EP1334166A1 - Production de distillats a faible teneur en soufre - Google Patents

Production de distillats a faible teneur en soufre

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Publication number
EP1334166A1
EP1334166A1 EP01925059A EP01925059A EP1334166A1 EP 1334166 A1 EP1334166 A1 EP 1334166A1 EP 01925059 A EP01925059 A EP 01925059A EP 01925059 A EP01925059 A EP 01925059A EP 1334166 A1 EP1334166 A1 EP 1334166A1
Authority
EP
European Patent Office
Prior art keywords
stage
hydrogen
hydrodesulfurization
stream
sulfur
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP01925059A
Other languages
German (de)
English (en)
Other versions
EP1334166B1 (fr
EP1334166A4 (fr
Inventor
Edward Stanley Ellis
Willim Ernest Lewis
Larry Lee Iaccino
Michele Sue Touvelle
Gordon Frederick Stuntz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
ExxonMobil Research and Engineering Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US09/553,107 external-priority patent/US7435335B1/en
Application filed by ExxonMobil Research and Engineering Co filed Critical ExxonMobil Research and Engineering Co
Publication of EP1334166A1 publication Critical patent/EP1334166A1/fr
Publication of EP1334166A4 publication Critical patent/EP1334166A4/fr
Application granted granted Critical
Publication of EP1334166B1 publication Critical patent/EP1334166B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING 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
    • C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/04—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps

Definitions

  • the present invention relates to a process for hydroprocessing a distillate stream to produce a stream exceptionally low in sulfur, with total aromatics and polynuclear aromatics being moderately reduced.
  • a distillate stream is hydrodesulfurized in a first hydrodesulfurization stage.
  • the product stream thereof is passed to a first separation stage wherein a vapor phase product stream and a liquid product stream are produced.
  • the liquid phase product stream is passed to a second hydrodesulfurization stage and the product stream thereof is passed to a second separation stage wherein a vapor phase product stream and a liquid product stream low in sulfur are produced. At least a portion of the vapor product stream from said second separation stage can be cascaded to the first hydrodesulfurization stage.
  • Hydrotreating or in the case of sulfur removal, hydrodesulfurization, is well known in the art and typically requires treating the petroleum streams with hydrogen in the presence of a supported catalyst at hydrotreating conditions.
  • the catalyst is usually comprised of a Group VI metal with one or more Group NIII metals as promoters on a refractory support.
  • Cobalt promoted molybdenum on alumina catalysts are most widely used when the limiting specifications are hydrodesulfurization, while nickel promoted molybdenum on alumina catalysts are the most widely used for hydrodenitrogenation, partial aromatic saturation, as well as hydrodesulfurization.
  • Two types of process schemes are commonly employed to achieve substantial hydrodesulfurization (HDS) and aromatics saturation (ASAT) of distillate fuels and both are operated at relatively high pressures.
  • One is a single stage process using Ni/Mo or Ni/W sulfide catalysts operating at pressures in excess of 800 psig. To achieve high levels of saturation, pressures in excess of 2,000 psig are required.
  • the other process scheme is a two stage process in which the feed is first processed over a Co/Mo, Ni/Mo or Ni/W sulfide catalyst at moderate pressure to reduce heteroatom levels while little aromatics saturation is observed. After the first stage, the product stream is stripped to remove H 2 S, NH 3 and light hydrocarbons. The first stage product is then reacted over a Group VIII metal hydrogenation catalyst at elevated pressure to achieve aromatics saturation.
  • Such two stage processes are typically operated between 600 and 1,500 psig.
  • a multi-stage process for reducing the sulfur content of a distillate feedstock having a sulfur content greater than about 3,000 wppm which process comprises:
  • step d) passing the liquid product stream of step d) above to a separation zone wherein a vapor phase stream and a liquid phase stream are produced.
  • At least a portion of the vapor product stream from the second separation stage is cascaded to said first hydrodesulfurization stage.
  • the invention further comprises combining at least a portion of the liquid phase stream of step (e) with at least one of (i) one or more lubricity aid, (ii) one or more viscosity modifier, (iii) one or more antioxidant, (iv) one or more cetane improver, (v) one or more dispersant, (vi) one or more cold flow improver, (vii) one or more metals deactivator, (viii) one or more corrosion inhibitor, (ix) one or more detergent, and (x) one or more distillate or upgraded distillate.
  • lubricity aid e.g., lubricity aid, ii) one or more viscosity modifier, (iii) one or more antioxidant, (iv) one or more cetane improver, (v) one or more dispersant, (vi) one or more cold flow improver, (vii) one or more metals deactivator, (viii) one or more corrosion inhibitor, (ix) one or more detergent, and (x) one or more distillate
  • the invention is a product made in accordance with the above processes.
  • Figure 1 hereof shows a preferred embodiment of the present invention and includes two co-current hydrodesulfurization stages with once-through hydrogen containing treat gas in the second hydrodesulfurization stage.
  • Figure 2 hereof is a plot of that defines the composition of distillate products of the present invention where the sulfur content is less than 50 ppm and the ratio of aromatics to polynuclear aromatics is greater than about 11.
  • Feedstreams suitable for being treated by the present invention are those petroleum based feedstocks boiling in the distillate range and above (i.e., "distillate"). Such feedstreams typically have a boiling range from about 150°C to about 400°C, preferably from about 175°C to about 370°C. These feedstreams usually contain greater than about 3,000 wppm sulfur. Non-limiting examples of such feedstreams include virgin distillates, light cat cycle oils, light coker oils, etc. It is highly desirable for the refiner to upgrade these types of feedstreams by removing heteroatoms such as sulfur, as well as to saturate aromatic compounds.
  • the process of the present invention can be better understood by a description of a preferred embodiment illustrated by Figure 1 hereof.
  • the embodiment of Figure 1 uses once-through hydrogen treat gas in a second hydrodesulfurization stage and optionally in a first hydrodesulfurization stage as well.
  • Relatively low amounts of hydrogen are utilized in the second hydrodesulfurization stage in such a way that very low levels of sulfur in the liquid product can be achieved while minimizing the amount of hydrogen consumed via saturation of the aromatics.
  • the first hydrodesulfurization stage will reduce the levels of both sulfur and nitrogen, with sulfur levels being less than about 1,000 wppm, preferably less than about 500 wppm.
  • the second hydrodesulfurization stage will reduce sulfur levels to less than about 100 wppm, preferably to less than about 50 wppm.
  • the hydrogen in the treat gas reacts with impurities to convert them to H 2 S, NH 3 ⁇ and water vapor, which are removed as part of the vapor effluent, and it also saturates olefins and aromatics.
