EP0333767A1 - Lit fluidise - Google Patents
Lit fluidiseInfo
- Publication number
- EP0333767A1 EP0333767A1 EP88900319A EP88900319A EP0333767A1 EP 0333767 A1 EP0333767 A1 EP 0333767A1 EP 88900319 A EP88900319 A EP 88900319A EP 88900319 A EP88900319 A EP 88900319A EP 0333767 A1 EP0333767 A1 EP 0333767A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tubes
- vessel
- fluidized bed
- gas
- tube
- 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.)
- Withdrawn
Links
- 239000007787 solid Substances 0.000 claims abstract description 25
- 239000002245 particle Substances 0.000 claims abstract description 19
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 16
- 230000000630 rising effect Effects 0.000 claims abstract description 13
- 239000007789 gas Substances 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 14
- 239000003054 catalyst Substances 0.000 claims description 12
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims description 8
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 5
- 238000007254 oxidation reaction Methods 0.000 claims description 5
- 239000012530 fluid Substances 0.000 claims description 4
- 238000004891 communication Methods 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 description 20
- 238000004519 manufacturing process Methods 0.000 description 8
- 238000005204 segregation Methods 0.000 description 5
- 239000011949 solid catalyst Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- -1 CIO hydrocarbons Chemical class 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000005465 channeling Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
-
- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/1836—Heating and cooling the reactor
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
-
- 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
- B01J2208/00008—Controlling the process
- B01J2208/00017—Controlling the temperature
- B01J2208/00026—Controlling or regulating the heat exchange system
- B01J2208/00035—Controlling or regulating the heat exchange system involving measured parameters
- B01J2208/00097—Mathematical modelling
-
- 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
- B01J2208/00008—Controlling the process
- B01J2208/00017—Controlling the temperature
- B01J2208/00106—Controlling the temperature by indirect heat exchange
- B01J2208/00115—Controlling the temperature by indirect heat exchange with heat exchange elements inside the bed of solid particles
- B01J2208/00132—Tubes
Definitions
- This invention relates to a fluidized bed, and the use thereof for contacting a gas phase with solid particles.
- This invention further relates to a new and improved process for effecting a reaction in a fluidized bed.
- This invention additionally relates to the production of maleic anhydride in a fluidized bed.
- Fluidized beds are generally known in the art as being suitable for effecting contact between a gas and solids.
- such fluidized beds are known to be suitable for effecting catalytic reactions wherein one or more gas reagents are contacted with a particulate solid catalyst.
- an improved fluidized bed vessel wherein the vessel is provided with a plurality of horizontal heat exchanger tubes positioned within the vessel in at least one horizontal row with the horizontal tubes having spaces therebetween to provide a free flow area between the tubes so that there is fluid flow communication between the portions of the vessel above and below the tubes.
- the spacing and arrangement of the tubes are selected in a manner such that the ratio of free area between the tubes to the free area of the vessel in the absence of tubes provides for breaking of rising bubbles.
- the free area between the tubes provides flow parameters whereby the gas flows through the bed in essentially plug flow, i.e., with gas backmix largely eliminated.
- the spacing is such that there is an exchange of solids between the portions above and below the tubes so as to enable adequate temperature control and to avoid particle size segregation.
- the heat exchanger tubes in the vessel have a total surface area such as to provide the heating or cooling requirements for the vessel; for example, if the vessel is employed for an endothermic reaction, then the heat exchanger tubes will have a surface area so as to provide for appropriate heating. Similarly, if the fluidized vessel is employed for an exothermic reaction, then the total surface area of the heat exchange tubes is sufficient to meet the cooling requirements for the reaction.
- the heat exchanger tubes will be placed in several vertically spaced horizontal banks, with each horizontal bank having at least one row of horizontal tubes and preferably each bank having several horizontal rows of tubes. The open spaces between vertically spaced tube banks and between a tube bank and either the feed inlet or the reactor outlet define compartments of chambers of fluidized solids.
- the open spaces or compartments assure that the fluidized bed is rehomogenized in the event that there is a tendency toward localized channeling or inhomogenity due to the presence of horizontal or vertical obstructions, and that lateral mixing is not impaired, thereby minimizing the possibilities of unwarranted lateral temperature and concentration gradients. Accordingly, in each of the superimposed compartments or chambers, there is continuous mixing of the solid phase.
- the horizontal and vertical spacing between tubes within a horizontal bank, and the vertical spacing between horizontal tube banks over the vertical length of the reactor are selected so as to effectively break rising bubbles, minimize gas backmix, and increase conversion and/or selectivity without causing a significant pressure drop or attrition or segregation of solid particles.
- the tube spacing and arrangements are optimized for the maximum possible bed-to-tube heat transfer coefficient, with minimum sacrifice of the bubble control and backmix prevention capability of tube banks.
