Zulia, Malaysia, and Indonesia Sumatra. Dealing with inferior crude oil can enhance the properties of inferior crude oil so that the crude oil can be accepted for transportation and / or processing. The crude oil and / or inferior crude oil to be processed herein is referred to as "" Crude feed, This crude feed can be a distillate as described herein. Crude products obtained from processing a crude feed as described herein are generally suitable for transportation and / or processing. As described herein The properties of the produced crude oil products are closer to the corresponding properties of West Texas Intermediate crude oil than crude oil feed, or Closer to the corresponding properties of Brent (Brent) crude oil, thereby increasing the economic value of the crude feed. This type of crude oil product can be refined with little or no pretreatment, thereby increasing the amount of 53 200532010 $ to the staff. Treatment can include desulfurization, demetallization and / or atmospheric distillation to remove impurities. 'Processing a crude oil feed in accordance with the present invention may include contacting the crude oil feed with a catalyst in a contact zone and / or a combination of two or more contact zones. In the contact zone, at least one property of the oil feed may be changed compared to the same property of the crude feed by contacting the crude feed with one or more catalysts. In several examples, the contact was performed in the presence of a hydrogen source. In several specific examples, the lice source provides a relatively small amount of hydrogen-or hydrocarbons to crude oil in order to react under specific exposure conditions. ° Figure 1 is a simplified diagram of a contact system 100, which includes a contact area 102. The crude oil feed enters the contact zone 102 via a conduit 104. The contact area may be an anti-cry, a part of a reactor, multiple parts of a reactor, or a combination thereof. Contact zone: Examples include stacked-bed reactors, fixed-bed reactors, 反应 bed reactors, ㈣ stirred tank reactors, ⑺Ca ”, fluidized bed reactions ^ spray reactions Z ′, and liquid / liquid contactors. In a specific embodiment, the contact system is located or connected to offshore equipment. In the contact system 100, the contact of the crude oil feed with the catalyst may be a continuous or batch process. This contact zone may contain one or more catalysts (eg Two catalysts). In several specific examples, the contact of the crude oil feed with the first catalyst of the two catalysts can reduce the crude oil feed into the TAN. The crude oil feed that has been reduced with the TAN and the first catalyst Subsequent contact is to reduce the heteroatom content and increase the specific gravity of the API. In other specific shots, after the crude oil is contacted with-or more catalysts, the TAN, viscosity, Nl / V / Fe content, heteroatom content, and residue of the crude oil feed Material content, API specific gravity, or a combination of these properties will change by at least 10% compared to the same properties of the crude oil feed 54 200532010. In certain specific examples, the contact (the contact media in I is between 10 and 60 months). Ugly product / 〇 '2G to 50% by volume, 3 () to 4Q% by volume of the total volume of crude oil feed in the contact zone. In some specific examples, the slurry of catalyst and crude oil feed may be included in each 100 grams of crude oil feed in the contact zone. Gu Ke 0.005 to 5 grams, or 0.01 to 3 grams of catalyst. The contact conditions in the dead zone may include, but are not limited to, temperature, pressure, hydrogen source flow, crude oil feed flow ', or a combination thereof. Control the contact conditions in several specific examples to produce characteristic crude oil products. The connection can be distributed in the range of 50 to 60, 60 to gift, 70 to _, or 80 to 42 C. The contact area The pressure can be distributed in the range of (M to 20MPa '; Erca' 4 to 10 cents or 6 to 8). Crude oil is imported, and the LHSV is usually distributed in the range of 0.1 to 3011-1, 0.5 to 2511-1 '1 to 20, LHSV 15 wide,' or 2 to 10 h 1 range. In some specific examples, LHSV is at least 5 h-1, at least! J 1, $ 丨 at least 2 0h 'to ^ is Old, at least 15h ·, or in specific examples where the hydrogen source is supplied as a gas (such as hydrogen), the ratio of gaseous hydrogen = original: 5 feed is typically distributed in ... Wide °, _ _, 1 to 8, _ Nm, 3, 2 to English, to 3,000 NmVm3 'or 10 to 800 Nm3 / m3 spot catalyst and It': Hydrogen is derived from several specific examples in combination with a carrier gas And == over-contact zone. The carrier gas can be, for example, nitrogen, gas, and / or airborne milk can promote the flow of crude oil feed in the zone of contact. The carrier gas can also increase the amount of 5 in the zone of contact. In some specific cases, the source of argon (such as hydrogen, methane or ethane) can be used as a carrier gas and recycled through the contact zone. The lice source may enter the contact zone 102 in parallel with the crude oil feed in the conduit 104 or via the conduit 106, respectively. In the contact zone 10 ", the contact system of the crude oil feed with the catalyst produces a total product containing crude oil products, and in some specific examples gas. In several specific examples, the carrier gas system and the crude oil feed or at V s 1 Combined with a hydrogen source in 06. The total product can leave the contact zone 1 and enter the separation zone 108 via the conduit 110.

\於分離區108巾,原油產物和氣體可使用一般已知的 勿離技術,例如氣-液分離,自總產物分離。原油產物可婉 由導管U2離開分離1 1〇8,;妾著輸送到輸送載具、管線、 儲存容器、精煉廠、其他處理區,或其組合。氣體可包括 處理期間所生成的氣體(例如硫化氫、二氧化碳,及/或一 氧化幻、過量氣態氫源,及/或載送氣體。過量氣體可再 騎至接觸t统⑽’可純化,輸送到其他處理區、儲存 容器,或其組合。 於若干具體實例中 產物係於兩個或更多個 生成原油產物和氣體。 ’使原油進料與觸媒接觸以生產總 接觸區内進行。可分離該總產物以In the separation zone 108, crude oil products and gases can be separated from the total product using generally known inseparable techniques, such as gas-liquid separation. Crude oil products may be separated by conduit U2 and separated by 108, and transported to transportation carriers, pipelines, storage containers, refineries, other processing areas, or a combination thereof. Gases may include gases generated during the process (such as hydrogen sulfide, carbon dioxide, and / or nitric oxide, excess gaseous hydrogen sources, and / or carrier gas. Excess gas may be re-ridden until contact with the system, can be purified, transported To other processing zones, storage containers, or a combination thereof. In several specific examples, the product is produced in two or more crude oil products and gases. 'Contacting the crude feed with the catalyst to produce a total contact zone can be performed. Isolate the total product to

圖2至3為包含兩個或二姻技Figures 2 to 3 contain two or two marriage techniques

飞一彳固接觸區的接觸系統1 0CContact system for flying contact area 1 0C

具體實例的簡圖。在圖2A知:)R A和2B中,接觸系統100包# 觸區102和114。圖3A和3B白人4立扣 β 3。接觸區 102、1 14、11 在圖2Α和3Α中’接觸區1〇2 』匕ίυ2、114、ΐι6係描繪成在_ 反應器中的個別接觸區。眉、%推Μy 原油進枓係經由導管1 04進7 56 200532010 觸區102。 於若干具體實例中’載送氣體切f 1()6巾與氣源站 合並且以混合物的形式導入接觸區。於特定具體實例中 如圖卜从和3B所示者,氣源及/或載送氣體可經由” H)6及/或經由如導管1Q6,以原油進料流動相反的方向,鱼 原油進料分料人—或多個接觸區。與原油進料流動反= 添加氫源及/或載送氣體可增進原油進料與觸媒 或接觸。 〇及/ 在接觸H 102巾’原油進料與觸媒的接觸會生成原料 ^此原料流係由接角㈣102流到接觸區ιΐ4。在圖 3B中,原料流係由接觸區U4流到接觸區H6。 一接觸區102、114、116可包含_或多種觸媒。如圖扣 所示’原料流係經由導t 118離開接駭1〇2而進入 區m。如圖3B所示’原料流係經由導管ιΐ8離開接觸區 1 14而進入接觸區丨丨6。 原料流可在接觸區114及/或接觸區116與附加觸 觸以生成總產物。總產物離開接觸區114及/或接觸區⑴ 經由導管no進人分離區1G8。原油產物及/或氣體係分離 自總產物。原油產物係經由導管112離開分離區1〇8。 圖4為分離區在接觸系統⑽上游之具體實例的簡圖。 劣質原油(蒸餘或非蒸餘者)係經由導管122 *入分離區 120。在分離區 ΐ2〇Φ,:τ, Π 至乂 一部分的劣質原油係使用該 項技術中已知的技術(你丨4為 入 T(例如贺佈、薄膜分離、減壓)分離以 生產原油進料。舉例而+ 牛W而3 ,水可從劣質原油中至少部分分 57 200532010A simplified diagram of a specific example. As shown in FIG. 2A :) In R A and 2B, the contact system 100 includes the contact areas 102 and 114. Figures 3A and 3B. Contact areas 102, 1 14, 11 In Figures 2A and 3A, the 'contact area 102' is depicted as individual contact areas in the reactor. Eyebrows and crude oil are fed into the area 102 through the conduit 1 04 to 7 56 200532010. In several specific examples, the 'carrying gas cut f 1 () 6 towel stands with the gas source and is introduced into the contact area as a mixture. In certain specific examples, as shown in Figs. 3 and 3B, the gas source and / or carrier gas can be passed through the "H) 6 and / or via the conduit 1Q6, in the opposite direction of the crude oil feed flow, the fish crude oil feed Distributor—or multiple contact zones. Reverse flow of crude oil feed = Addition of hydrogen source and / or carrier gas can promote crude oil feed with catalyst or contact. 〇 and / In contact with H 102 towels, crude oil feed and The contact of the catalyst will generate raw materials ^ This raw material stream flows from the contact angle ㈣102 to the contact zone ιΐ 4. In Figure 3B, the raw material stream flows from the contact zone U4 to the contact zone H6. A contact zone 102, 114, 116 may include _ Or multiple catalysts. As shown in the figure, the 'raw material flow leaves the receiving area 102 through the guide t 118 and enters the area m. As shown in FIG. 3B' the raw material flow leaves the contact area 1 14 through the conduit 8 and enters the contact. Zone 丨 丨 6. The raw material stream may be in additional contact with the contact zone 114 and / or the contact zone 116 to generate a total product. The total product leaves the contact zone 114 and / or the contact zone 进 enters the separation zone 1G8 via a conduit no. Crude product And / or the gas system is separated from the total product. The crude product leaves the separation zone 108 via a conduit 112. Fig. 4 is a simplified diagram of a specific example of the separation zone upstream of the contact system 。. Inferior crude oil (distilled or non-distilled) is introduced into the separation zone 120 via the conduit 122. In the separation zone ΐ2Φ ,: τ, Π to乂 A part of the inferior crude oil is separated using a technique known in the technology (such as Hebu, membrane separation, and decompression) to produce crude oil feed. For example, + cattle W and 3, water can be At least partly from inferior crude oil 57 200532010

離。於另一實例中,具有沸程分佈低於951或低於i〇(TC 的成7刀可從劣質原油中至少部分分離以生產原油進料。於 若干具體實例中,至少一部分的石腦油及比石腦油更具揮 發性的化合物係從劣質原油中分離。於若干具體實例中, 至少一部分經過分離的成分係經由導管124離開分離區 120。from. In another example, a knife having a boiling range distribution below 951 or below 10 ° C can be at least partially separated from inferior crude oil to produce a crude feed. In several specific examples, at least a portion of naphtha And compounds that are more volatile than naphtha are separated from inferior crude oil. In some specific examples, at least a portion of the separated components leave the separation zone 120 via the conduit 124.

由分離區120所得到的原油進料於若干具體實例中係 ^含沸程分佈至少$ 1〇(rc,或於若干具體實例中,沸程 刀佈至夕為120 c之成分的混合物。典型而言,經過分離 的原油進料包含沸程分佈介於100至1000 〇c,120至9〇〇 C,或200至8〇〇 t之成分的混合物。至少一部分的原油 進料經由導管126離開分離區120進入接觸系統(參見 如圖1至3中的接觸區)以進一步處理生成原油產物。於若 干具體實例中,分離區12〇可位於脫鹽單元的上游或下游。 處理之後,原油產物係經由導管"2離開接觸系統1〇〇。 於若干具體實例中,使原油產物與原油進料相同或 同的1油摻合。舉例而言,原油產物可與具有不同黏度 原油結合’藉此產生具有黏度介於該原油產物黏度與該 由J度之間的摻合產品。於另一實例中,原油產物可與 有不同TAN白勺原、油摻合,藉此產生具有介於該原 產物與該原油ΤΑΝ之間的產品。此摻合產品可適用 及/或處理。 'The crude oil feed obtained from the separation zone 120 is, in some embodiments, a mixture of components having a boiling range distribution of at least $ 10 (rc, or in some embodiments, the boiling range knife cloth to 120 c. Typical. In terms of separation, the separated crude oil feed comprises a mixture of components having a boiling range distribution of 100 to 1000 OC, 120 to 900 C, or 200 to 800 t. At least a portion of the crude oil feed leaves via conduit 126 The separation zone 120 enters the contact system (see the contact zone in Figures 1 to 3) for further processing to produce crude oil products. In several specific examples, the separation zone 120 may be located upstream or downstream of the desalination unit. After the treatment, the crude oil product is Exit the contact system 100 via a conduit " 2. In several specific examples, the crude oil product is blended with the same or the same oil as the crude oil feed. For example, the crude oil product can be combined with crude oil having different viscosities. A blended product having a viscosity between the viscosity of the crude product and the degree of origin is produced. In another example, the crude product may be blended with raw materials and oils with different TANs, thereby producing a product having a viscosity between Produce Between the product and the crude TAN. This blended product may be suitable and / or processed. '

如圖5所示, 104進入接觸系 於特定具體實例中,原油進料係經由 統100,而至少一部分的原油產物經 導 由 58 200532010 導官128離開接觸系統1〇〇導入摻合區13〇。於摻合區 中,使至少一部分的原油產物與一或多個工業生產液流(例 如烴流,如分離一或多種原油進料所產生的石腦油)、原油、 原油進料,或其混合物結合以產生摻合產品。將工業生產 液流、原油進料、原油,或其混合物經由導管132直接導 入摻合區1 30或這類摻合區的上游。混合系統可位於或接 近摻合區130。摻合產品可符合精煉廠及/或輸送載具所指 定的產品規格。產品規格包括,但不限於Αρι比重、ταν、As shown in FIG. 5, 104 enters the contact system in a specific embodiment, and the crude oil feed is via system 100, and at least a part of the crude product is guided by 58 200532010, and the director 128 leaves the contact system 100 and is introduced into the blending zone 13. . In the blending zone, at least a portion of the crude oil product is combined with one or more industrial production streams (eg, hydrocarbon streams such as naphtha produced by separating one or more crude feeds), crude oil, crude feeds, or The mixtures are combined to produce a blended product. Industrial production streams, crude feeds, crude oil, or mixtures thereof are directed via conduit 132 into blending zone 130 or upstream of such blending zone. The mixing system may be located at or near the blending zone 130. The blended product can meet the product specifications specified by the refinery and / or conveyor. Product specifications include, but are not limited to, Αρι specific gravity, ταν,

黏度,或其組合的範圍或限制。摻合產品係經由導管Η# 離開摻合區1 30以進行輸送或處理。 在圖6中,劣質原油係通過導管122進入分離區, 如先前所述使劣質原油分離以生成原油進料。原油進料接 著通過導f m進入接觸系統1〇〇。該劣質原油的至少若 干成分係經由導管124離開分離區12〇。至少一部分的原 油產物係經由導管128離開接觸系統1〇〇進入摻合區 其他工業生產液流及/或原油係直接或經由導管132進入摻Viscosity, or range or limit of combinations. The blended product leaves the blending zone 1 30 for delivery or processing via a catheter ##. In FIG. 6, the inferior crude oil is introduced into the separation zone through the conduit 122, and the inferior crude oil is separated to generate a crude oil feed as previously described. The crude oil feed then enters the contact system 100 through the guide fm. At least some of the components of the inferior crude oil leave the separation zone 120 via the conduit 124. At least a portion of the crude oil product exits the contact system 100 via the conduit 128 and enters the blending zone. Other industrial production streams and / or crude oil enter the blending directly or via the conduit 132.

合區130與原油產物結合生成摻合產品。摻合產品係經由 導管1 3 4離開摻合區1 3 〇。 於若干具體實例中,原油產物及/或推合產品係輸送到 精煉廠及/或處理設備。原油產物及/或摻合產品可加工以 生f工業產品,如運輸用燃料、加熱用燃料、#滑由或化 子°°。加工可包括蒸餾及/或分餾原油產物及/或摻合產品 以產生I多種鶴分。於若干具體實例中,原油產物、推 合產品,及/或—或多種餾分可加氫處理。 ’ 59 200532010 於若干具體實例中,原油產物具有TAN最多為9〇%, 最多為鄕,最多為30%,或最多& 1〇%之原油進料的 TAN。於若干具體實例中’原油產物具有則在!至80%, ^至7〇% ’ 30至6〇%,或至50%之原油進料的TAN之 軏圍内。於特定具體實例中,原油產物具有最多為卜最 多為〇·5,最多為0.3,最多為〇2,最多為〇1,或最多為 〇.〇5的TAN。原油產物的TAN通常至少為〇_卜更常 見者’至少為G.GG1。於若干具體實例中,原油產物的tan 可在0.001至0.5,〇 〇1至〇 2,或〇 〇5至〇」的範圍内。The combined zone 130 is combined with the crude product to produce a blended product. The blended product exits the blended zone 130 via a conduit 134. In some specific examples, crude oil products and / or push products are delivered to refineries and / or processing equipment. Crude products and / or blended products can be processed to produce industrial products, such as transportation fuels, heating fuels, skimmers or chemicals. Processing may include distilling and / or fractionating the crude product and / or blending the product to produce more than one crane fraction. In several specific examples, crude products, push products, and / or multiple fractions may be hydrotreated. ′ 59 200532010 In several specific examples, the crude oil product has a TAN of up to 90%, up to 鄕, up to 30%, or up to & 10% of the TAN of the crude oil feed. In several specific examples, the 'crude product' has To 80%, ^ to 70% ′ 30 to 60%, or within 50% of the TAN of the crude oil feed. In certain specific examples, the crude oil product has a TAN of at most 0.5, at most 0.3, at most 02, at most 01, or at most 0.05. The TAN of the crude product is usually at least 0. More commonly, 'is at least G.GG1. In several specific examples, the tan of the crude product can be in the range of 0.001 to 0.5, 0.001 to 0.02, or 005 to 0 ".

於若干具體實例中,原油產物具有總Ni/V/Fe含量最 =為90%,最多為5G%,最多為1()%,最多為外,或最 多為3%之原油進料的Ni/V/Fe含量。此原油產物於若干具 奴只例中具有總Ni/V/Fe含量在1至8〇%,1〇至7〇%,2〇In some specific examples, crude oil products have a total Ni / V / Fe content of 90%, 5G% at most, 1 ()% at most, Ni / Vout at most, or 3% of crude oil feed. V / Fe content. This crude oil product has a total Ni / V / Fe content of 1 to 80%, 10 to 70%, and 20% in several slaves.

至6〇%,或30至50%之原油進料的Ni/V/Fe含量之範圍内。 於特定具體實例中,原油產物在每克原油產物中具有在lx 克至 5 X 1〇 克’ 3 χ 1〇-7 克至 2 X ι〇 5 克,或 1 X 1〇 6 克至1 X 10-5克之範圍内的總Ni/v/Fe含量。於特定具體實 ::,此原油含有最多為2 χ 1〇·5克的Ni/V/Fe。於若干具 月且只例中,原油產物的總Ni/V/Fe含量為7〇至 至120%或90至ι1〇%之原油進料的Ni/v/Fe含量。 若干八肢' 只例中’原油產物具有有機酸金屬鹽形態 的金屬總含量最多&列%,最多為5G%,最多為10%,或 =夕為5%之原《由進料中有機酸金屬鹽形態的金屬總含量。 钐定具κ例中,原油產物具有有機酸金屬鹽形態的金 60 200532010 屬總含里在1至80%’ 1〇至70%’ 20至60%’或30至50% 之原油進料中有機酸金屬鹽形態的金屬總含量之範圍内。 常用來生成金屬鹽的有機酸包括,但不限於羧酸、硫醇、 亞胺、磺酸和磺酸鹽。羧酸的實例包括,但不限於環烷酸、 菲酸和苯曱酸。金屬鹽的金屬部分可包括鹼金屬(例如鋰、 鈉和鉀),鹼土金屬(例如鎂、鈣和鋇),第丨2攔金屬(例如 鋅和錢)’第1 5欄金屬(例如坤),第6欄金屬(例如鉻),或 其混合物。To 60%, or 30 to 50% of the Ni / V / Fe content of the crude feed. In a specific embodiment, the crude oil product has from 1x grams to 5 X 10 grams' 3 x 10-7 grams to 2 X ι05 grams per gram of crude oil product, or 1 X 106 grams to 1 X Total Ni / v / Fe content in the range of 10-5 grams. In a specific embodiment ::, this crude oil contains up to 2 x 10.5 g of Ni / V / Fe. In several months and by way of example only, the total Ni / V / Fe content of the crude product is 70 to 120% or 90 to 10% of the Ni / v / Fe content of the crude feed. In some examples, the total content of metals in the form of organic acid metal salt in crude oil products is the most & column%, the maximum is 5G%, the maximum is 10%, or = 5% of the original "Organic from feed Total metal content in the form of an acid metal salt. In the case of κ, the crude oil product has the form of a metal salt of organic acid 60 200532010 The total content is 1 to 80% '10 to 70% 20 to 60%' or 30 to 50% of the crude oil feed The total metal content in the form of a metal salt of an organic acid. Organic acids commonly used to form metal salts include, but are not limited to, carboxylic acids, thiols, imines, sulfonic acids, and sulfonates. Examples of carboxylic acids include, but are not limited to, naphthenic acid, phenanthronic acid, and phenylarsinic acid. The metal part of the metal salt may include alkali metals (such as lithium, sodium, and potassium), alkaline earth metals (such as magnesium, calcium, and barium), metals (such as zinc and money), and metals (such as zinc) , Column 6 metals (such as chromium), or mixtures thereof.

〜符疋具體貫例中,原油產物在每克原油產物中具 有機酸金屬鹽形態的金屬總含量為在每克原油產物中 00001 克至 〇 00005 克,〇 000Q003 克至 0 00002 克 〇⑻〇 1克至〇·〇⑼〇 1克的有機酸金屬鹽形態之金屬 :圍内於右干具體貫例中,原油產物之有機酸金屬鹽 態的金屬總含量為70至13〇%,8〇至12〇%,或9〇至 之原油進料中有機酸金屬鹽形態的金屬總含量。 觸所:特疋具體貫例中’在接觸條件下原油進料與觸媒:~ In the specific examples, the total content of the metal in the form of organic acid metal salt per gram of crude oil product is from 0,001 grams to 00005 grams, and 0000Q003 grams to 0,000 grams per gram of crude oil products. 1 gram to 0.000 gram of metal in the form of a metal salt of an organic acid: In the specific example of the right-hand dry wall, the total metal content of the metal salt of the organic acid in the crude product is 70 to 13%, 8 To 120%, or 90% to the total metal content of organic acid metal salt in the crude oil feed. Contact: In the specific example of the specific example, ’crude oil feed and catalyst under contact conditions:

^生產的原油產物之API比重為70至i3Q%,8〇 i20/〇,90 至 110%,或 1〇〇 -^ The API gravity of the crude product produced is 70 to i3Q%, 80i20 / 〇, 90 to 110%, or 100-

王1 之原油進料的API I :特定具體實例中,原油產物 1 …或 16至25。 ^4 14^40 於特定具體實例中,;5《 最多為f^。/ ^ 、,物/、有黏度最多為90%, 夕為80/〇,或最多$ 7〇%之API 1 of King 1's crude oil feed: In a specific embodiment, crude oil product 1… or 16 to 25. ^ 4 14 ^ 40 In certain specific examples, 5 <at most f ^. / ^,, / / Have a viscosity of up to 90%, evening is 80 / 〇, or up to $ 70%

體實例中,;5a d ,、進科的黏度。於若干J 或3〇Γ 物具有黏度在心帆,2()至50%, 次30至術之原油進料 乾阗内。於若干具體實 61 200532010 例中’原油產物的黏 士,^ #從取多為90%之原油進料的黏度,同 日守此原油產物的API比重為7G至麵, 财二%之原油進料的Αρι比重。 或 為若=體實例巾,原油產物具有雜原子總含量最多 ,最多為,或最多為5%之原油 進料的原子确今吾 雜原子總含量:;特定具體實例中’原油產物具有 至少為_之,二:,至少為3°%,至少為8〇%,或 κ 4 原,由進枓的雜原子總含量。 於若干具體實例中,原油產 90%,最多為5〇%, 里J月匕取夕為 的含炉量。於胜 夕為1〇%,或最多為5%之原油產物 為以,至少為3〇%,至原油產物具有含硫量至少 至夕為80%,或至少a Q()0/ 進料的含硫量。於若干 戈至&quot;為99/。之原油 70至130。/ qa —貫1j中,原油產物的含硫量為 硫量。 一 至U0/❹之原油進料的含 於若干具體實例中, 9〇〇/ , - ^ ^ 〇 ,、油產物的總含氮量可能最多為 9〇/。,取多為80%,最多為1〇% 取夕马 的總含氮量。於特定且體 ;取夕'、、、5%之原油進料 ^ f , ®月例中,原油產物具有洎含焉旦 至少為1%,至少為30%,至少為8〇〇/ /、有,,心3氮里 原油進料的總含氮量。 或至少為99%之 於若干具體實例中,原油產物的 為95%,最多為㈣,最 ^里了此取多 Λ ,0/ ^ ^ 為50/〇,攻多為】〇%,或最吝 匕5/。之原油進料的驗性氯含量。於 取: ㈣具有驗性氮含量至,至少為二少為原 200532010 80%,或至少為 …°之原油進料的鹼性氮含量。 灰右干具體實例 9〇%,最多為50%一 產物的含氧量可能最多為 ° 取多為30%,最多為lf)0/,式#夕炎 5%之原油進料的含 取夕4 10/。,或取多為 有含氧量至少》。於衫具體實例中,原油產物具 為99%之h 至少為30%,至少為80%,或至少 马y y /〇之原油進料的 物的含氧量在…吖二於若干具體實例中,原油產 鳩之原油進料的含!^曰G至7G%,2G至6G%,或30至In the physical example, 5a d, the viscosity of the department. In some J or 〇Γ objects have viscosity in the heart sail, 2 () to 50%, 30 to the crude oil feed dry. In some specific examples, 61 200532010, the stickiness of crude oil products, ^ #From the viscosity of 90% of the crude oil feed, the API proportion of this crude product on the same day was 7G, and the crude oil feed was 2%. The specific gravity of Aρι. Or if it is a specific example, the crude oil product has the largest total heteroatom content, at most, or a maximum of 5% of the atomic total crude heteroatom content of the crude oil feed: in a specific embodiment, the crude oil product has at least Among them, at least: 3 °%, at least 80%, or κ 4 proton, from the total content of heteroatoms. In some specific examples, the crude oil production is 90%, and the maximum is 50%. The crude oil product at Shengxi is 10%, or at most 5%, at least 30%, until the crude oil product has a sulfur content of at least 80%, or at least a Q () 0 / Sulfur content. In a few Gezhi "quote is 99 /. Crude oil 70 to 130. / qa — In 1j, the sulfur content of crude oil products is the sulfur content. The crude oil feed from 1 to U0 / ❹ is included in several specific examples, 900 /,-^^, and the total nitrogen content of the oil product may be up to 90 /. The maximum nitrogen content is 80% and the maximum is 10%. In a specific system; take the crude oil feed ^ f, 5%, in the monthly example, the crude oil product has a content of at least 1%, at least 30%, at least 800 //, The total nitrogen content of the crude oil feed in Xin 3 nitrogen. Or at least 99%. In some specific examples, the crude oil product is 95%, the maximum is ㈣, the maximum is Λ, 0 / ^ ^ is 50 / 〇, and the attack is】 0%, or the most. Dagger 5 /. The chlorine content of the crude oil feed. Take: ㈣ Have a test nitrogen content to, at least two less than the original 200532010 80%, or at least the basic nitrogen content of crude oil feed. Gray right dry concrete example is 90%, the maximum is 50%. The oxygen content of a product may be at most °, which is 30% at most, and at most lf) 0 /, formula #xiyan 5% crude oil feed 4 10 /. , Or take as much as having at least oxygen content. In the specific example of the shirt, the crude oil product has an oxygen content of 99%, at least 30%, at least 80%, or at least yy / 0 of the crude oil feed. The oxygen content in ... The crude oil production of the dove of crude oil contains! ^ G to 7G%, 2G to 6G%, or 30 to

..,.範圍内。於若干具體實例中, 原油產物的羧酸化合物 5〇%,最多為10%,或最:3二取“ 9。%,最多為 物含量。於特定呈體^/中為之原油進料中㈣酸化合 含量至少為”/5原油產物具有叛酸化合物總 ”、、0 ^為3〇%,至少為8〇%,或至少為99% 之原油進料中的羧酸化合物總含量。..,. Within range. In some specific examples, the carboxylic acid compound of the crude oil product is 50%, up to 10%, or up to 3: 9%, up to the material content. In the crude oil feed in a specific form ^ / The phosphonate compound content is at least "/ 5 crude oil products with total acid compounds", 0 ^ is 30%, at least 80%, or at least 99% of the total carboxylic acid compound content in the crude feed.