  • FIG. 1 shows hydrodesulfurization reaction vessel Rl that contains reaction zones 12a and 12b, each of which is comprised of a bed of hydrodesulfurization catalyst. Although two zones are shown in Rl, it will be understood that this reaction stage may contain only one reaction zone or alternatively two or more reaction zones. It is preferred that the catalyst be in the reactor as a fixed bed, although other types of catalyst arrangements can be used, such as slurry or ebullating beds. Downstream of each reaction zone is a non-reaction zone, 14a and 14b.
  • the non-reaction zone is typically void of catalyst, that is, it will be an empty section in the vessel with respect to catalyst.
  • a liquid distribution means upstream of each reaction stage.
  • the type of liquid distribution means is believed not to limit the practice of the present invention, but a tray arrangement is preferred, such as sieve trays, bubble cap trays, or trays with spray nozzles, chimneys, tubes, etc.
  • a vapor-liquid mixing device (not shown) can also be employed in non-reaction zone 14a for the purpose of introducing a quench fluid (liquid or vapor) for temperature control.
  • the feedstream is fed to reaction vessel Rl via line 10 along with a hydrogen-containing treat gas via line 18, which treat gas will typically be from another refinery process unit, such as a naphtha hydrofiner. It is within the scope of this invention that treat gas can also be recycled via lines 20, 22, and 16 from separation zone SI .
  • the term "recycled" when used herein regarding hydrogen treat gas is meant to indicate a stream of hydrogen-containing treat gas separated as a vapor effluent from one stage that passes through a gas compressor 23 to increase its pressure prior to being sent to the inlet of a reaction stage. It should be noted that the compressor will also generally include a scrubber to remove undesirable species such as H 2 S from the hydrogen recycle stream.
  • the feedstream and hydrogen-containing treat gas pass, co-currently, through the one or more reaction zones of hydradesulfurization stage Rl to remove a substantial amount of the heteroatoms, preferably sulfur, from the feedstream.
  • the first hydrodesulfurization stage contain a catalyst comprised of Co-Mo, or Ni-Mo on a refractory support.
  • hydrodesulfurization refers to processes wherein a hydrogen- containing treat gas is used in the presence of a suitable catalyst which is primarily active for the removal of heteroatoms, preferably sulfur, and nitrogen, and for some hydrogenation of aromatics.
  • Suitable hydrodesulfurization catalysts for use in the reaction vessel Rl of the present invention include conventional hydrodesulfurization catalysts such as those comprised of at least one Group VIII metal, preferably Fe, Co or Ni, more preferably Co and/or Ni, and most preferably Co; and at least one Group VI metal, preferably Mo or W, more preferably Mo, on a relatively high surface area refractory support material, preferably alumina.
  • hydrodesulfurization catalyst supports include refractory oxides such as silica, zeolites, amorphous silica-alumina, and titania-alumina. Additives such as P can also be present. It is within the scope of the present invention that more than one type of hydrodesulfurization catalyst be used in the same reaction vessel and in the same reaction zone.
  • the Group VIII metal is typically present in an amount ranging from about 2 to 20 wt.%, preferably from about 4 to 15 wt.%.
  • the Group VI metal will typically be present in an amount ranging from about 5 to 50 wt.%, preferably from about 10 to 40 wt.%, and more preferably from about 20 to 30 wt.%).
  • All metals weight percents are based on the total weight of the catalyst.
  • Typical hydrodesulfurization temperatures range from about 200°C to about 400°C with a total pressures of about 50 psig to about 3,000 psig, preferably from about 100 psig to about 2,500 psig, and more preferably from about 150 to 500 psig. More preferred hydrogen partial pressures will be from about 50 to 2,000 psig, most preferably from about 75 to 800 psig.
  • a combined liquid phase/vapor phase product stream exits hydrodesulfurization stage Rl via line 24 and passes to separation zone SI wherein a liquid phase product stream is separated from a vapor phase product stream.
  • the liquid phase product stream will typically be one that has components boiling in the range from about 150°C to about 400°C, but will not have an upper boiling range greater than the feedstream.
  • the vapor phase product stream is collected overhead via line 20.
  • the liquid reaction product from separation zone SI is passed to hydrodesulfurization stage R2 via line 26 and is passed downwardly through the reaction zones 28a and 28b. Non-reaction zones are represented by 29a and 29b.
  • Fresh hydrogen-containing treat gas is introduced into reaction stage R2 via line 30.
  • this figure shows the treat gas flowing cocurrent with the liquid feedstream, it is also within the scope of this invention that the treat gas can be introduced into the bottom section of reactor R2 and flowed countercurrent to the downward flowing liquid feedstream. It is preferred that the rate of introduction of hydrogen contained in the treat gas be less than or equal to 3 times the chemical hydrogen consumption rate of this stage, more preferably less than about 2 times, and most preferably less than about 1.5 times.
  • the feedstream and hydrogen- containing treat gas pass, preferably co-currently, through the one or more reaction zones of hydrodesulfurization stage R2 to remove a substantial amount of remaining sulfur, preferably to a level wherein the feedstream now has less than about 100 wppm sulfur, more preferably less than about 50 wppm sulfur.
