JP2002263476A - Method of equalizing heat distribution in reactor tube - Google Patents
Method of equalizing heat distribution in reactor tubeInfo
- Publication number
- JP2002263476A JP2002263476A JP2001393138A JP2001393138A JP2002263476A JP 2002263476 A JP2002263476 A JP 2002263476A JP 2001393138 A JP2001393138 A JP 2001393138A JP 2001393138 A JP2001393138 A JP 2001393138A JP 2002263476 A JP2002263476 A JP 2002263476A
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- monolith
- heat
- tube
- catalytic
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 18
- 238000009826 distribution Methods 0.000 title claims abstract description 7
- 239000003054 catalyst Substances 0.000 claims abstract description 34
- 230000003197 catalytic effect Effects 0.000 claims abstract description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000006356 dehydrogenation reaction Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000919 ceramic Substances 0.000 claims description 2
- 150000002118 epoxides Chemical class 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 1
- 229910017052 cobalt Inorganic materials 0.000 claims 1
- 239000010941 cobalt Substances 0.000 claims 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 229910052750 molybdenum Inorganic materials 0.000 claims 1
- 239000011733 molybdenum Substances 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 229910052709 silver Inorganic materials 0.000 claims 1
- 239000004332 silver Substances 0.000 claims 1
- 239000012808 vapor phase Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 13
- 238000012856 packing Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 102100024522 Bladder cancer-associated protein Human genes 0.000 description 1
- 101150110835 Blcap gene Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 101100493740 Oryza sativa subsp. japonica BC10 gene Proteins 0.000 description 1
- 102100031083 Uteroglobin Human genes 0.000 description 1
- 108090000203 Uteroglobin Proteins 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/248—Reactors comprising multiple separated flow channels
- B01J19/2485—Monolithic reactors
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/2415—Tubular reactors
- B01J19/2425—Tubular reactors in parallel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
- B01J35/56—Foraminous structures having flow-through passages or channels, e.g. grids or three-dimensional monoliths
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3332—Catalytic processes with metal oxides or metal sulfides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/02—Processes carried out in the presence of solid particles; Reactors therefor with stationary particles
- B01J2208/023—Details
- B01J2208/024—Particulate material
- B01J2208/025—Two or more types of catalyst
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/48—Silver or gold
- B01J23/50—Silver
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/74—Iron group metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
- C07C2523/74—Iron group metals
- C07C2523/745—Iron
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、触媒を収容してい
る反応管における熱分布の均等化方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for equalizing heat distribution in a reaction tube containing a catalyst.
【0002】[0002]
【発明の背景】触媒を充填している恒温管型反応器の性
能は触媒充填管における熱伝達により制限されている。
吸熱反応では、熱は管の中心から除去され、管壁の温度
は管中心の温度よりも実質的に高くなる。発熱反応で
は、反応熱により触媒床の中心ゾーンの触媒の温度は管
壁近くの触媒床の外側領域の温度よりも実質的に高くな
る。温度差によりいろいろな悪影響が生じる恐れがあ
る。充填物の低温部分は効果的接触処理のためには余り
に低いままであり得、充填物の高温部分は予想以上に短
い寿命を有し得る。いずれの場合にも、処理効率は低下
する。BACKGROUND OF THE INVENTION The performance of a constant temperature tube reactor packed with catalyst is limited by heat transfer in the catalyst packed tube.
In an endothermic reaction, heat is removed from the center of the tube and the temperature at the tube wall is substantially higher than at the tube center. In an exothermic reaction, the heat of reaction causes the temperature of the catalyst in the central zone of the catalyst bed to be substantially higher than the temperature in the outer region of the catalyst bed near the tube wall. Various adverse effects may occur due to the temperature difference. The cold part of the filling may remain too low for effective contact treatment, and the hot part of the filling may have a shorter life than expected. In either case, processing efficiency is reduced.