於若干具體實例中,可還原原油進料中的選定有機氧 化合物。於若干具體實例中,_及/或_金屬鹽可在含 非羧酸有機氧化合物之前使其化學還原。原油產物中含羧 酸與非羧酸的有機氧化合物可使用一般已知的光譜法(例如 紅外線分析、質譜分析’及/或氣相層析法)藉由分析原油 產物而鑑別。 此原油產物於特定且體f你丨φ 1 竹疋η篮具例中具有含氧量最多為 90%’最多為8G%,以為观,或最多4观之原油進 料的含氧量’而此原油產物的TAN最多為9〇%,最多為 70%’最多為50%,或最多為40%之原油進料的丁八/於 特定具體實例中,原油產物具有含氧量至少為ι%,至少 63 200532010 為30% ’至少為8〇%,或至少為㈧❹/❹之原油進料的含氧量, . 而此原油產物具有TAN至少$ ι%,至少為,至少為 80 /〇或至少為99〇/〇之原油進料的TAN。 此外,原油產物可具有羧酸及/或羧酸金屬鹽含量佔原 油進料最多為9〇%,最多為70%,最多為50%,或最多為 4〇/〇 3非羧酸有機氧化合物的含量是在70至130。/。,80 至120%,或90至11〇%之原油進料中含非羧酸有機氧化 合物的範圍内。 於右干具體貫例中,原油產物於其分子結構中包含每 _ 克原油產物有0·05至〇·15克或〇〇9至〇13克的氫。此原 油產物於其分子結構中可包含每克原油產物有〇 8至0.9 克或U2 i 〇·88克的碳。原油產物之原子氮和原子碳的 比(H/C)可在70至130%,80至120%,或90至110%之原 油進料的原子H/C比之範圍内。在1〇至3〇%之原油進料 的原子H/C比之範圍内的原油產物之原子H/c比係顯示出 在過耘中吸取及/或消耗的氫相當地少,及/或氫係現場生 產。 · 原油產物包含某個沸點範圍内的成分。於若干具體實 例中’原油產物在每克原油產物中包含:至少〇·〇〇 1克, 或0.001至〇·5克之沸程分佈在〇 下最多為^⑼它 的k,至少0.001克,或〇·〇01至〇 5克之沸程分佈在〇 1〇1 MPa下;丨於i〇〇c和200C之間的烴;至少0001克,或0001 至〇‘5克之沸程分佈在〇·ι〇1 MPa下介於2〇(Γ(:和3〇〇t:之 間的烴;至少〇·〇〇1克,或0·001至〇 5克之沸程分佈在〇1〇1 64 200532010 MPa下介於300°C和400°C之間的烴;及至少0.001克,或 0.001至0.5克之沸程分佈在o.ioi MPa下介於400〇C和538 °C之間的烴。 於若干具體實例中,原油產物在每克原油產物中包含 至少0.001克之沸程分佈在0.101 MPa下最多為l〇〇°C的烴 及/或至少0.001克之沸程分佈在〇1〇1 Mpa下介於i〇〇°c 和200°C之間的烴。In several specific examples, selected organic oxygen compounds in a crude oil feed can be reduced. In several specific examples, the _ and / or _ metal salt may be chemically reduced before the non-carboxylic acid-containing organic oxygen compound. Organic oxygen compounds containing carboxylic acids and non-carboxylic acids in crude oil products can be identified by analyzing the crude oil products using generally known spectroscopic methods (e.g., infrared analysis, mass spectrometry ', and / or gas chromatography). This crude oil product has a specific oxygen content of φ 1 in the bamboo case. It has an oxygen content of at most 90% 'and a maximum of 8G%. The TAN of this crude oil product is at most 90%, at most 70%, at most 50%, or at most 40% of the crude oil feed Ding Ba / In a specific embodiment, the crude product has an oxygen content of at least ι% , At least 63 200532010 is 30% 'at least 80%, or at least the oxygen content of the crude oil feed, and this crude oil product has a TAN of at least $ ι%, at least, at least 80/0 or The TAN of the crude oil feed is at least 99/0. In addition, crude oil products may have a carboxylic acid and / or metal carboxylic acid salt content of up to 90%, up to 70%, up to 50%, or up to 40/03 non-carboxylic organic oxygen compounds in the crude feed. The content is between 70 and 130. /. , 80 to 120%, or 90 to 110% of the crude oil feed contains non-carboxylic acid organic oxides. In the specific example of the right stem, the crude oil product contained in its molecular structure 0.05 to 0.15 g or 009 to 013 g of hydrogen per gram of crude oil product. This crude oil product may contain, in its molecular structure, 0.8 to 0.9 grams or U2i of 0.88 grams of carbon per gram of crude product. The atomic nitrogen to atomic carbon ratio (H / C) of the crude oil product may be in the range of 70 to 130%, 80 to 120%, or 90 to 110% of the atomic H / C ratio of the crude oil feed. The atomic H / c ratio of the crude oil product in the range of 10 to 30% of the atomic H / C ratio of the crude oil feed shows that relatively little hydrogen is absorbed and / or consumed during overworking, and / or Hydrogen-based on-site production. · Crude oil products contain components in a range of boiling points. In several specific examples, the 'crude oil product contains per gram of crude oil product: at least 0.0001 g, or a boiling range distribution of 0.001 to 0.5 g, and at most ^ its k, at least 0.001 g, or 〇01 ~ 05 grams of boiling range distribution at 010 MPa; 丨 hydrocarbons between 〇OOc and 200C; at least 0001 grams, or 0001 to 〇5 grams of boiling range distribution at 〇ι Hydrocarbons between 〇 (Γ (: and 300t :) at 〇1 MPa; at least 0.001 g, or 0.001 to 0.05 g boiling range distribution at 001 64 200532010 MPa Hydrocarbons between 300 ° C and 400 ° C; and hydrocarbons with a boiling range of at least 0.001 g, or 0.001 to 0.5 g, distributed between 400 ° C and 538 ° C at o.ioi MPa. In a specific example, the crude oil product contains at least 0.001 grams of boiling range distribution per gram of crude oil product, hydrocarbons of up to 100 ° C at 0.101 MPa and / or at least 0.001 grams of boiling range distribution between 0.101 MPa Hydrocarbons between 100 ° C and 200 ° C.

於若干具體實例中,原油產物在每克原油產物中可含 有至少0.001克,或至少0·01克的石腦油。在其他具體實 例中,原油產物可具有石腦油含量為每克原油產物中最多 〇·6克,或最多0.8克。 ν /工·々穴巧獨,刀言篁马 7ϋ 130〇/。’80至120%,或90至11〇%之原油進料的館分含量 原油產物的館分含量於每克原油產物中可在0 00_至( 克,0.001至0.3克,或0.002克至〇 2的範圍内。 於特定具體實例中,原油產物具有VG〇含量為%In several specific examples, the crude product may contain at least 0.001 grams, or at least 0.01 grams of naphtha per gram of crude product. In other specific examples, the crude product may have a naphtha content of up to 0.6 g, or up to 0.8 g, per gram of crude product. ν / Gong · Xiao acupoint cleverly, swordsmanship 7 篁 130〇 /. '80 to 120%, or 90 to 11% of the crude oil feed fraction content Crude oil fraction content per gram of crude oil product can be between 0 00_ to (g, 0.001 to 0.3 g, or 0.002 g to In the specific embodiment, the crude product has a VG content of%

r%,8G至厲,或9G至UG%之原油進料的VGO ^於W實例中,原油產物在每克原 請_至㈣克,,或〇〇〇2至二二 0.001至0.3克之範圍内的VG〇含量。 於若干具體實例中,原油產物具 ⑽,,至叫或9。至 :?里為… 量。此眉、、Α $ μ 1 ^ ^ 原油達科的殘留物4 =此原油產物可在每克原油產物令具有〇_ 克 至 0.5 克,〇._ 至 〇 · 凡υ.οοι至〇 3克, 65 200532010 0. 005至0.2克,或〇 〇1至〇1克之範圍内的殘留物含量。· 於知'疋具體實例中,原油產物具有MCR含量為7〇至 13 0%,80至120%,或9〇至110%之原油進料的Mcr含 量,同時此原油產物具有q瀝青質含量最多為9〇%,最多 為80%’或最多為5G%之原油進料的〜歷青質含量。於特 定具體實例中,原油進料的C5瀝青質含量至少為1〇%,至 少為60%’或至少&amp; 7〇%之原油進料的Cs遞青質含量,同 時,油產物的MCR含量在1〇至3〇%之原油進料的mcr 含罝之範圍内。於若干具體實例中,減少原油進料的q瀝參 青質含量且同時保持相對穩定的MCR含量可增加原油進 料/總產物混合物的穩定度。 於右干具體實例中,可結合Cs瀝青質含量和mcr含 1、 產生人原油進料中的尚黏度成分相比介於原油產物的 度成分之間的數學關係。舉例而言,原油進料之q瀝 青質含量和原油進料之MCR含量的和可表示為S。原油產 物之C5渥青質含量和原油產物之mcr含量的和可表示為 比較這些和(s,與s)以估算原油進料中高黏度成分的 籲 淨減少量1油產物的s’可在1至99%,10至90%,或20 一 之S的範圍内。於若干具體實例中,原油產物之mcr 含置和C5瀝青質含量的比在1〇至3·〇,1·2至2 〇,或1·3 至1 · 9的範圍内。 方、特疋具體實例中,原油產物具有MCR含量最多為 最夕為80%,最多為50%或最多為1〇%之原油進料 ' R S里。於若干具體實例中,原油產物具有MCR含 66 200532010 量在1至80%,10至70% ’ 20至60%,或3〇至5〇%之原 油進料的MCR含量之範圍内。原油產物於若干具於〒例 中在每克原油產物中含有0.0001至(M克,〇〇〇5至〇⑽ 克,或0.01至0.05克的MCR。 於若干具體實例中,原油產物在每克原油產物中包含 大於0克,但小於0.01克,0.000001至0.001克,或〇 〇⑻Μ 至0.0001克的觸媒總量。觸媒在輸送及/或處理期間可幫 助使原油產物穩定化。觸媒可抑制腐蝕,抑制摩擦,及/或 長:升原油產物的分水能力。可配置本文中所述的方法在户 理期間將本文中所述的一或多種觸媒添加至原油產物。 與接觸系統1 〇〇接觸所產生的原油產物具有和原、、由進 料性質不同的性質。這類性質可包括,但不限於:a)降低 TAN ; b)降低黏度;c)降低的總Ni/V/Fe含量;d)降低 的硫、氧、氮,或其組合之含量;e)降低的殘留物含量; 0降低的瀝青質含量;g)降低的MCR含量;h)辦力 的API比重;i)降低的有機酸金屬鹽形態之金屬含量·戍 J)其組合。於若干具體實例中,原油產物的一或多種性質 與原油進料相比可選擇性地改變,而其他性質並沒有同樣 多的改變或者實質上未改變。舉例而言,可能希望只選擇 性地減少原油進料中的TAN而不會顯著地改變其他成分 (例如硫、殘留物、Nl/V/Fe,或VGO)的量。用這種方式, 接觸期間的氫吸取可依TAN的減少而被“濃縮,,,而不會作 用在其他成分的減少。因此,雖然使用較少的氫,但仍可 減少原油進料的TAN,因為較少量的這類氫同樣會用來減 67 200532010 少原油進料中的其他成分。舉例而言,如果劣質原油具有 高TAN ’但含硫量為符合處理及/或輸送規格所能接受者, 則這類原油進料可更有效地處理以減少TAN而不需同樣也 減少硫。 本發明之一或多個具體實例中所用的觸媒可包含一或 多種塊狀金屬及/或載體上的一或多種金屬。該金屬可呈元 素形態或呈金屬化合物形態。本文中所述的觸媒可以前驅 物的形式導入接觸區,然後在接觸區中變成具有活性的觸 媒(舉例而言當硫及/或含硫的原油進料與前驅物接觸時)。 如本文敘述所使用的觸媒或觸媒組合可能是或可能不是商 品觸媒。涵蓋本文敘述所使用的商品觸媒實例包括HDS3 ; HDS22 ; HDN60 ; C234 ; C31 1 ; C344 ; C411 ; C424 ; C344 ; C444 ; C447 ; C454 ; C448 ; C524 ; C534 ; DN110 ; DN120 ; DN130; DN140; DN190; DN200; DN800; DN2118; DN2318 DN3100 ; DN3110 ; DN3300 ; DN3310 ; RC400 ; RC410 RN412 ; RN400 ; RN420 ; RN440 ; RN450 ; RN650 ; RN5210 RN5610 ; RN5650 ; RM430 ; RM5030 ; Z603 ; Z623 ; Z673 ; Z703; Z713; Z723; Z753;和 Z763,其可得自 CRI International, Inc. (Houston, Texas,U.S.A·) 〇 於若干具體實例中,用來改變原油進料性質的觸媒包 含載體上的一或多種第5至10攔金屬。第5至10欄金屬 包括,但不限於叙、鉻、鉬、鐫、猛、錯、銖、鐵、始、 錄、釕、Ιε、姥、鐵、錶、翻,或其混合物。該觸媒在每 克觸媒中可具有至少0.0001克,至少0_001克,至少0.01 200532010 克或是在0·0001至n AA ^ 古,urn ·6 克,〇·005 至 0.3 克,〇·_ 至(Μ 克 或 〇·〇 至 〇.〇8 券 ήθ® &lt; 1/% 一 、 至1 〇攔金屬總含量◦於若干 具體貫例中,該觸媒除τ坌 笛—本 系除了弟5至10搁金屬之外,還包含 弟15欄兀素。第15欄元素的者 ”貝Η匕括磷。該觸媒可具有 弟1 5攔兀素的總含晋尤灰古 里在母克觸媒中為0.000001至〇·1克, 0.00001 至 0.06 克,〇 〇〇〇〇5 王 υ·ϋ3 克’或 〇 〇〇〇1 至 〇 〇〇1 克的範圍内。 於特疋具體實例中’觸媒包含第6攔金屬。該觸㈣V% of the crude oil feed at r%, 8G to 8g, or 9G to UG% ^ In the W example, the crude oil product is in the range of _ to ㈣ grams per gram, or 0.002 to 22 0.001 to 0.3 grams VG0 content within. In several specific examples, the crude oil product has ⑽, 叫 or 9. to :? Here is ... This eyebrow, A $ μ 1 ^ ^ Residues of crude oil Dakota 4 = This crude oil product can have 0_ grams to 0.5 grams per gram of crude oil product, and _ to 〇. Where υ.οοι to 〇3 grams , 65 200532010 A residual content in the range of 0.005 to 0.2 g, or 0.001 to 0.001 g. · In the specific examples of known crude oil products, the crude oil product has an MCR content of 70 to 130%, 80 to 120%, or 90 to 110% of the crude oil feed, and the crude product has a q asphaltene content Up to 90%, up to 80% ', or up to 5G% of crude oil feed ~ Alexandrite content. In specific examples, the C5 asphaltene content of the crude oil feed is at least 10%, at least 60% ', or at least &amp; 70% of the Cs cyanocyanine content of the crude oil feed, and at the same time, the MCR content of the oil product Within the range of 10 to 30% of the mcr content of crude oil feed. In several specific examples, reducing the q-leaching cyanide content of the crude oil feed while maintaining a relatively stable MCR content can increase the stability of the crude oil feed / total product mixture. In the specific example of the right stem, the mathematical relationship between the Cs asphaltene content and the mcr content can be used to generate the viscosity component of the crude oil feed compared to the degree component of the crude oil product. For example, the sum of the q cyanide content of the crude feed and the MCR content of the crude feed can be expressed as S. The sum of the C5 cyanocyanine content of the crude oil product and the mcr content of the crude oil product can be expressed as a comparison of these sums (s, and s) to estimate the net reduction in high viscosity components in the crude oil feed. To 99%, 10 to 90%, or 20 to S. In some specific examples, the ratio of the mcr content to the C5 asphaltene content of the crude product is in the range of 10 to 3.0, 1.2 to 20, or 1.3 to 1.9. In the specific examples of formulas and formulas, crude oil products have a maximum MCR content of at most 80%, at most 50%, or at most 10% of the crude feed. In several specific examples, the crude oil product has an MCR content of 66 200532010 ranging from 1 to 80%, 10 to 70% ′ 20 to 60%, or 30 to 50% of the MCR content of the crude oil feed. The crude oil product contains 0.0001 to (M grams, 0.05 to 0.005 grams, or 0.01 to 0.05 grams of MCR per gram of crude oil product in several examples. In several specific examples, the crude oil product is present in each gram. Crude products contain more than 0 grams, but less than 0.01 grams, 0.00001 to 0.001 grams, or 0.0000 to 0.0001 grams of total catalyst. The catalyst can help stabilize the crude product during transportation and / or processing. Catalyst Can inhibit corrosion, inhibit friction, and / or increase the water-separation capacity of crude oil products. The methods described herein can be configured to add one or more of the catalysts described herein to crude oil products during household management. Contact The crude oil product produced by the system 1000 contact has different properties from the original and feed properties. Such properties can include, but are not limited to: a) reduced TAN; b) reduced viscosity; c) reduced total Ni / V / Fe content; d) reduced sulfur, oxygen, nitrogen, or a combination thereof; e) reduced residue content; 0 reduced asphaltene content; g) reduced MCR content; h) API weight ; I) Reduced metal content of organic acid metal salt form 戍 J) Its combination. In several specific examples, one or more properties of the crude product may be selectively changed compared to the crude feed, while other properties are not changed as much or substantially unchanged. For example, it may be desirable to selectively reduce only the TAN in a crude oil feed without significantly altering the amount of other components such as sulfur, residues, Nl / V / Fe, or VGO. In this way, the hydrogen uptake during the contact can be "concentrated" according to the decrease in TAN without affecting the reduction of other components. Therefore, although less hydrogen is used, the TAN of the crude oil feed can still be reduced , Because a smaller amount of this hydrogen will also be used to reduce other components in the crude oil feed. 67 200532010. For example, if inferior crude oil has a high TAN 'but the sulfur content is within the processing and / or transportation specifications Recipients, this type of crude feed can be processed more efficiently to reduce TAN without also reducing sulfur. The catalyst used in one or more embodiments of the present invention may include one or more bulk metals and / or One or more metals on the carrier. The metal can be in the form of an element or a metal compound. The catalyst described herein can be introduced into the contact zone as a precursor, and then becomes an active catalyst in the contact zone (for example, and (When the sulfur and / or sulfur-containing crude feed is in contact with the precursor). The catalyst or catalyst combination used as described herein may or may not be a commodity catalyst. It covers the commodities used in the description Examples of catalysts include HDS3; HDS22; HDN60; C234; C31 1; C344; C411; C424; C344; C444; C447; C454; C448; C524; C534; DN110; DN120; DN130; DN140; DN190; DN200; DN800; DN800; DN800; DN2318 DN3100; DN3110; DN3300; DN3310; RC400; RC410 RN412; RN400; RN420; RN440; RN450; RN650; RN5210 RN5610; RN5650; RM430; RM5030; Z763; Z603753; Z603713; Z603753; Z603753; Z603753; Z603673; Z603753 It can be obtained from CRI International, Inc. (Houston, Texas, USA). In several specific examples, the catalyst used to change the properties of the crude oil feed comprises one or more metals 5 to 10 on the carrier. Columns 5 to 10 include, but are not limited to, chrome, molybdenum, rhenium, fierce, erroneous, baht, iron, starting, recording, ruthenium, Ιε, thorium, iron, watch, iron, or mixtures thereof. Each gram of the catalyst may have at least 0.0001 grams, at least 0_001 grams, at least 0.01 200532010 grams, or in the range of 0.0001 to n AA ^ ancient, urn 6 grams, 0.005 to 0.3 grams, 〇_ to (M grams or · 〇 ~ 〇〇〇〇〇〇〇〇〇〇〇〇〇〇。 Total metal content in metal ◦ In some specific examples, the catalyst except τ 坌 flute—this series except for 5 to 10 metal In addition, it contains 15 columns. The element of the 15th column is "bei dagger". The catalyst may have a total content of 15 5% of the element. Jinyou Gray Guli in the mother gram catalyst is 0.000001 to 0.1 g, 0.00001 to 0.06 g, 〇〇〇〇〇〇 Wang υ · ϋ 3 grams 'or 0.001 to 001 grams in the range. In the specific example of the catalyst' catalyst contains the sixth metal. The catalyst

母克觸媒中可具有至少0 0001克,至少〇〇1克,至少㈣ ^及/或在〇._至0.6克,〇.〇〇1至〇 3克,〇 〇〇5至〇 —或0.01至0.08克的第6攔金屬總含量。於若干具楚 實例中’觸媒在每克觸媒中包含〇.〇〇〇1至〇〇6克的第( 搁金屬。於若干具體實财,_除了第6欄金屬之外, 還包含第15欄元素。The master gram catalyst may have at least 0 0001 grams, at least 0.001 grams, at least ^^ and / or between .0 to 0.6 grams, from 0.001 to 〇3 grams, and from 005 to 0— 0.01 to 0.08 grams of total 6th metal. In several examples, the 'catalyst contains from 0.00001 to 0.006 grams of metal in each gram of catalyst. In some specific financial matters, in addition to the metal in column 6, it also contains Column 15 element.

。、一方、右干具體貫例中’觸媒包含第6攔金屬與第5欄及/ 或第7至1 G攔之-或多種金屬的組合。第6欄金屬與第」 欄金屬的莫耳比可在〇1至2〇,i至1〇,或2至$的範圍 内第6攔金屬與第7至丨〇攔金屬的莫耳比可在〇· 1至, 1 t 1〇,或2至5的範圍内。於若干具體實例中,觸媒除 了第6搁金屬與第5攔及/或第7至丨〇欄之一或多種金屬 勺、、且3之外,還包含第1 5攔元素。於其他具體實例中, 觸媒包含g 6欄金屬和第1〇攔金屬。觸媒中第1〇欄金屬 總量與第6攔金屬總量的莫耳比可在1至1〇,或2至5的 範圍内。於特定具體實例中,觸媒包含第5欄金屬和第ι〇 69 200532010 棚金屬。觸媒中第10攔金屬總量與第5攔金屬總量的莫 耳比可在1至10,或2至5的範圍内。 、於若干具體實財,第5至1G欄金屬係併人或沈積於 載體上以形成觸媒。在某些具體實例中,第5 i ι〇搁金 屬與第15欄元素之組合被併入或沉積在载體上以形成觸 媒。於金屬及/或元素受載的具體實例中,觸媒的重量包括 所有載體,所有金屬和所有元素。該载體可為多孔性而且 可包括对火性氧化物,多孔性碳基材料,沸石,或其組合。 耐火性氧化物可包括,但不限於氧化鋁、氧化矽、氧化矽_ 5化鋁、氧化鈦、氧化鍅、氧化鎂,或其混合物。載體可 伃自工業製造商’例如Criteri〇n Catalysts㈣丁“hn〇1〇細 LP (Houston,Texas,us.A)。多孔性碳基材料包括,但不 限於活性碳及/或乡孔石墨。沸石的實例包括y弗石1沸 1、絲光彿石、ZSM-5沸石和鎮驗濟石。沸石可得自工業 衣每商,例如Zeolyst (Valley F〇rge,卜加巧卜扣υ $ a ) 〇、 於若干具體實例中係製備載體以便使該載體具有至少 150 A,至少170 A ’或至少、18〇 A的平均孔徑。於特定具 體貫例中’載體係藉由形成载體的水漿而製備。於若干2 體實例中,將酸添加至漿料以促進漿料的擠出:具 的酸係以所需要的量並藉由所需要的方法添加,以2釋 擠出漿料期望的稠度。酸的實例包括,但不限於硝萨:、了 酸、硫酸和鹽酸。 文、乙 漿料可使用一般已知的觸媒擠出法和觸媒切割 出和切告,i以形成擠出物。該擠出物可在5至2的 知 L或85 70 200532010 士 5 C之範圍内的溫度下熱處理—段時間(例如〇.5至8 小日守)及/或直到擠出物的濕度達到期望值為止。孰處理過 的撥出物可在_至1扇。〇或_ more‘I範圍内 的溫度下進-步熱處理以形成具有平均孔徑至少為15〇入 的載體。 於特,具體實例中,載體包含γ氧化銘、㊀氧化紹、§氧 化鋁(X乳化鋁’或其混合物。γ氧化鋁、δ氧化鋁、α氧化 鋁’或其混合物的量於每克觸媒載體中可在0.0001至〇.99 克’0.001至〇·5克,〇〇15 〇1古 · •克的範圍内,或最多為0.1 克,其藉由X射線繞射測定。於若干具體實例中,載體係 早獨含有或結合其他形態的氧化紹,θ氧化銘含量於每克 ί體中在0·1至〇.99克,〇·5至0.9克,或0.6至0.8克的 乾圍内’其藉自X射線繞射敎。於料具體實例中,載 體可含有至少G.U,至少G.3克,至少⑴…或至少〇8 克的Θ氧化鋁,其藉由χ射線繞射測定。 受载觸媒可使用-般已知的觸媒製備技術製備。觸媒 製備法的實例係見述於頒予GabdelQv等人的美國專利案 f 6,21 8,333;頒予 Gabriel〇v 等人的 6,29〇,841;頒予 ⑽ 寺人的5,744,G25,及頒予Bhan的美國專利中請案公告案 號 20030111391 。 … 於若干具體實例中,載體可用金屬浸潰以形成觸媒。 於特定具體實例中,在浸潰金屬之前,使載體於彻至 c ’ 450至1000 t ’或600至9〇〇 t之範圍内的溫度下 進订,4處理。於若干具體實例中,浸潰助劑可在製備觸媒 71 200532010 期間使用。浸潰助劑的實例包括檸檬酸成分、乙二胺四乙 酸(EDTA)、氨,或其混合物。. In the specific example of the one side, the right side, the catalyst includes a combination of the sixth metal and the fifth column and / or the seventh to the first G-metal. The molar ratios of the metal in the sixth column and the metal in the second column may be in the range of 0 to 20, i to 10, or 2 to $. In the range of 0.1 to 1, 1 t 10, or 2 to 5. In some specific examples, the catalyst includes the 15th element in addition to the 6th metal and the 5th and / or one or more metal spoons in the 7th to 10th columns, and 3. In other specific examples, the catalyst includes a G6 column metal and a 10th metal. The molar ratio of the total amount of metal in column 10 to the total amount of metal in column 6 in the catalyst can be in the range of 1 to 10, or 2 to 5. In a specific embodiment, the catalyst includes the fifth column of metal and the second column of metal. The molar ratio of the total amount of the 10th metal to the total amount of the 5th metal in the catalyst can be in the range of 1 to 10, or 2 to 5. In some specific real money, the metals in columns 5 to 1G are merged or deposited on a carrier to form a catalyst. In some specific examples, the combination of the 5th metal and the 15th column element is incorporated or deposited on a carrier to form a catalyst. In the specific example of metal and / or element loading, the weight of the catalyst includes all carriers, all metals and all elements. The support may be porous and may include a refractory oxide, a porous carbon-based material, a zeolite, or a combination thereof. Refractory oxides can include, but are not limited to, aluminum oxide, silicon oxide, aluminum oxide, titanium oxide, hafnium oxide, magnesium oxide, or mixtures thereof. The support may be obtained from an industrial manufacturer, such as Criterion Catalysts, "hn〇10 Fine LP (Houston, Texas, us. A). Porous carbon-based materials include, but are not limited to, activated carbon and / or terracotta graphite. Examples of zeolites include zeolite 1 fused, mercerized zeolite, ZSM-5 zeolite, and zeolite. Zeolites are available from industrial clothing manufacturers, such as Zeolyst (Valley Forge, Bu Jia Qiao Bu υ $ a ) 〇. In several specific examples, the carrier is prepared so that the carrier has an average pore size of at least 150 A, at least 170 A ', or at least 18 A. In specific embodiments, the' carrier is formed by water forming the carrier. The slurry is prepared. In several 2-body examples, acid is added to the slurry to promote the extrusion of the slurry: the acid is added in the required amount and by the required method to extrude the slurry in 2 releases. Desirable consistency. Examples of acids include, but are not limited to, nitric acid, sulfuric acid, and hydrochloric acid. Paper and slurry can be cut out and reported using commonly known catalyst extrusion methods and catalysts. Forms an extrudate. The extrudate can be in the range of 5 to 2 or 85 70 200532010 ± 5 C Heat treatment at a temperature-for a period of time (for example, 0.5 to 8 small day guards) and / or until the humidity of the extrudate reaches the desired value. 孰 processed dials can be in _ to 1 fan. 〇 or _ more ' Further heat treatment is performed at a temperature in the range of I to form a support having an average pore size of at least 150. Ute, in specific examples, the support includes gamma oxide, tritium oxide, § alumina (X emulsified aluminum 'or its Mixtures. The amount of gamma alumina, delta alumina, alpha alumina 'or mixtures thereof may be between 0.0001 and 0.99 grams per gram of catalyst support, and between 0.001 and 0.5 grams, and 0.015 grams per year. • Within the range of gram, or up to 0.1 gram, it is determined by X-ray diffraction. In some specific examples, the carrier contains alone or in combination with other forms of oxide, and the content of θ oxide is in per gram of body. 0.1 to 0.99 grams, 0.5 to 0.9 grams, or 0.6 to 0.8 grams within the dry range 'which is borrowed from X-ray diffraction. In specific examples of the material, the carrier may contain at least GU, at least G. 3 grams, at least ⑴ ... or at least 0 8 grams of Θ alumina, which is determined by X-ray diffraction. -Generally known catalyst preparation techniques. Examples of catalyst preparation methods are described in U.S. Patent No. f 6,21 8,333 issued to GabdelQv et al .; ; 5,744, G25 awarded to the Temple Temple, and US Patent Application Publication No. 20030111391 issued to Bhan.… In several specific examples, the carrier can be impregnated with metal to form a catalyst. In specific specific examples, in Before the metal is impregnated, the carrier is ordered at a temperature ranging from c ′ 450 to 1000 t ′ or 600 to 900 t, and 4 is processed. In several specific examples, the impregnation aid can be used during the preparation of the catalyst 71 200532010. Examples of the impregnation aid include a citric acid component, ethylenediaminetetraacetic acid (EDTA), ammonia, or a mixture thereof.