  • Suitable hydrodesulfurization catalysts for use in the reaction vessel R2 in the present invention include conventional hydrodesulfurization catalyst such as those described for use in Rl .
  • Noble metal catalysts may also be employed, and preferably the noble metal is selected from Pt and Pd or a combination thereof. Pt, Pd or the combination thereof is typically present in an amount ranging from about 0.5 to 5 wt.%), preferably from about 0.6 to 1 wt.%.
  • Typical hydrodesulfurization temperatures range from about 200°C to about 400°C with a total pressures of about 50 psig to about 3,000 psig, preferably from about 100 psig to about 2,500 psig, and more preferably from about 150 to 1,500 psig. More preferred hydrogen partial pressures will be from about 50 to 2,000 psig, most preferably from about 75 to 1,000 psig.
  • R2 outlet pressure ranges from about 500 to about 1000 psig.
  • second reaction stage R2 contain two or more reaction zones wherein at least one of the reaction zones is operated at least 25°C, preferably at least about 50°C cooler than the other reaction zone(s). It is preferred that the lower temperature zone(s) be operated at a temperature of at least about 50°C lower than the higher temperature zone(s). It is preferred that the lower temperature zone be the last downstream zone(s) with respect to the flow of feedstock. It is also within the scope of this invention that the second reaction stage be operated in either cocurrent or countercurrent mode. By countercurrent mode we mean that the treat gas will flow counter to the downflowing feedstock.
  • the reaction product from second hydrodesulfurization stage R2 is passed via line 35 to a second separation zone S2 wherein a vapor product, containing hydrogen, is preferably recovered overhead via line 32 and may be removed from the process via line 36.
  • a vapor product containing hydrogen
  • the treat gas is referred to as a "once-through" treat gas.
  • all or a portion of the vapor product may be cascaded to hydrodesulfurization stage Rl via lines 34 and 16.
  • cascaded when used in conjunction with treat gas, is meant to indicate a stream of hydrogen- containing treat gas separated as a vapor effluent from one stage that is sent to the inlet of a reaction stage without passing through a gas compressor. That is, the treat gas flows from a downstream reaction stage to an upstream stage that is at the same or lower pressure, and thus there is no need for the gas to be compressed.
  • Figure 1 also shows several optional processing schemes.
  • line 38 can carry a quench fluid that may be either a liquid or a gas. Hydrogen is a preferred gas quench fluid and kerosene is a preferred liquid quench fluid.
  • reaction stages used in the practice of the present invention are operated at suitable temperatures and pressures for the desired reaction.
  • typical hydroprocessing temperatures will range from about 200°C to about 400°C at pressures from about 50 psig to about 3,000 psig, preferably 50 to 2,500 psig, and more preferably about 150 to 1,500 psig.
  • reaction stage R2 can be operated in two or more temperature zones wherein the most downstream temperature zone is at least about 25°C , preferably about 35°C, cooler than the upstream temperature zone(s).
  • hydroprocessing and in the context of the present invention, the terms "hydrogen” and “hydrogen-containing treat gas” are synonymous and may be either pure hydrogen or a hydrogen-containing treat gas which is a treat gas stream containing hydrogen in an amount at least sufficient for the intended reaction, plus other gas or gasses (e.g., nitrogen and light hydrocarbons such as methane) which will not adversely interfere with or affect either the reactions or the products.
  • gas or gasses e.g., nitrogen and light hydrocarbons such as methane
  • Impurities such as H2S and NH3 are undesirable and, if present in significant amounts, will normally be removed from the treat gas, before it is fed into the Rl reactor.
  • the treat gas stream introduced into a reaction stage will preferably contain at least about 50 vol.% hydrogen, more preferably at least about 75 vol.%> hydrogen, and most preferably at least 95 vol.% hydrogen.
  • unreacted hydrogen in the vapor effluent of any particular stage is used for hydroprocessing in any stage, there must be sufficient hydrogen present in the fresh treat gas introduced into that stage, for the vapor effluent of that stage to contain sufficient hydrogen for the subsequent stage or stages.
  • the first stage vapor effluent will be cooled to condense and recover the hydrotreated and relatively clean, heavier (e.g., C4+) hydrocarbons.
  • the liquid phase in the reaction vessels used in the present invention will typically be comprised of primarily the higher boiling point components of the feed.
  • the vapor phase will typically be a mixture of hydrogen-containing treat gas, heteroatom impurities like H 2 S and NH 3 , and vaporized lower-boiling components in the fresh feed, as well as light products of hydroprocessing reactions. If the vapor phase effluent still requires further hydroprocessing, it can be passed to a vapor phase reaction stage containing additional hydroprocessing catalyst and subjected to suitable hydroprocessing conditions for further reaction. Alternatively, the hydrocarbons in the vapor phase products can be condensed via cooling of the vapors, with the resulting condensate liquid being recycled to either of the reaction stages, if necessary.
  • the liquid phase products may be combined with other distillate or upgraded distillate.