- the horizontal tubes in at least one tube bank are arranged in a manner such that the free cross-sectional area of spaces between the tubes in the bank, as projected in a plan view of the at least one tube bank (the "Projected Free Area") is less than 60% and preferably less than 50% of the cross-sectional area of the vessel without tubes.
- the total open space or free area between tubes in a horizontal plane through the tube bank is generally at least 10% and preferably at least 20% of the cross-sectional area of the vessel without tubes.
- the "Projected Free Area" for a tube bank can be 0%, even though the free area in each horizontal plane through the tube bank is at least 10%.
- the "Projected Free Area” for the tube bank which is less than the free area between the tubes in each horizontal plane through the tube bank.
- the at least one tube bank preferably contains at least two rows of horizontal tubes, and the reactor preferably includes at least two vertically spaced banks of horizontal tubes.
- the size and number of tubes, and the spacings between the tubes, as well as the possible staggering of the tube arrangement in each bank will be such as to provide for essentially plug flow of the gas through the vessel, while maintaining a good exchange rate of solids between compartments.
- such arrangement will cause effective redistribution and breaking of the rising bubbles, without causing a significant pressure drop, or attrition or segregation of solid particles.
- the tube spacings and arrangements are optimized for the maximum sacrifice of the bubble control and backmix prevention capability of the tube banks.
- the vertical spacing between the tube banks is selected so as to maximize conversion and/or selectivity by providing for effective breaking of rising bubbles and an essentially plug flow of gas through the vessel.
- the conditions are such that the number of heat exchanger tubes required for breaking of rising bubbles is greater than the heat exchange requirements. In such a case it is possible to use "dummy" tubes or appropriate baffling to provide for breaking of rising bubbles and essentially plug flow of gas through the vessel.
- the breaking of rising bubbles also reduces back-mixing of solids between compartments defined by the horizontal tube wall.
- some back-mixing of solids is desirable in that such back-mixing improves heat transfer and prevents segregation of the solid particles.
- the use of spaced banks of heat exchanger tubes allows for optimum temperature control in that each bank may be separately controlled.
- the tubes in each bank can have the same or different diameters.
- the tubes may be circular, elliptical, etc., and may be employed with or without fins.
- the tubes are preferably arranged in a heat exchanger coil having a hairpin shape which adjusts to large changes in temperature without creating mechanical stresses.
- the axis of tubes in a tube bank need not be aligned with each other; i.e., criss-crossing of tube rows in a bank. The selection of a particular type of tube and arrangement is deemed to be within the scope of those skilled in the art from the teachings herein.
- the horizontal tubes are placed in the vessel in a manner so as to form banks which are located at predetermined heights of the bed.
- Such tube banks in effect, form a wall having a plurality of passages therethrough defined by the free area between the tubes.
- the relative position of the tubes within each bank, as well as the diameter of the tubes, determines the fraction of the cross section of the reactor which is left free for circulation between the compartments formed by the horizontal tube wall.
- the diameter and relative placement of the tubes within the bank control the degree to which the gas bubbles arriving from the compartment below the bank will be redisbursed into small bubbles while passing through the bank.
- the horizontal tubes are spaced in the tube bank so as to provide a tube bank having a reduced flow area, as hereinabove described, to redistribute and break rising bubbles, while minimizing pressure drop, as well as attrition and segregation of solid particles.
- the fluidized bed is employed as a reactor, and at least a portion of the fluidized bed of solids within the reactor is comprised of solid catalyst particles. It is to be understood, however, that the fluidized bed may be employed for other purposes.
- the gas which is passed through the bed may be comprised of one, two or more components.
- the fluidized bed reactor is particularly suitable for use in an exothermic reaction; however, the fluid bed may also be employed for an endothermic reaction.
- the fluidized bed has particular applicability to the production of maleic anhydride.
- the reactor is divided into three or more compartments by the horizontal tube banks.
- the bottommost tube bank is preferably placed as close to the inlet means, such as a gas sparger or grid, as is physically possible to remove the heat generated in an intense reaction zone close to the inlet means.
- the uppermost tube bank is preferably placed within the fluidized bed of solids but below the top surface thereof so that there is some entrainment of solids into the free space immediately above the bed. Such an arrangement creates a free board (splash) zone in which the solids and gas more intimately contact each other. In the case where the vessel is used as a reactor, conversion and/or yield can be increased. However, if it is desired to minimize additional gas-solid contact, then the uppermost tube bank is placed at, and even extending above, the top surface of the bed.
- the drawing is a simplified schematic diagram of a fluidized bed vessel in accordance with the invention.
