WO2003047741A1 - Procede et dispositif de reaction chimique entre un gaz et au moins un compose en solution, mis en oeuvre en presence d'un catalyseur solide - Google Patents
Procede et dispositif de reaction chimique entre un gaz et au moins un compose en solution, mis en oeuvre en presence d'un catalyseur solide Download PDFInfo
- Publication number
- WO2003047741A1 WO2003047741A1 PCT/FR2002/004159 FR0204159W WO03047741A1 WO 2003047741 A1 WO2003047741 A1 WO 2003047741A1 FR 0204159 W FR0204159 W FR 0204159W WO 03047741 A1 WO03047741 A1 WO 03047741A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- solution
- reactor
- reacted
- gas
- primary filter
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 34
- 239000011949 solid catalyst Substances 0.000 title claims abstract description 15
- 238000006243 chemical reaction Methods 0.000 title claims abstract description 14
- 150000001875 compounds Chemical class 0.000 title claims abstract description 13
- 238000004064 recycling Methods 0.000 claims abstract description 19
- 238000001914 filtration Methods 0.000 claims abstract description 11
- 239000000725 suspension Substances 0.000 claims abstract description 7
- 238000011084 recovery Methods 0.000 claims abstract description 6
- 239000000243 solution Substances 0.000 claims description 92
- 239000003054 catalyst Substances 0.000 claims description 29
- 239000007789 gas Substances 0.000 claims description 28
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 11
- 238000005984 hydrogenation reaction Methods 0.000 claims description 9
- 238000005086 pumping Methods 0.000 claims description 9
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 8
- 238000011001 backwashing Methods 0.000 claims description 8
- 239000006185 dispersion Substances 0.000 claims description 8
- 150000004056 anthraquinones Chemical class 0.000 claims description 6
- 238000011144 upstream manufacturing Methods 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 239000012527 feed solution Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 230000000717 retained effect Effects 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract description 16
- 238000000926 separation method Methods 0.000 abstract description 5
- 238000002386 leaching Methods 0.000 abstract 1
- 239000012224 working solution Substances 0.000 description 27
- 238000013019 agitation Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
- -1 cyclic anthraquinone Chemical class 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000011256 aggressive treatment Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
- C01B15/01—Hydrogen peroxide
- C01B15/022—Preparation from organic compounds
- C01B15/023—Preparation from organic compounds by the alkyl-anthraquinone process
-
- 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
- B01J19/18—Stationary reactors having moving elements inside
- B01J19/1868—Stationary reactors having moving elements inside resulting in a loop-type movement
- B01J19/1881—Stationary reactors having moving elements inside resulting in a loop-type movement externally, i.e. the mixture leaving the vessel and subsequently re-entering it
-
- 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
- B01J8/005—Separating solid material from the gas/liquid stream
- B01J8/006—Separating solid material from the gas/liquid stream by filtration
-
- 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
- B01J8/20—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles with liquid as a fluidising medium
- B01J8/22—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles with liquid as a fluidising medium gas being introduced into the liquid
- B01J8/224—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles with liquid as a fluidising medium gas being introduced into the liquid the particles being subject to a circulatory movement
- B01J8/228—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles with liquid as a fluidising medium gas being introduced into the liquid the particles being subject to a circulatory movement externally, i.e. the particles leaving the vessel and subsequently re-entering it
Definitions
- the subject of the present invention is:
- the present invention has been more particularly developed, in the context of the production of hydrogen peroxide (H 2 0 2 ) by the anthraquinone process, at the level of the catalytic hydrogenation of the working solution (or "working solution”). Its scope is however not limited to said context.
- a person skilled in the art will readily understand, on reading the following, that the invention has as a field of application any context of gas / liquid reaction (G / L), the liquid (L) containing in solution at least one chemical compound capable of reacting with the gas (G), in the presence of a solid catalyst, kept in suspension in said liquid (L).
- the context of the invention is more precisely that of gas / liquid reactions (G / L), the liquid (L) containing in solution at least one chemical compound capable of reacting with the gas (G), in the presence of a solid catalyst, kept in suspension in said liquid (L), placed used with separation (recovery) of said solid catalyst by filtration.
- a WS solution (containing at least one compound capable of reacting with the intervening gas G) is treated, continuously, in the reactor 1, with a gas G, in the presence of a solid catalyst.
- Said solution WS is put into circulation, at the flow rate Q, by the pumps PI and P2.
- the WS solution is efficiently treated in the stirred reactor 1 in which solid catalyst and reactive gas (G) are dispersed and kept in suspension.