  • the products are compatible with effective amounts of fuel additives such as lubricity aids, cetane improvers, and the like. While a major amount of the product is preferably combined with a minor amount of the additive, the fuel additive may be employed to an extent not impairing the performance of the fuel. While the specific amount(s) of any additive employed will vary depending on the use of the product, the amounts may generally range from 0.05 to 2.0 wt.% bas.ed on the weight of the product and additive(s), although not limited to this range.
  • the additives can be used either singly or in combination as desired.
  • distillate fuel products that are characterized as having relatively low levels of sulfur and polynuclear aromatics (PNAs) and a relatively high ratio of total aromatics to PNAs may be formed in accordance with such processes.
  • Such distillate fuels may be employed in compression-ignition engines such as diesel engines, particularly so-call "lean-burn" diesel engines.
  • Such fuels are compatible with: compression-ignition engine systems such as automotive diesel systems utilizing (i) sulfur-sensitive NOx conversion exhaust catalysts, (ii) engine exhaust particulate emission reduction technology, including particulate traps, and (iii) combinations of (i) and (ii).
  • Such distillate fuels have moderate levels of total aromatics, reducing the cost of producing cleaner-burning diesel fuel and also reducing C0 2 emissions by minimizing the amount of hydrogen consumed in the process.
  • the distillate fuel products made in accordance with the process of the invention contain less than about 100 wppm, preferably less than about 50 wppm, more preferably less than about 10 wppm sulfur.
  • the distillate fuels of the present invention have relatively low amounts of low boiling material with a T10 distillation point of at least about 205°C. They will also have a total aromatics content from about 15 to 35 wt.%, preferably from about 20 to 35 wt.%, and most preferably from about 25 to 35 wt.%.
  • the PNA content of the distillate product compositions obtained by the practice of the present invention will be less than about 3 wt.%, preferably less than about 2 wt.%, and more preferably less than about 1 wt.%. Such weight percents and weight ppms are based on the weight of the product.
  • the aromatics to PNA ratio will be at least about 11, preferably at least about 13, and more preferably at least about 15. In another embodiment, the aromatics to PNA ratio ranges from 11 to about 50, preferably from 11 to about 30, and more preferably from 11 to about 20.
  • PNA polynuclear aromatics that are defined as aromatic species having two or more aromatic rings, including alkyl and olefin- substituted derivatives thereof.
  • Naphthalene and phenanthrene are examples of PNAs.
  • aromatics is meant to refer species containing one or more aromatic ring, including alkyl and olefm-substituted derivatives thereof.
  • naphthalene and phenanthrene are also considered aromatics along with benzene, toluene and tetrahydronaphthalene. It is desirable to reduce PNA content of the liquid product stream since PNAs contribute significantly to emissions in diesel engines. However, it is also desirable to minimize hydrogen consumption for economic reasons and to minimize C0 2 emissions associated with the manufacture of hydrogen via steam reforming. Thus, the current invention achieves both of these by obtaining a high aromatics to PNA ratio in the liquid product.
  • a virgin distillate feed containing from about 10,000 to 12,000 wppm sulfur was processed in a commercial hydrodesulfurization unit (first hydrodesulfurization stage) using a reactor containing both conventional commercial NiMo/ A1 2 0 3 (Akzo-Nobel KF842/840) and CoMo/Al 2 0 3 (Akzo-Nobel KF-752) catalyst under the following typical conditions: 300-350 psig; 150-180 psig outlet H 2 ; 75% H 2 treat gas; 500-700 SCF/B treat gas rate; 0.3-0.45 LHSV; 330-350°C.
  • the liquid product stream from this first hydrodesulfurization stage was used as feedstream to the second hydrodesulfurization stage, which product stream is described under the feed properties heading in Table 1 below.
  • the process conditions for this second hydrodesulfurization stage are also shown in the table below.
  • a commercial NiMo catalyst (Criterion C-411 containing 2.6 wt.% Ni and 14.3 wt.% Mo) was used in all of the runs.
  • Examples 1 - 5 demonstrate that products with less than 100 wppm sulfur can be produced wherein the rate of introduction of hydrogen in the treat gas in the second reaction stage is less than or equal to three times the chemical hydrogen consumption.
  • the area to the right of the vertical line in the Figure 2 defines the products made in accordance with the present invention.
  • the product total aromatics to PNA ratio of the invention can be greater than 20.
  • the invention provides a method for regulating the total aromatics to PNA ratio by regulating the tieat gas rate in R2. Such regulation may be accomplished for a constant sulfur amount in the product by, for example, decreasing the liquid space velocity in R2 as the treat gas rate is reduced.
  • Comparative Examples A-F in Table 2 below are all conventional fuel compositions containing less than 100 ppm sulfur and total aromatics levels greater than 15 wt.%. All of them, however, have a ratio of total aromatics to PNAs less than 10 which is outside the range of the fuel compositions of the present invention.
  • FIA fluorescence indicator analysis
  • MS mass spectiophotometry
  • SFC supercritical fluid chromatography
  • the area to the right of the vertical line in the Figure 2 hereof defines the preferred products formed in the process of this invention. While figure 2's abscissa is truncated at 20, it should be understood that the preferred product's total aromatics to PNA ratio of the invention may exceed 20. In addition to the total aromatics (15-35 wt.%) and total aromatics/PNA criteria, the preferred products have S levels less than about 100 wppm and a T10 point of >205°C.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