於特定具體實例中,觸媒可藉由將第5至1〇欄金屬添 加或摻入已熱處理成形的載體混合物(“覆蓋,,)而形成。在 已熱處理成形的載體頂面上覆蓋金屬以具有實質或相對均 勻濃度的金屬通常會賦予觸媒有利的催化性質。在每次覆 蓋金屬後熱處理已成形的載體會有改善觸媒催化活性的傾 向。使用覆蓋法製備觸媒的方法係見述於頒予Bhan的美 國專利申請案公告案號200301 1 1391。 第5至1〇攔金屬和載體可用適當的混合設備混合以 成第5至1 〇攔金屬/載體混合物。第5至! 〇棚金屬/載 混合物可使用適當的混合設備混合。適當的混合設備實 包括滾筒、固定殼或槽、研磨混合機(例如分批式或連 式)、衝擊式混合機,以及能適當形成第5至1〇攔金屬/ 體混合物的任何其他一般已知混合器,或一般已知裝置In a specific embodiment, the catalyst may be formed by adding or mixing columns 5 to 10 of the metal into a heat-treated formed carrier mixture ("cover,"). The top surface of the heat-treated formed carrier is covered with metal to form Metals with a substantially or relatively uniform concentration usually give the catalyst favorable catalytic properties. Heat treating the formed support after each coating of the metal tends to improve the catalytic activity of the catalyst. The method of preparing the catalyst by the coating method is described in the description In U.S. Patent Application Publication No. 20031 1 1391 issued to Bhan. The 5th to 10th metal and carrier can be mixed with a suitable mixing device to form the 5th to 10th metal / support mixture. 5th to 10th! The metal / loaded mixture can be mixed using suitable mixing equipment. Suitable mixing equipment includes rollers, fixed shells or tanks, grinding mixers (such as batch or continuous), impact mixers, and can form the 10 Any other generally known mixer or generally known device for blocking metal / body mixtures

::特定具體實例中,使材料混合直到第5至1〇欄金屬: 貝上均勾分散在載體中為止。 於若干具體實例中,在結合載體與金屬之後,使觸士 在150至75〇 t,2〇〇至74〇艺,或4〇〇至7川t的公 度下進行熱處理。 於若干具體實例中,觸媒可在熱空氣及/或富氧空氣名 :下’於介於400。。和1000 t之範圍内的溫度下進行索 处理,以移除揮發性物質,以便使至少一部分的第$至卫丨 搁金屬轉化成對應的金屬氧化物。 72 200532010 '、、'而在其他具體實例中’觸媒可在空氣存在 (例如低於· t,低於·。^低於州、。^ 乾圍内的溫度下熱處理達1至3小時之範圍内的—段時 間,以移除大多數的揮發性物質而不會使第…〇欄金 :轉二成金屬氧化物。#由此種方法所製備的觸媒通常稱 備觸宜f過的”觸媒° #以這種方式結合形成硫化物法製 :觸媒4 ’活性金屬實質上可分散在載體中。這類觸媒的 :備係見述於頒予Gabnelov等人的美國專利案號 ,2 1 8,333,及頒予 Gabriel〇v 等人的 6,29〇,841。 於特定具體實例t,Θ氧化銘載體可結合帛5至ι〇攔 金屬以形成Θ氧化鋁載體/第5 i 1〇攔金屬混合物。㊀氧化 鋁載體/第5至10攔金屬混合物可在至少4〇〇 ^的溫度下 熱處理以形成具有中位孔徑至少&amp; 23〇 Α之孔徑分佈的觸 媒。典型而言,這類熱處理在最高為12〇〇 t的溫度下進 行。:: In a specific embodiment, the materials are mixed until the 5th to 10th columns of metal: shell are uniformly dispersed in the carrier. In some specific examples, after combining the support and the metal, the Tentacle is heat-treated at a temperature of 150 to 7500 t, 2000 to 7400 art, or 400 to 7 t. In some specific examples, the catalyst may be between 400 and 400 under the name of hot air and / or oxygen-enriched air. . And a temperature in the range of 1000 t to remove volatile substances, so as to convert at least a part of the first metal to the corresponding metal oxide. 72 200532010 ',,' and in other specific examples, the catalyst may be heat treated in the presence of air (for example, less than · t, less than ... Within a period of time, to remove most of the volatile substances without turning column…… gold: into metal oxides. # Catalysts prepared by this method are usually called catalysts.的 的 catalyst ° #Combined in this way to form a sulfide process: the catalyst 4 'active metal can be substantially dispersed in the carrier. For this type of catalyst: see the US patent case issued to Gabnelov et al. No. 2 1 8,333, and 6,29〇, 841 awarded to Gabriel ov et al. In specific examples t, the Θ oxide support can be combined with 帛 5 to ι ^ metal to form a Θ alumina support / No. 5 i 10 metal mixture. The alumina support / 5 to 10 metal mixture can be heat treated at a temperature of at least 400 ^ to form a catalyst with a pore size distribution with a median pore size of at least & 23 〇A. Typical In terms of this type of heat treatment, a temperature of up to 12,000 t is performed.

於若干具體實例中,«體(商品載體或如本文敛述所製 備之載體)可與受載觸媒及/或塊狀金屬觸媒結合。於若干 具體實例中’受載觸媒可包含第15攔金屬。舉例而言, 受載觸媒及/或塊狀金屬觸媒可壓碎成平均粒徑為i至5〇 微米’ 2至45 或5至4G微米的粉末。該粉末可與 載體結合以形成埋入金屬觸媒。於若干具體實例中,粉末 可與載體結合,然後使用標準技術擠出,以形成具有中位 孔徑在80至200 A或90至〗80 A,或丨2〇至n〇 a的範 圍内之孔徑分佈的觸媒。 73 200532010 使觸媒與載體接觸於若干具體實例中可&amp; “ 分的金屬存在於埋入金屬觸媒表面下 +至V —部 中)’而導致在表面上比用其他方法存在,士埋入載體 者有更少的金屬。於若干具體實例中,在埋入金屬觸媒 較少金屬者會由於在使用期間容許至少—2表面上具有 觸媒表面而延長觸媒的壽命及/或催化活性。:的金屬移到 媒與原油進料接觸期間觸媒表面的侵蝕而移到屬可藉由觸 夾雜及/或混合觸媒成分於若干具體 估:面。 氣化物曰μ社娃士给 j Τ會使弟6欄 =物…構中弟6攔金屬的結構順 體結構中第6攔金屬的實質隨機順序 =觸媒日曰 可使用粉末X射線繞射法決定。與金屬氧化:=的順: :序相比’觸媒中金屬元素的順序可藉由比較第、= 物之X射線繞射光譜中第6攔金屬波峰的順序和觸媒之 X射線繞射光譜中帛6攔金屬波峰的順序而決定。從盘X :、線繞射㈣中第6攔金屬有關的圖案增寬及/或無圖案來 ,可估算在晶體結構中實質上無規排列的第6攔金屬。 ^舉例而言,三氧化鉬與具有中位孔徑至少為1 80人的 氧化鋁载體可結合形成氧化鋁/三氧化鉬混合物。三氧化鉬 具有明確圖案(例如明確的Di〇〇、D2〇〇及㈣d_波—峰氧 化鋁/第6攔二氧化物混合物可在至少5 3 8它(丨〇〇〇卞)的 咖度下熱處理以產生在χ射線繞射光譜中不會顯示出二氧 化鉬圖案(例如沒有D丨。。波峰)的觸媒。 於若干具體實例中,觸媒的特徵可能是孔隙結構。各 種孔隙結構的參數包括,但不限於孔徑、孔體積、表面積, 74 200532010 或其組σ觸媒可具有與孔徑相對的孔徑總量分佈。孔徑 分佈的中位孔徑可在30至1000人、5〇至5〇〇人,或6〇至 300 Α的範圍内。於若干具體實例中,每克觸媒中包含至 少〇·5克γ氧化鋁的觸媒具有中位孔徑在6〇至2〇〇 A; 9〇 至180 A 100至140 A,或120至13〇 A之範圍内的孔徑 分佈。於其他具體實例中,每克觸媒中包含至少01克㊀氧 化鋁的觸媒具有中位孔徑在180至500 A,200至300 A,In some specific examples, the «body (commercial carrier or carrier prepared as described herein) may be combined with a supported catalyst and / or a bulk metal catalyst. In several specific examples, the 'supported catalyst may include a 15th metal. For example, the supported catalyst and / or bulk metal catalyst can be crushed into a powder having an average particle diameter of i to 50 microns' 2 to 45 or 5 to 4G microns. This powder can be combined with a carrier to form an embedded metal catalyst. In several specific examples, the powder can be combined with a carrier and then extruded using standard techniques to form a pore size with a median pore size in the range of 80 to 200 A or 90 to 80 A, or 20 to noa Distributed catalyst. 73 200532010 Contacting the catalyst with the carrier in a number of specific examples may &amp; &quot; separate metals exist beneath the surface of the buried metal catalyst + to V-in the part) 'and cause it to exist on the surface than by other methods. There is less metal in the carrier. In some specific examples, those who have less metal catalyst in the buried metal will extend the life and / or catalysis of the catalyst by allowing at least -2 surfaces to have a catalyst surface during use. Activity .: The metal is moved to the surface of the catalyst during the contact with the crude oil during the contact with the catalyst, and the catalyst surface can be removed by contacting and / or mixing the catalyst components at a number of specific estimates: surface. j Τ will make the 6th column = material ... the structure of the 6th metal in the cis structure of the random random order of the metal = catalyst can be determined using powder X-ray diffraction method. And metal oxidation: = The order of the :: order comparison of the order of the metal elements in the catalyst can be compared by comparing the order of the 6th metal peak in the X-ray diffraction spectrum of the object and the 6th block in the X-ray diffraction spectrum of the catalyst. The order of the metal peaks. From the disk X :, the line diffraction ㈣ With the widening and / or non-patterning of 6 metal-related patterns, it is possible to estimate the 6th metal that is substantially randomly arranged in the crystal structure. ^ For example, molybdenum trioxide and those with a median pore size of at least 1 80 people Alumina support can be combined to form an alumina / molybdenum trioxide mixture. Molybdenum trioxide has a clear pattern (such as clear Di00, D200, and ㈣d_wave-peak alumina / 6th dioxide mixture) Heat treatment at a temperature of at least 5 3 8 (丨 〇〇〇 卞) to produce a catalyst that does not show a molybdenum dioxide pattern in the X-ray diffraction spectrum (for example, without D 丨 ... wave peak). In specific examples, the catalyst may be characterized by a pore structure. Various parameters of the pore structure include, but are not limited to, pore size, pore volume, and surface area. 74 200532010 or a group of sigma catalysts may have a total pore size distribution relative to the pore size. Pore size The median pore size of the distribution can be in the range of 30 to 1,000 people, 50 to 500 people, or 60 to 300 A. In several specific examples, each gram of catalyst contains at least 0.5 grams of gamma alumina The catalyst has a median pore size of 60 to 2 A; pore size distribution in the range of 90 to 180 A, 100 to 140 A, or 120 to 13 A. In other specific examples, a catalyst containing at least 01 g of gadolinium alumina per gram of catalyst has a median pore size At 180 to 500 A, 200 to 300 A,

或230至250 A之範圍内的丨你八A 心祀囷門扪孔徑分佈。於若干具體實例中,Or within the range of 230 to 250 A, your eight A heart sacrifice the pore size distribution. In several specific examples,

孔徑分佈的中位孔徑至少為1 9 Λ X J 丁 1扎仕王/馬12〇 Α,至少為15〇人,至少為 ⑽人,至少為200 Α,至少為22〇 Α,至少為23〇人,或 至少為3〇〇Α。這類中位孔捏典型而言最多為議入。 觸媒可具有中位孔徑至少Α λ 夕馬60 Α或至少為90 Α的孔 徑分佈。於若干具體實例中,觸拔 嘴媒具有中位孔徑在90至1 80The median pore size of the pore size distribution is at least 19 Λ XJ Ding 1 Zashi Wang / Ma 12〇A, at least 150 people, at least ⑽, at least 200 Α, at least 22 〇A, at least 23 〇 , Or at least 300A. This type of median pinch is typically at most negotiated. The catalyst may have a pore size distribution with a median pore size of at least A λ Xi Ma 60 A or at least 90 A. In some specific examples, the touch-out nozzle media has a median aperture of 90 to 1 80

A,100 至 140 人,或 120 至 X 一 i 3 〇人之乾圍内的孔徑分佈, 該孔徑分佈中至少60%的總孔盤A, the pore size distribution within 100 to 140 people, or 120 to X-i 30 people, at least 60% of the total pore plate in the pore size distribution

〜札數具有在45 A、35 A,或25 A 之中位孔徑範圍内的孔徑。於# 、特疋具體貫例中,觸媒具有 中位孔徑在70至180 A之範囹出t 圍内的孔徑分佈,該孔徑分佈 中至少60%的總孔數具有在λ , x 一 45人、35 A,或25 A之中位 孔徑範圍内的孔徑。 於孔徑分佈之中位孔徑至少 王夕為180 A,至少為2〇〇人, 或至少為230人的具體實例中 ^ 、 中,该孔徑分佈中有超過6〇% 的總孔數具有在50 A、70 A,式 一 或9 〇 A之中位孔徑範圍内 的孔徑。於若干具體實例中,角 觸媒具有中位孔徑在180至 500 A,200 至 400 A,或 230。1 5 23〇至300人之範圍内的孔徑分 75 200532010 佈,該孔徑分佈中至少6〇%的總孔數具有在A、川 或9 0 Α之中位孔也範圍内的孔徑。 於若干具體實例中,孔的孔體積可為至少、3 至少 0.7 cm3/g或至少立。0 3 / .. 、m /g g 夕為0·9 cm/g。於特定具體實例中, 孔的孔體積可在0·3至〇·99 cmVg,〇·4至〇•“ 至0.7 cm3/g的範圍内。 g ,〇·5The 数 number has a pore size in the range of 45 A, 35 A, or 25 A median pore size. In the specific examples of #, the catalyst has a pore size distribution with a median pore size ranging from 70 to 180 A. At least 60% of the total number of pores in the pore size distribution has a lambda x x 45. Aperture in the median aperture range of human, 35 A, or 25 A. In the pore size distribution, the median pore size is at least 180 A, at least 200 people, or at least 230 people. In the specific example ^, in which more than 60% of the pore size distribution has a total number of 50 A, 70 A, pore size within the median pore size range of Formula One or 90A. In some specific examples, the angular catalyst has a median pore size in the range of 180 to 500 A, 200 to 400 A, or 230. 1 5 230 to 300 people with a pore size of 75 200532010. The pore size distribution is at least 6 0% of the total number of pores has a pore size that is also in the range of A, Chuan, or 90 A. In several specific examples, the pore volume of the pore may be at least, 3 at least 0.7 cm3 / g, or at least cubic. 0 3 / .., m / g g and 0.9 cm / g. In a specific embodiment, the pore volume of the pores can be in the range of 0.3 to 0.99 cmVg, 0.4 to 0.7 cm to 0.7 cm3 / g. G, 0.5

具有中位孔徑在90至18〇Α之範圍内的孔徑分佈之觸 媒於若干具體實例中可具有至少為100 m2/g,至少 m /g,至少為17〇 m2/g,至少為22〇 m2 认* r 士 S 乂主夕為270 m2/j 的表面積。這類表面積可在100至300 m 至 27( m/g,130至250 m2/g,或17〇至細心㈣範圍内。 於特定具體實例中,具有中位孔徑在18〇至3〇〇 A之 範圍内的孔徑分佈之觸媒可具有至少為6〇m2 : 吟至&gt;、為1〇〇m2/g,至少為120m2/g,或至少為謂… 的表面積。這類表面積可在60至30〇1112仏,9〇至 100 至 270 mVg,或 120 至 250 m2/g 的範圍内。 gCatalysts having a pore size distribution with a median pore size in the range of 90 to 18 OA may have at least 100 m2 / g, at least m / g, at least 170 m2 / g, and at least 22 in some specific examples. The surface area of m2 is determined to be 270 m2 / j. Such surface areas can range from 100 to 300 m to 27 (m / g, 130 to 250 m2 / g, or 170 to attentive pressure). In specific embodiments, median pore sizes range from 180 to 300A. The catalyst with a pore size distribution within the range may have a surface area of at least 60 m2: ≧ 100 m2 / g, at least 120 m2 / g, or at least a surface area of this type. Such surface area may be at 60 To 30〇1112 仏, 90 to 100 to 270 mVg, or 120 to 250 m2 / g. G

。於特定具體實例中,觸媒係以成形形態,例如片粒狀、 圓柱狀,及/或擠出物存在。該觸媒典型而言具有在至 5〇〇 N/cm,60 至 400 N/cm ’ 1〇〇 至 350 N/cm,200 至 3〇〇 N/cm,或220至280 N/cm之範圍内的平板抗碎強度。 於若干具體實例中,觸媒及/或觸媒前驅物係使用該項 技術中已知的技術(例如ACTICATtm法,CRI International,. In a specific embodiment, the catalyst exists in a shaped form, such as a pellet shape, a cylindrical shape, and / or an extrudate. The catalyst typically has a range of up to 500 N / cm, 60 to 400 N / cm '100 to 350 N / cm, 200 to 300 N / cm, or 220 to 280 N / cm. Shatter strength of the inner plate. In some specific examples, catalysts and / or catalyst precursors use technologies known in the technology (such as ACTICATm method, CRI International,

Inc.)硫化以形成金屬硫化物(在使用之前)。於若干具體實 例中,觸媒可乾燥然後使其硫化。或者,觸媒可藉由觸媒 76 200532010 與包含含硫化合物夕语、山、ώ t, 物之原油進料的接觸而在現場硫化。 硫化可在氫存在下使用$ 尸 匆 吏用虱心4化晟,或液相硫化劑 有機硫化合物(包括貌基硫、 …^例如 場外硫化法係見述於 ^ 亞楓) 5 468 377,u , mans寺人的美國專利案號 ,,,頒予Sea職ns等人的5,688,736。 與載:::具體實例中,第-類觸媒(“第-種觸媒,,)包含 ΐ 25ΓΓ 口的第5至1〇攔金屬,且具有令位孔徑在150 至250 A之範圍内的孔 锸勰讲叮曰士 , 刀伸弟一種觸媒可具有至少1〇〇Inc.) is vulcanized to form metal sulfides (before use). In several specific examples, the catalyst can be dried and then vulcanized. Alternatively, the catalyst can be vulcanized on-site by contacting the catalyst 76 200532010 with a crude oil feed containing sulfur-containing compounds. Vulcanization can be performed in the presence of hydrogen with a cadaver, or a liquid-phase vulcanizing agent, an organic sulfur compound (including surface sulfur, ... ^ For example, the off-site vulcanization method is described in ^ Yafeng) 5 468 377, The U.S. Patent No. of Mans Temples, issued to Sea, ns and others 5,688,736. With ::: In the specific example, the first-type catalyst ("the first-type catalyst,") contains the 5th to 10th metal of the ΐ 25ΓΓ mouth, and has an order aperture within the range of 150 to 250 A. Kong Yan talked about scholars, Dao Shendi a catalyst can have at least 100

„插又面積帛一種觸媒的孔體積可至少為0.5 cm3/g。 =重觸射具有γ氧化銘含量在每克的第一種觸媒中至少 马υ·5克的γ氧化鋁,血 ” 最多為〇·9999克的Υ氧化鋁。 昂 種觸媒於若干呈雕奋 η Ί , ” 貝例中在每克觸媒中具有0.0001至„Insertion area: The pore volume of a catalyst can be at least 0.5 cm3 / g. = Heavy shots have a gamma oxide content of at least 5 g of gamma alumina per gram of first catalyst, A maximum of 0.099 grams of rhenium alumina. There are several catalysts in Ang 雕 奋, "In the case, there are 0.0001 to

ο·1克之範圍内的第6捫人H ^ ,, .. α1 攔孟屬總含量。第一種觸媒能移除 ^ Γ — ^Ni/v/Fe,移除造成原油進料之則 Γ;:成分’移除原油進料中至少-部分…青質, 矛夕除原油進料中至小一 5 或1 4 A 少一 刀的有機酸金屬鹽形態之金屬,ο · 1 gram range of the 6th person H ^ ,, .. α1 total content of Mon. The first catalyst can remove ^ Γ — ^ Ni / v / Fe, remove the rule that caused the crude oil feed Γ ;: component 'removed at least-part of the crude oil in the crude oil feed ... Medium to small one 5 or 1 4 A less than one metal in the form of a metal salt of an organic acid,

〆”且6 〇當原油 如八访曰 /、弟一種觸媒接觸時,其他性質(例 3石爪$、VGO含量、 可能只表現出相當少二重、殘留物含量’或其組合) 的性# &amp; + 里、艾化。能選擇性地改變原油進料 J丨王貝而同時·口 士0 Α , 進行更有效地:理改變其他性質可容許原油進料 觸媒可以任意:序使::干具體實例中’-或多種第-種 於特定具體實例中,楚—ί 與載體处人的兹ς 弟一頒觸媒(“第二種觸媒,,)包含 且、、口 口的第5至ί 〇細a η ⑶攔金屬,具有中位孔徑在90至180 77 200532010 A之h圍内的孔徑分佈。 的總孔數且有在的孔經分佈尹至少 致具有在45 A之中位孔徑範圍 當接觸條件下原、▲ W』,t 孝图Μ的孔偟。在適 、 卞件下原油進料與第二種觸媒的接觸 進料的同樣性質相比,且— 產與原油 、 ^有U者改變之選定性暂^ , 而同時其他性質 &amp; 生貝(例如TAN) /IA ^ 乂里改變的原油產物。於若千且雕承 例中,在接觸期間可存在氫源。 干,… 第:種觸媒可減少造成原油進料之Μ 成分’造成相對高黏度的至少—部分成 刀 物之至少一部分的N /夕原油產 3里。此外,原油進料盥第-重:媒的接觸可生產與原油進料的含硫量相比,1二; 量改變的原油產物。舉例而言,原油產物;具:含 瓜里為70%至130%之原油進料的含硫 原油進料相比,在餾分含量、ν ::一產物與 3里VCj〇合Ϊ,和殘留物含量方 ,也可能只表現出相當少量的變化。 於若干具體實例中,原油進料可具有相對低的驗/Fe :里(例如最多為50 wtppm),但相對高的TAN、瀝青質含 量,或有機酸金屬鹽形態的金屬含量。相對高白勺Μ、⑽ 如至少為〇·3白勺ΤΑΝ)可能使得原油進料為輸送及/或精煉 所不能接受。具有相對高。5遞青質含量的劣質原油在處理 期間與具有相對低溽音皙今晷&amp; # π ,仲幻必% &amp;月貝3里的其他原油相比,可能會 表現出較低的穩定性。原油進料與第二種觸媒的接觸可移 除原油進料中造成TAN的酸性成分及/或C5瀝青質。於若 干具體實例中’減少c5瀝青質及/或造成TAN的成分與原 油進料的黏度相比,可能會降低原油進料/總產物混合物的 78 200532010 黏度。於特定具體實例中 用來處理本文中所、+、AA —種觸媒的一或多種組合當 + 乂甲所述的原油 物混合物的穩定性,辦 ^ 可^面總產物/原油產 最小淨吸取。 W加觸媒壽命,提供原油進料之氫的 π右卞具 員· 合丨J 中 ,Αλ. 一 “ 由使载體與第6欄金屬結:::觸媒:第三種觸媒”)可藉 前驅物可在一或夕 ° 觸媒前驅物而獲得。觸媒 (例如低於482。〇 =化合物的存在下在低於500 t 未煅燒過的第:種觸:…熱—段相當短的時間以生成 至少10 0 〇C、素9丨士 D ,觸媒洳驅物係加熱到 ^ k °於特定具體實例中,第二種觸拔, 母克觸媒中可具有0 001石 弟一種觸媒在 〇 008 · 至 〇·03 克,0.005 至 0.02 克,或 •01克之範圍内的第 二 當用來處理本文中所过… 攔疋素含夏。弟三種觸媒 μ . r ^ .. 勺原油進料時,可表現出顯著的活 陡和%疋性。於若干具奋 ^ ”且貝例中’觸媒前驅物係於一或多 種硫化合物的存在下在 4夕 — 隹下在低於500 t的溫度下加熱。 弟三種觸媒可減少造成原油進料之UN的至少 成分,減少至少—八^ i 刀 s ^ ^ D刀的有機酸金屬鹽形態之金屬,減少 :油產物的卿Fe含量,及降低原油產物的黏度。此外, 士、油進料與第三種觸媒的接觸可生產與原油進料的含硫量 曰目比 ':其含硫量相當少量改變及具有原油進料之氫的相對 旦r吸取的原油產物。舉例而言,原油產物可具有含硫 為70%至130%之原油進料的含硫量。使用第三種觸媒 所生產的原油產物盘眉A 、 旦 I职原油進枓相比,在API比重、餾分含 里VGO 3里,和殘留物含量方面,也可能只表現出相當 79 200532010 2的變化。降低原油進料&amp; TAN、有機酸金屬鹽形態之 Ni/V/Fe s里,及黏度且同時只少量改變A&quot;比重、 :::里⑽含董,和殘留物含量的能力可容許原油產 物為各種處理設備所使用。 一/三種觸媒於若干具體實例中可降低原油進料之至少 :部t的紅R含量,而同時保持原油進料/總產物的穩定 。於特定具體實例中,第三種觸媒在每克觸媒中可呈有 在-^至克,請5至⑽克,或⑽丨至請1 之祀圍内的第6攔金屬含量以及在G咖至Q G5克,〇 〇〇5 至0·03克,或〇·〇〇〗至0 01克筋 旦^ 見之乾圍内的弟1 〇攔金屬含 里。弟Y和10欄金屬觸媒可促使減少至少一部分在3〇〇 ^ 500 1或350至450 t之範圍内的溫度和〇·1至10 二進1料至φ8 MPa’或2至5 Mpa之範圍内的壓力下造成 原/由進料中之MCR的成分。 於:定具體實例中,第四類觸媒(“第四種觸媒,,包含 孔平、.呂載體結合的第5攔金屬。第四種 :=…的孔徑分佈。於若干具體實例中,第四 的中位孔經可至少為22。入,至少為—,至少為 〇1古或至少為_A°該載體在每克載體中可包含至少 •見’至少〇·5克,至少古 少 &quot;。第四種觸媒於若干具體實例中可或二 為丁姐只例中可包含每克觸媒中最多 第5.的第5攔金屬,且每克觸媒中至少為〇〇〇〇1克的 屬。於特定具體實例中,第5攔金屬為鈒。 ;右干具體實射’在與第四種觸媒接觸之後,原油 80 200532010 進料可與附加觸媒接觸。 者··第一種觸媒、第二種觸 第五種觸媒、第六種觸媒、 品觸媒,或其組合。 該附加觸媒可為下列一或多種 媒、第三種觸媒、第四種觸媒、 第七種觸媒、本文中所述的商 於若干具體實例中 J r 風可在原油進料與第四種觸媒接 觸期間於3 0 0至4 0 〇。广,q A 1 4⑽ C,32〇 至 38〇 t,或 33〇 至 370 〇c 的溫度下產生。由這類接總〆 ”and 〇 When the crude oil such as Hachiman / Yi was exposed to a catalyst, other properties (eg, Stone claw $, VGO content, may show only a relatively small amount of double, residue content 'or a combination thereof). Sex # &amp; Li, Aihua. Can selectively change the crude oil feed J 丨 Wang Bei while at the same time · mouth 0 Α, to perform more effectively: change other properties can allow crude oil feed catalyst can be arbitrary: sequence Use :: in the specific example '-or multiple first-species in a specific specific example, Chu — ί and the carrier's enthusiast, the first catalyst (“the second catalyst,”) contains and, The 5th to 15th a η ⑶ metal of the mouth has a pore size distribution with a median pore diameter within the range of h from 90 to 180 77 200532010 A. The total number of pores and the distribution of pores are at least such that they have a median pore size range of 45 A. Under contact conditions, the original, ▲ W ″, t are the holes of Figure M. Under the appropriate conditions, the crude oil feed has the same properties as the contact feed of the second catalyst, and-the production and crude oil, ^ the selection is subject to change, and at the same time other properties &amp; raw shellfish ( For example, TAN) / IA ^ 改变 changes in crude oil products. In the case of Yu Qianqian, the source of hydrogen may be present during the contact. Dry, ... The first kind of catalyst can reduce the M component that causes the crude oil feed ′ which results in a relatively high viscosity of at least-part of the knife, at least a part of the N / X crude oil production 3 miles. In addition, the contact of the crude oil feed-heavy: medium contact can produce crude oil products with varying amounts of sulfur compared to the sulfur content of the crude oil feed. For example, crude oil products; compared with sulfur-containing crude oil feeds containing 70% to 130% of crude oil feeds in Guari, the distillate content, ν :: a product and 3 miles VCj〇 combined, and residual In terms of material content, it may show only a small change. In several specific examples, the crude oil feed may have a relatively low I / F: (e.g., up to 50 wtppm), but a relatively high TAN, asphaltene content, or metal content in the form of a metal salt of an organic acid. Relatively high M, (e.g., at least 0.3 A) may make crude oil feed unacceptable for transportation and / or refining. Has relatively high. Inferior crude oils with 5 cyanin content may show lower stability during processing compared with other crude oils with relatively low 溽 音 皙 晷 &amp;# π, Zhong Huan must% & Yuebei 3 . The contact of the crude feed with the second catalyst can remove the acidic components of the crude feed that cause TAN and / or C5 asphaltenes. In some specific examples, 'reducing c5 asphaltenes and / or the constituents that cause TAN compared to the viscosity of the crude oil feed may reduce the viscosity of the crude feed / total product mixture by 78 200532010. In specific examples, it is used to deal with the stability of one or more combinations of +, AA, and various catalysts described in this article. draw. W plus catalyst life, π right-hander who provides hydrogen for crude oil feed. · In J, Aλ. "" By the carrier and the metal in column 6 :: catalyst: third catalyst " ) Can be obtained by the precursors can be obtained at one or the night ° catalyst precursors. Catalyst (for example, less than 482. 0 = less than 500 t of uncalcined in the presence of a compound: ... heat: a relatively short period of time to produce at least 100 ° C, prime 9 D, The catalyst flooding system is heated to ^ k °. In the specific embodiment, the second type is pulled out, and the mother gram catalyst can have 0 001 stone. One type of catalyst is 〇008 · to 0.03 g, 0.005 to 0.02. Gram, or the second within the range of • 01 grams, when used to deal with what has been done in this article ... Blocker containing Xia. The three catalysts μ. R ^ .. can show significant activity and sharpness when feeding crude oil. %. In some cases, the catalyst precursor is heated in the presence of one or more sulfur compounds on the night of the night-at temperatures below 500 t. The three catalysts can be Reduce at least the components of the UN that cause crude oil feed, reduce the metal in the form of organic acid metal salt of at least -eight ^ i knife s ^ ^ D knife, reduce: Fe content of oil products, and reduce the viscosity of crude oil products. In addition, The contact of taxis, oil feeds and a third catalyst can produce a sulfur ratio with crude oil feeds': its sulfur content A relatively small change in crude oil product with relative absorption of hydrogen with crude oil feed. For example, a crude oil product may have a sulfur content of 70% to 130% of the crude oil feed. Use a third catalyst Compared with the crude oil produced by Panmei A, and crude oil, the crude oil product may also show only changes in the proportion of API, fraction VGO 3, and residue content that are comparable to 79 200532010 2. Reduce crude oil input The ability to feed &amp; TAN, organic acid metal salt in the form of Ni / V / Fe s, and the viscosity while only slightly changing the A &quot; specific gravity, ::: ⑽⑽, and residue content can allow crude oil products to be various Used by processing equipment. One or three catalysts can reduce the red R content of crude oil feed by at least: part t in several specific examples, while maintaining the stability of the crude oil feed / total product. In a specific specific example, the third The catalyst can present the metal content of the 6th block in the range of-^ to g, please 5 to ⑽, or ⑽ 丨 to please 1 and the amount of G to Q G5 gram per gram of catalyst. 〇〇5 to 0. 03 grams, or 〇〇〇〗 to 0 01 grams Jindan ^ See the dry fence Brother 1 〇 metal ri. Brother Y and 10 columns of metal catalyst can promote reducing at least a part of the temperature in the range of 300 ^ 500 1 or 350 to 450 t and 0.1 to 10 2 feed 1 to φ 8 MPa 'or the pressure in the range of 2 to 5 Mpa caused the composition of the original / from the MCR in the feed. In: specific examples, the fourth type of catalyst ("fourth catalyst, including Kong Ping, The fifth metal block combined with the Lv carrier. The fourth type: = pore size distribution. In some specific examples, the fourth median pore length can be at least 22. The carrier may be at least-, at least 〇1, or at least _A °. The carrier may contain at least 0.5 g, at least ancient &quot; per gram of carrier. The fourth catalyst may or may be Ding Jie in some specific examples. The example may contain up to 5.5% of the metal in each gram of catalyst, and at least 0.0001 grams per gram of catalyst. Of the genus. In a specific embodiment, the fifth metal is thallium. ; The right dry concrete shot ’After contact with the fourth catalyst, the crude oil 80 200532010 feed can be contacted with the additional catalyst. The first catalyst, the second catalyst, the fifth catalyst, the sixth catalyst, the product catalyst, or a combination thereof. The additional catalyst may be one or more of the following catalysts, a third catalyst, a fourth catalyst, a seventh catalyst, and a number of specific examples described in this article. J r wind can be used in crude oil feed and The fourth catalyst contact period is from 300 to 400. Wide, q A 1 4⑽C, 32 ° to 38 ° t, or 33 ° to 370 ° C. From this type

、 類接觸所生產的原油產物可具有丁A1S 隶多為90%,最多為只〇0/ 田々 夕馮80/。,取多為5〇%,或最多為1〇%之The crude oil products produced by such contact may have 90% of D1S, most of which are only 0 / Tian Yu Xifeng 80 /. , The maximum is 50%, or up to 10%

原油進料的TAN。氫氣發生可在45〇Nm3/m3,i〇jL4〇The TAN of the crude feed. Hydrogen generation can occur at 45 ° Nm3 / m3, i0L4.