【0003】熱伝達の問題により、断熱系に比して恒温
反応器の効率は低下し、その商業的魅力も低下する。こ
れは、管の中心に対して十分な熱を与えるために恒温反
応器において高い管壁温度を必要とする吸熱系で特に当
てはまり、その結果高い温度勾配が生じ、最適性能では
ない。[0003] Heat transfer problems reduce the efficiency of isothermal reactors and their commercial appeal as compared to adiabatic systems. This is especially true for endothermic systems that require high tube wall temperatures in a thermostatic reactor to provide sufficient heat to the center of the tube, resulting in high temperature gradients and non-optimal performance.
【0004】[0004]
【発明の要旨】触媒モノリスを使用すると、熱は所望方
向に向けられ得、よって熱勾配が低下し、効率及び触媒
性能が向上する。管型反応器における触媒上の熱分布の
均等化方法が提供され、その方法は管型反応器の各管に
1つ以上の触媒モノリスを充填することを特徴とする。SUMMARY OF THE INVENTION With the use of a catalytic monolith, heat can be directed in the desired direction, thus reducing thermal gradients and improving efficiency and catalytic performance. A method is provided for equalizing the heat distribution on a catalyst in a tubular reactor, the method comprising charging each tube of the tubular reactor with one or more catalytic monoliths.
【0005】[0005]
【詳細な説明】「モノリス触媒」は、単方向もしくは多
方向チャネルを有する通常セラミック支持体を含む触媒
を意味する。前記支持体に1つ以上の触媒反応性金属を
含浸させてもよく、或いは支持体材料そのものが触媒反
応性材料(例えば、酸化鉄)であってもまたは触媒反応
性材料を含んでいてもよい。モノリス触媒は、容器の形
に近い形に形成され得るという利点を有する。よって、
管型反応器用モノリス触媒は十分に長い(数インチ〜数
フィートの長さ)円筒形であってもよく、通常その直径
はモノリス触媒を配置する管の内径よりもやや小さい。
単方向もしくは多方向チャネルは供給物が所望通りに流
れるようにモノリスに成形され得る。このようにして、
各チャネルは多くのルーズ触媒粒子に等しい表面積を有
する。DETAILED DESCRIPTION "Monolith catalyst" means a catalyst comprising a conventional ceramic support having unidirectional or multidirectional channels. The support may be impregnated with one or more catalytically reactive metals, or the support material itself may be a catalytically reactive material (eg, iron oxide) or may include a catalytically reactive material. . Monolithic catalysts have the advantage that they can be formed in a shape close to that of a container. Therefore,
Monolithic catalysts for tubular reactors may be sufficiently long (several inches to several feet long) cylindrical and usually have a diameter slightly smaller than the inside diameter of the tube in which the monolithic catalyst is located.
Unidirectional or multidirectional channels can be formed into a monolith so that the feed flows as desired. In this way,
Each channel has a surface area equal to many loose catalyst particles.
【0006】チャネルの表面に触媒活性金属または金属
化合物を含浸させて、各チャネルを該チャネルの表面積
に等しい表面積を有する触媒として有効なものとしても
よい。或いは、モノリスを触媒反応性材料から構成して
もよい。[0006] The surfaces of the channels may be impregnated with a catalytically active metal or metal compound to render each channel effective as a catalyst having a surface area equal to the surface area of the channel. Alternatively, the monolith may be composed of a catalytically reactive material.
【0007】管型反応器における触媒上の熱分布は、管
型反応器の管に充填したモノリス触媒のチャネルに熱を
所望のように下方に向けることにより均等化される。熱
は、吸熱反応器の管の温度プロフィルを均等化するため
には内向きに、または発熱反応の管の温度プロフィルを
均等化するためには外向きに向けられ得る。[0007] The heat distribution on the catalyst in a tubular reactor is equalized by directing heat as desired downward to the channels of the monolith catalyst packed in the tubes of the tubular reactor. The heat may be directed inward to equalize the temperature profile of the tubes of the endothermic reactor or outward to equalize the temperature profile of the tubes of the exothermic reaction.