- the catalyst is separated from the solution WS ', using a series of filters, successively comprising:
- At least one primary filter FI generally of the carbon or sintered metal candle type (coarse filter, with a porosity adapted to that of the catalyst grains to be blocked, for example with a porosity close to 5 ⁇ m).
- At least one secondary filter generally of the cartridge filter type, of finer porosity (for example, close to 0.5 ⁇ m), intended to stop the finer particles which have inexorably, due to the strong agitation necessary in the reactor, was generated by abrasion of the catalyst grains.
- secondary filters F2 and F3, connected in series.
- the total flow Q of the incoming solution to be treated in the reactor 1 is sent to and passes through said filters FI, F2 and F3.
- Said flow rate Q effectively crosses the single IF filter in service (single intervening IF filter or single IF filter in service with a battery of at least two filters mounted in parallel) or is shared between at least two IF filters in service such a battery of filters. In the latter case, it is considered that said flow Q passes through said filters in service, considered as a whole.
- the primary filters FI are sequentially washed against the current, to avoid clogging of their pores and to bring back the grains of catalyst blocked in the reactor 1. This sequential washing involves a flow q, taken, according to the variant shown, from the flow Q of solution treated and filtered WS ".
- said primary filters FI must regularly (once every three weeks in the context of the production of H 2 0 2 ) undergo a chemical washing (acid and / or basic) to remain clean. Said primary filters FI are highly stressed insofar as, overall, the entire flow rate Q of treated solution WS ′ passes through them and where chemical washes are relatively aggressive treatments. They must be changed frequently.
- each backwashing disrupts the operation of the reactor, by returning within said reactor of solution WS "and catalyst.
- said invention therefore relates to a chemical reaction process between a gas and at least one compound in solution, carried out continuously, in a stirred reactor, in the presence of a solid catalyst maintained, dispersed, in suspension at within the solution containing said compound.
- said method comprises:
- said method of the invention further comprises recycling a fraction of the reacted solution to the lower part of said reactor, at a flow rate greater than that of supply said reactor into the solution to be reacted; said recycling being ensured by the implementation, within said reactor, of adequate agitation and said fraction of the reacted solution being diverted, for said recycling, at the level of said primary filter (s) (s) and thus ensuring a tangential licking of said primary filter (s).
- a tangential licking of the primary filter (s) is ensured with a substantial flow of reacted solution, recycled in the lower part of the reactor; agitation within said reactor alone ensuring said recycling at the consequent flow rate.
- this rate of recycling of the reacted solution is generally 3 to 10 times greater than the rate of supply of the reactor with the solution to be reacted. It is advantageously 5 to 10 times greater than said feed rate.
- the key point for implementing the process of the invention is agitation within the reactor. Said agitation is conventionally responsible for the intensity of the gas / liquid / catalyst contacts. It must moreover, in a more original way, ensure the expected pumping effect (the recycling of part of the reacted solution). In the context of an optimized implementation of the method of the invention, said stirring must, at the same time, ensure:
- the filter (s) is (are) crossed by a flow rate of treated solution corresponding to the feed flow rate of the reactor and licked (s) by a flow rate of more treated solution. This licking minimizes any accumulation of grains and fines of catalyst, continuously cleans said filter (s), recycles said grains and fines to the reactor.
- the catalyst concentration within the reactor is optimized; the service life of the primary and secondary filters is considerably increased (the frequency of chemical washes of the candles of the primary filters is greatly reduced as well as that of the changes of the secondary filter cartridges.
- the process of the invention is very particularly suitable for carrying out hydrogenations.
- the gas involved consists of hydrogen or, in any event, contains hydrogen; the intervening solution contains, for its part, at least one compound capable of reacting with said hydrogen.
- the process of the invention is very particularly suitable for the hydrogenation of at least one anthraquinone derivative, in solution in the working solution, in the context of the preparation of hydrogen peroxide (H 2 0 2 ).
- This framework is specified in particular in applications WO98 / 28225 and EP016 622. In said framework, by implementing the method of the invention, the applicant has obtained very interesting results.
- Said device comprises, conventionally: - a reactor equipped with stirring means, means for supplying solution, means for supplying gas and means for delivering the reacted solution; said means for supplying solution and gas being arranged in the lower part of said reactor while said means for delivering the reacted solution are arranged in the upper part;
- a filtration assembly mounted, at the outlet of said reactor, on said means for delivering the reacted solution and comprising at least one primary filter (generally, a battery of at least two primary filters, mounted in parallel, so that the it is possible to pass from one filter to another filter without stopping the process) and at least one secondary filter (generally, several secondary filters, connected in series);
- at least one primary filter generally, a battery of at least two primary filters, mounted in parallel, so that the it is possible to pass from one filter to another filter without stopping the process
- at least one secondary filter generally, several secondary filters, connected in series
- the device of the invention is of the type of that of the prior art, as shown diagrammatically in FIG. 1.