Nm /m3 ’或15至25 Nm3/m3的範圍内。原油產物可具有 總Ni/V/Fe含量最多為9〇0/ 异夕 ^ 取夕马90/〇取多為80。/〇,最多‘為70〇/〇, 袁夕為50%’最多兔in〇/ -vs »从 取夕為10/〇,或至少為1%之原油進料Nm / m3 'or 15 to 25 Nm3 / m3. Crude products may have a total Ni / V / Fe content of up to 900 / day. ^ Take Xima 90 / 〇 take 80. / 〇, up to ‘is 70〇 / 〇, Yuan Xi is 50%’ up to rabbit in〇 /-vs »from 10 / 〇, or at least 1% of crude oil

Ni/V/Fe含量。Ni / V / Fe content.

於特定具體實例中,第五類觸媒(“第五種觸媒,,… 與θ氧化㈣體結合的第6攔金屬。第五種觸媒具有中4 孔徑至少為180 A,至少為220 A,至少為23〇 a,至少』 250 A ’至少為3〇〇 A ’或最多為5〇〇 A的孔徑分佈 體在每克載體中可包含至少〇.丨克,至少〇·5克,或 0.999—克的θ氧化在呂。於若干具體實例+,載體具有 鋁含量為每克觸媒中有低於〇」克的α氧化鋁。該觸媒於」 干具體實例中係包含每克觸媒中最多為Q1克的 、、/ 屬,且母克觸媒中至少為0 0001克的第6搁金屬K 具體實例中,第6欄金屬為鉬及/或鎢。 、右 於特定具體實例中,當原油進料與第五種觸媒在3 81 200532010 至400 t:,320至370 t;,或33〇至36〇它的溫度下接 觸時’原油進料之氫的淨吸取可能相當地低(例如0.01至 100 Nm3/m3,1 至 8〇 Nm3/m3,5 至 5〇 Nm3/m3,或 1〇 至 3〇In a specific specific example, the fifth type of catalyst ("the fifth catalyst, ... the sixth metal that is combined with theta oxide body. The fifth catalyst has a meso 4 pore size of at least 180 A and at least 220 A, at least 23〇a, at least "250 A 'at least 300 A' or at most 500 A, the pore size distribution body may contain at least 0.1 g, at least 0.5 g per gram of carrier, Or 0.999—gram of θ oxidation in Lu. In some specific examples +, the carrier has an alumina content of less than 0 ″ g per gram of catalyst. Α catalyst is included in the specific examples. In the catalyst, there is a maximum of 1 gram of the /, and /, and the mother gram catalyst has at least 0 0001 grams of the sixth metal K. In the specific example, the metal in column 6 is molybdenum and / or tungsten. In the example, when the crude oil feed is in contact with the fifth catalyst at a temperature of 3 81 200532010 to 400 t :, 320 to 370 t ;, or 33 to 36, the net absorption of hydrogen from the crude feed may be Quite low (e.g. 0.01 to 100 Nm3 / m3, 1 to 80 Nm3 / m3, 5 to 50 Nm3 / m3, or 10 to 30.

Nm3/m3)。原油進料之氫的淨吸取於若干具體實例中可在工 至 20 Nm /m,2 至 15 Nm3/m3,或 3 至 10 Nm3/ni3 的範圍Nm3 / m3). The net uptake of hydrogen from crude oil feeds can range from 20 Nm / m, 2 to 15 Nm3 / m3, or 3 to 10 Nm3 / ni3 in several specific examples.

内。由原油進料與第五種觸媒接觸所生產的原油產物可具 有TAN最多為90%,最多為8〇%,最多為5〇%,或最多為 ίο%之原油進料的TAN。原油產物的TAN可在〇 〇1至, 0.03至0.05,或〇·〇2至0 03的範圍内。Inside. The crude oil product produced by contacting the crude oil feed with the fifth catalyst may have a TAN of up to 90%, a maximum of 80%, a maximum of 50%, or a maximum TAN of the crude feed. The TAN of the crude product may be in the range of 0.01 to 0.03 to 0.05, or 0.02 to 0.03.

於特定具體實例中,第六類觸媒(“第六種觸媒,,)包兔 與Θ氧化鋁載體結合的第5欄金屬和第6搁金屬。第六禮 觸媒具有中位孔徑至少$ 18〇 Α的孔徑分佈。於若干具靡 實例中,孔徑分佈的中位孔徑可至少為22〇 Α,至少為 A,至少為250 A,至少為300 A,或最多為5〇〇 A。該載 體在每克載體中可包含至少〇」克,至少〇·5克,至少〇》 克,至少〇·9克,或最多為〇·99克的θ氧化銘。該載體於 若干具體實例中可包含每克觸媒中最多為Q i 1之第$搁 金屬和第6欄金屬的總量,且每克觸媒中至少為克 之第5攔金屬和第6攔金屬的總量。於若干具體實例中, 第6攔金屬總量與第5攔金屬總量的莫耳比可在ο」至μ, 1至’或2至5的範圍内。於特定具體實例中,第$棚 金屬為鈒而第6攔金屬為鉬及/或鎢。 。當原油進料與第六種觸媒在310至4〇〇。〇,32〇至37〇 °C,或330至360。⑽溫度下接觸時,原油進料之氣 82 200532010 吸取可在-10 Nm3/m3 至 2〇 Nm3/m3,·7 Nm3/m3 至In a specific specific example, the sixth type of catalyst ("the sixth catalyst,") includes the fifth column metal and the sixth shelf metal combined with a Θ alumina carrier. The sixth ceremony catalyst has a median pore size of at least $ 18〇A pore size distribution. In several examples, the median pore size of the pore size distribution can be at least 22 OA, at least A, at least 250 A, at least 300 A, or up to 500 A. The carrier may contain at least 0 "grams, at least 0.5 grams, at least 0" grams, at least 0.9 grams, or at most 0.99 grams of theta oxide per gram of carrier. In some specific examples, the carrier may include the total amount of the first metal and the sixth metal of column Q i 1 per gram of the catalyst, and at least the fifth metal and the sixth metal per gram of the catalyst. The total amount of metal. In some specific examples, the molar ratio of the total amount of the 6th metal to the total amount of the 5th metal may be in the range of ο ″ to μ, 1 to ′, or 2 to 5. In a specific embodiment, the first metal is rhenium and the sixth metal is molybdenum and / or tungsten. . When crude oil is fed with the sixth catalyst at 310 to 400. 0, 32 to 37 ° C, or 330 to 360. When contacted at ⑽ temperature, the gas of crude oil feed 82 200532010 can be absorbed from -10 Nm3 / m3 to 20 Nm3 / m3, 7 Nm3 / m3 to

Nm3/m3 ’或·5 Nm3/m3至5 NmVm3的範圍内。氮的負值淨 吸取為氫在現場產生的跡象。由原油進料與第六種觸媒接 觸所生產的原油產物可具有TAN最多為90%,最多為, 取多為50%,最多為10%,或至少為1%之原油進料的。 原油產物的TAN可在〇.〇1至ο」,〇·〇2至〇 〇5, 至0.04的範圍内。 〆 在原油進料與第四種、第五種,或第六種觸媒接觸期 間氫的少量淨吸取會減少在生產輸送及/或處理可接受之原 油產物的加工期間氫的總需求。由於生產及/或輸送氫的成 本昂貴,因此使製程中氫的使用減至最小量會降低加工總 成本。 於特定具體實例中,第七類觸媒(“第七種觸媒”)具有 第6欄金屬總含量在每克觸媒中有〇 〇〇〇1至〇 〇6克之第6 攔金屬的範圍内。第6攔金屬為鉬及/或鎢。第七種觸媒係 有利於生產具有TAN最多為90%之原油進料的ΤΑΝ之原 油產物。 、 第一種、第二種、第三種、第四種、第五種、第六種 和第七種觸媒的其他具體實例也可像本文中另外敘述一樣 地製造及/或使用。 遥擇本申請案之觸媒及控制操作條件可容許生產具有 與原油進料相比改變的ΤΑΝ及/或選定性質而同時原油進 料的其他性質沒有顯著改變的原油產物。所得原油產物與 原油進料相比可能會具有強化性質,因此更為輸送及/或精 83 200532010 煉所能接受。 按選擇順序配置兩種或更多種觸媒可控制原油進料的 性質改善順序。舉例而言,原油進料中的TAN、比重、 至少一部分的q瀝青質、至少一部分的鐵、 、 ^ #分的 、,、,及/或至少一部分的釩能在減少原油進料中至少一部八 的雜原子之前減少。 刀 配置及/或選擇觸媒於若干具體實例中可提高觸媒壽命 及/或原油進料/總產物混合物的穩定性。在加工期間提高Nm3 / m3 'or · 5 Nm3 / m3 to 5 NmVm3. Negative net uptake of nitrogen is an indication that hydrogen is being produced on site. The crude oil product produced by contacting the crude oil feed with the sixth catalyst may have a TAN of at most 90%, at most, at most 50%, at most 10%, or at least 1% of crude oil feed. The TAN of the crude product may be in the range of 0.001 to ο ", 0.02 to 0.05, and 0.04.的 A small net uptake of hydrogen during contact of the crude feed with the fourth, fifth, or sixth catalyst will reduce the overall demand for hydrogen during processing to produce and / or process acceptable crude oil products. Since the cost of producing and / or transporting hydrogen is expensive, minimizing the amount of hydrogen used in the process will reduce the overall processing cost. In a specific specific example, the seventh type of catalyst (the "seventh catalyst") has a total metal content in the sixth column of the sixth metal barrier ranging from 0.001 to 0.66 grams per gram of catalyst. Inside. The sixth metal is molybdenum and / or tungsten. The seventh catalyst system is conducive to the production of crude oil products of TAN with a crude oil feed of TAN of up to 90%. Other specific examples of the first, second, third, fourth, fifth, sixth, and seventh catalysts can also be manufactured and / or used as described elsewhere herein. The remote selection of the catalysts and control of operating conditions of this application may allow the production of crude oil products with altered TAN and / or selected properties compared to the crude oil feed while other properties of the crude oil feed do not change significantly. The resulting crude oil product may have enhanced properties compared to the crude oil feed and is therefore more transportable and / or refined. Configuring two or more catalysts in a selected order can control the order of improving the properties of the crude oil feed. For example, TAN, specific gravity, at least a portion of q asphaltenes, at least a portion of iron, ^ #,, ,, and / or at least a portion of vanadium in a crude oil feed can reduce at least one of the crude oil feed. The heteroatoms in Part 8 were reduced before. Knife configuration and / or selection of catalyst in several specific examples can improve catalyst life and / or stability of crude oil feed / total product mixture. Improve during processing

觸媒壽命及/或原油進料/總產物混合物的穩定性可容許: 觸系統在不更換接觸區中觸媒的情況下,運轉至少3個月, 至少6個月,或至少1年。 尨合遥疋觸媒可在原油進料的其他性質改變之前,令 由進料中至少_部分的Ni/v/Fe,至少—部分的^遞^ :,至少一部分的有機酸金屬鹽形態之金屬,至少一部名 造成TA士N的成分,至少一部分的殘留物,或其組合減少, 同了在加工期間保持原油進料/總產物混合物的穩定伯The life of the catalyst and / or the stability of the crude feed / total product mixture may allow: The catalyst system to operate for at least 3 months, at least 6 months, or at least 1 year without changing the catalyst in the contact zone. Before the other properties of the crude oil feed are changed, the coupling catalyst can make at least a part of Ni / v / Fe in the feed, at least a part of ^^^, and at least a part of the organic acid metal salt form. Metals, at least a portion of the ingredients that cause TA + N, at least a portion of the residue, or a combination thereof are reduced, as well as maintaining a stable crude oil feed / total product mixture during processing

(J、保持间方、1 ·5的原油進料p值)。或者,C5瀝青質、ΤΑΪ 及/或A P I比重可rt» 7K 、 稽由原油進料與選定觸媒的接觸而逐漸減 夕。漸進式及/或選摆柯 释14改變原油進料性質的能力可容許在 加工期間保持原油進料/總產物混合物的穩定性。 干八體只例中,第一種觸媒(上述者)可配置在一 連串觸媒的上游。箓一絲雜 2曰 種觸媒的此種配置可容許移除高分 子置污染物、金屬污迅 、,R门 木物’及/或有機酸金屬鹽形態之金屬, 亚且同時保持原油進料 寸十/〜產物混合物的穩定性。 84 200532010 第一種觸媒於若干具體實例中係容許移除原油進料中 至少一部分的ISH/V/Fe,移除酸性成分,移除造成系統中 其他觸媒壽命減短的成分,或其組合。舉例而言,與原油 進料相比,減少原油進料/總產物混合物中至少一部分的 瀝青質會抑制配置於下游之其他觸媒的堵塞,因此會增加5 接觸系統在沒有補充觸媒的情況下仍可運轉的持續時間。 移除原油進料中至少一部分的Ni/V/Fe於若干具體實例中 可增加配置在第一種觸媒後面之一或多種觸媒的壽命。 第二種觸媒及/或第三種觸媒可配置在第一種觸媒的下 游。原油進料/總產物混合物與第二種觸媒及/或第三種觸 媒的進一步接觸可進一步降低TAN,降低Ni/v/Fe含量, 争低S瓜里,降低含氧!,及/或降低有機酸金屬鹽形態的 金屬含量。 〜 方、若干具體貫例中,原油進料與第二種觸媒及/或第三 種觸媒的接觸可生產原油進料/總產物混合物,與原油進料 的個別性質相比,其具有降低的TAN,降低的含硫量,降 低的3氧里,降低的有機酸金屬鹽形態之金屬含量,降低 的瀝青質含量,降低的黏度’或其組合,i同時在加工期 間保持原油進料/總產物混合物的穩定性。第二種觸媒可並 聯配置’第二種觸媒係位於第三種觸媒上游,或者反過來 也可以。 、使氫輸运至4寺定接角蜀區的能力會傾向於使接觸期間氯 ^吏用減至最小量。結合在接觸期間促使氫氣發生的觸媒 吳在接觸期間吸取相當少量氫氣的觸媒可用來改變與原油 85 200532010 進料的同樣性質相比之下原油產 一笼^ ^ 初的璉定性質。舉例而 : 觸媒可與第-種觸媒、第二種觸媒、第:種觸 媒、第五種觸媒、第六種觸媒,及/或第七種觸媒合== 以改變原油進料的選定性質,而同時只有選擇量地改變原 :進料的其他性質,及/或同時保持原油進料/總產物的轉 :性。可4擇觸媒的順序及/或數目使氫的淨吸取減至最小 :二ΓΓ原油進料/總產物的穩定性。氫的最小淨吸取 係使原油進科的殘留物含量、VG〇含量、餾分含量、(J, keep the marginal, p-value of crude oil feed of 1.5). Alternatively, the specific gravity of C5 asphaltenes, TAH and / or AP may be rt »7K, which is gradually reduced by the contact between the crude oil feed and the selected catalyst. The ability to change the properties of the crude feed incrementally and / or selectively 14 may allow the stability of the crude feed / total product mixture to be maintained during processing. In the case of dried octopuses, the first catalyst (the above) can be arranged upstream of a series of catalysts. This configuration of the catalyst can allow the removal of high-molecular pollutants, metal fouling, metals in the form of R-wood, and / or organic acid metal salts, while maintaining crude oil feed Inch ten / ~ Product mixture stability. 84 200532010 The first catalyst, in several specific examples, allows the removal of at least a part of the ISH / V / Fe in the crude oil feed, the removal of acidic components, the removal of components that shorten the life of other catalysts in the system, or combination. For example, compared to crude feed, reducing at least a portion of the asphaltenes in the crude feed / total product mixture will inhibit the clogging of other catalysts placed downstream, thus increasing the number of contact systems in the absence of supplemental catalyst Down for the duration of operation. Removal of at least a portion of the Ni / V / Fe in the crude oil feed in several specific examples can increase the life of one or more catalysts placed behind the first catalyst. The second catalyst and / or the third catalyst may be arranged downstream of the first catalyst. Further contact of the crude oil feed / total product mixture with the second catalyst and / or the third catalyst can further reduce the TAN, reduce the Ni / v / Fe content, fight for low S, and reduce oxygen content! And / or reduce the metal content in the form of metal salts of organic acids. In some specific examples, the contact of the crude oil feed with the second catalyst and / or the third catalyst can produce a crude oil feed / total product mixture. Compared with the individual properties of the crude oil feed, it has Reduced TAN, reduced sulfur content, reduced oxygen content, reduced metal content in the form of metal salts of organic acids, reduced asphaltene content, reduced viscosity 'or a combination thereof, while maintaining crude oil feed during processing / Total product mixture stability. The second catalyst can be arranged in parallel. The second catalyst is located upstream of the third catalyst, or vice versa. The ability to transport hydrogen to the 4th corner of Jiaoshu District will tend to minimize the amount of chlorine used during contact. Combined with the catalyst that promotes the occurrence of hydrogen during the contact Wu's catalyst that absorbed a relatively small amount of hydrogen during the contact can be used to change the initial properties of crude oil compared to the same properties of the crude oil 85 200532010 feed. For example: The catalyst can be combined with the first catalyst, the second catalyst, the first catalyst, the fifth catalyst, the sixth catalyst, and / or the seventh catalyst == to change Selected properties of the crude oil feed, while at the same time only changing the other properties of the original: feed in a selected amount, and / or maintaining the conversion of the crude oil feed / total product at the same time. The order and / or number of catalysts can be selected to minimize the net uptake of hydrogen: the stability of the crude oil feed / total product. The minimum net absorption of hydrogen is the residue content, VG0 content, fraction content,

比重’或其組合保持在鳩的原油進料之個別性質的範圍 内,而原油產物的TAN及/或黏度最多為90%之原油進料 的TAN及/或黏度。 減少原油進料之氫的淨吸取可生產具有與原油進料 彿點分佈類似㈣程㈣,與原油進料之tan相比降&gt; tan的原油產物。原油產物的原子H/c也可只比原油進$ 的原子H/C有相當少量的改變。The specific gravity 'or a combination thereof is kept within the range of individual properties of the crude oil feed, and the TAN and / or viscosity of the crude oil product is at most 90% of the TAN and / or viscosity of the crude oil feed. Reducing the net uptake of hydrogen by crude oil feed can produce crude oil products that have a process similar to the distribution of the fodder point of the crude oil feed, compared with the tan of the crude oil feed> tan. The atomic H / c of crude oil products can also be changed only slightly compared to the atomic H / C of crude oil.

特定接觸區中的氫氣發生可容許氯選擇性添加至其他 接觸區及/或容許選擇性減少原油進料的性質。於若干具體 二例中’第四種觸媒可配置在本文中所述的附加觸媒上 游、下游或介於其間。氫可在原油進料與第四種觸媒接觸 -月間t生,可將氫輸送至包含附加觸媒的接觸區。氫的輸 运可與原油進料的流動反向。於若干具體實例中,氫的輪 送可與原油進料的流動同向。 舉例而言,在堆疊結構中(參見如圖2B),氫可在接觸 期間於一接觸區中(例如圖2B中的接觸區102)生成,氫可 86 200532010 以原油進料流動相反的方向輸送至附加接觸區(例如圖2β 中的接觸區114)。於若干具體實例中,氫流動可與原油進 料的流動同向。或者,在堆疊結構中(參見如圖3B),氫可 在接觸期間於一接觸區中(例如圖3B中的接觸區1〇2)生 成。氫源可以原油進料流動相反的方向輸送至第一附加接 觸區(例如在圖3B中,使氫經由導管1〇6,添加至接觸區 Π4) ’以原油進料流動相同的方向輸送至第二附加接觸區 (例如在圖3B巾,使氫經由導f 1〇61添加至接觸區ιι6)。 於若干具體實例中,第四種觸媒與第六種觸媒係並聯 使用,第四種觸媒係位於第六種觸媒上游’或者反過來也 2以。結合第四種觸媒與附加觸媒可在原油進料之氫的少 量淨吸取的情況下’降低TAN,降低⑽職含量,及/或 降低有機酸金屬鹽形態的金屬含量。氣的少量淨吸取可容 許原油產物的其他性質盥 有少量改變。I原油進枓的同樣性質相比之下只 於若干具體實例中,兩種 用。力μ » π 个U的弟七種觸媒可合併使 在上游所用的第七種觸媒而非下 克觸媒中可具有〇至G G6克彳觸媒在母 總含量。下游的第七種觸 ⑽内的第6攔金屬 且有箄Η 士A 媒在母克下游的第七種觸媒中可 或大於上游的第七種觸媒中 或母克觸媒中至少〇.〇2支 ]金屬t 3里 量。於若干且+ 攔金屬的第六攔金屬總含 右干具體貫例中,上游 種觸媒可顛倒過來。於下 種觸媒和下游的第七 之催化活性金屬的能力可 :觸媒中使用相當少量 μ ’產物的其他性質與原油 87 200532010 進料的同樣性質相比 σ API t卜f 夕里改變(例如雜原子含量、 ΑΡί比重、殘留物含量、VG〇含 于3里 改變)。 或/、、、且a的相當少量 原油進料與上游和下 有TAN最多為·最二?弟七種觸媒之接觸可生產具 或至少為】。 夕為8〇%,最多為5〇%,最多為㈣, 〆 /為1 /〇之原油進料的TAN之屌、、占弇仏 實例中,原油進料的丁 於若干具體 Μ ^ 4. - ^ Τ糟由/、上游和下游的第七種觸 媒之接觸而逐漸降低(例如, 盘屌 原,由進科與觸媒的接觸以生成 產物幻/ 有改變性質的初原油產物’接著初原油 性質的、i ΓΓ媒的接觸係產生與初原油產物相比具有改變 :=產物)。漸進式降低TAN的能力可在加工期間 保持原油進料/總產物混合物的穩定性。 干八體貝例中’觸媒選擇及/或觸媒順序與控制接 觸條件(例如溫度及/或 ^ 次原,由進枓流率)的結合可幫助減少原 、、e人;之氯的吸取’在加工期間幫助保持原油進料/總產物 、勿的n n ’並且與原油進料的個別性質相比,改變 /、口 j物㈤或夕種性質。原油進料/總產物混合物的穩定 w Z % θ又到來自原油進料/總產物混合物之各種相分離的 影響。相分離可能由例如原油進料/總產物混合物中原油進 或原油產物的不溶性,原油進料/總產物混合物之遞 、勺絮减原油進料/總產物混合物之成分的沈澱,或其 組合所導致。 、在接觸期間的-定次數下,原油進料/總產物混合物中 原油進料及/或總產物的濃度可能會改變。當原油進料/總 88 200532010 產物混合物中的總產物濃度因為生成原油產物而改變時, 原油進料/總產物混合物中原油進料成分及/或總產物成分 的溶解度會有改變的傾向。舉例而言,原油進料可能含: 於加工-開始可溶於原油進料的成分。當原油進料的^質 (例如TAN、MCR、C5瀝青質、p值,或其組合)改變時,、 這些成分可能會有變得較不易溶於原油進料/總產物混合物 的傾向。於若干實例中,原油進料和總產物可能會形成兩 相及/或變成彼此不溶。溶解度改變也可能導致原油進料/ 總產物混合物形成兩個或更多個相。由於瀝青質的絮凝, 原油進料和總產物濃度的改變,及/或成分的沈㈣形成兩 相會傾向於減短-或多種觸媒的壽命。此外,製程效率也 可此會降低舉例而言,可能f要重複處理原 物混合物以生產具有期望性質的原油產物。 +〜產 ▲在加工期間,可監測原油進料/總產物混合物的p值, 製程、原油進料,及/或原油進料/總產物混合物的 ='。典型而言,最多為MMP值係表示原油進料之 遞'質的絮凝通常會發生。如果P值一開始至少為15, 值在接觸期間會增加或相當穩定,那麼這表示原 /'、在接觸期…目當敎。原油進料/總產物混合物的穩 疋}生,如 p稽% ▲ —斤砰估者,可藉由控制接觸條件,藉由觸媒 =’糟由觸媒的選擇性排序,或其组合而加以控制。 ^才工制接觸條件可包括控制 LHSV、溫度、壓力、氕的 吸取::油進料流率,或其組合。 2、 於右干具體實例中,控制接觸溫度以便移除c5遞青質 89 200532010 及/或其他瀝青質,祐 ,^ ^寸保持原油進料的MCR含量。藉 致形成兩相,其可二降觸溫度降低MCR含量可能會導 性及/或-或多種觸媒;壽1原;:進料/總產物混合㈣ ^ ^ ^ x ^ ^ p抆制接觸溫度和氫的吸取並 —本文中料的觸媒可容許降低 少量地改變原油進料的MCR含量。 n 於若干具體實例中,押 觸區中的溫度可為相里去制接觸條件以便使一或多個接 ^ 、 ,、、、4,、者。不同溫度下的操作可容許選擇 性改變原油進料性暂而η 士 、 Λ — 貝而冋呀保持原油進料/總產物混合物的 穩定性。原油進料在μ 十在裏転開始時進入第一接觸區。第一接 觸溫二為第一接觸區中的溫度。其他接觸溫度(例如第二溫 度、第三溫度、第四溫度等)為配置在第一接觸區後面之: 觸區中的溫度。第一接觸溫度可在1〇〇至42〇 t的範圍内, 第二接觸溫度可在與第-接觸溫度相差20至100。。,3〇 至90 C或40至60 t的範圍内。於若干具體實例中, 第二接觸溫度大於第一接觸溫度。具有不同的接觸溫度可 使原油產物中@ TAN及/或c5遞青質含量與原油進料的 TAN及/或A瀝青質含量相比之下降低至比,如果有的話, 在第一和第二接觸溫度彼此相同或相差為1〇亡以内時的 TAN及/或C5瀝青質減少量更大的程度。 舉例而言,第一接觸區可包含第一種觸媒及/或第四種 觸媒’而弟二接觸區可包含本文中所述的其他觸媒。第一 接觸溫度可為350 °C,第二接觸溫度可為300 t。原油 進料在第一接觸區中與第一種觸媒的接觸及/或在與第二接 200532010 觸區中舆其他觸媒接觸之前於較高溫度下與第四種觸媒的 接觸可導致在原油進料中’與在第一和第二接觸溫度相差 為1 〇 C以内時相同原油進料中TAN及/或q瀝青質的減 少相比,有更多TAN及/或匚5瀝青質的減少。 實施例 以下k出載體製備、觸媒製備,及具有選定觸媒配置 與控制接觸條件之系統的非限定實施例。 f施例1 ·掣備觸媼和艚。 載體係利用585克的水和8克的冰硝酸將576克的氧 _ 化鋁(Criterion Catalysts and Techn〇1〇gies Lp,廳吨抓The generation of hydrogen in a particular contact zone may allow selective addition of chlorine to other contact zones and / or allow selective reduction of the properties of the crude feed. In several specific examples, the fourth catalyst may be disposed upstream, downstream, or between the additional catalysts described herein. Hydrogen can be brought into contact with the fourth catalyst in the crude feed-within a month, hydrogen can be transported to the contact zone containing additional catalyst. The transport of hydrogen can be reversed from the flow of the crude feed. In several specific examples, the rotation of hydrogen may be in the same direction as the flow of crude oil feed. For example, in a stacked structure (see Figure 2B), hydrogen may be generated during a contact in a contact zone (such as contact zone 102 in Figure 2B), and hydrogen may be transported in the opposite direction of the crude oil feed flow 86 200532010 To additional contact areas (such as contact area 114 in Figure 2β). In several specific examples, the hydrogen flow may be in the same direction as the flow of the crude oil feed. Alternatively, in a stacked structure (see Fig. 3B), hydrogen may be generated in a contact region (such as the contact region 102 in Fig. 3B) during the contact. The hydrogen source can be transported to the first additional contact zone in the opposite direction of the crude oil feed flow (for example, in FIG. 3B, hydrogen is added to the contact zone Π4 via the conduit 106). Two additional contact areas (for example, in FIG. 3B, hydrogen is added to the contact area ιι6 via the conductive f 061). In several specific examples, the fourth catalyst is used in parallel with the sixth catalyst system, and the fourth catalyst system is located upstream of the sixth catalyst 'or vice versa. The combination of the fourth catalyst and the additional catalyst can reduce the TAN, reduce the job content, and / or reduce the metal content in the form of a metal salt of an organic acid in the case of a small net absorption of hydrogen from the crude oil feed. The small net uptake of gas allows for minor changes in other properties of the crude product. The same properties of I crude oil are compared in only a few specific examples, two of which are used. The force μ »π U of the seven catalysts can be combined so that the seventh catalyst used upstream instead of the lower catalyst can have 0 to G G6 gram catalyst in the total mother content. The sixth metal in the seventh kind of catalyst in the downstream and the metal A in the seventh kind of catalyst in the mother gram can be at least larger than the seventh kind of catalyst in the upstream or the mother gram catalyst in the seventh. .〇2 支] Metal t 3 miles. In some concrete examples of the sixth metal block that contains + metal, the upstream catalyst can be reversed. The ability of the next catalyst and the seventh seventh catalytically active metal can be as follows: other properties of the catalyst using a relatively small amount of μ 'products are compared to the same properties of the crude oil 87 200532010 feed σ API t 卜 f (for example Heteroatom content, APί specific gravity, residue content, and VG0 content were changed in 3). Or a relatively small amount of crude oil feed with upstream and downstream has a maximum of TAN? The contact of the seven different catalysts can be produced or at least]. It is 80%, up to 50%, and up to ㈣. In the example of TAN, 弇 仏, and 弇 仏, which are 1/0 of the crude oil feed, the crude oil feed is divided into several specific M ^ 4. -^ Τ 糟 is gradually reduced by the contact of /, the upstream and downstream seventh catalyst (for example, Panyuyuan, the contact between Jinke and the catalyst to produce the product magic / virgin crude oil products with altered properties' then The contact system of i ΓΓ media produced by the crude oil has a change compared with the crude oil product: = product). The ability to progressively reduce the TAN maintains the stability of the crude feed / total product mixture during processing. The combination of 'catalyst selection and / or catalyst sequence and control of contact conditions (such as temperature and / or primary flow rate by flow rate) in dried octopus cases can help reduce the amount of chlorine It absorbs 'helps to maintain the crude oil feed / total products during processing' and changes compared to the individual properties of the crude oil feed. The stability of the crude feed / total product mixture w Z% θ in turn affects the various phase separations from the crude feed / total product mixture. Phase separation may be caused by, for example, the insolubility of crude oil feed or crude product in the crude oil feed / total product mixture, the transfer of crude oil feed / total product mixture, precipitation of ingredients in the reduced crude oil feed / total product mixture, or a combination thereof resulting in. The concentration of crude oil feed and / or total product in the crude oil feed / total product mixture may vary during a certain number of contact periods. When the total product concentration in the crude oil feed / total 88 200532010 product mixture changes due to the formation of crude oil products, the solubility of the crude oil feed ingredients and / or total product ingredients in the crude oil feed / total product mixture will tend to change. For example, a crude oil feed may contain: components that are soluble in the crude oil feed at the beginning of processing. When the quality of the crude oil feed (such as TAN, MCR, C5 asphaltenes, p-values, or a combination thereof) changes, these ingredients may tend to become less soluble in the crude oil feed / total product mixture. In several examples, the crude feed and total product may form two phases and / or become insoluble with each other. Changes in solubility may also cause the crude feed / total product mixture to form two or more phases. Due to the flocculation of asphaltenes, changes in the crude oil feed and total product concentration, and / or sedimentation of the constituents, two phases tend to reduce the life of one or more catalysts. In addition, process efficiency can also decrease. For example, the raw material mixture may be repeatedly processed to produce a crude product with desired properties. + ~ Product ▲ During processing, the p value of crude oil feed / total product mixture, process, crude oil feed, and / or crude oil feed / total product mixture = 'can be monitored. Typically, the maximum MMP value indicates that the flocculation of the crude oil feed usually occurs. If the P value is at least 15 at first, the value will increase or be fairly stable during the contact period, then this means that the original / ', during the contact period ... Stability of crude oil feed / total product mixtures, such as %%, can be controlled by controlling the contact conditions, by the catalyst = 'selective ordering of the catalyst, or a combination of Be controlled. ^ The contact conditions of the industrial system may include controlling the LHSV, temperature, pressure, and hydration. Absorption :: oil feed flow rate, or a combination thereof. 2. In the specific example of the right stem, control the contact temperature in order to remove c5 cyanide 89 200532010 and / or other asphaltenes, and keep the MCR content of the crude oil feed. If two phases are formed, it can reduce the MCR content by lowering the contact temperature, which may be conductive and / or-or multiple catalysts; Shou 1 Yuan ;: mixed feed / total product 产物 ^ ^ ^ x ^ ^ p The combination of temperature and hydrogen uptake-the catalysts charged herein may allow for a small change in the MCR content of the crude oil feed. n In several specific examples, the temperature in the contact zone can be used to make contact conditions in order to make one or more contacts ^, ,,,, 4 ,, etc. Operation at different temperatures may allow selective changes in the feedability of the crude oil for a period of time η, Λ—belt to maintain the stability of the crude oil feed / total product mixture. The crude feed enters the first contact zone at the beginning of μ. The first contact temperature is the temperature in the first contact zone. Other contact temperatures (e.g., second temperature, third temperature, fourth temperature, etc.) are the temperatures in the contact area disposed behind the first contact area. The first contact temperature may be in a range of 100 to 420,000 t, and the second contact temperature may be 20 to 100 different from the first contact temperature. . , In the range of 30 to 90 C or 40 to 60 t. In some specific examples, the second contact temperature is greater than the first contact temperature. Having different contact temperatures can reduce the @TAN and / or c5 cyanide content in the crude product to a ratio compared to the TAN and / or A asphaltene content of the crude feed, if any, in the first and The TAN and / or C5 asphaltenes are reduced to a greater extent when the second contact temperatures are the same or differ by less than 10 ° C. For example, the first contact area may include a first catalyst and / or a fourth catalyst &apos; and the second contact area may include other catalysts described herein. The first contact temperature can be 350 ° C, and the second contact temperature can be 300 t. Contact of the crude oil feed with the first catalyst in the first contact zone and / or contact with the fourth catalyst at a higher temperature before contact with other catalysts in the second contact zone 200532010 may result in In the crude feed, there are more TAN and / or 匚 5 asphaltenes compared to the decrease in TAN and / or q asphaltenes in the same crude oil feed when the first and second contact temperatures differ by less than 10 ° C. Reduction. Examples The following are non-limiting examples of carrier preparation, catalyst preparation, and a system having a selected catalyst configuration and controlled contact conditions. fExample 1 · Prepare for contact and contact. The carrier system uses 585 grams of water and 8 grams of glacial nitric acid to reduce 576 grams of aluminum oxide (Criterion Catalysts and Technogies Lp).