【0008】上記したように使用されるモノリス触媒
は、触媒床中の圧力低下を抑えるという別の利点を有す
る。[0008] The monolithic catalyst used as described above has another advantage in that the pressure drop in the catalyst bed is suppressed.
【0009】本発明の方法は特に、吸熱反応であるエチ
ルベンゼンの脱水素化によりスチレンを製造するための
市販の恒温反応器に使用される。前記反応器は下記する
3つの重大な問題を有する:反応のために液空間速度は
低くなければならず、直径がより大きい管が必要とな
る。スチレン反応は吸熱反応であるので、熱を加えなけ
ればならず、大きな管では管の外側から触媒床の中心ま
での温度差が大きくなり、その結果触媒性能は悪くな
る。更に、熱を充填物の中心に加えるべく管壁の温度を
上昇させると、管壁の温度はエチルベンゼン及びスチレ
ンが分解し、よって望ましくない副生成物が生ずる恐れ
があるレベルに達し得る;管型恒温反応器は本質的に半
径流断熱反応器に比して高い圧力低下を示す。このため
に、活性及び選択性の点で管型反応器は不利である;供
給材料(エチルベンゼン)1モルが生成物(スチレン+
水素)2モルとなるので、上記した問題が顕著になる。The process according to the invention is used in particular in a commercial thermostatic reactor for the production of styrene by the endothermic dehydrogenation of ethylbenzene. The reactor has three major problems: the liquid space velocity must be low for the reaction, and a larger diameter tube is required. Since the styrene reaction is an endothermic reaction, heat must be applied, and in large tubes the temperature difference from the outside of the tube to the center of the catalyst bed is large, resulting in poor catalyst performance. Furthermore, as the temperature of the tube wall is increased to apply heat to the center of the fill, the temperature of the tube wall can reach levels at which ethylbenzene and styrene can decompose and thus produce undesirable by-products; Isothermal reactors exhibit a substantially higher pressure drop compared to radial adiabatic reactors. For this reason, tubular reactors are disadvantageous in terms of activity and selectivity; one mole of feed (ethylbenzene) is converted to product (styrene +
(Hydrogen) 2 mol, so that the above-mentioned problem becomes remarkable.
【0010】モノリス触媒を使用すると、熱は各管中の
触媒床の中心に向けられ、管壁の温度が低下し、供給材
料及び生成物の望ましくない副生成物への分解が抑えら
れる。また、生ずる圧力低下はスチレン反応にとって有
利である。With the use of monolith catalysts, heat is directed to the center of the catalyst bed in each tube, reducing the temperature of the tube walls and reducing the decomposition of feedstock and products into unwanted by-products. The resulting pressure drop is also advantageous for the styrene reaction.
【0011】前記したモノリス触媒は、他の吸熱反応
(例えば、脱水素化方法及びオレフィン分解方法)の管
温度プロフィールをコントロールするのに有用である。
モノリス触媒を、チャネルにより反応管の中心から放熱
させ、よってエポキシドの気相製造、他の酸化方法及び
ヒドロクラッキング方法のような発熱反応にも有用とな
るように改質してもよい。The monolithic catalysts described above are useful for controlling the tube temperature profile of other endothermic reactions (eg, dehydrogenation and olefin cracking processes).
The monolith catalyst may be modified to radiate heat from the center of the reaction tube through the channel and thus be useful for exothermic reactions such as epoxide gas phase production, other oxidation methods and hydrocracking methods.
【0012】本明細書に記載の本発明の趣旨または範囲
を逸脱することなく本発明に対して多くの変更及び改変
をなし得ることは当業者に自明である。It will be apparent to those skilled in the art that many changes and modifications can be made to the present invention without departing from the spirit or scope of the invention described herein.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4G075 AA03 AA45 AA62 AA63 BA05 BA06 BD01 BD14 CA02 CA03 CA54 EE33 4H006 AA02 AC12 BA05 BA14 BA18 BA30 BC10 BC11 BD20 4H039 CA21 CC10 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4G075 AA03 AA45 AA62 AA63 BA05 BA06 BD01 BD14 CA02 CA03 CA54 EE33 4H006 AA02 AC12 BA05 BA14 BA18 BA30 BC10 BC11 BD20 4H039 CA21 CC10
Claims (5)
リスを充填することを特徴とする管型反応器における触
媒上の熱分布の均等化方法。1. A method for equalizing heat distribution on a catalyst in a tubular reactor, wherein each tube of the tubular reactor is filled with one or more catalyst monoliths.