- said device of the invention further comprises means for recycling, with tangential licking of the primary filter (s), a flow of solution having reacted downwards from said reactor and the means for agitating said reactor alone ensure said recycling.
- Said means consist of an adequate circuit which makes it possible to ensure, successively: - the diversion, of a fraction of the reacted solution, at the top outlet of the reactor;
- This fraction can be reintroduced into said reactor, independently or not, from the supply of said reactor with the solution to be reacted.
- a single supply in the lower part of the reactor, with a mixture of said recycled fraction and of said solution to be reacted; said mixture having been formed upstream.
- the means for agitating the reactor capable of ensuring said agitation and recycling of the diverted fraction, are also advantageously capable of ensuring internal recirculation. They advantageously consist of a multistage agitator (generally at least three stages).
- said stirring means comprise:
- a dispersion mobile active in the lower part of the reactor; - an intermediate stage, capable of ensuring internal recirculation in the reactor and helping to pump the reacted solution to the primary filter (s);
- Said dispersion mobile ensures good dispersion of the catalyst and of the gas within the solution, containing the reagent (s) in solution.
- Said intermediate stage (other mobile) provides a little pumping but above all an internal recirculation of the reaction mixture in the reactor (it makes it possible to increase the residence time of said mixture in said reactor).
- Said upper stage ensures the pumping of the reacted solution towards the primary filter (s).
- the guaranteed flow must be high in order to continuously recycle the catalyst to the bottom of the reactor.
- said intermediate and upper stages have blades inclined downward and upward respectively.
- the device of the invention as described above is advantageously arranged in a loop for producing hydrogen peroxide, by the cyclic anthraquinone process, at the level of the hydrogenation reactor of the working solution.
- Figure 1 illustrates the prior art closest to said invention. It was commented on in the introductory part of this text.
- Figure 2 illustrates a preferred embodiment of said invention. It should be considered in parallel with said Figure 1.
- the solution to be reacted, WS is brought to a flow rate Q, by means of the pump PI. It is introduced into the bottom of the reactor after having been mixed with a fraction of the reacted solution WS ', fraction recycled at a flow rate Q'.
- Q ′ advantageously 3 Q.
- the mixture additionally sequentially contains the flow q of treated and filtered solution WS ". This flow q has been used to wash the primary filter (s) sequentially FI.
- the stirring means 2 of said reactor 1 are of the optimum type specified above. They comprise a lower or mobile dispersion stage 2 ', an intermediate stage 2 "which mainly ensures recirculation of the solution in the reactor 1 and an upper stage 2""which mainly ensures pumping of the reacted solution WS'.
- the pump PI ensures the flow of the flow rate Q of solution WS while the upper stage 2 '"of the stirring means 2 mainly provides circulation of the flow rate Q' of solution WS '. There is no longer a need for a second pump P2, according to FIG. 1.
- Said reactor was equipped with a three-stage agitator, comprising from bottom to top: - a Rushton turbine with 6 fixed blades;
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02799769A EP1450940B1 (fr) | 2001-12-04 | 2002-12-03 | Procede et dispositif de reaction chimique entre un gaz et au moins un compose en solution, mis en oeuvre en presence d'un catalyseur solide |
CA2469171A CA2469171C (fr) | 2001-12-04 | 2002-12-03 | Procede et dispositif de reaction chimique entre un gaz et au moins un compose en solution, mis en oeuvre en presence d'un catalyseur solide |