- a vessel 10 which includes a first gas inlet, in the form of a sparger 11, and a second gas inlet, in the form of a sparger 12. It is to be understood that other gas inlets could be used.
- the reactor is described with respect to the production of maleic anhydride, wherein a hydrocarbon such as n-butane would be introduced into one of the spargers 11 and 12, and air would be introduced into the other of the spargers 11 and 12.
- the vessel 10 is divided into a plurality of compartments, 13B through 13N, each of which contains a fluidized bed of catalyst suitable for producing maleic anhydride by oxidation of a hydrocarbon.
- the compartments are limited above and below by partitions comprised of banks of horizontal heat exchanger tubes, generally designated as 14A through 14M.
- the heat exchanger banks 14A through 14M are formed from a plurality of horizontally disposed tubes, which are sized and spaced from each other, as hereinabove described, so as to break rising bubbles and provide for essentially plug flow of the gas through the vessel 10 while maintaining a good exchange rate of solids between compartments above and below the banks.
- Across each of the horizontal tube banks, 14A through 14M there is a backmixing of catalyst; however, the fluid phase flows across said tube banks in essentially plug flow; i.e., without backmixing between compartments.
- the vertical spacing between successive banks 14A - 14M is set based on the desired conversion, with conversion being increased provided the total bed height is maintained constant (thus, there is an increase in the number of compartments).
- the vertical space between successive tube banks is in the order of from 0.2 to 4.0 meters, preferably less than 2.0 meters. It is to be understood that the space between any two successive banks can vary or be the same over the length of the vessel. Bubbles grow more rapidly in beds of high density and large particle size, and in such beds a closer spacing between successive tube banks may be required to achieve a desired conversion. For beds of smaller particle size, a desired conversion may be achieved with a larger spacing between successive tube banks.
- the tubes are arranged in each tube bank so as to provide a "Projected Free Area" in each bank of less than 60% of the cross-sectional area of the vessel, with the total free area between tubes in each individual horizontal row of tubes in each tube bank being at least 10% of the cross-sectional area of the vessel so as to insure adequate flow between the tubes.
- the specific "Projected Free Area" for a tube bank is selected within the hereinabove described range so as to cause significant bubble breaking while large enough for a good exchange rate of solids between adjoining compartments.
- a closer spacing of tubes in a bank results in smaller bubbles, higher pressure drops and more difficult exchange of solids between compartments.
- a decreased bubble size increases conversion.
- the spacing of tubes in each bank is selected to provide desired conversion consistent with pressure drop, heat transfer and solid exchange.
- the lowermost bank 14A is spaced from the uppermost sparger 11 as hereinabove described.
- the uppermost bank 14M is positioned near the top of the bed but below the top surface of the bed, whereby there is some entrainment of the catalyst particles in the splash zone 15 above the top of the expanded bed.
- the reaction product, as well as any unreacted starting material is withdrawn from the top of reactor 10 through an outlet conduit 16.
- the outlet portion of the vessel 10 may be provided with a conventional cyclone separator system, either external or internal, so as to return any catalyst fines which are entrained in the outlet gas.
- Other catalyst recovery systems e.g., sintered metal mesh, ceramic, fabric filter systems
- the fluidized bed vessel of the present invention may be employed for effecting contact between a wide variety of solids and gases; however, such vessel has particular use as a fluidized bed reactor wherein one or more reactants are contacted with a solid catalyst.
- the fluidized bed reactor has particular applicability to exothermic reactions, such as the production of maleic anhydride.
- the present invention will be further described with respect to the production of maleic anhydride from n-butane; however, as know in the art, saturated or unsaturated C4 to CIO hydrocarbons or mixtures thereof, in addition to n-butane, may be employed as a feed for producing maleic anhydride; for example, 1,3-butadiene or a C4 cut from a refinery.
- Conditions under which maleic anhydride may be produced using the reactor of the present invention are temperatures of from 330 ⁇ C-490 ⁇ C, particularly 370-450 ⁇ C. Although a uniform temperature profile along the length of the reactor is ordinarily desired; in some situations, a profile may be desired and is achievable by the present invention.
- a concentration of hydrocarbon (butane) in air generally is 1-20 volume percent, or higher, particularly 2-8 volume percent.
- Superficial gas velocities of from 0.5 to 5 feet/second may be used.
- the catalyst used may be any catalyst effective for oxidizing a hydrocarbon to maleic anhydride, particularly one containing vanadium and phosphorus, as known in the art.
- the catalyst particle size distribution will by typical of those used in a fluidized bed process, with an average particle size being from 20-500 microns, preferably less than 150 microns.
- the present invention is particularly advantageous in that it is possible to use a fluidized bed at higher conversions at acceptable selectivities.