City,Michigan,U.S.A·)研磨35分鐘製備。所得到的研磨 混合物係透過1.3 Tril〇beTM模板擠出,於9〇至i25 1之 間乾燥,接著在918 °C下煅燒,得到65〇克具有中位孔徑 為I82人的煅燒載體。將此煅燒載體放入Lindberg爐中。 使爐溫於1.5小時過程中升到1〇〇〇至11〇〇它,然後保持 在此範圍内2小時以生產載體。此载體在每克载體中包含 0-0003克的γ氧化鋁,0·0008克的以氧化鋁,〇〇2〇8克的s _ 氧化鋁,和0.978丨克的θ氧化鋁,其藉由\射線繞射測定。 此載體具有110m2/g的表面積和〇·821 cmVg的總孔體積。 此載體具有中位孔徑為232 A的孔徑分佈,該孔徑分佈中 有66.7%的總孔數具有在85人之中位孔徑範圍内的孔徑。 此實施例說明如何製備具有孔徑分佈至少為18〇 A且 包含至少0 · 1克Θ氧化鋁的載體。 宽座例製備县徑至少為―之孔徑分 91 200532010 1的鈒觸嫫。 鈒觸媒係以下列方式製備。由實施例!所述之方法f 備的氧化銘載體用鈒浸潰溶液浸潰,其藉由結合7 69克的 vosw與82克的去離子水而製備。該溶液的值為2 27。 氧化紹載體(100 g)係利用鈒浸潰溶液浸潰,以偶然授 動老化2小日守’於! 25 °c下乾燥數小時,接著在彻。。 下煆燒2小時。所得觸媒在每克觸媒中含有〇 克的釩, ^部分為載體。此鈒觸媒具有中位孔徑$别A的孔捏 分佈’ 0.69cm3/g的孔體積’ * n〇m2/g的表面積。此外, 銳觸媒的孔徑分佈中有66 7%的總孔數具有在Μ a之中位 孔捏範圍内的孔徑。 此實施例說明製備具有中位孔徑至少4 230 A之孔徑 分佈的第5欄觸媒。 徑至少為j3〇 A之孔姆^ iilii觸媒。 銦觸媒係以下列方式製備。由實施例1所述之方法製 =的乳化紹載體用錮浸潰溶液浸潰。此翻浸潰溶液係藉*籲 結合 4.26 克的(ΝΗ4)2Μ〇2〇7、6·38 克的 M〇〇3、112 克的 3〇% H2〇2、0.27克的單乙醇胺(MEA),貞6.51克的去離子水形 成’灸液而製備。此漿液係加熱至65。。直到固體溶解為止。 使加熱溶液冷卻至室溫。該溶㈣pH值為5 36。用離子 水將溶液體積調整至82 mL。 氧化鋁載體(1 00克)係利用鉬浸潰溶液浸潰,以偶然攪 動老化2小時,於125它下乾燥數小時,接著在480 t 92 200532010 下取k 2小日守。所彳于觸媒在每克觸媒中含有〇 · 克的鉑, 其餘部分為載體。此鉬觸媒具有中位孔徑為25〇 Α的孔徑 刀佈Ο·77 cm /g的孔體積,和j J 6 m2/g的表面積。此外, 鉬觸媒的孔徑分佈中有67·7%的總孔數具有在86人之中位 孔徑範圍内的孔徑。 此實施例說明製備具有中位孔徑至少為23〇 Α之孔徑 分佈的第6攔觸媒。 九^例七——製A具有中位孔您至少為230 A之孔徑分 搜土鉬/鈕觸嬅。 鉬/釩觸媒係以下列方式製備。由實施例丨所述之方法 製備的氧化鋁載體用如下製備的鉬/釩浸潰溶液浸潰。第一 種〉谷液係藉由結合2.14克的(NH4)2M〇2〇7、3 21克的M〇〇3、 0·56克的30%過氧化氫(n)、〇14克的單乙醇胺(MEA), 與3.28克的去離子水形成漿液而製造。此漿液係加熱至65 C直到固體溶解為止。使加熱溶液冷卻至室溫。 第二種溶液係藉由結合3·57克的从〇8〇4與4〇克的去 離子水而製造。使第一種溶液和第二種溶液結[添加足 =的去離子水使結合溶液的體積達到82 ml以產生鉬/釩浸 潰溶液。將氧化紹用翻/鈒浸潰溶液浸潰,以偶然授動老化 2小時,於125 t下乾燥數小時,接著在48〇 t下煅燒2 小時。所得觸媒在每克觸媒中含# 〇〇2 {的釩#口 〇〇2克City, Michigan, U.S.A.) was prepared by milling for 35 minutes. The resulting milled mixture was extruded through a 1.3 TrilobeTM template, dried between 90 and 25, and then calcined at 918 ° C to obtain 650 g of a calcined support with a median pore size of I82 people. This calcined support was placed in a Lindberg furnace. The temperature of the furnace was raised to 1,000 to 11,000 during 1.5 hours, and then kept in this range for 2 hours to produce a carrier. This carrier contains 0-0003 grams of gamma alumina, 0.008 grams of alumina, 0.0008 grams of s_alumina, and 0.978 grams of theta alumina per gram of carrier. Determined by \ ray diffraction. This support has a surface area of 110 m2 / g and a total pore volume of 0.82 cmVg. This carrier had a pore size distribution with a median pore size of 232 A, and 66.7% of the total number of pores in the pore size distribution had a pore size in the range of 85 people. This example illustrates how to prepare a support having a pore size distribution of at least 180 A and containing at least 0.1 g of Θ alumina. For example, the diameter of the wide seat should be at least ― pore size 91 200532010 1. The rhenium catalyst was prepared in the following manner. By example! The prepared oxide carrier was impregnated with a rhenium immersion solution, which was prepared by combining 7,69 g of vosw and 82 g of deionized water. The value of this solution was 2 27. Oxide Shao carrier (100 g) was impregnated with osmium immersion solution to accidentally induce aging for 2 hours. Dry at 25 ° c for several hours, and then thoroughly. . Simmer for 2 hours. The obtained catalyst contained 0 g of vanadium per gram of catalyst, and a part was used as a carrier. This rhenium catalyst has a surface area with a pore pinch distribution of a median pore size of $ A and a pore volume of 0.69 cm3 / g '* nom2 / g. In addition, in the pore size distribution of the sharp catalyst, 66 7% of the total number of pores had a pore size within the range of the meso pore pinch. This example illustrates the preparation of a column 5 catalyst having a pore size distribution with a median pore size of at least 4 230 A. Kongm ^ iilii catalyst with a diameter of at least j3〇 A. The indium catalyst is prepared in the following manner. The emulsified carrier prepared by the method described in Example 1 was impregnated with a rhenium immersion solution. This infusion solution was combined with 4.26 grams of (ΝΗ4) 2MO207, 6.38 grams of MO3, 112 grams of 30% H202, and 0.27 grams of monoethanolamine (MEA). , 6.51 grams of deionized water was prepared to form a 'moxibustion solution. This slurry was heated to 65. . Until the solids are dissolved. The heating solution was allowed to cool to room temperature. The pH of the solvent was 5 36. Adjust the solution volume to 82 mL with ionized water. The alumina carrier (100 g) was impregnated with a molybdenum impregnating solution, aged by accidental agitation for 2 hours, dried at 125 hours for several hours, and then taken at 2 480 t 92 200532010. The catalyst contained in the catalyst contains 0. g of platinum per gram of catalyst, and the remainder is a carrier. This molybdenum catalyst has a pore volume of a median pore diameter of 25 Å, a pore volume of 0.77 cm / g, and a surface area of j J 6 m2 / g. In addition, the pore size distribution of the molybdenum catalyst had a total number of pores of 67.7% having a pore size in the median pore size range of 86 persons. This example illustrates the preparation of a sixth catalyst having a pore size distribution with a median pore size of at least 23 A. Nine ^ Example 7-System A has a median hole. You must have a hole diameter of at least 230 A. Search for earth molybdenum / button contact. The molybdenum / vanadium catalyst was prepared in the following manner. The alumina support prepared by the method described in Example 丨 was impregnated with a molybdenum / vanadium impregnation solution prepared as follows. The first one is that by combining 2.14 g of (NH4) 2M0207, 3 21 g of M03, 0.56 g of 30% hydrogen peroxide (n), and 14 g of single Ethanolamine (MEA) is manufactured by forming a slurry with 3.28 grams of deionized water. This slurry was heated to 65 C until the solids were dissolved. The heating solution was allowed to cool to room temperature. The second solution was made by combining 3.57 grams of deionized water from 0804 and 40 grams. The first solution was combined with the second solution [adding sufficient = deionized water to bring the volume of the binding solution to 82 ml to produce a molybdenum / vanadium immersion solution. The oxide was impregnated with a flip / plump immersion solution, aged by accident for 2 hours, dried at 125 t for several hours, and then calcined at 48 0 t for 2 hours. The obtained catalyst contained # 〇〇2 {of vanadium # 口 〇〇2 g per gram of catalyst

的鉬,其餘部分為載體。此鉬/釩觸媒具有中位孔徑為3㈧A 的孔徑分佈。 此實施例說明製備具有中位孔徑至少為23〇 A之孔徑 93 200532010 分佈的第6攔金屬和第5攔金屬觸媒。 t施例5·~~MJtJM料輿三箱觸媳的 在中央配置有測溫插套的管式反應器係配備熱電偶以 測里整個觸媒床的溫度。此觸媒床係藉由在測溫插套和内 壁之間的空間填充觸媒和碳化矽(20_grid,stanford Matenals; AllS0 Vlej〇, CA)而形成。咸信此種碳化矽如果 有的話,在本文中所述的操作條件下具有低的催化性質。 在將混合物放入反應器的接觸區部位之前,使所有觸媒與 等體積量的碳化矽摻合。Molybdenum, the rest is the carrier. This molybdenum / vanadium catalyst has a pore size distribution with a median pore size of 3㈧A. This example illustrates the preparation of a 6th metal and a 5th metal catalyst having a pore size with a median pore size of at least 230 A. Example 5 · ~~ MJtJM is equipped with a three-box reactor. A tubular reactor equipped with a temperature measuring sleeve at the center is equipped with a thermocouple to measure the temperature of the entire catalyst bed. The catalyst bed is formed by filling the space between the temperature measuring sleeve and the inner wall with catalyst and silicon carbide (20_grid, stanford Matenals; AllS0 Vlej0, CA). It is believed that this silicon carbide, if any, has low catalytic properties under the operating conditions described herein. Prior to placing the mixture in the contact zone of the reactor, all catalysts were blended with an equal volume of silicon carbide.

反應為的原油進料流動係由反應器的頂部至反應器白^ 底邛石反化矽係配置在反應器的底部作為底部載體。底旬 的觸媒/碳化矽混合物(42 cm3)係配置在該碳化矽上方以= 成底部接觸區。底部觸媒具有中位孔徑為77 A的孔徑分 佈,5亥孔徑分佈中有66 7%的總孔數具有在A之中位孔 #範圍内的孔徑。該底部觸媒在每克觸媒中含冑0.095克 的鉬和0.025克的# ’其餘部分為氧化鋁載體。The reaction crude oil feed flow system is from the top of the reactor to the reactor white bottom flint reversed silica system is arranged at the bottom of the reactor as a bottom carrier. The catalyst / silicon carbide mixture (42 cm3) at the end of the year is placed above the silicon carbide to form a bottom contact area. The bottom catalyst has a pore size distribution with a median pore size of 77 A, and 66 7% of the total number of pores in the 50 pore size distribution has a pore size within the range of A's median pore #. The bottom catalyst contained 0.095 g of molybdenum and 0.025 g of # 'per gram of catalyst, and the remainder was an alumina carrier.

中間的觸媒/碳切混合物(56 em3)係配置在底部接觸 區上方以形成中間接觸區。中間觸媒具有中位孔徑為98 Λ 的孔徑分佈’該孔徑分佈中“6.7%的總孔數具有在24 Α 之中位孔徑乾圍内的孔徑。t亥中間觸媒在每克觸媒中含有 〇2克的錄和〇.〇8克的翻,其餘部分為氧化銘載體。 &amp;頁。P的觸媒/奴化矽混合物(42 cm3)係配置在中間接觸 區上方以形成頂部接觸區。頂部觸媒具有中位孔徑為192A 勺孔k刀佈’在每克觸媒中含有G G4克的鉬,其餘部分主 94 200532010 要為γ氧化鋁載體。 石反化石夕係配置在頂部接觸區上方以填充空位並且作為 預熱區。觸媒床係裝入Lindberg爐,其包括對應於預熱區、 頂&quot;卩、中間’和底部接觸區,及底部載體的五個加熱區。 觸媒係藉由將5體積%硫化氫和95體積%氫氣的氣態 混合物以每單位體積(mL)觸媒總量(碳化矽並不視為觸媒的 體積部分)1.5升之氣態混合物的速率導入接觸區而形成硫 化物接觸區的溫度於1小時過程中提高到204 °C (400。1?) 並且保持在204 °C下2小時。保持在204 °C下之後,接 觸區以每小時10 °C (5〇 °F)的速率逐漸提高到316 t (600 F)。使接觸區保持在316。。下一小時,们小時過 Μ逐漸升到370。。(7〇〇 τ)並且保持在37〇七下兩小 % °使接觸區冷卻至周圍溫度。 過濾Gulf〇fMexico中Mars鑽臺的原油,接著在% t (扇。F)下’於供箱中加熱12至24小時以生成具有摘要 方、表1 7之性質的原油進料。將原油進料饋入反應器 頂部。原油進料係流過反應器的預熱區、頂部接觸區、中 ^接觸區、底部接觸區和底部載體。原油進料係於氯氣存 ^與每-種觸媒接觸。接觸條件如下:氫氣與供應至反 應杰之原油進料的比率為328 Nm3/m3 (2〇〇〇 SUB),薦V 為1 h-、及壓力為69Mpa〇〇l4 為石。w 。 U 一個接觸區係加 …、至3 70 C (700。|?)並且伴持a 3 7Λ。广 y ^且俅符在370 C下500小時。三 個接觸區的溫度係接著以 j貝序增加和保持·· 379 °C F) 500小時,接著為388。 u (/30 F) 500 小時, 95 200532010 接著為390 t (734 T) 18〇〇小時,接著為外 T ) 2400 小時。 (?42 總產物(換言之為原油產物和氣體)離開觸媒床。將總 產物導人氣液相分離器。於氣液相分離器巾,將總產物八 離成原油產物和氣體。系統的氣體輸入係由質量流量心 器測定。離開系統的氣體係由測濕計測定。原油產物係定 期分析以敎原油產物成分的重量百分率。所列結果 分之實測重量百分率的平均值。原油產物性質係摘要於圖 7的表1中。 如表1所示,原油產物在每克原油產物中具有〇〇〇75 克的含硫量,0.255克的殘留物含量,〇 〇〇〇7克的含氧量。 原油產物具有MCR含量與C5瀝青質含量的比率為h9及 〇.〇9的TAN。錄和釩的總量為22·4 ^沖㈤。 觸媒壽命係藉由測量加權平均床溫度(“WABT”)對原、、由 進料的運轉時間而決定。觸料命可能與觸媒床的溫度相 關。咸^當觸媒壽命減短時,WABT會增加。目8為本實 “,,丨中所述用於改善接觸區中的原油進料之wabt對時間 ()的圖不。曲線136係表示三個接觸區的平均WAB 丁對 、由進料與頂部、中間,和底部觸媒接觸之運轉時間的時 約2方、大夕數的運轉時間過程中,接觸區的WABT僅改變 、、、C。攸相當穩定的WABT來看,可判斷觸媒的催化 活性並未受到影響。典型而言,3_至3500小時的中門 工廠運轉時間與1年的工業操作相關。 此貫施例說明在控制接觸條件的情況下,使原油進料 96 200532010 契具有t位孔#至少為! 8Q A之孔徑分佈的—種觸媒接觸 以及與具有中位孔徑介於⑽至i8GA範圍内之孔徑分佈, =孔徑分佈中至少60〇/〇的總孔數具有在45 A之中位孔徑 I巳圍内的孔;U之附加觸媒接觸,以生產含有原油產物的總 產物,如同p值所測定者,係保持了原油進料/總產物混合 物的L疋1± .亥原油產物與原油進料相比,具有降低的 TAN,降低的Ni/V/Fe各旦ίΐ夂从上人人 里’降低的§硫量,及降低的含 氧量,而原油產物的殘留物含量和VGO含量為90%至11〇% ❿ 之原油進料的該等性質。 一 介於 90 黾 180Α 接觸。 反應器設備(除了接_ ρ ^ 接觸&amp;的數目和内容以外)、觸媒形 成硫化物法、分離物吝私+ 心產物的方法和分析原油產物的方法係 與實施例5所述者相同。备一 母種觸媒係與等體積的碳化矽 混合。 反應器的原油進料详叙#丄&lt; + 抖机動係由反應器的頂部至反應器的 底部。該反應器係以下列方式由底部填充至頂部。碳化石夕 係配置在反應器的底部作為底部載體。底部的觸媒/碳化矽 混合物(80 cm3)係配置在嗜舻 隹”亥石反化矽上方以形成底部接觸 區。底部觸媒具有中位孔和盍 扎彳工為127 A的孔徑分佈,該孔徑 分佈中有㈣的總孔數具有在32 A之中位孔徑以内的孔 徑。該底部觸媒在每克觸媒中包含〇·η克的在目和〇〇2克 的鎳,其餘部分為載體。 頂部的觸媒/碳化矽混合物 I cm )係配置在底部接觸 97 200532010The middle catalyst / carbon cut mixture (56 em3) is placed above the bottom contact area to form the middle contact area. The intermediate catalyst has a pore size distribution with a median pore size of 98 Λ. In this pore size distribution, "6.7% of the total number of pores has a pore size within the range of 24 Α median pore diameter. Contains 0.02 gm and 0.08 gm, and the rest is an oxide carrier. &Amp; Page. The catalyst / silicon compound (42 cm3) of P is arranged above the middle contact area to form the top contact area. The top catalyst has a median pore size of 192A scoop hole k-knife cloth '. Each gram of the catalyst contains 4 g of molybdenum, and the rest is mainly 94 200532010. It is a gamma alumina carrier. The top of the zone is filled with vacancies and serves as a preheating zone. The catalyst bed is loaded into the Lindberg furnace, which includes five heating zones corresponding to the preheating zone, top &quot; 卩, middle 'and bottom contact zones, and the bottom carrier. The medium is introduced by introducing a gaseous mixture of 5 vol% hydrogen sulfide and 95 vol% hydrogen at a rate of 1.5 liters of the gaseous mixture per unit volume (mL) of the catalyst (silicon carbide is not considered as a volume part of the catalyst). Contact zone to form a sulfide contact zone at a temperature of 1 During the process, the temperature was increased to 204 ° C (400.1?) And kept at 204 ° C for 2 hours. After holding at 204 ° C, the contact zone gradually increased at a rate of 10 ° C (50 ° F) per hour. To 316 t (600 F). Keep the contact area at 316. In the next hour, they gradually rose to 370 in the next hour (700) and kept at 2700% to make the contact area. Cool to ambient temperature. Filter crude oil from the Mars rig in GulfOfMexico, then heat it in a supply tank for 12 to 24 hours at% t (fan. F) to generate a crude oil with the properties shown in Table 17 in summary. Feed the crude oil feed to the top of the reactor. The crude oil feed flows through the preheating zone, the top contact zone, the middle contact zone, the bottom contact zone, and the bottom carrier of the reactor. The crude oil feed is stored in the chlorine gas reservoir and Each catalyst is contacted. The contact conditions are as follows: the ratio of hydrogen to the crude oil feed to the reaction is 328 Nm3 / m3 (200 SUB), the recommended V is 1 h-, and the pressure is 69 MPa. It is a stone. W. U A contact area is added ... to 3 70 C (700. |?) And is accompanied by a 3 7 Λ. Guangy ^ and the symbol is 500 hours at 370 C. The temperature in each contact zone was then increased and maintained in the order of j shells (· 379 ° CF) for 500 hours, followed by 388. u (/ 30 F) for 500 hours, 95 200532010 followed by 390 t (734 T) for 180 hours , Followed by the outer T) 2400 hours. (? 42 total products (in other words, crude oil products and gases) leave the catalyst bed. The total products are led to a gas phase liquid separator. In a gas-liquid separator, the total product is separated into a crude product and a gas. The system's gas input is measured by a mass flow cardiac device. The gas system leaving the system is determined by a hygrometer. Crude oil products are regularly analyzed to determine the weight percentage of crude oil product components. Results listed are averages of measured weight percentages. Crude product properties are summarized in Table 1 of FIG. As shown in Table 1, the crude oil product has a sulfur content of 0.0075 grams per gram of crude oil product, a residue content of 0.255 grams, and an oxygen content of 0.0007 grams. The crude oil product has TANs with a ratio of MCR content to C5 asphaltene content of h9 and 0.09. The total amount of recorded and vanadium is 22.4 ^ Chong. The catalyst life is determined by measuring the weighted average bed temperature ("WABT") against the original and the feed operating time. The catalyst life may be related to the temperature of the catalyst bed. As the catalyst life decreases, WABT increases. Figure 8 shows the graph of wabt versus time () used to improve the crude oil feed in the contact zone as described in Figure 1, and curve 136 shows the average WAB Ding pair of the three contact zones. The contact time of the top, middle, and bottom catalysts is about 2 squares. During the operating hours of the large number of hours, the WABT in the contact area only changes,, and C. From the perspective of the relatively stable WABT, the catalyst can be judged. The catalytic activity is not affected. Typically, 3 to 3500 hours of operation at the Zhongmen plant is related to one year of industrial operation. This example shows that crude oil is fed under controlled contact conditions 96 200532010具有 有 t 位 孔 # at least! 8Q A pore size distribution-a catalyst contact and a pore size distribution with a median pore size ranging from ⑽ to i8GA, = the total number of pores in the pore size distribution of at least 60/0 Have holes within the median pore diameter I 巳 of 45 A; additional catalyst contact of U to produce total products containing crude oil products, as determined by p-value, maintains L of crude oil feed / total product mixture ± 1 ± .Ha crude oil product has Reduced TAN, reduced Ni / V / Fe, and reduced the amount of sulphur and oxygen content from the above, and the residue content and VGO content of crude oil products are 90% to 11%. % Of these properties of crude oil feed. One between 90 黾 180 Α contact. Reactor equipment (except for the number and content of _ ρ ^ contact &amp; contact), catalyst formation sulfide method, isolates privacy + heart The method of the product and the method of analyzing the crude oil product are the same as those described in Example 5. A parent catalyst system was mixed with an equal volume of silicon carbide. The crude oil feed to the reactor is described in detail. From the top of the reactor to the bottom of the reactor. The reactor is filled from the bottom to the top in the following way. Carbide is arranged at the bottom of the reactor as a bottom carrier. The catalyst / silicon carbide mixture at the bottom (80 cm3) It is arranged above the Si-Hexite reversed silicon to form the bottom contact area. The bottom catalyst has a median hole and a pore size distribution of 127 A. The total number of holes in the pore size distribution has a pore size within the 32 A median pore size. The bottom catalyst contained ηg of on-mesh and 0.02g of nickel per gram of catalyst, and the remainder was a carrier. The catalyst / silicon carbide mixture at the top (I cm) is configured at the bottom contact 97 200532010

= 成頂部接觸區。頂部觸媒具有中位孔徑為1。。A= Into the top contact area. The top catalyst has a median aperture of 1. . A

之中:該孔徑分佈中有66·7%的總孔數具有在20 A 之中位孔徑以内的莉僻# ^ ^ ° A 工。以頂部觸媒在每克觸媒中包含〇 〇3 克的鎳和0.12克的鉬,且 山 在第一接觸區上方以填充^ 乳化1呂1化石夕係配置 狀 、充二位並且作為預熱區。觸媒床係 衣、111叫爐,其包括對應於預熱區、兩個接觸區,及 底部載體的四個加熱區。Middle: 66.7% of the total number of pores in this pore size distribution have a solitary # ^ ^ ° A operation within a median pore size of 20 A. The top catalyst contains 0.003 grams of nickel and 0.12 grams of molybdenum per gram of catalyst, and the mountain is filled above the first contact area with ^ emulsified 1 Lu 1 fossil evening system configuration, filled two positions and used as Hot zone. The catalyst bed garment, 111 is called a furnace, and includes four heating zones corresponding to a preheating zone, two contact zones, and a bottom carrier.