L'invention concerne un procédé d'hydrotraitement d'un écoulement du type distillat visant à produire un écoulement à teneur en soufre exceptionnellement faible, la teneur en aromatiques totaux et polynucléaires étant modérément réduite. A cet effet, on hydrodésulfure un écoulement du type distillat au cours d'une première étape d'hydrodésulfuration. L'écoulement obtenu subit une première étape de séparation donnant lieu à la production d'un écoulement en phase vapeur et d'un écoulement liquide. L'écoulement en phase liquide subit une seconde étape d'hydrodésulfuration, et l'écoulement obtenu passe par une seconde étape de séparation donnant lieu à la production d'un écoulement en phase vapeur et d'un écoulement liquide à faible teneur en soufre. Un partie au moins de l'écoulement en phase vapeur tiré de la seconde étape de séparation peut être réintroduit en cascade au niveau de la première étape d'hydrodésulfuration.
EP01925059.6A 2000-04-20 2001-04-17 Production de distillats a faible teneur en soufre Expired - Lifetime EP1334166B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US553107 2000-04-20
US09/553,107 US7435335B1 (en) 1998-12-08 2000-04-20 Production of low sulfur distillates
PCT/US2001/012516 WO2001081506A1 (fr) 2000-04-20 2001-04-17 Production de distillats a faible teneur en soufre