DE60203930T DE60203930T2 (de) | 2001-12-04 | 2002-12-03 | Verfahren und vorrichtung für eine in anwesenheit eines feststoffkatalysators durchgeführte chemische reaktion zwischen einem gas und mindestens einer gelösten komponente |
AU2002364414A AU2002364414A1 (en) | 2001-12-04 | 2002-12-03 | Method and device for chemical reaction between a gas and at least a compound in solution, carried out in the presence of a solid catalyst |
US10/497,771 US7276223B2 (en) | 2001-12-04 | 2002-12-03 | Method and device for chemical reaction between a gas and at least one compound in solution carried out in the presence of a solid catalyst |
ZA2004/03964A ZA200403964B (en) | 2001-12-04 | 2004-05-21 | Method and device for chemical reaction between a gas and at least a compound in solution carried out in the presence of a solid catalyst |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR01/15660 | 2001-12-04 | ||
FR0115660A FR2832937B1 (fr) | 2001-12-04 | 2001-12-04 | Procede et dispositif de reaction chimique entre un gaz et au moins un compose en solution, mis en oeuvre en presence d'un catalyseur solide |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003047741A1 true WO2003047741A1 (fr) | 2003-06-12 |
Family
ID=8870091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2002/004159 WO2003047741A1 (fr) | 2001-12-04 | 2002-12-03 | Procede et dispositif de reaction chimique entre un gaz et au moins un compose en solution, mis en oeuvre en presence d'un catalyseur solide |
Country Status (10)
Country | Link |
---|---|
US (1) | US7276223B2 (fr) |
EP (1) | EP1450940B1 (fr) |
AU (1) | AU2002364414A1 (fr) |
CA (1) | CA2469171C (fr) |
DE (1) | DE60203930T2 (fr) |
ES (1) | ES2242094T3 (fr) |
FR (1) | FR2832937B1 (fr) |
MY (1) | MY133272A (fr) |
WO (1) | WO2003047741A1 (fr) |
ZA (1) | ZA200403964B (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005005038A1 (fr) * | 2003-07-15 | 2005-01-20 | Sasol Technology (Proprietary) Limited | Procede de separation d'un catalyseur contenu dans un liquide |
CN103007834A (zh) * | 2012-11-27 | 2013-04-03 | 飞潮(无锡)过滤技术有限公司 | 利用陶瓷滤管过滤器回收气相催化剂的装置及方法 |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2444055B (en) * | 2006-11-23 | 2011-11-23 | Gtl F1 Ag | Gas to liquids plant with consecutive Fischer-Tropsch reactors and hydrogen make-up |
WO2009121366A2 (fr) * | 2008-04-03 | 2009-10-08 | Povl Kaas | Unité de filtration avec banc filtrant |
GB2465554B (en) | 2008-11-18 | 2013-03-13 | Gtl F1 Ag | Slurry bubble column reactor |
GB2466315B (en) * | 2008-12-22 | 2013-01-09 | Gtl F1 Ag | Apparatus and method for conducting a Fischer-Tropsch synthesis reaction |
CN102458636B (zh) * | 2009-06-05 | 2015-02-25 | 索尔维公司 | 用于从一种多相混合物中分离液体的方法 |
GB2471338B (en) | 2009-06-26 | 2014-12-24 | Gtl F1 Ag | Apparatus and process for three-phase reacton |
CN110975784A (zh) * | 2019-10-31 | 2020-04-10 | 黄冈师范学院 | 甲硝唑羟化反应中环氧乙烷的加料装置及其加料工艺 |
CN112370856B (zh) * | 2020-11-10 | 2022-06-14 | 西部宝德科技股份有限公司 | 一种干法回收乙烯齐聚催化剂细粉的过滤分离系统及方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3423176A (en) * | 1965-12-04 | 1969-01-21 | Degussa | Process for carrying out catalytic hydrogenation reactions in the presence of suspension catalysts |
WO2001068519A1 (fr) * | 2000-03-17 | 2001-09-20 | Atofina | Procede d'obtention directe du peroxyde d'hydrogene |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
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US4258025A (en) * | 1979-02-26 | 1981-03-24 | E. I. Du Pont De Nemours And Company | Pd/SiO2 Hydrogenation catalyst suitable for H2 O2 manufacture |
US4374820A (en) * | 1981-07-29 | 1983-02-22 | E. I. Du Pont De Nemours And Company | Manufacture of H2 O2 |
SE431532B (sv) * | 1982-09-08 | 1984-02-13 | Eka Ab | Forfarande vid framstellning av veteperoxid |
US4428923A (en) * | 1982-11-09 | 1984-01-31 | Degussa Aktiengesellschaft | Continuous process for the production of hydrogen peroxide according to the anthraquinone process |