具有摘要於表2,«9之性質的BS-4原油(Venezuela) 係供給人反應器頂部。原油進料係流過反應器的預熱區、 料㈣H部㈣區和底部載體。原油進料係於氣氣 存在下與每-種觸媒接觸。接觸條件如下:氯氣與供應至 反應器之原油進料的比率為160 NmVmMl〇〇〇 SCFB), 。 為lh ,及壓力為6·9 MPa (1014.7 psi)。兩個接觸 區係加熱至260 t (500卞)並且保持在26〇 t (5〇〇 τ) 下287小時。兩個接觸區的溫度係接著以下列順序增加和 保持· 270 C (525 Τ ) 190 小時,接著為 288 °c (55〇 下)The BS-4 crude oil (Venezuela) with properties summarized in Table 2, «9, was supplied to the top of the reactor. The crude oil feed flows through the preheating zone of the reactor, the H zone of the feedstock and the bottom carrier. The crude oil feed is contacted with each catalyst in the presence of gas. The contact conditions were as follows: the ratio of chlorine gas to the crude oil feed to the reactor was 160 NmVmM (100 SCFB). Is lh, and the pressure is 6.9 MPa (1014.7 psi). The two contact zones were heated to 260 t (500 ° F) and maintained at 260 t (500 τ) for 287 hours. The temperature of the two contact zones was then increased and maintained in the following order: 270 C (525 Τ) for 190 hours, followed by 288 ° c (55 ° C)

216小日守,接著為315它(6〇〇卞)36〇小時,接著為343。〇 (650 F) 120小時,以達到1173小時的總運轉時間。 總產物離開反應器並且像實施例5所述一樣地分離。 原油產物在加工期間具有〇·42的平均TAN和12.5的平均 API比重。該原油產物在每克原油產物中含有〇 〇〇23克的 硫’ 0.0034克的氧,0.441克的VGO,和0.378克的殘留 物。原油產物的額外性質係列於圖9的表2中。 此實施例顯示使原油進料與具有中位孔徑介於90至 98 200532010 1 8 0人範圍内之孔經公 刀佈的觸媒接觸以生產原油產物,其 與原油進料的性質相比, 具有降低的TAN,降低的Ni/V/Fe 含量,及降低的含氧晋, 而原油產物的殘留物含量和V G Ο 含量為99%和100%之为 眾油進料的個別性質。 f旌&gt; 例7. 原油淮粗命工 ~^觸媒的接觸。 反應器設備(除了拉緬π a 接觸£的數目和内容以外)、觸媒、 總產物分離法、原油產物八 — 座物刀析’和觸媒形成硫化物法係與 實施例6所述者相同。 具有摘要於表3,圖in Q 10之性質的原油進料(BC-10原油) 係供給入反應器頂部。屑 原油進枓係流過反應器的預熱區、 頂部接觸區、底部接觸p $ 丨筏觸區和底部載體。接觸條件如下··氫 氣與供應至反應器之肩、、由隹 原/由進枓的比率為80 NmVm3 (5〇〇 SCFB),LHSV 為 2 Ir1,π 茂上达 及麼力為 6.9 MPa (1014.7 psi)。 兩個接觸區係逐漸加熱至343。「、 土 王C (650 F)。總運轉時間 為1007小時。 原油產物在加工期間具有0.16的平均TAN和162的 平均AH比重。該原油產物含有! 9 wtppm _,6 ,納,〇.6wtppm的辞,和3卿㈣的卸。該原油產物在 母克原油產物中含有㈣33克的硫,G.002克的t,〇376 克的VGO,和〇.4〇1克的殘留物。原油產物的額外 列於圖10的表3中。 、“ 此實施例顯示使原油進料與具有孔徑分佈在9〇至 A之範圍内的選定觸媒接觸以生產原油產物,其具 的TAN,降低的總妈、納、辞,和卸含量,而原油產物的 99 200532010 含硫量、VGO含量和殘留物含量為76%、94%和ι〇3%之 · 原油進料的個別性質。 t施例8至11.__觸嫫系統在各種接 觸條件下的接觸。 母個反應裔’设備(除了接觸區的數目和内容以外)、每 個觸媒形成硫化物法、每個總產物分離法和每個原油產物 分析係與實施例5所述者相同。除另有說明外,所有觸媒 係以2份碳化矽對丨份觸媒的體積比與碳化矽混合。通過 每個反應器的原油進料流動係由反應器的頂部至反應器的 · 底部。碳化矽係配置在每個反應器的底部作為底部載體。 每個反應器具有底部接觸區和頂部接觸區。在觸媒/碳化矽 混合物放入每個反應器的接觸區之後,碳化矽係配置在頂 部接觸區上方以填充空位並且作為每個反應器的預熱區。 每個反應器係裝人LindbergM,其包括對應於預熱區、兩 個接觸區,及底部載體的四個加熱區。 於實施例8中,未煅燒過的鉬/鎳觸媒/碳化矽混合物 ⑽3)係配置在底部接觸區中^該觸媒在每克觸媒中包含鲁 0.146克的翻,0.047克的錄,和〇〇21克的鱗,其餘部分 為氧化鋁載體。 包含具有中位孔徑為180 A的孔徑分佈之觸媒的鉬觸 媒/碳化矽混合物(12 cm3)係配置在頂部接觸區中。該鉬觸 媒具有每克觸媒中含〇.〇4克鉬的總含量,其餘部分為包含 每克載體中至少為〇.5〇克丫氧化鋁的載體。 貝知例9中,未锻燒過的#目/銘觸媒/碳化石夕混合物(4 8 100 200532010 ⑽3)係配置在兩個接觸區中。該未锻燒過的鉑/姑觸媒包含 0.⑷克的錮,(MM3克祕,和⑴吻克的磷,其餘部分 為氧化鋁载體。 钥觸媒/碳化石夕混合物(12 cm3)係配置在頂部接觸區 中。該鉬觸媒與實施例8之頂部接觸區者相同。 於貫施例10中’如實施例8之頂部接觸區中所述的翻 觸媒係與碳化矽混合並配置在兩個接觸區中(6〇 cy)。 於貝施例11中,未煅燒過的鉬/鎳觸媒/碳化矽混合物 (48 cm3)係配置在底部接觸㊣中。該未锻燒過的翻/錄觸媒 在每克觸媒中包含0.09克的銷,〇 〇25克的錄,和〇 〇ι克 的鱗’其餘部分為氧化鋁載體。 銦觸媒/碳化石夕混合物(12 cm3)係配置在頂部接觸區 。忒鉬觸媒與實施例8之頂部接觸區者相同。 。過濾來自Mars鑽臺(Gulf〇fMexic〇)的原油,接著在% ^ (200 F)下’於烘箱中加熱以24小時以生成用於實 她例8至11之具有摘要於表4,圖11之性質的原油進料。 =原油進料供給入此等實施例的反應器頂部。原油進料係 机過反應裔的預熱區、頂部接觸區、底部接觸區和底部載 月丑。原油進料係於氫氣存在下與每一種觸媒接觸。每個實 施例的接觸條件如下:氫氣與接觸期間之原油進料的比率 為160 Nm3/m3 (1_ SCFB),及每個系統的總壓力為㈠ MPa (1014·7 PS1)。在接觸的前200小時期間,LHSV為2.〇 h而接著在剩下的接觸時間LHSV降低至i〇 。所有 接觸區的溫度丨343 °C (650 T)接觸500小時。在5〇〇 101 200532010 小時後,所有接觸區的溫度係控制如下:使接觸區的溫度 ’ 升到354 C (670 °F ),保持在354 °C下200小時;升到 3 66 C (690 F ),保持在 366 °C 下 200 小時;升到 371 。〇 (700 F)’ 保持在 371 °C 下 1000 小時;升到 385。〇 (725 F )保持在3 8 5 C下2 0 0小時;然後升到3 9 9 °C (7 5 0 ) 的最終溫度並保持在399 °C下200小時,以達到23〇〇小 時的總接觸時間。 原油產物係定期分析以測定TAN、原油進料之氫的吸 取p值、VGO含量、殘留物含量,及含氧量。實施例8 _ 至11所生產之原油產物性質的平均值係列於目U的表5 中。 ”、、貫施例8至11的每個蜩琛糸統之原油產物之 P值(“P”)對運轉時間(“t”)的圖示。原油進料具有至少工5 :二值I曲線140、142、144,# 146係表示藉由使原油 進料個別與實施例8至n的四種_系統接 原I油產物之?值。對於實施例的觸❹統而言, 達到23 00小時的搭、丄女&quot; 例η中,多數剩下至少為於實施 ,數運轉時間的Ρ值大於1.5。在實施例u運 之2p3:i:)結束時’ P值為Μ。從每個試驗的原油產物 持相當穩定(例:=τ中原油進料於接觸期間保 了實施例!。中的:值1分離)。如圖12所示,除 值^加之外,原油產物之ρ值在 分的每個試驗中均保持相當固定。 在大4 圖13為氫氣存在下四種觸媒系統的原油進料之氫的淨 102 200532010 吸取(“h2”)對運轉時間(“t”)的圖示。曲線i48、i5〇、⑴、 154係表示藉由使原油進料個別與實施例8至u的每個觸 媒乐統接觸所得到之氫的淨吸取。原油進料之氫的淨吸取 在2300小時的運轉期間係於7至48 SCFB)的範圍内。如圖 ' Ώ 3所不,原油進料之氫的淨吸取在 每個試驗中相當固定。216 small day guards, followed by 315 it (6000) 36 hours, then 343. 〇 (650 F) 120 hours to achieve a total operating time of 1173 hours. The total product left the reactor and was separated as described in Example 5. Crude products have an average TAN of 0.42 and an average API specific gravity of 12.5 during processing. This crude product contained 0.0023 grams of sulfur '0.0034 grams of oxygen, 0.441 grams of VGO, and 0.378 grams of residue per gram of crude product. Additional properties of the crude product series are shown in Table 2 of FIG. This example shows that contacting a crude oil feed with pores having a median pore size in the range of 90 to 98 200532010 180 people through a catalyst of a male knife cloth to produce a crude oil product, compared with the properties of the crude oil feed, It has the characteristics of reduced TAN, reduced Ni / V / Fe content, and reduced oxygen content, while crude oil product residue content and VG 0 content are 99% and 100%. fijing &gt; Example 7. Crude oil crude oil ~ ~ contact with catalyst. Reactor equipment (except the number and content of Ramon π a contact), catalyst, total product separation method, crude product eight-block analysis, and catalyst sulfide formation method are as described in Example 6. the same. A crude oil feed (BC-10 crude oil) with properties summarized in Table 3, figure in Q 10, was fed to the top of the reactor. Crude crude oil enters the preheating zone, the top contact zone, the bottom contact zone, and the bottom carrier of the reactor. The contact conditions are as follows: · The ratio of hydrogen to the shoulder supplied to the reactor is 80 NmVm3 (500SCFB) from Liaoyuan / Longjin, LHSV is 2 Ir1, π Moshangda and Moduli is 6.9 MPa ( 1014.7 psi). The two contact zones were gradually heated to 343. ", King C (650 F). The total operating time is 1007 hours. The crude product has an average TAN of 0.16 and an average AH specific gravity of 162 during processing. This crude product contains! 9 wtppm _, 6, nano, 0.6 wtppm The crude product and the unloading of 3 ㈣. The crude product contains 33 g of sulfur, G.002 g of t, 0376 g of VGO, and 0.41 g of residue in the crude oil product of crude oil. Crude oil The products are additionally listed in Table 3 of Figure 10. "This example shows that a crude oil feed is contacted with a selected catalyst having a pore size distribution in the range of 90 to A to produce a crude product, which has a lower TAN, The individual properties of crude oil feeds are 99 200532010 sulfur content, VGO content and residue content of crude oil products of 76%, 94% and ι03%. tExamples 8 to 11 .__ Contact of the palatal system under various contact conditions. The parent reaction apparatus (except for the number and content of contact zones), each catalyst-forming sulfide method, each total product separation method, and each crude oil product analysis system are the same as those described in Example 5. Unless otherwise stated, all catalysts were mixed with silicon carbide in a volume ratio of 2 parts silicon carbide to 1 part catalyst. The crude feed flow through each reactor is from the top of the reactor to the bottom of the reactor. The silicon carbide system is arranged at the bottom of each reactor as a bottom carrier. Each reactor has a bottom contact zone and a top contact zone. After the catalyst / silicon carbide mixture was placed in the contact area of each reactor, the silicon carbide system was arranged above the top contact area to fill the voids and serve as a preheating area for each reactor. Each reactor was fitted with LindbergM, which included four heating zones corresponding to a preheating zone, two contact zones, and a bottom carrier. In Example 8, the uncalcined molybdenum / nickel catalyst / silicon carbide mixture was arranged in the bottom contact area. The catalyst contained 0.146 g of per gram of catalyst and 0.047 g of per gram of catalyst. And 〇21 grams of scale, the rest is alumina support. A molybdenum catalyst / silicon carbide mixture (12 cm3) containing a catalyst having a pore size distribution with a median pore diameter of 180 A was arranged in the top contact area. The molybdenum catalyst has a total content of 0.04 g of molybdenum per gram of the catalyst, and the remainder is a carrier containing at least 0.50 g of alumina per gram of the carrier. In Known Example 9, the unburned # 目 / 明 catalyst / carbonized carbide mixture (4 8 100 200532010 ⑽3) is arranged in two contact areas. The uncalcined platinum / catalyst contains 0.1 g of gadolinium, (MM3 g of mythium, and gallium of phosphorus, and the rest is an alumina carrier. Key catalyst / carbonized carbide mixture (12 cm3 ) Is arranged in the top contact area. The molybdenum catalyst is the same as that in the top contact area of Example 8. In the tenth embodiment, the flip catalyst system and silicon carbide described in the top contact area of Example 8 are used. Mix and arrange in two contact areas (60cy). In Example 11, the uncalcined molybdenum / nickel catalyst / silicon carbide mixture (48 cm3) was placed in the bottom contact ridge. The unwrought The burned turning / recording catalyst contains 0.09 grams of pins per gram of catalyst, 0.25 grams of recordings, and 100,000 grams of scale. The rest is an alumina carrier. Indium catalyst / carbide carbide mixture (12 cm3) is arranged in the top contact area. The rhenium-molybdenum catalyst is the same as that in the top contact area of Example 8. The crude oil from the Mars rig (Gulf〇fMexic〇) is filtered, and then at% ^ (200 F) 'Heated in an oven for 24 hours to generate a crude oil feed having the properties summarized in Table 4, Figure 11 for Examples 8 to 11. = Crude oil feed supply Feed to the top of the reactors of these examples. Crude oil feed is the preheating zone, top contact zone, bottom contact zone and bottom of the reactor. The crude oil feed is in the presence of hydrogen and each catalyst. Contact. The contact conditions of each example were as follows: the ratio of hydrogen to the crude oil feed during the contact was 160 Nm3 / m3 (1_SCFB), and the total pressure of each system was ㈠ MPa (1014 · 7 PS1). During the first 200 hours, the LHSV was 2.0 hours, and then the remaining contact time LHSV was reduced to i 0. The temperature of all contact zones was 343 ° C (650 T) for 500 hours of contact. At 50001 200532010 hours After that, the temperature of all contact zones was controlled as follows: the temperature of the contact zone was raised to 354 C (670 ° F) and kept at 354 ° C for 200 hours; it was raised to 3 66 C (690 F) and kept at 366 ° 200 hours at C; rose to 371.0 ° (700 F) '1000 hours at 371 ° C; rose to 385 ° (725 F) 2000 hours at 3 8 5 C; then rose to 3 9 A final temperature of 9 ° C (750) was maintained at 399 ° C for 200 hours to achieve a total contact time of 23,000 hours. Crude oil products are regularly analyzed to determine the TAN, the hydrogen absorption p-value of the crude oil feed, the VGO content, the residue content, and the oxygen content. The average values of the properties of the crude oil products produced in Examples 8 to 11 are shown in head U. Table 5. "A graph showing the P value (" P ") versus the operating time (" t ") of the crude oil products of each system in Examples 8-11. The crude oil feed has at least 5: binary I-curves 140, 142, 144, and # 146 means that the crude oil feed is individually connected to the four _ systems of Examples 8 to n to the original I oil product? value. For the contact system of the embodiment, in the case of reaching 23,200 hours, most of the cases η, most of the remaining is at least for implementation, and the P value of the running time is greater than 1.5. At the end of Example 2p3: i :) ', the P value is M. The crude product from each test remained fairly stable (e.g., the crude oil feed in τ was maintained during the contact example! Medium: value 1 separation). As shown in Figure 12, in addition to the value ^ added, the ρ value of the crude oil product remained fairly constant in each test. In Big 4 Figure 13 is a graph showing the net hydrogen of crude oil feed for four catalyst systems in the presence of hydrogen. The curves i48, i50, ⑴, 154 represent the net uptake of hydrogen obtained by contacting the crude oil feed individually with each of the catalysts of Examples 8 to u. The net uptake of hydrogen from the crude feed is in the range of 7 to 48 SCFB during a 2,300-hour operation. As shown in Figure Ώ3, the net uptake of hydrogen from the crude feed was fairly constant in each experiment.

圖14為實施例8至&quot;的每個觸媒系統之以重量百分 率表示的原油產物之殘留物含量(“R”)對運轉時間(“t”)的圖 不。於四個試驗的每一個之中,原油產物具有殘留物含量 為88至90%之原油進料的殘留物含量。曲線156、158、1M、 162係表示藉由使原油進料個別與實施例8至η的觸媒系 、、’充接觸所得到之原油產物的殘留物含量。如圖14所示y,、 原油產物的殘留物含量在大部分的每個試驗中均保持相當Fig. 14 is a graph showing the residual content ("R") of crude oil products as a percentage of the weight of each catalyst system of Examples 8 to "&quot; versus operating time (" t "). In each of the four tests, the crude oil product had a residue content of the crude oil feed with a residue content of 88 to 90%. Curves 156, 158, 1M, and 162 show the residual content of the crude oil product obtained by bringing the crude oil feeds individually into contact with the catalyst systems of Examples 8 to η. As shown in Figure 14, the residual content of the crude oil product remained comparable in most of the experiments.