Publications (3)

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EP1334166A1 true EP1334166A1 (fr) 2003-08-13
EP1334166A4 EP1334166A4 (fr) 2004-10-20
EP1334166B1 EP1334166B1 (fr) 2017-11-29

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EP (1) EP1334166B1 (fr)
JP (1) JP5469791B2 (fr)
AU (2) AU5165701A (fr)
CA (1) CA2405019C (fr)
NO (1) NO20025020L (fr)
WO (1) WO2001081506A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8632675B2 (en) * 2008-12-24 2014-01-21 Exxonmobil Research And Engineering Company Co-processing of diesel biofeed and heavy oil
DE102011101503A1 (de) * 2011-05-16 2012-11-22 Schott Ag Sensorbauteilgehäuse
US10273420B2 (en) 2014-10-27 2019-04-30 Uop Llc Process for hydrotreating a hydrocarbons stream

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5114562A (en) * 1990-08-03 1992-05-19 Uop Two-stage hydrodesulfurization and hydrogenation process for distillate hydrocarbons
US5292428A (en) * 1989-05-10 1994-03-08 Davy Mckee (London) Ltd. Multi-step hydrodesulphurization process
EP0727474A2 (fr) * 1995-02-14 1996-08-21 Nippon Oil Co., Ltd. Méthode et catalyseur d'hydrogénation d'hydrocarbures aromatiques dans les huiles hydrocarbonées
EP0902078A2 (fr) * 1997-09-11 1999-03-17 Jgc Corporation Méthode et appareillage pour le traitement de pétrole
WO2000034416A1 (fr) * 1998-12-08 2000-06-15 Exxon Research And Engineering Company Production de distillats a faible teneur en soufre et en aromatiques
US6231753B1 (en) * 1996-02-02 2001-05-15 Exxon Research And Engineering Company Two stage deep naphtha desulfurization with reduced mercaptan formation

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2530498B2 (ja) * 1989-08-31 1996-09-04 東燃株式会社 石油蒸留物の低イオウ化方法
JP2519191B2 (ja) * 1990-04-10 1996-07-31 触媒化成工業株式会社 灯軽油の水素化処理方法
JP2921379B2 (ja) * 1993-12-30 1999-07-19 株式会社コスモ総合研究所 軽油の水素化脱硫方法
JP3634041B2 (ja) * 1995-12-26 2005-03-30 財団法人石油産業活性化センター 軽油の高品質化処理法
FR2757532B1 (fr) * 1996-12-20 1999-02-19 Inst Francais Du Petrole Procede de transformation d'une coupe gazole pour produire un carburant a haute indice de cetane, desaromatise et desulfure
US6103104A (en) * 1998-05-07 2000-08-15 Exxon Research And Engineering Company Multi-stage hydroprocessing of middle distillates to avoid color bodies
JP4282118B2 (ja) * 1998-10-05 2009-06-17 新日本石油株式会社 軽油の水素化脱硫方法

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5292428A (en) * 1989-05-10 1994-03-08 Davy Mckee (London) Ltd. Multi-step hydrodesulphurization process
US5114562A (en) * 1990-08-03 1992-05-19 Uop Two-stage hydrodesulfurization and hydrogenation process for distillate hydrocarbons
EP0727474A2 (fr) * 1995-02-14 1996-08-21 Nippon Oil Co., Ltd. Méthode et catalyseur d'hydrogénation d'hydrocarbures aromatiques dans les huiles hydrocarbonées
US6231753B1 (en) * 1996-02-02 2001-05-15 Exxon Research And Engineering Company Two stage deep naphtha desulfurization with reduced mercaptan formation
EP0902078A2 (fr) * 1997-09-11 1999-03-17 Jgc Corporation Méthode et appareillage pour le traitement de pétrole
WO2000034416A1 (fr) * 1998-12-08 2000-06-15 Exxon Research And Engineering Company Production de distillats a faible teneur en soufre et en aromatiques

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO0181506A1 *

Also Published As

Publication number Publication date
EP1334166B1 (fr) 2017-11-29
EP1334166A4 (fr) 2004-10-20
AU2001251657B2 (en) 2006-05-18
WO2001081506A1 (fr) 2001-11-01
JP5469791B2 (ja) 2014-04-16
CA2405019A1 (fr) 2001-11-01
NO20025020L (no) 2002-12-19
NO20025020D0 (no) 2002-10-18
AU5165701A (en) 2001-11-07
CA2405019C (fr) 2010-06-22
JP2003531274A (ja) 2003-10-21

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