AU584743B2 (en) * | 1986-01-31 | 1989-06-01 | Schewitz, Jonathan | Filtering unit |
SE464867B (sv) * | 1989-02-23 | 1991-06-24 | Eka Nobel Ab | Foerfarande vid framstaellning av vaeteperoxid enligt antrakinonprocessen |
US5217629A (en) * | 1990-09-10 | 1993-06-08 | Kemira Oy | Procedure for cleaning filter used in production of hydrogen peroxide from anthraquinone |
DE4217245A1 (de) * | 1992-05-25 | 1993-12-02 | Degussa | Verfahren zur Abtrennung katalysatorfreier Arbeitslösung aus dem Hydrierkreislauf des Anthrachionverfahrens zur Herstellung von Wasserstoffperoxid |
DE4418931C2 (de) * | 1994-05-31 | 1997-06-19 | Degussa | Verfahren zur Abtrennung katalysatorfreier Arbeitslösung aus dem Hydrierkreislauf des Anthrachinonverfahrens zur Herstellung von Wasserstoffperoxid |
US5772977A (en) * | 1994-12-14 | 1998-06-30 | E. I. Du Pont De Nemours And Company | Anthraquinone process |
US5853693A (en) * | 1996-04-03 | 1998-12-29 | Mitsubishi Gas Chemical Company, Inc. | Hydrogenation catalyst for production of hydrogen peroxide, and method for preparation of same |
ES2192883T3 (es) * | 1998-09-12 | 2003-10-16 | Degussa | Procedimiento para la realizacion de reacciones gas-liquido y reactor de circulacion para el mismo. |
DE19956859A1 (de) * | 1999-11-25 | 2001-06-07 | Hydac Filtertechnik Gmbh | Rückspülfiltervorrichtung |
-
2001
- 2001-12-04 FR FR0115660A patent/FR2832937B1/fr not_active Expired - Fee Related
-
2002
- 2002-12-03 DE DE60203930T patent/DE60203930T2/de not_active Expired - Lifetime
- 2002-12-03 AU AU2002364414A patent/AU2002364414A1/en not_active Abandoned
- 2002-12-03 WO PCT/FR2002/004159 patent/WO2003047741A1/fr not_active Application Discontinuation
- 2002-12-03 ES ES02799769T patent/ES2242094T3/es not_active Expired - Lifetime
- 2002-12-03 EP EP02799769A patent/EP1450940B1/fr not_active Expired - Lifetime
- 2002-12-03 MY MYPI20024528A patent/MY133272A/en unknown
- 2002-12-03 US US10/497,771 patent/US7276223B2/en not_active Expired - Lifetime
- 2002-12-03 CA CA2469171A patent/CA2469171C/fr not_active Expired - Lifetime
-
2004
- 2004-05-21 ZA ZA2004/03964A patent/ZA200403964B/en unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3423176A (en) * | 1965-12-04 | 1969-01-21 | Degussa | Process for carrying out catalytic hydrogenation reactions in the presence of suspension catalysts |
WO2001068519A1 (fr) * | 2000-03-17 | 2001-09-20 | Atofina | Procede d'obtention directe du peroxyde d'hydrogene |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005005038A1 (fr) * | 2003-07-15 | 2005-01-20 | Sasol Technology (Proprietary) Limited | Procede de separation d'un catalyseur contenu dans un liquide |
GB2418626A (en) * | 2003-07-15 | 2006-04-05 | Sasol Tech Pty Ltd | Process for separating a catalyst from a liquid |
GB2418626B (en) * | 2003-07-15 | 2007-03-14 | Sasol Tech Pty Ltd | Process for separating a catalyst from a liquid |
CN100404118C (zh) * | 2003-07-15 | 2008-07-23 | 萨索尔技术(控股)有限公司 | 从液体分离催化剂的方法 |
US7488760B2 (en) | 2003-07-15 | 2009-02-10 | Sasol Technology (Proprietary) (Limited) | Process for separating a catalyst from a liquid |
CN103007834A (zh) * | 2012-11-27 | 2013-04-03 | 飞潮(无锡)过滤技术有限公司 | 利用陶瓷滤管过滤器回收气相催化剂的装置及方法 |
CN103007834B (zh) * | 2012-11-27 | 2015-03-18 | 飞潮(无锡)过滤技术有限公司 | 利用陶瓷滤管过滤器回收气相催化剂的装置及方法 |
Also Published As
Publication number | Publication date |
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DE60203930D1 (de) | 2005-06-02 |
MY133272A (en) | 2007-10-31 |
DE60203930T2 (de) | 2006-02-23 |
US7276223B2 (en) | 2007-10-02 |
CA2469171C (fr) | 2010-02-09 |
AU2002364414A1 (en) | 2003-06-17 |
FR2832937A1 (fr) | 2003-06-06 |
ZA200403964B (en) | 2005-07-27 |
FR2832937B1 (fr) | 2004-01-16 |
CA2469171A1 (fr) | 2003-06-12 |
ES2242094T3 (es) | 2005-11-01 |
EP1450940B1 (fr) | 2005-04-27 |
US20050047992A1 (en) | 2005-03-03 |
EP1450940A1 (fr) | 2004-09-01 |
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