圖15為實施例8至u的每個觸媒系統之原油產物 API比重改變(“ΔΑΡΙ,,)對運轉時間(“t”)的圖示。曲線 166、168、17〇係表示藉由使原油進料個別與實施例8 11的觸媒系統接觸所得到之原油產物的Αρι比重。於四 試驗的每一個之中,每個原油產物具有在58.3至72 7 c 之範圍内的黏度。每個原油產物的Αρι比重係增加工$ 4·1度。增加的API比重係對應於21·7至22·95範圍内 原油產物之API比重。此範圍内的Αρι比重為ιι〇至Η? 之原油進料的API比重。 圖1 6為實施例8至1 1的每個觸媒系統之以重量百 103 200532010 率表示的原油產物之含氧量r 孔里(〇2 )對運轉時間(‘‘t,,)的 示。曲線 172、174、176、178 在矣-μ 山 &amp; π 8係表不猎由使原油進料個 別=施例8至U的觸媒系統接觸所得到之原油產物的 含虱量。每個原油產物具有含氧量最多為原油進料的“%。 每個原油產物在每個試驗期間具有含氧量為每克原油產。物 中請Μ至〇.〇〇15克的範圍内。如圖16所示,原油產物 的含氧量纟小時的接觸時間之後仍保持相當固定。原 油產物相當固定的含氧量顯示選定的有機氧化合物在接觸 期間減少。因為在這些實施例中ΤΑΝ也降低,所以可推斷 至少-冑分的含叛酸有冑氧化合物比含非幾酸有機氧化合 物選擇性減少的更多。 於實施例11中,反應條件為·· 371它(7〇〇卞卜壓 力為6.9 MPa (ΗΗ4.7 psi),及氫和原油進料的比率為二 (1_ SCFB),以原油進料重量計,原油進料 含量的降低為17.5 wt%。在399 °C (750卞)的溫度下, 方、相同壓力及氫和原油進料的比率下,以原油進料重量 計,原油進料MCR含量的降低為25·4 wt%。 於實施例9中,反應條件為:371它(7〇〇卞),粟 力為6·9 MPa (1014·7 psi),及氫和原油進料的比率為 ^/以(1〇〇〇 SCFB),以原油進料重量計,原油進料 含量的降低為17_5 wt%。在399 °C (750 °F)的溫度下, 於相同壓力及氫和原油進料的比率下,以原油進^重量 計’原油進料MCR含量的降低為19 wt%。 原油進料MCR含量中此等降低的增加係顯示未煅燒 104 200532010 過的第6和l〇攔金屬觸媒於較高溫度下比未椴燒過的第6 和9攔金屬觸媒更能促使MCR含量的降低。 這些實施例顯示具有相對高TAN (〇 8 @ TAN)的原油 進料與-或多種觸媒接觸係生產原油產物,而同時保持原 油進料/總產物混合物的穩定性並且具有相當少量氫的淨吸 =°選定的原油產物性質最多為7〇%之原油進料的同樣性 負’同時原油產物的選定性質在2〇 i 3〇%之原油進料的 同樣性質範圍内。 具體而t,如表4所示,每個原油產物係以最多為料 NmW (275 SCFB)的原油進料之氫的淨吸取生產。這類產 物具有平均TAN最多為原油進料的4%,平均總Ni/v含量 最多為61%之原油進料的總Ni/V含量,而同時保持高於3 的原油進料之P值。每個原油產物的平均殘留物含量為'88 至90%之原油進料的殘留物含量。每個原油產物的平均 VGO含量為1 15至117%之原油進料的VG〇含量。每個原 油產物的平均API比重為11〇至117%之原油進料的Αρι 比重,而每個原油產物的黏度最多為45%之原油進料的黏 度。 ' 施例 1 2至14 · 原油淮斜 1情況下 中位至少為」j〇A之孔徑分佈的觸撼夕 於實施例12至14中,每個反應器設備(除了接觸區的 數目和内容以外)、每個觸媒形成硫化物法、每個總產物分 離法和每個原油產物分析係與實施例5所述者相同。所有 觸媒係與等體積的碳化矽混合。每個反應器的原油進料流 105 200532010 動係由反應器的頂部至反應器的底部。碳化矽係配置在每 個反應器的底部作為底部載體。每個反應器包含一個接觸 區。在觸媒/碳化矽混合物放入每個反應器的接觸區之後, 石厌化矽係配置在頂部接觸區上方以填充空位並且作為每個 反應器的預熱區。每個反應器係裝入Lindberg爐,其包括 對應於預熱區、接觸區,及底部載體的三個加熱區。使原 油進料於氫氣存在下與每一種觸媒接觸。 觸媒/碳化矽混合物(40 cm3)係配置在碳化矽上方以形 、接觸區用於貫施例12的觸媒係如實施例2所製備的 ⑩ 5媒用於實施例13的觸媒係如實施例3所製備的鉬 蜀某用於貝施例14的觸媒係如實施例4所製備的鉬/釩 觸媒。 貝轭例12至14的接觸條件如下··氫與供應至反應器 】原由進料的比率為160 Nm3/m3 (1〇〇〇 SCFB),LHSV為1 、,及壓力為6_9 MPa (ΐ〇14·7 psi)。接觸區係於一段時間 過程中,漸加熱至343 °C (650 T)並且保持在343 t;下 2〇小日寸,以達到36〇小時的總運轉時間。 _ 總產物_接觸區並且像實施例5所述—樣地分離。 12 j門係’則定每値觸媒系統之氫的淨吸取。於實施例 氫的'尹吸取為_10·7 Nm3/m3 (·65 SCFB),原油產物 具有 6 · 7 5 的 τ Δ Μ 一 7 Λ ' 。於貫施例13中,氫的淨吸取在2.2至 3·〇 Nm3/m3 (13 A •至18·7 SCFB)的範圍内,原油產物具有 在〇.3至〇·5之^ Μ 7 &amp;圍内的TAN。於實施例14中,在原油進 枓與銦/飢觸媒的 、妾觸L,氫的淨吸取在_〇·〇5 Nm3/m3至 106 200532010 原油產物 〇·6 NmVm3 (-0.36 SCFB 至 4.0 SCFB)的範圍内 具有在0.2至0.5之範圍内的tan。 從接觸期間氫的淨吸取值來看,估計在原油進料與叙 觸媒接觸期間,氫係以! 0.7 Nm3/m3 (65 SCFB)的速率發^。 接觸期間的氫氣發生與習知製程中所用的氫量心,x可容 許在製程中使用較少的氫來改善劣質原油的性f。接觸: 間需要較少的氫會傾向於降低加工原油的成本。 / 此外,原油進料與鉬/釩觸媒的接觸係生產具有低於由 單獨:觸媒所生產之原油產物的TAN之TAN的原油產物。 15 ^ 1S __ 每個反應器設備(除了接觸區的數目和内容以外)、每 個觸媒形成硫化物法、每個總產物分離法和每個原油產物 分析係與實施例5所述者相同。除另有說明外,所有觸媒 係以2份碳化石夕對!份觸媒的體積比與碳化石夕混合。每個 反應1的原油進料流動係由反應器的頂部至反應器的底 卩厌化石夕心配置在每個反應器的底部作為底部載體。每籲 個反應器具有底部接觸區和頂部接觸區。在觸媒/碳化石夕混 合物放入每個反應器的接觸區之後,碳化矽係、配置在頂部 接觸區上方以填充空位並且作為每個反應器的預熱區。每 個反應器係裝人Lindberg爐,其包括對應於預熱區、兩個 接觸區’及底部載體的四個加熱區。 在每個實施例中,飢觸媒像實施例2所述一樣地製備 並且和附加觸媒一起使用。 107 200532010 方'貝軛例15中,附加觸媒/碳化矽混合物(45 cm3)係配 5底部接觸區中,該附加觸媒為藉由實施例3所述之方 ▲備的麵觸媒。飢觸媒/碳化石夕混合物(1 5 cm3)係配置在 頂部接觸區中。 ' 〗16中’附加觸媒/碳化石夕混合物(3〇 cm3)係配 在底接觸區中,該附加觸媒為藉由實施例3所述之方 製備的銦觸媒。飢觸媒/碳化石夕混合物(3〇⑽3)係配置在 了頁部接觸區中。 於貫施例17中’附加觸媒/碳化矽混合物(30 cm3)係配 籲 置在底部接觸區中,該附加觸媒係如實施例4所製備的鉬/ 釩觸媒。釩觸媒/碳化矽混合物(3() cm3)係配置在頂部接觸 區中。 於實施例 1 8 中,Pyrex® (Glass works Corporation,New Y〇rk,U.S·Α·)小珠(30 cm3)係配置在每個接觸區中。 用於實施例1 5至1 8之具有摘要於表5,圖1 7之性質 的原油(Santos Basin,Brazil)係供給入反應器頂部。原油進 料係流過反應器的預熱區、頂部接觸區、底部揍觸區和底 春 部載體。原油進料係於氫氣存在下與每一種觸媒接觸。每 個貫施例的接觸條件如下:氫氣與供應至反應器之原油進 料的比率在前86小時為160 Nm3/m3 (1000 SCFB)而在剩下 的時限為 80 Nm3/m3 (500 SCFB),LHSV 為 1 h·1,及壓力 為6.9 MPa (1014.7 psi)。接觸區係於一段時間過程中逐漸 加熱至343 °C (650 °F)並且保持在343 °C下以達到1400 小時的總運轉時間。 108 200532010 這些實施例顯示於氫源存在下,原油進料與具有中位 孔徑為35G A之孔徑分佈的第5攔金屬觸媒與結合且有中 位孔徑在250至300 A範圍内之孔狎八欲,a 、 ^工刀佈的附加觸媒接觸 以生產原油產物,其與原油進料之 』樣性質相比具有改變 的性貝’而該原油產物的其他性質盘 、〃原油進料之同樣性質 相比只有少量改變。此外,在加 牡 期間係觀察到原油進料 之相當少量氫的吸取。 具體而言,如表5,圖17所示,實施例15至17的原 油產物具有TAN最多為15%之原油進料的tan。實施例Η =1 7中所生產的原油產物與原油進料的同樣性質相比, 3具有最多Α 44%的總請/Fe含量,最多為观的含 氧量’及最多A 75%的黏度。此外,實施例15至17中所 生產的原油產物分別具有API比重為1〇〇至1〇3%之原油 進料的API比重。 對比之下,在非催化條件(實施例18)下所生產的原油 產物與原油進料的黏度# Αρι比重相&amp;,係生成具有增加 占度和降低API比重的產物。從增加黏度和降低A&quot;比重 來看,可推斷已引發原油進料的焦化及/或聚合。 料在各種lhsν下的接觸。 接觸系統和觸媒係與實施例6所述者相同。原油進料 、1'貝列於圖1 8中的表6。接觸條件如下:氫氣與供應至 〜之原油進料的比率為16〇 Nm3/m3 (1〇〇〇 SCFB),壓 力為6.9MPa(1014.7Psi),及接觸區的溫度為371 X: (700 F )達總運轉時間。於實施例1 9中,接觸期間的LHSV於 109 200532010 一,時間過程中由1 h-丨增加到12 h·〗,保持在12 h-】下48 ' ^ 接著使增加到20.7 h·1,保持在20.7 h·1下96 小時。 方、貝苑例1 9中’分析原油產物以測定在LHSV為1 2 1Γ1 和20.7 h 1之時限期間的TAN、黏度、密度、vG〇含量、 玟甾物3量、雜原子含量,及有機酸金屬鹽形態的金屬含 里。原油產物性質的平均值示於表6,圖丨8。 ^ 士表6,圖18所示,實施例丨9的原油產物與原油進 料的TAN和黏度相比具有降低的TAN和降低的黏度,而參 原油產物的ApI比重為104至110%之原油進料的Apl比Fig. 15 is a graph showing the change in API specific gravity of crude oil products ("ΔΑΡΙ ,," versus operating time ("t") for each catalyst system of Examples 8 to u. The crude oil feeds were individually contacted with the catalyst systems of Examples 8 and 11 and the Aρm specific gravity of the crude oil products. In each of the four tests, each crude oil product had a viscosity in the range of 58.3 to 72 7 c. Each The crude oil product's Aρ specific gravity increased by $ 4.1 degrees. The increased API specific gravity corresponds to the API specific gravity of crude oil products in the range of 21.7 to 22.95. The APF specific gravity in this range is ιι0 to Η? The API specific gravity of the crude oil feed. Figure 16 shows the oxygen content of the crude oil product expressed in terms of weight percent 103 200532010 for each catalyst system of Examples 8 to 11 in pores (0 2) versus operating time (' The curves of 172, 174, 176, and 178 in the 矣 -μ mountain & π 8 series show that the crude oil obtained by contacting the catalyst system of the crude oil feed individually = Examples 8 to U Product lice content. Each crude product has an oxygen content of at most "% of the crude feed. Each crude oil product had an oxygen content per gram of crude oil production during each test period. The content should be in the range of M to 0.015 g. As shown in Figure 16, the oxygen content of the crude product remained fairly constant after a contact time of 纟 hours. The relatively constant oxygen content of the crude oil product shows a reduction in the selected organic oxygen compounds during the contact. Because TAN is also reduced in these examples, it can be concluded that at least -fractionate-reactive acid-containing oxygenated compounds have a more selective reduction than non-acid-containing organic oxides. In Example 11, the reaction conditions were 371. It (700 MPa pressure is 6.9 MPa (4.7 psi), and the ratio of hydrogen and crude oil feed was two (1 SCFB), based on the weight of the crude oil feed. The reduction in crude oil feed content was 17.5% by weight. At a temperature of 399 ° C (750 ° F), the same pressure and the ratio of hydrogen and crude oil feed, the crude oil feed MCR was calculated based on the weight of the crude oil feed. The reduction of the content was 25 · 4 wt%. In Example 9, the reaction conditions were: 371 (700 卞), Su Li force was 6.9 MPa (1014 · 7 psi), and hydrogen and crude oil were fed. The ratio is ^ / (1000SCFB), based on the weight of the crude oil feed, the reduction in crude oil feed content is 17_5 wt%. At the temperature of 399 ° C (750 ° F), the same pressure and hydrogen and At the ratio of crude oil feed, the reduction in MCR content of crude oil feed was 19 wt% by weight of crude oil feed. The increase in these reductions in the MCR content of crude oil feed was shown to be uncalcined. Metal barrier catalysts are more capable of reducing MCR content at higher temperatures than unburned metal barrier catalysts 6 and 9. These examples show that TAN (〇8 @ TAN) crude oil feed in contact with-or multiple catalysts to produce crude oil products while maintaining the stability of the crude oil feed / total product mixture and having a net absorption of a relatively small amount of hydrogen = ° selected crude oil products The identity of the crude oil feed with a maximum of 70% is negative. At the same time, the selected properties of the crude oil product are within the same range of the crude oil feed of 20%. Specifically, as shown in Table 4, each t Crude oil products are produced by the net absorption of hydrogen from crude oil feeds up to NmW (275 SCFB). Such products have crude oils with an average TAN of up to 4% of the crude oil feed and an average total Ni / v content of up to 61%. The total Ni / V content of the feed, while maintaining the P value of the crude oil feed above 3. The average residue content of each crude oil product is '88 to 90% of the residue content of the crude oil feed. Each crude oil The average VGO content of the product is VG0 content of the crude oil feed of 115 to 117%. The average API specific gravity of each crude oil product is the Aρι specific gravity of the crude oil feed of 11 to 117%, and each crude oil product has the highest viscosity Viscosity of 45% crude oil feed. 'Example 1 2 to 14 · Original In the case of Huaixie 1, the pore size distribution with a median of at least "j〇A is shocking. In Examples 12 to 14, each reactor device (except the number and content of contact areas) and each catalyst formed sulfur. The physical method, each total product separation method, and each crude oil product analysis system are the same as those described in Example 5. All catalyst systems are mixed with an equal volume of silicon carbide. Crude oil feed stream 105 200532010 per reactor From the top of the reactor to the bottom of the reactor. The silicon carbide system is arranged at the bottom of each reactor as a bottom carrier. Each reactor contains a contact zone. After the catalyst / silicon carbide mixture was placed in the contact area of each reactor, the lithogranite system was arranged above the top contact area to fill the voids and serve as a preheating area for each reactor. Each reactor was charged into a Lindberg furnace, which included three heating zones corresponding to a preheating zone, a contact zone, and a bottom carrier. The crude oil feed was contacted with each catalyst in the presence of hydrogen. The catalyst / silicon carbide mixture (40 cm3) is arranged above the silicon carbide in a shape and contact area for the catalyst system of Example 12 as described in Example 2 and the catalyst is used for the catalyst system of Example 13. The molybdenum catalyst prepared as in Example 3 was used in the catalyst of Beishi Example 14 as the molybdenum / vanadium catalyst prepared in Example 4. The contact conditions of yoke examples 12 to 14 are as follows: Hydrogen and supply to the reactor] The original feed ratio was 160 Nm3 / m3 (100 SCFB), the LHSV was 1, and the pressure was 6-9 MPa (ΐ〇 14.7 psi). The contact zone is gradually heated to 343 ° C (650 T) during a period of time and maintained at 343 t; the next 20 hours, to reach a total operating time of 36 hours. _ Total product_ Contact zone and isolated as described in Example 5. The 12 gate system ’sets the net uptake of hydrogen per catalyst system. In the example, the 'Yin absorption of hydrogen is -10 · 7 Nm3 / m3 (· 65 SCFB), and the crude oil product has a τ Δ Μ-7 Λ' of 6 · 7 5. In Example 13, the net absorption of hydrogen was in the range of 2.2 to 3.0 Nm3 / m3 (13 A • to 18.7 SCFB), and the crude oil product had a ^ 7 &amp; 0.3 to 0.5 ; TAN inside. In Example 14, when crude oil was in contact with indium / catalyst, and L contacted, the net absorption of hydrogen was from _〇.05 Nm3 / m3 to 106 200532010 crude oil product 0.6 NmVm3 (-0.36 SCFB to 4.0 SCFB) has a tan in the range of 0.2 to 0.5. From the point of view of the net hydrogen absorption during the contact period, it is estimated that during the contact between the crude oil feed and the catalyst, the hydrogen system will start with! The rate is 0.7 Nm3 / m3 (65 SCFB). The hydrogen generation during the contact time and the amount of hydrogen used in the conventional process, x allows the use of less hydrogen in the process to improve the properties of poor crude oil f. Contact: The need for less hydrogen will tend to reduce the cost of processing crude oil. In addition, the contact of the crude oil feed with the molybdenum / vanadium catalyst is to produce a crude oil product having a TAN lower than the TAN of the crude oil product produced by the catalyst alone. 15 ^ 1S __ Each reactor equipment (except the number and content of contact zones), each catalyst sulfide formation method, each total product separation method, and each crude oil product analysis system are the same as those described in Example 5 . Unless otherwise stated, all catalysts are paired with 2 sets of carbides! The volume ratio of the catalyst is mixed with the carbide. The crude oil feed flow of each reaction 1 is from the top of the reactor to the bottom of the reactor. An anthracite fossil is arranged at the bottom of each reactor as a bottom carrier. Each reactor has a bottom contact zone and a top contact zone. After the catalyst / carbonite mixture was placed in the contact area of each reactor, the silicon carbide was placed above the top contact area to fill the voids and served as a preheating area for each reactor. Each reactor is housed in a Lindberg furnace and includes four heating zones corresponding to a preheating zone, two contact zones' and a bottom carrier. In each example, the catalyst was prepared as described in Example 2 and used with an additional catalyst. 107 200532010 In Fang's yoke example 15, the additional catalyst / silicon carbide mixture (45 cm3) is used in the bottom contact area. The additional catalyst is the surface catalyst prepared by the method described in Example 3. The catalyst / carbon fossil evening mixture (15 cm3) was placed in the top contact area. '〖16' An additional catalyst / carbonized carbide mixture (30 cm3) is arranged in the bottom contact area, and the additional catalyst is an indium catalyst prepared by the method described in Example 3. The Hungry Catalyst / Carbonite Mixture (30⑽3) was placed in the contact area of the sheet. In Example 17, the 'additional catalyst / silicon carbide mixture (30 cm3) was arranged in the bottom contact area. The additional catalyst was the molybdenum / vanadium catalyst prepared in Example 4. A vanadium catalyst / silicon carbide mixture (3 () cm3) is placed in the top contact area. In Example 18, Pyrex® (Glass works Corporation, New York, U.S.A.) beads (30 cm3) were arranged in each contact area. Crude oil (Santos Basin, Brazil) having the properties summarized in Table 5 and Table 17 for Examples 15 to 18 was fed to the top of the reactor. Crude oil feeds flow through the reactor's preheat zone, top contact zone, bottom contact zone, and bottom carrier. The crude feed is contacted with each catalyst in the presence of hydrogen. The contact conditions for each example are as follows: the ratio of hydrogen to crude oil feed to the reactor was 160 Nm3 / m3 (1000 SCFB) for the first 86 hours and 80 Nm3 / m3 (500 SCFB) for the remaining time period , LHSV is 1 h · 1, and pressure is 6.9 MPa (1014.7 psi). The contact zone is gradually heated to 343 ° C (650 ° F) over a period of time and maintained at 343 ° C to achieve a total operating time of 1400 hours. 108 200532010 These examples show that in the presence of a hydrogen source, crude oil feed and a fifth metal catalyst with a pore size distribution with a median pore size of 35G A are combined with pores with a median pore size in the range of 250 to 300 A. Bayu, a, knives, additional catalyst contact to produce crude oil products, which have changed properties compared to the "like properties" of crude oil feeds, and other properties of the crude oil products, There are only small changes in the same properties. In addition, a relatively small amount of hydrogen uptake from the crude feed was observed during the feed. Specifically, as shown in Table 5, and FIG. 17, the crude oil products of Examples 15 to 17 have tan of a crude oil feed having a TAN of at most 15%. Compared with the same properties of the crude oil feed, the crude oil product produced in Example Η = 1 has a total content of 44% of Fe / Fe, a maximum oxygen content of 75%, and a viscosity of A 75%. . In addition, the crude oil products produced in Examples 15 to 17 have API gravity of a crude oil feed having an API gravity of 100 to 103%, respectively. In contrast, the viscosity of the crude oil product and crude oil feed produced under non-catalytic conditions (Example 18) # Αρι Specific Gravity Phase &amp; produces products with increased occupancy and reduced API specific gravity. From increasing viscosity and decreasing A &quot; specific gravity, it can be concluded that coking and / or polymerization of the crude oil feed has been initiated. Contact of materials at various lhsν. The contact system and the catalyst system are the same as those described in the sixth embodiment. The crude feed, 1 ', is listed in Table 6 in Figure 18. The contact conditions were as follows: the ratio of hydrogen to the crude oil feed to ~ was 160 Nm3 / m3 (1000 SCFB), the pressure was 6.9 MPa (1014.7 Psi), and the temperature in the contact zone was 371 X: (700 F ) To reach the total operating time. In Example 19, the LHSV during the contact period was increased from 1 h- 丨 to 12 h in the course of time, and maintained at 12 h-] at 48 ′ ^, and then increased to 20.7 h · 1, Hold at 20.7 h · 1 for 96 hours. Fang and Beiyuan Example 19 'Analyze crude oil products to determine TAN, viscosity, density, vG0 content, steroid 3 content, heteroatom content, and organic content during the time periods when LHSV is 1 2 1Γ1 and 20.7 h 1 The metal in the form of an acid metal salt is contained. The average values of the properties of the crude oil products are shown in Table 6 and Figures 8-8. ^ As shown in Table 6, Figure 18, the crude oil product of Example 丨 9 has a reduced TAN and a reduced viscosity compared to the TAN and viscosity of the crude oil feed, and the crude oil product has an ApI specific gravity of 104 to 110% of the crude oil. Apl ratio of feed

重MCR έ i與C:5瀝青質含量的重量比至少為i ·5。MCR 3里與C5瀝青質含量的和比原油進料之MCR含量與c5瀝 青質含量的和減少。從MCR含量與C5瀝青質含量的重量 2及MCR含量與q瀝青質的和減少來看,可推斷是瀝青 貝而不疋具有形成焦炭傾向的成分會減少。原油產物也具 有鉀、納、鋅和巧的總含量最多&amp; 6〇%的原油進料之相同 孟屬的、、心s里。原油產物的含硫量為8〇至9〇〇乂之原油進 籲 料的含硫量。 實施例6和19顯示可控制接觸條件以便與具有lHSV 為1 h」的製程相比,使通過接觸區的lhsv大於⑺^, 以生產具有類似性質的原油產物。在液體空間速度大於⑺ h下k擇〖生改變原油進料性質的能力可容許接觸法在比市 售可得容器縮小尺寸的容器中進行。較小的容器尺寸可容 許劣質原油的處理在具有尺寸限制的生產場所(例如近海設 110 200532010 備)進行。 接觸系統和觸媒係與實施例6所述者相同。將具有列 於圖19的表7之性質的原油進料加到反應器頂部,於氫 存在下與兩個接觸【中的兩種觸媒接觸以生產原油產物。 兩個接觸區係於不同溫度下操作。 頂部接觸區的接觸條件如下:LHSV為丨;頂部接 觸區的溫度為26G °C ( °F);氫和原油進料的比率為 16〇 NmVW ⑽〇 SCFB);及壓力為 6 9 咖(ι〇ΐ4 7 ㈣。 底邛接觸區的接觸條件如下·· LHSV為〗h·〗;底部接 觸區的溫度為315 °C (_ ”;氫和原油進料的比率為 Nm /m (1〇〇〇 SCFB);及壓力為 6 9 Mpa ㈣)。 八總產物離開底部接觸區並導入氣液相分離器。於氣液 相分離器中’將總產物分離成原油產物和氣體。原油產物 係定期分析以測定TAN和C5瀝青質含量。 運轉期間所得到之原油產物性質的平均值列於表7, = 19。原油進料具有9.^⑽及A瀝青質含量為 :油進料中有0.055克的C5遞青質。原油產物具有”的 = AN及C5瀝青質的平均含量為每克原油產物中有 〇39克的c5瀝青質。原油產物的q瀝青質含量最多為η% 之原油進料的C5瀝青質含量。 原油產物中鉀和鈉的總含量最多4 53%之原油進料 料:玉屬的總合篁。原油產物的TAN最多為10%之原油進 ”勺TAN。在接觸期間係保持15或更高的p值。 111 200532010 如貫施例6和20所示,具有低於第二(在此實例中為 底部)區之接觸溫度50。。的第一(在此實例中為頂部)接觸 溫度會傾向於使原油產物之q瀝f f含量比原油進料之c 瀝青質含量更為降低。 5 曰此外,使用控制溫差會使有機酸金屬鹽形態的金屬含 量降低的更多。舉例而·r,在每個實施例具有相#固定的 原油^掏產物混合物之穩定性(如p㈣測定者)的情況The weight ratio of heavy MCR i to C: 5 asphaltene content is at least i · 5. The sum of MCR 3 and C5 asphaltene content is lower than the sum of MCR content and c5 asphaltene content of crude oil feed. From the reduction of the weight 2 of the MCR content and the C5 asphaltene content, and the reduction of the sum of the MCR content and the q asphaltene, it can be inferred that the components that have a tendency to form coke will be reduced by bitumen. Crude oil products also have the same total content of potassium, sodium, zinc, and magnesium, and 60% of the crude oil feed is the same. The crude product has a sulfur content of 80 to 900 乂, and the sulfur content of the crude feed is appealing. Examples 6 and 19 show that the contact conditions can be controlled so that lhsv through the contact zone is greater than ⑺ ^ compared to a process with lHSV of 1 h "to produce crude products with similar properties. The ability of k to change the properties of the crude oil feed at liquid space velocities greater than ⑺ h allows the contact method to be performed in a container that is smaller in size than a commercially available container. The smaller container size allows the treatment of inferior crude oil to be carried out at production sites with size restrictions (eg offshore facilities 110 200532010). The contact system and the catalyst system are the same as those described in the sixth embodiment. A crude oil feed having the properties listed in Table 7 of Fig. 19 was added to the top of the reactor and contacted with two catalysts in the presence of hydrogen to produce crude oil products. The two contact zones operate at different temperatures. The contact conditions of the top contact zone are as follows: the temperature of the top contact zone is 丨; the temperature of the top contact zone is 26G ° C (° F); the ratio of hydrogen to crude oil feed is 16〇NmVW ⑽SCFB); and the pressure is 6 9 coffee (ι 〇ΐ4 7 ㈣. The contact conditions in the bottom contact zone are as follows: · The LHSV is 〖h ·〗; the temperature in the bottom contact zone is 315 ° C (_); the ratio of hydrogen to crude oil feed is Nm / m (1〇〇 〇SCFB); and the pressure is 6 9 Mpa ㈣). Eight total products leave the bottom contact area and are introduced into a gas-liquid separator. In the gas-liquid separator, the total product is separated into crude oil products and gases. Crude oil products are regularly Analyze to determine the TAN and C5 asphaltene content. The average value of the properties of the crude oil products obtained during operation is shown in Table 7, = 19. The crude oil feed has 9. ^ ⑽ and A asphaltene content: 0.055 in the oil feed Grams of C5 asphaltenes. Crude oil products have an average content of = AN and C5 asphaltenes of 0.39 grams of c5 asphaltenes per gram of crude oil products. The crude asphaltenes have a maximum asphaltene content of q% of crude oil. C5 asphaltene content of the feedstock. The total potassium and sodium content in the crude oil product is up to 4 53% of the crude oil feed. : Total sum of jade genus. The TAN of the crude oil product is at most 10% of the crude oil into the spoon of TAN. The p value is maintained at 15 or higher during the contact. 111 200532010 As shown in Examples 6 and 20, it has a low The contact temperature in the second (bottom in this example) zone is 50. The first (top in this example) contact temperature tends to make the q lff content of the crude oil product better than the c asphaltenes of the crude oil feed. The content is more reduced. In addition, the use of a controlled temperature difference will reduce the metal content of the organic acid metal salt form. For example, r, in each embodiment, has the stability of a crude oil product mixture with a fixed phase. (E.g. p㈣ tester)

下,貝鈿例20之原油產物的鉀和鈉總含量降低比實施例6 之原油產物的鉀和鈉總含量降低的更多。 使用純溫度的第一接觸區可容許⑽高分子量化合 物(例如C5瀝青質及/或有機酸金屬鹽),其會有形成聚合物 及/或具有柔軟性及/或黏性的物理性質之化合物(例如膠及/ 、'油)的傾向。於較低溫度下移除這些化 化合物在它們堵塞和被㈣媒之前被移除,藉此:配置 在弟-接觸區後面於較高溫度下操作的觸媒壽命。 --W W 觸媒的接觸In the following, the total potassium and sodium content of the crude product of Example 20 was reduced more than the total potassium and sodium content of the crude product of Example 6. The first contact zone using pure temperature can tolerate high molecular weight compounds (such as C5 asphaltenes and / or organic acid metal salts), which will have compounds that form polymers and / or have physical properties that are soft and / or sticky (Such as gum and / or 'oil). Removal of these compounds at lower temperatures is removed before they become clogged and catalyzed, thereby: configuring the catalyst lifetime to operate at higher temperatures behind the brother-contact zone. --W W Catalyst contact

本申請案之塊狀金屬觸媒及/或觸媒100克的居 =料中含0侧至5克或〇〇2至4克的觸媒)於若干肩 例中可用原油進料使其懸浮並且於下列條件下反應: 度在85至425 °C 085至797 T)的範圍内,壓力在 至1 〇 MPa的摩&amp;圍内,及氫源和原油進料的比率為1 6至1( 一段時間。在足以生產原油產物的反應時間 原油產物係使用分離設備,如過渡器及/或離心機, 尋媒及/或殘留的原油進料分離。原油產物與原油進料相 112 200532010 可具有改變的TAN,鐵、铉,芬/斗、z l 及降低的C5 ^ 螺,及/或釩的含量 瀝青質含量。 熟習該項技術者鑑於本說明書應顯 種恶樣的進一步修飾和替代具 x之各 :為方::…達到教,該項二施:::r λ又方法之目的。應瞭解本中 能m 又中所表不和敘述的本發明之形 :“乍為具體貫例的範例。可取代本文中所圖示和敘述的 几件和材料’可顛倒本發明的部分和程序,可單獨使The bulk metal catalyst of this application and / or the catalyst (100 grams of catalyst = 0 side to 5 grams or 002 to 4 grams of catalyst in the material) can be suspended in crude oil in some cases And the reaction under the following conditions: degrees in the range of 85 to 425 ° C (085 to 797 T), pressure in the Mo &amp; range to 10 MPa, and the ratio of hydrogen source and crude oil feed is 16 to 1 (A period of time. The crude oil product is separated at a reaction time sufficient to produce the crude oil product using separation equipment such as a transitional device and / or centrifuge, mediator and / or residual crude oil feed. Crude oil product and crude oil feed phase 112 200532010 may It has altered TAN, iron, osmium, fen / bucket, zl and reduced C5 ^ snails, and / or vanadium content. Asphaltene content. Those skilled in the art should further modify and substitute for the appearance of bad things in this specification. Each of the x: means: ... to achieve the purpose of teaching two terms: :: r λ and method. It should be understood that the form of the present invention can not be expressed and described in the m: Examples of examples. Can replace several pieces and materials illustrated and described in this article 'can reverse parts and procedures of the present invention , May be used alone

發明的某些特徵,以上全部在兹 王口丨在獲致本發明說明書的效益之 後’應為熟習該項技術者所顯而易見。可進行本文中所述 之元件的改變而不致脫離如後附中請專利範圍所述之本發 明的精神與範疇。 【圖式簡單說明】 圖式簡單說明 對於热習该項技術者而言,本發明具有下列詳細說明 之效益的優點在參照附圖後將變得顯而易見,其中: 圖1為接觸系統之具體實例的簡圖。 鲁 圖2 A和2B為包含兩個接觸區的接觸系統之具體實例 的簡圖。 圖3 A和3B為包含三個接觸區的接觸系統之具體實例 的簡圖。 圖4為結合接觸系統的分離區之具體實例的簡圖。 圖5為結合接觸系統的摻合區之具體實例的簡圖。 圖6為結合分離區、接觸系統和摻合區之具體實例的 113 200532010 間圖。 圖7為使原油進料盘:r猶總^甘 進斜“丄* 化、-種觸媒接觸的具體實例之原油 進科與原油產物的代表性質列表。 圖8為使原油進料盘一或客 加權平均± 種觸媒接觸的具體實例之 卞习尿/m度對運轉時間的圖示。 圖9為使原油進料與兩種觸媒接觸的具體實例 料與原油產物的代表性質列表。 ’ 圖10為使原油進料與兩種觸 進料盥周、山立此、 安觸之具體K例的原油 ,、原油產物之代表性質的另一個列表。 圖Π為使原油進料與四種不 例夕 J觸媒系統接觸的具體實 原油進料與原油產物的列表。 圖1 2為使原油進料與四種不 例的眉4^ j觸媒糸統接觸之具體實 原油產物之P值對運轉時間的圖示。 例的Γ3為使原油進料與四種不同觸媒系統接觸之具體-油進料之氫的淨吸取對運轉時間的圖示。 只 圖U為使原油進料與四種不同觸媒系 門,重量百分率表示的原油產物之殘留物含量對運:: 間的圖示。 田切s里對運轉時 例的:15為使原油進料與四種不同觸媒系統接觸之呈體· 的原油產物之API比重改變對運轉時間的圖示。只 圖16為使原油進料與四種不同觸媒系統接觸的 从重量百分率表示的原油產物二Λ 圖示。 乳里對運轉時間的 圖Π為使原油進料與觸媒系統接觸的具體實例之原油 114 200532010 進料與原油產物的代表性質列表,該觸媒系統包含各種量 的翻觸媒和銳觸媒,與包含鈒觸媒和翻/銳觸媒的觸媒系 統,以及玻璃珠。 圖18為在各種液體空間速度下使原油進料與 觸媒接觸的具體實例之原油進料與原油產物的性質列表。 〜圖19為在各種接觸溫度下使原油進料進行接觸的具體 貫例之原油進料與原油產物的性質列表。 發明容許各種修飾與替代形式,但其特定具體 制 〇 只妁衣不省荨圖不可能未按比例繪 衣。應瞭解其圖示和詳細說明並非 # — 兀A上非用來將本發明限制在所 ^不的特定形&lt;,但相反地,則意圖涵蓋^人如後附申請 專利範圍所限定之精神與範#内 代物。 7 Ί W ^有修飾、等效物和替 【主要元件符號說明】 100 :接觸系統 102 :接觸區 104 :導管 106 ;導管 106…導管 108 :分離區 110 :導管 112 :導管 11 4 :接觸區 11 6 :接觸區 115 200532010 1 18 :導管 120 :分離區 122 :導管 124 :導管 126 :導管 128 :導管 130 :摻合區 132 :導管 134 :導管 # 136 :加權平均床溫度(WABT)對運轉時間的曲線 140-146 :原油產物之P值對運轉時間的曲線 148-154:氫的淨吸取對運轉時間之曲線 15 6-162 :原油產物之殘留物含量對運轉時間之曲線 164-170 :原油產物之API比重對運轉時間之曲線 172-178 :原油產物之含氧量對運轉時間之曲線 • 116Certain features of the invention, all of which are described at Wangkou, after obtaining the benefits of the description of the present invention 'should be apparent to those skilled in the art. Changes may be made in the elements described herein without departing from the spirit and scope of the invention as described in the appended claims. [Brief description of the drawings] For the technical person who is eager to learn the drawings, the advantages of the present invention having the following detailed description will become apparent after referring to the drawings, where: Figure 1 is a specific example of a contact system Simple diagram. Figures 2A and 2B are simplified diagrams of a specific example of a contact system including two contact areas. 3A and 3B are diagrams showing a specific example of a contact system including three contact areas. Fig. 4 is a schematic diagram of a specific example of a separation zone incorporating a contact system. Fig. 5 is a schematic diagram of a specific example of a blending zone of a contact system. Figure 6 is a diagram of the specific example of the combined separation zone, contact system, and blending zone. Fig. 7 is a list of representative properties of crude oil processing and crude oil products for specific examples of the crude oil feed tray: a specific example of the contact of catalysts and catalysts. Fig. 8 shows a crude oil feed tray. Or the weighted average ± the specific example of catalyst contact, the graph of the urine / m degree versus the running time. Figure 9 is a specific example of the contact between crude oil feed and two catalysts. 'Figure 10 is another list of the representative properties of crude oil and crude oil with two kinds of crude oil feeds, two specific examples of contacting feed tanks, Shanli this, and An Touch. Figure Π is the crude oil feed and A list of the four specific crude oil feeds and crude oil products contacted by the four example J catalyst systems. Figure 12 is the specific real crude oil products that brought the crude oil feed into contact with the four example 4 ^ j catalyst systems. The graph of P value vs. running time. Example Γ3 is the specific drawing of the net absorption of hydrogen from the oil feed to the running time of the specific crude oil feed in contact with four different catalyst systems. Residues of crude oil products in feed and four different catalyst systems, expressed as weight percentages Content vs. transportation: Graphical representation of the time. Tianqian s on the operating time example: 15 is the API gravity ratio of crude oil products in which the crude oil feed is brought into contact with four different catalyst systems. Graphical representation of the operating time Fig. 16 is a diagram showing the crude oil product Λ, expressed as a percentage by weight, when the crude oil feed is brought into contact with four different catalyst systems. The graph of the operating time in the milk is the specific example of the crude oil feed that contacts the catalyst system Examples of crude oil 114 200532010 List of representative properties of feed and crude oil products. The catalyst system contains various amounts of flip catalyst and sharp catalyst, and catalyst systems containing thallium catalyst and flip / sharp catalyst, and glass beads. Figure 18 is a list of properties of crude oil feeds and crude oil products for specific examples of contacting crude oil feeds with catalysts at various liquid space velocities. ~ Figure 19 is a specific example of contacting crude oil feeds at various contact temperatures. List of properties of crude oil feeds and crude oil products. The invention allows for various modifications and alternative forms, but its specific specific system. It is not possible to draw pictures without scale. You should understand its diagrams and details. The description is not # — Wu A is not used to limit the present invention to the specific forms &lt;, but on the contrary, it is intended to cover the spirit and scope # within the scope of the patent application as appended. 7 Ί W ^ Modifications, equivalents, and substitutions [Description of main component symbols] 100: contact system 102: contact area 104: conduit 106; conduit 106 ... conduit 108: separation area 110: conduit 112: conduit 11 4: contact area 11 6: Contact zone 115 200532010 1 18: Catheter 120: Separation zone 122: Catheter 124: Catheter 126: Catheter 128: Catheter 130: Blend zone 132: Catheter 134: Catheter # 136: Weighted average bed temperature (WABT) vs. operating time Curve 140-146: P value of crude oil product versus operating time curve 148-154: Net absorption of hydrogen versus operating time curve 15 6-162: Residual content of crude oil product versus operating time curve 164-170: crude oil Product API gravity vs. running time curve 172-178: Oxygen content of crude oil product vs. running time • 116