属を含浸させたセラミックモノリス支持体を含むことを
特徴とする請求項1に記載の方法。2. The method according to claim 1, wherein the catalytic monolith comprises a ceramic monolith support impregnated with one or more catalytically reactive metals.
ンへの接触脱水素化に有用な酸化鉄を含み、熱が各管の
中心に向かうように触媒モノリス中の流路が配列されて
いることを特徴とする請求項1に記載の方法。3. The catalyst monolith contains iron oxide useful for catalytic dehydrogenation of ethylbenzene to styrene, and the channels in the catalyst monolith are arranged so that heat is directed toward the center of each tube. The method of claim 1, wherein
びモリブデンからなる群から選択され、触媒モノリスが
炭化水素の脱水素化に有用であり、熱が各管の中心に向
かうように触媒モノリス中の流路が配列されていること
を特徴とする請求項2に記載の方法。4. The catalyst-reactive metal is selected from the group consisting of nickel, cobalt and molybdenum, wherein the catalyst monolith is useful for hydrocarbon dehydrogenation and the heat in the catalyst monolith is such that heat is directed to the center of each tube. 3. The method according to claim 2, wherein the channels are arranged.
スがエポキシドの気相製造に有用であり、熱が各管の中
心から去るように触媒モノリス中の流路が配列されてい
ることを特徴とする請求項2に記載の方法。5. The method of claim 1, wherein the catalytically reactive metal is silver, the catalytic monolith is useful for the vapor phase production of epoxides, and the channels in the catalytic monolith are arranged so that heat leaves the center of each tube. 3. The method according to claim 2, wherein the method comprises:
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US754793 | 2001-01-04 | ||
US09/754,793 US20020085975A1 (en) | 2001-01-04 | 2001-01-04 | Method to equalize heat distribution in reactor tube |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2002263476A true JP2002263476A (en) | 2002-09-17 |
Family
ID=25036361
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001393138A Pending JP2002263476A (en) | 2001-01-04 | 2001-12-26 | Method of equalizing heat distribution in reactor tube |
Country Status (3)
Country | Link |
---|---|
US (1) | US20020085975A1 (en) |
JP (1) | JP2002263476A (en) |
DE (1) | DE10200050A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018531969A (en) * | 2015-11-04 | 2018-11-01 | エクソンモービル ケミカル パテンツ インコーポレイテッド | Heating tube conversion system and method |
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CN110312571A (en) * | 2017-01-24 | 2019-10-08 | 巴斯夫公司 | For epoxidised integral catalyzer |
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US4912077A (en) * | 1988-07-15 | 1990-03-27 | Corning Incorporated | Catalytically active materials and method for their preparation |
SK279333B6 (en) * | 1989-10-16 | 1998-10-07 | Haldor Topsoe A/S | Catalyst for preparing aldehydes |
US6005143A (en) * | 1998-08-07 | 1999-12-21 | Air Products And Chemicals, Inc. | Use of a monolith catalyst for the hydrogenation of dinitrotoluene to toluenediamine |
MY124615A (en) * | 1998-09-03 | 2006-06-30 | Dow Global Technologies Inc | Autothermal process for the production of olefins |
US6623707B1 (en) * | 2000-06-19 | 2003-09-23 | Corning Incorporated | Monolithic catalyst dehydrogenation reactor |
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JP2018531969A (en) * | 2015-11-04 | 2018-11-01 | エクソンモービル ケミカル パテンツ インコーポレイテッド | Heating tube conversion system and method |
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