- the present invention for the production of maleic anhydride, it is possible to achieve conversions in excess of 70% and as high as 90% or more, while maintaining selectivity of at least 50% and in some cases at least 70%.
- fluidized bed vessel has particular applicability to the production of maleic anhydride, it is to be understood that the scope of the invention is not limited to such production in that the fluidized bed vessel may be used for other purposes.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
- Furan Compounds (AREA)
Abstract
Une enceinte à lit fluidisé (10) comprend des rampes horizontales de tubes échangeurs de chaleur (14A, 14B, 14M), ces tubes étant espacés les uns des autres afin d'assurer un écoulement pratiquement idéal du gaz à travers l'enceinte et la rupture des bulles montantes tout en permettant également un transfert thermique et un échange de particules solides appropriés. Cette enceinte est particulièrement utile pour produire de l'anhydride maléique.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US94024886A | 1986-12-10 | 1986-12-10 | |
US940248 | 1986-12-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0333767A1 true EP0333767A1 (fr) | 1989-09-27 |
Family
ID=25474490
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88900319A Withdrawn EP0333767A1 (fr) | 1986-12-10 | 1987-12-07 | Lit fluidise |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0333767A1 (fr) |
JP (1) | JPH01503211A (fr) |
KR (1) | KR910006861B1 (fr) |
CN (1) | CN87108228A (fr) |
BR (1) | BR8707910A (fr) |
WO (1) | WO1988004199A1 (fr) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4987239A (en) * | 1988-04-06 | 1991-01-22 | The Boc Group, Inc. | Process for the production of anhydrides |
CA2243402A1 (fr) * | 1997-07-22 | 1999-01-22 | Hideo Suwa | Methode pour la production d'anhydride maleique |
US6657097B1 (en) | 1999-03-08 | 2003-12-02 | Mitsubishi Chemical Corporation | Fluidized bed reactor |
DE10055810A1 (de) | 2000-11-10 | 2002-05-23 | Aventis Res & Tech Gmbh & Co | Verfahren zur Herstellung von Essigsäure |
CN101528338B (zh) * | 2006-09-19 | 2013-03-27 | 巴斯夫欧洲公司 | 用于进行气相反应的流化床反应器 |
US8044244B2 (en) * | 2006-09-19 | 2011-10-25 | Basf Se | Process for preparing aromatic amines in a fluidized-bed reactor |
JP5840822B2 (ja) * | 2006-09-27 | 2016-01-06 | 旭化成ケミカルズ株式会社 | 流動層反応器の温度制御方法 |
JP2012515133A (ja) | 2009-01-09 | 2012-07-05 | レック シリコン インコーポレイテッド | 粒状シリコンを製造する方法及び装置 |
US9404177B2 (en) | 2014-08-18 | 2016-08-02 | Rec Silicon Inc | Obstructing member for a fluidized bed reactor |
FR3029802B1 (fr) * | 2014-12-11 | 2022-01-07 | Axens | Dispositif permettant de limiter l'entrainement de particules solides en sortie d'un lit fluidise triphasique |
CN109467195B (zh) * | 2017-09-08 | 2021-10-29 | 中国石化工程建设有限公司 | 反硝化膨胀床及含硝氮废水处理方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2983259A (en) * | 1955-02-09 | 1961-05-09 | Combustion Eng | Method and apparatus of steam generation |
US4351773A (en) * | 1980-12-31 | 1982-09-28 | The Standard Oil Company | Preparation of maleic anhydride from butane using fluidized vanadium-phosphorous-oxide containing catalysts |
-
1987
- 1987-12-07 JP JP88500696A patent/JPH01503211A/ja active Pending
- 1987-12-07 KR KR1019880700935A patent/KR910006861B1/ko not_active IP Right Cessation
- 1987-12-07 EP EP88900319A patent/EP0333767A1/fr not_active Withdrawn
- 1987-12-07 BR BR8707910A patent/BR8707910A/pt active Search and Examination
- 1987-12-07 WO PCT/US1987/003194 patent/WO1988004199A1/fr not_active Application Discontinuation
- 1987-12-10 CN CN198787108228A patent/CN87108228A/zh active Pending
Non-Patent Citations (1)
Title |
---|
See references of WO8804199A1 * |
Also Published As
Publication number | Publication date |
---|---|
KR910006861B1 (ko) | 1991-09-09 |
CN87108228A (zh) | 1988-06-29 |
KR890700045A (ko) | 1989-03-02 |
JPH01503211A (ja) | 1989-11-02 |
WO1988004199A1 (fr) | 1988-06-16 |
BR8707910A (pt) | 1989-10-03 |
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Legal Events
Date | Code | Title | Description |
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PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19890424 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE FR GB IT NL |
|
17Q | First examination report despatched |
Effective date: 19900503 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 19900914 |