Claims (1)

200532010 十、申請專利範圍: 1 · 一種生產原油產物之方法, 使原油進料與一或多其包括: 的總產物,其中該原油產物在:接觸以生產含有原油產物 態混合物,該原油進料包含5。〇和〇·101 Mpa下為液 金屬鹽,一或多種有機酸的一2種有機酸的一或多種驗 合物,該原油進料在每克原 夕種鹼土金屬帛,或其混 之有機酸金屬鹽形態的驗金屬和^中^有至少曰0.00001克 -種觸媒在每克觸媒中,以金i /屬總含篁’s亥至少 克之: 屬重置計’含有至少請! 週期表第6攔的一或多種今 喱金屬,週期表第6攔之一 ^ 多種金屬的一或多種化合物,或其混合物;及200532010 X. Scope of patent application: 1 · A method for producing crude oil products, the crude oil feed is made with one or more of the total products including: where the crude oil products are in contact to produce a mixture containing crude oil products, the crude oil feed Contains 5. 〇 and 〇.101 Mpa are liquid metal salts, one or more organic acids, one or more test compounds of two organic acids, the crude oil is fed per gram of the alkaline earth metal hafnium, or mixed organic There are at least 0.00001 grams of metals in the test of the acid metal salt form. There is at least 0.00001 grams of catalyst in each gram of catalyst, with gold i / total content containing 篁 's at least grams of: gen reset meter' contains at least please! One or more of the present gels in Table 6 and one of the six in the Periodic Table ^ one or more compounds of multiple metals, or a mixture thereof; and 控制接觸條件以便使接觸區中的液體空間速度超過工 h-l,使該原油產物具有有機酸金屬鹽形態的鹼金屬和鹼』 金屬總含量最多為90%之該原油進料中有機酸金屬鹽形慰 的鹼金屬和鹼土金屬含量,其中有機酸金屬鹽形態的鹼名 屬和鹼土金屬含量係藉由ASTM法D1 3 1 8測定。 2_如申請專利範圍第丨項之方法,其中該原油產物中 有機酸金屬鹽形態的鹼金屬和鹼土金屬總含量最多為 50%,最多為10%,或最多為5%之該原油進料中有機酸金 屬鹽形態的鹼金屬和鹼土金屬含量。 3.如申請專利範圍第1項之方法’其中該原油產物中 有機酸金屬鹽形態的鹼金屬和鹼土金屬總含量是在從丨至 80%’ 10至70%’ 20至60%’或3〇至50%之該原油進料 117 200532010 中有機酸金屬鹽形態的鹼金屬 々园双工孟屬含夏之範圍内。 4·如申請專利範圍第…項中任—項之方法,立中 該原油產物在每克原油產物中含有從〇〇__克'至 克’從 〇.〇〇〇〇〇〇3 克至 〇.〇〇〇〇2克,或從 〇 〇〇〇謝 屬。Μ,1克之有機酸金屬鹽形態的驗金屬和驗土金 一 5.如申請專利範圍第(項中任—項之方法,1中 一或多種第ό攔的金屬為鉬及/或鎢。 —6.如申請專利範圍第…項中任一項之方法… 的金相媒具有中位孔徑至少為㈣,至少為μ, 或至夕為1 80 Α的孔徑分佈。 Μ 7.如申請專利範圍第…項中任一項之方法,其中 的觸媒另外包含週期表第5欄的一或多種金屬,一 或多種第5欄金屬的一或多種化合物,週期表 搁的一或多種金屬,一或多 Α夕種弟7至1〇欄金屬的一或多 種化合物,及/或其混合物。 8.如申請專利範圍第1 i 7項中任一項之方法,其中 6攔的金屬觸媒另外包含週期表第15攔的—或多種元 、及7或一或多種第15攔元素的一或多種化合物。 兮—9.如申請專利範圍第丨至8項中任一項之方法,其中 —或夕種觸媒另外包含附加觸媒,該附加觸媒具有中位 ^至少為6〇A或至少為i8〇A的孔徑分佈。 上1〇·如申請專利範圍第丨至9項中任一項之方法,其中 使4原油進料在位於或連接到近海設備的接觸區中進行接 118 200532010 觸。 π寸们视固第 1至丨ϋ項〒任一項之方、去, 中接觸包括於氫源存在下進行接觸。 ” 12.如申請專利範圍第η項之方法,其中,在 間’ δ亥原油進料係以選定速率吸取分子氫以抑制接觸/ 原油進料的相分離。 &quot;丨接觸期間 如申請專利範圍第i至12項中任 中:方法尚包括使該原油產物與該原油進料相=其 原油結合以形成摻合物。 门或不同的 I4·-種原油產物或摻合物 1至13項中任-項之方法獲得。、猎由申^專利範圍第 1 5. —種生產運輸用燃料、 品之方法’其包括加 、用燃料、潤滑油或化學 或摻合物。 專利範圍第“項之原油產物 16.如申請專利範圍第15項 使該原油產物或摻合物蒸館成為、法’其中該加工包括 17·如申請專利範圍第】 或广分。 包括加氫處理。 一 16項之方法1中該加工 十一、圓式: 如次頁 119The contact conditions are controlled so that the liquid space velocity in the contact zone exceeds the industrial hl, so that the crude oil product has an alkali metal and an alkali in the form of an organic acid metal salt. The content of alkali metals and alkaline earth metals, among which the alkali name and alkaline earth metals in the form of metal salts of organic acids are determined by ASTM method D1 3 1 8. 2_ The method according to the scope of patent application, wherein the total content of alkali metals and alkaline earth metals in the form of organic acid metal salts in the crude oil product is at most 50%, at most 10%, or at most 5% of the crude oil feed Alkali and alkaline earth metal content in organic acid metal salt form. 3. The method according to item 1 of the scope of patent application, wherein the total content of alkali metals and alkaline earth metals in the form of organic acid metal salts in the crude oil product is from 丨 to 80%, 10 to 70%, 20 to 60%, or 3 0 to 50% of the crude oil feed 117 200532010 in the form of organic acid metal salt alkali metal Gion duplex Meng belongs to the range of summer. 4. According to the method of any of the items in the scope of applying for a patent, the crude oil product contains gram of crude product per gram of crude product from gram to gram to gram. 0.00000 gram, or from the genus 100,000. M, 1 gram of organic acid metal salt in the form of metal test and earth test-5. If the scope of the application for a patent (any of the-method), one or more of the metals in 1 is molybdenum and / or tungsten. —6. The metallurgical medium according to the method of any one of the scope of applying for a patent… has a pore size distribution with a median pore size of at least ㈣, at least μ, or 1 80 Α. Μ 7. If a patent is applied for The method of any one of the scope of ..., wherein the catalyst further comprises one or more metals in column 5 of the periodic table, one or more compounds of one or more metals in column 5 and one or more metals on the periodic table, One or more compounds of one or more metals in columns 7 to 10, and / or mixtures thereof. 8. The method according to any one of claims 1 i 7 in the patent application scope, wherein 6 metal catalysts In addition, one or more compounds of the 15th block of the periodic table—or one or more elements and 7 or one or more elements of the 15th block. Xi—9. The method according to any one of the claims 1 to 8 in which —Or the catalysts additionally include additional catalysts which have a median ^ at least A pore size distribution of 60A or at least 80A. The method according to any one of claims 1 to 9 in which the crude oil feed is brought to a contact zone located or connected to offshore equipment Intermediate contact 118 200532010. π-inches are determined according to any one of items 1 to ϋ, and intermediate contact includes contact in the presence of a hydrogen source. "12. Methods such as applying item η in the scope of patent applications Among them, the 'δ' Hai crude oil feedstock absorbs molecular hydrogen at a selected rate to suppress contact / phase separation of the crude oil feed. &Quot; 丨 During contacting, if any of the scope of applications for patents i to 12: any method: the method still includes The crude oil product is combined with the crude oil feed phase = its crude oil to form a blend. It is obtained by a method of any one of items 1 to 13 of different I4 · -type crude oil products or blends. ^ No. 1 in the scope of patents 5. —A method for producing fuels and products for transportation ', which includes the addition, use of fuel, lubricating oil or chemicals or blends. To make the crude product or blend , France '· 17 wherein the processing comprises as patent wide range of the partial} or hydrotreating process comprising a 16 1 of the process XI Circular: page 119 such as hypophosphorous
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Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0405587A (en) * 2003-12-19 2005-10-04 Shell Int Research Methods of Producing a Transportable Fuel and Crude Oil Product, Heating Fuel, Lubricants or Chemicals, and Crude Oil Product
US7736490B2 (en) 2003-12-19 2010-06-15 Shell Oil Company Systems, methods, and catalysts for producing a crude product
WO2006110660A1 (en) * 2005-04-11 2006-10-19 Shell Internationale Research Maatschappij B.V. Method and catalyst for producing a crude product having a reduced mcr content
CA2604015C (en) * 2005-04-11 2014-02-18 Shell International Research Maatschappij B.V. Systems, methods, and catalysts for producing a crude product
EP2001976A1 (en) * 2006-04-04 2008-12-17 Shell Internationale Research Maatschappij B.V. A process for reducing the total acid number (tan) of a liquid hydrocarbonaceous feedstock
US20080087575A1 (en) * 2006-10-06 2008-04-17 Bhan Opinder K Systems and methods for producing a crude product and compositions thereof
MX2010005855A (en) * 2007-11-28 2010-09-07 Saudi Arabian Oil Co Process for upgrading heavy and highly waxy crude oil without supply of hydrogen.
BRPI0704443B1 (en) 2007-11-30 2018-09-11 Petroleo Brasileiro S/A Petrobras system and process for separating spent catalyst suspensions and hydrocarbons formed in a multi-reaction upstream fluid catalytic cracking unit
US7862708B2 (en) 2007-12-13 2011-01-04 Exxonmobil Research And Engineering Company Process for the desulfurization of heavy oils and bitumens
KR100931036B1 (en) * 2008-03-18 2009-12-10 한국화학연구원 Catalyst for Hydrocracking of Crude Oil and Hydrocracking Method Using the Same
US8114806B2 (en) * 2008-04-10 2012-02-14 Shell Oil Company Catalysts having selected pore size distributions, method of making such catalysts, methods of producing a crude product, products obtained from such methods, and uses of products obtained
EP2321046A4 (en) * 2008-04-10 2013-12-18 Shell Int Research Catalyst systems and methods for converting a crude feed with such catalyst systems
EP2628780A1 (en) * 2012-02-17 2013-08-21 Reliance Industries Limited A solvent extraction process for removal of naphthenic acids and calcium from low asphaltic crude oil
JP2013057075A (en) * 2012-11-19 2013-03-28 Shell Internatl Research Maatschappij Bv Lowering process of total acid number (tan) of liquid hydrocarbon quality feedstock
US10604709B2 (en) 2017-02-12 2020-03-31 Magēmā Technology LLC Multi-stage device and process for production of a low sulfur heavy marine fuel oil from distressed heavy fuel oil materials
US12071592B2 (en) 2017-02-12 2024-08-27 Magēmā Technology LLC Multi-stage process and device utilizing structured catalyst beds and reactive distillation for the production of a low sulfur heavy marine fuel oil
US12025435B2 (en) 2017-02-12 2024-07-02 Magēmã Technology LLC Multi-stage device and process for production of a low sulfur heavy marine fuel oil
US20180230389A1 (en) 2017-02-12 2018-08-16 Mag&#275;m&#257; Technology, LLC Multi-Stage Process and Device for Reducing Environmental Contaminates in Heavy Marine Fuel Oil
US11788017B2 (en) 2017-02-12 2023-10-17 Magëmã Technology LLC Multi-stage process and device for reducing environmental contaminants in heavy marine fuel oil

Family Cites Families (119)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US587636A (en) * 1897-08-03 Blacking-brush and dauber
US2850435A (en) * 1956-02-06 1958-09-02 Pure Oil Co Method of removing high molecular weight naphthenic acids from hydrocarbon oils
US2921023A (en) * 1957-05-14 1960-01-12 Pure Oil Co Removal of naphthenic acids by hydrogenation with a molybdenum oxidesilica alumina catalyst
US3025231A (en) * 1959-06-03 1962-03-13 Texaco Inc Catalytic hydrogenation of heavy oils such as shale oil
NL275200A (en) 1961-07-31
GB1115122A (en) * 1965-08-23 1968-05-29 Universal Oil Prod Co Hydrotreatment of alkyl aromatic hydrocarbons
US3488716A (en) * 1967-10-03 1970-01-06 Exxon Research Engineering Co Process for the removal of naphthenic acids from petroleum distillate fractions
US3547585A (en) * 1968-11-26 1970-12-15 Universal Oil Prod Co Combination of a hydrocarbon conversion process with a waste water treating process
US3576737A (en) * 1969-03-25 1971-04-27 Chevron Res Vanadium removal from hydrocarbons
GB1232173A (en) * 1969-11-18 1971-05-19
US3696027A (en) * 1970-01-12 1972-10-03 Chevron Res Multi-stage desulfurization
GB1364238A (en) * 1970-08-04 1974-08-21 Topsoe H F A Process for the hydrodesulphurisation of heavy hydrocarbon oils
US3712861A (en) * 1970-10-19 1973-01-23 Mobil Oil Corp Upgrading a hydrocarbon utilizing a catalyst of metal sulfides dispersed in alumina
US3730876A (en) 1970-12-18 1973-05-01 A Sequeira Production of naphthenic oils
US3766054A (en) * 1970-12-23 1973-10-16 Mobil Oil Corp Demetalation of hydrocarbon charge stocks
US3684688A (en) * 1971-01-21 1972-08-15 Chevron Res Heavy oil conversion
US3876532A (en) * 1973-02-27 1975-04-08 Gulf Research Development Co Method for reducing the total acid number of a middle distillate oil
US3948759A (en) 1973-03-28 1976-04-06 Exxon Research And Engineering Company Visbreaking a heavy hydrocarbon feedstock in a regenerable molten medium in the presence of hydrogen
US3902991A (en) * 1973-04-27 1975-09-02 Chevron Res Hydrodesulfurization process for the production of low-sulfur hydrocarbon mixture
US3960712A (en) * 1973-04-30 1976-06-01 Universal Oil Products Company Hydrodesulfurization of asphaltene-containing black oil with a gamma-alumina composite catalyst of specified particle density
IN142203B (en) * 1973-04-30 1977-06-11 Uop Inc
US3846288A (en) * 1973-07-05 1974-11-05 Gulf Research Development Co Acid number reduction of hydrocarbon fractions using a solid catalyst and methanol
US3876523A (en) * 1973-08-29 1975-04-08 Mobil Oil Corp Catalyst for residua demetalation and desulfurization
US3891541A (en) * 1973-08-29 1975-06-24 Mobil Oil Corp Process for demetalizing and desulfurizing residual oil with hydrogen and alumina-supported catalyst
US3931052A (en) * 1973-08-29 1976-01-06 Mobil Oil Corporation Alumina-supported catalyst for residua demetalation and desulfurization
US3920538A (en) 1973-11-30 1975-11-18 Shell Oil Co Demetallation with nickel-vanadium on silica in a hydrocarbon conversion process
JPS51122105A (en) * 1975-04-18 1976-10-26 Toa Nenryo Kogyo Kk Process for hydrofining of hydrocarbon oil
US4062757A (en) * 1975-07-18 1977-12-13 Gulf Research & Development Company Residue thermal cracking process in a packed bed reactor
US4196102A (en) * 1975-12-09 1980-04-01 Chiyoda Chemical Engineering & Construction Co., Ltd. Catalysts for demetallization treatment of _hydrocarbons supported on sepiolite
US4048060A (en) * 1975-12-29 1977-09-13 Exxon Research And Engineering Company Two-stage hydrodesulfurization of oil utilizing a narrow pore size distribution catalyst
US4067799A (en) 1976-07-02 1978-01-10 Exxon Research And Engineering Company Hydroconversion process
US4127470A (en) * 1977-08-01 1978-11-28 Exxon Research & Engineering Company Hydroconversion with group IA, IIA metal compounds
US4225421A (en) * 1979-03-13 1980-09-30 Standard Oil Company (Indiana) Process for hydrotreating heavy hydrocarbons
US4446244A (en) * 1979-09-26 1984-05-01 Chevron Research Company Hydrocarbons hydroprocessing with imogolite catalyst
US4358361A (en) * 1979-10-09 1982-11-09 Mobil Oil Corporation Demetalation and desulfurization of oil
JPS595011B2 (en) * 1979-11-27 1984-02-02 千代田化工建設株式会社 Catalyst for hydrotreating heavy hydrocarbon oil and its production method
US4301037A (en) 1980-04-01 1981-11-17 W. R. Grace & Co. Extruded alumina catalyst support having controlled distribution of pore sizes
US4306964A (en) * 1980-09-16 1981-12-22 Mobil Oil Corporation Multi-stage process for demetalation and desulfurization of petroleum oils
US4411824A (en) * 1981-05-12 1983-10-25 Chevron Research Company Method of making a catalyst suitable for hydrometalation of hydrocarbonaceous feedstocks
US4549957A (en) * 1981-06-17 1985-10-29 Amoco Corporation Hydrotreating catalyst and process
US4456699A (en) * 1981-06-17 1984-06-26 Standard Oil Company (Indiana) Catalyst and support, and their methods of preparation
AU547464B2 (en) * 1981-06-17 1985-10-24 Amoco Corporation Catalyst for hydrotreating hydrocarbon feed
US4447314A (en) * 1982-05-05 1984-05-08 Mobil Oil Corporation Demetalation, desulfurization, and decarbonization of petroleum oils by hydrotreatment in a dual bed system prior to cracking
FR2528721B1 (en) * 1982-06-17 1986-02-28 Pro Catalyse Ste Fse Prod Cata SUPPORTED CATALYST HAVING INCREASED RESISTANCE TO POISONS AND ITS USE IN PARTICULAR FOR THE HYDROTREATMENT OF OIL FRACTIONS CONTAINING METALS
US4405441A (en) * 1982-09-30 1983-09-20 Shell Oil Company Process for the preparation of hydrocarbon oil distillates
US4886594A (en) * 1982-12-06 1989-12-12 Amoco Corporation Hydrotreating catalyst and process
JPS59150537A (en) * 1982-12-06 1984-08-28 アモコ コーポレーション Hydrotreating catalyst and hydrotreating of hydrocarbon
US4450068A (en) 1982-12-20 1984-05-22 Phillips Petroleum Company Demetallization of hydrocarbon containing feed streams
JPS59132945A (en) * 1983-01-21 1984-07-31 Shokubai Kasei Kogyo Kk Hydro-demetalation catalyst and use thereof
US4592827A (en) * 1983-01-28 1986-06-03 Intevep, S.A. Hydroconversion of heavy crudes with high metal and asphaltene content in the presence of soluble metallic compounds and water
US4525472A (en) * 1983-02-23 1985-06-25 Intevep, S.A. Process for catalyst preparation for the hydrodemetallization of heavy crudes and residues
JPS6065092A (en) * 1983-09-21 1985-04-13 Res Assoc Petroleum Alternat Dev<Rapad> Removal of metal from oil sand oil and residual oil
US4587012A (en) * 1983-10-31 1986-05-06 Chevron Research Company Process for upgrading hydrocarbonaceous feedstocks
US4588709A (en) * 1983-12-19 1986-05-13 Intevep, S.A. Catalyst for removing sulfur and metal contaminants from heavy crudes and residues
US4520128A (en) * 1983-12-19 1985-05-28 Intevep, S.A. Catalyst having high metal retention capacity and good stability for use in the demetallization of heavy crudes and method of preparation of same
US4572778A (en) * 1984-01-19 1986-02-25 Union Oil Company Of California Hydroprocessing with a large pore catalyst
US4844792A (en) * 1984-08-07 1989-07-04 Union Oil Company Of California Hydroprocessing with a specific pore sized catalyst containing non-hydrolyzable halogen
NL8402997A (en) * 1984-10-01 1986-05-01 Unilever Nv CATALYST MATERIAL.
GB2167430B (en) * 1984-11-22 1988-11-30 Intevep Sa Process for hydroconversion and upgrading of heavy crudes of high metal and asphaltene content
US4600503A (en) * 1984-12-28 1986-07-15 Mobil Oil Corporation Process for hydrotreating residual petroleum oil
US4729826A (en) * 1986-02-28 1988-03-08 Union Oil Company Of California Temperature controlled catalytic demetallization of hydrocarbons
US4738884A (en) * 1986-03-03 1988-04-19 Owens-Corning Fiberglas Corporation Asphalt adhesives superimposed on asphalt-based roofing sheet
US4670134A (en) * 1986-05-02 1987-06-02 Phillips Petroleum Company Catalytic hydrofining of oil
US4830736A (en) * 1986-07-28 1989-05-16 Chevron Research Company Graded catalyst system for removal of calcium and sodium from a hydrocarbon feedstock
JP2631712B2 (en) * 1988-08-18 1997-07-16 コスモ石油株式会社 Catalyst composition for hydrotreating heavy hydrocarbon oil and hydrotreating method using the same
US4992157A (en) * 1988-08-29 1991-02-12 Uop Process for improving the color and color stability of hydrocarbon fraction
JP2609301B2 (en) * 1988-08-31 1997-05-14 工業技術院長 Method for producing hydrotreating catalyst
EP0367021B1 (en) * 1988-10-19 1993-12-29 Research Association For Petroleum Alternatives Development Process for hydrogenation of heavy oil
US5124027A (en) 1989-07-18 1992-06-23 Amoco Corporation Multi-stage process for deasphalting resid, removing catalyst fines from decanted oil and apparatus therefor
US4992163A (en) 1989-12-13 1991-02-12 Exxon Research And Engineering Company Cat cracking feed preparation
US4988434A (en) 1989-12-13 1991-01-29 Exxon Research And Engineering Company Removal of metallic contaminants from a hydrocarbonaceous liquid
JPH03292395A (en) * 1989-12-28 1991-12-24 Chevron Res & Technol Co Removal of calcium from hydrocarbon supply material
US5053117A (en) * 1990-07-25 1991-10-01 Mobil Oil Corporation Catalytic dewaxing
US5851381A (en) 1990-12-07 1998-12-22 Idemitsu Kosan Co., Ltd. Method of refining crude oil
US5200060A (en) * 1991-04-26 1993-04-06 Amoco Corporation Hydrotreating process using carbides and nitrides of group VIB metals
US5215954A (en) 1991-07-30 1993-06-01 Cri International, Inc. Method of presulfurizing a hydrotreating, hydrocracking or tail gas treating catalyst
US5210061A (en) * 1991-09-24 1993-05-11 Union Oil Company Of California Resid hydroprocessing catalyst
US5215955A (en) * 1991-10-02 1993-06-01 Chevron Research And Technology Company Resid catalyst with high metals capacity
JP2966985B2 (en) * 1991-10-09 1999-10-25 出光興産株式会社 Catalytic hydrotreating method for heavy hydrocarbon oil
US5399259A (en) * 1992-04-20 1995-03-21 Texaco Inc. Hydroconversion process employing catalyst with specified pore size distribution
EP0569092A1 (en) 1992-05-05 1993-11-10 Shell Internationale Researchmaatschappij B.V. Hydrotreating process
US5322617A (en) * 1992-08-07 1994-06-21 Her Majesty The Queen In Right Of Canada As Represented By The Minister Of Energy, Mines And Resources Upgrading oil emulsions with carbon monoxide or synthesis gas
JPH0753968A (en) * 1993-08-09 1995-02-28 Idemitsu Kosan Co Ltd Hydrotreatment of heavy hydrocarbon oil
US5928601A (en) * 1994-02-28 1999-07-27 Honda Giken Kogyo Kabushiki Kaisha Method for producing silicon nitride reaction sintered body
NO303837B1 (en) * 1994-08-29 1998-09-07 Norske Stats Oljeselskap Process for removing substantially naphthenic acids from a hydrocarbon oil
JP3504984B2 (en) * 1994-09-19 2004-03-08 日本ケッチェン株式会社 Hydrodesulfurization demetallization catalyst for heavy hydrocarbon oil
US5635056A (en) * 1995-05-02 1997-06-03 Exxon Research And Engineering Company Continuous in-situ process for upgrading heavy oil using aqueous base
US5807469A (en) * 1995-09-27 1998-09-15 Intel Corporation Flexible continuous cathode contact circuit for electrolytic plating of C4, tab microbumps, and ultra large scale interconnects
JP3315314B2 (en) 1996-05-30 2002-08-19 矢崎総業株式会社 Low insertion force connector
JPH1060456A (en) * 1996-08-15 1998-03-03 Catalysts & Chem Ind Co Ltd Hydrogenation treatment of heavy oil and device for hydrogenation treatment
FR2758278B1 (en) * 1997-01-15 1999-02-19 Inst Francais Du Petrole CATALYST COMPRISING A MIXED SULFIDE AND USE IN HYDRO-REFINING AND HYDROCONVERSION OF HYDROCARBONS
US5744025A (en) 1997-02-28 1998-04-28 Shell Oil Company Process for hydrotreating metal-contaminated hydrocarbonaceous feedstock
US6162350A (en) * 1997-07-15 2000-12-19 Exxon Research And Engineering Company Hydroprocessing using bulk Group VIII/Group VIB catalysts (HEN-9901)
US5871636A (en) 1997-08-29 1999-02-16 Exxon Research And Engineering Company Catalytic reduction of acidity of crude oils in the absence of hydrogen
US5910242A (en) * 1997-08-29 1999-06-08 Exxon Research And Engineering Company Process for reduction of total acid number in crude oil
US5928502A (en) 1997-08-29 1999-07-27 Exxon Research And Engineering Co. Process for reducing total acid number of crude oil
US5897769A (en) 1997-08-29 1999-04-27 Exxon Research And Engineering Co. Process for selectively removing lower molecular weight naphthenic acids from acidic crudes
US5914030A (en) * 1997-08-29 1999-06-22 Exxon Research And Engineering. Co. Process for reducing total acid number of crude oil
RU2184762C2 (en) * 1997-08-29 2002-07-10 Экссон Рисерч энд Энджиниринг Компани Method of lowering summary acid number of oil feedstock
US5928501A (en) * 1998-02-03 1999-07-27 Texaco Inc. Process for upgrading a hydrocarbon oil
JP2000005609A (en) * 1998-06-26 2000-01-11 Idemitsu Kosan Co Ltd Method for regeneration of hydrotreating catalyst
US6096192A (en) 1998-07-14 2000-08-01 Exxon Research And Engineering Co. Producing pipelinable bitumen
US6258258B1 (en) * 1998-10-06 2001-07-10 Exxon Research And Engineering Company Process for treatment of petroleum acids with ammonia
FR2787040B1 (en) * 1998-12-10 2001-01-19 Inst Francais Du Petrole HYDROTREATMENT OF HYDROCARBON CHARGES IN A BOILING BED REACTOR
FR2787041B1 (en) 1998-12-10 2001-01-19 Inst Francais Du Petrole HYDROCARBON CHARGE HYDROTREATMENT CATALYST IN A FIXED BED REACTOR
US6218333B1 (en) 1999-02-15 2001-04-17 Shell Oil Company Preparation of a hydrotreating catalyst
US6554994B1 (en) * 1999-04-13 2003-04-29 Chevron U.S.A. Inc. Upflow reactor system with layered catalyst bed for hydrotreating heavy feedstocks
JP3824464B2 (en) * 1999-04-28 2006-09-20 財団法人石油産業活性化センター Method for hydrocracking heavy oils
FR2792851B1 (en) * 1999-04-29 2002-04-05 Inst Francais Du Petrole LOW-DISPERSE NOBLE METAL-BASED CATALYST AND USE THEREOF FOR THE CONVERSION OF HYDROCARBON CHARGES
JP2003171671A (en) * 2000-06-08 2003-06-20 Japan Energy Corp Method for hydrogenation refining of heavy oil
US20020056664A1 (en) * 2000-09-07 2002-05-16 Julie Chabot Extension of catalyst cycle length in residuum desulfurization processes
US6547957B1 (en) 2000-10-17 2003-04-15 Texaco, Inc. Process for upgrading a hydrocarbon oil
JP4260477B2 (en) * 2000-10-24 2009-04-30 日揮株式会社 Refined oil and method for producing the same
US20020112987A1 (en) * 2000-12-15 2002-08-22 Zhiguo Hou Slurry hydroprocessing for heavy oil upgrading using supported slurry catalysts
US6759364B2 (en) 2001-12-17 2004-07-06 Shell Oil Company Arsenic removal catalyst and method for making same
GB0209222D0 (en) 2002-04-23 2002-06-05 Bp Oil Int Purification process
JP2003181292A (en) * 2002-12-25 2003-07-02 Chevron Research & Technology Co Highly active catalyst for treating residual oil
BRPI0405587A (en) * 2003-12-19 2005-10-04 Shell Int Research Methods of Producing a Transportable Fuel and Crude Oil Product, Heating Fuel, Lubricants or Chemicals, and Crude Oil Product
US10535462B2 (en) 2007-04-05 2020-01-14 Hans Wennerstrom Flat winding / equal coupling common mode inductor apparatus and method of use thereof

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