JP2022534671A - プロセス - Google Patents
プロセス Download PDFInfo
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- JP2022534671A JP2022534671A JP2021565865A JP2021565865A JP2022534671A JP 2022534671 A JP2022534671 A JP 2022534671A JP 2021565865 A JP2021565865 A JP 2021565865A JP 2021565865 A JP2021565865 A JP 2021565865A JP 2022534671 A JP2022534671 A JP 2022534671A
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- 238000000034 method Methods 0.000 title claims abstract description 42
- 239000007789 gas Substances 0.000 claims abstract description 133
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 76
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 75
- 239000001257 hydrogen Substances 0.000 claims abstract description 66
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 66
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 61
- 239000003054 catalyst Substances 0.000 claims abstract description 50
- 238000006243 chemical reaction Methods 0.000 claims abstract description 40
- 150000001336 alkenes Chemical class 0.000 claims abstract description 38
- 239000007788 liquid Substances 0.000 claims abstract description 37
- 239000000203 mixture Substances 0.000 claims abstract description 27
- 229910052703 rhodium Inorganic materials 0.000 claims abstract description 27
- 239000010948 rhodium Substances 0.000 claims abstract description 27
- 238000010926 purge Methods 0.000 claims abstract description 6
- 238000004064 recycling Methods 0.000 claims abstract description 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims abstract 14
- 238000000926 separation method Methods 0.000 claims description 38
- 239000012528 membrane Substances 0.000 claims description 13
- 230000015572 biosynthetic process Effects 0.000 claims description 11
- 238000003786 synthesis reaction Methods 0.000 claims description 11
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 10
- 238000001704 evaporation Methods 0.000 claims description 6
- 238000007037 hydroformylation reaction Methods 0.000 abstract description 9
- 150000001299 aldehydes Chemical class 0.000 description 46
- 239000000047 product Substances 0.000 description 20
- 239000000243 solution Substances 0.000 description 14
- 239000003446 ligand Substances 0.000 description 10
- 239000011552 falling film Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 239000012808 vapor phase Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 235000019256 formaldehyde Nutrition 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- -1 triphenylphosphine Chemical class 0.000 description 3
- OPNUROKCUBTKLF-UHFFFAOYSA-N 1,2-bis(2-methylphenyl)guanidine Chemical compound CC1=CC=CC=C1N\C(N)=N\C1=CC=CC=C1C OPNUROKCUBTKLF-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000012466 permeate Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000004088 simulation Methods 0.000 description 2
- 239000006200 vaporizer Substances 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
-
- 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
- B01J19/2455—Stationary reactors without moving elements inside provoking a loop type movement of the reactants
- B01J19/2465—Stationary reactors without moving elements inside provoking a loop type movement of the reactants 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/04—Purification; Separation; Use of additives by distillation
-
- 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
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
-
- 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
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/822—Rhodium
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
a.配位子-ロジウム触媒の存在下、反応ゾーン内で水素及び一酸化炭素によって1つ以上のオレフィンをヒドロホルミル化することと、
b.反応ゾーンから、生成物アルデヒド及び配位子-ロジウム触媒を含む反応器流出物を回収することと、
c.反応器流出物及びストリップガスを蒸発器へ送ることであって、ストリップガスが、一酸化炭素を含み、かつ再利用ストリップガス流及びメークアップストリップガス流から形成され、生成物アルデヒドが、蒸発器内でストリップガス中に蒸発して、ストリップガス及び生成物アルデヒドを含む蒸気混合物、並びに配位子-ロジウム触媒を含む液体混合物を生じさせる、送ることと、
d.液体混合物を回収し、配位子-ロジウム触媒を反応ゾーンへ再利用することと、
e.蒸気混合物を回収し、蒸気混合物から生成物アルデヒドを分離して、生成物アルデヒド流及び工程(c)に戻すための再利用ストリップガス流を生成することと、
f.再利用ストリップガス流の一部を、パージされたストリップガス流としてパージすることと、
g.パージされたストリップガス流を水素含有流と組み合わせて、水素及び一酸化炭素を含む再形成された合成ガス流を生成し、再形成された合成ガス流を工程(a)における反応ゾーンへフィードすることと、を含む。
Claims (12)
- オレフィンをアルデヒドにヒドロホルミル化するプロセスであって、
a.配位子-ロジウム触媒の存在下、反応ゾーン内で水素及び一酸化炭素によって1つ以上のオレフィンをヒドロホルミル化することと、
b.前記反応ゾーンから、生成物アルデヒド及び前記配位子-ロジウム触媒を含む反応器流出物を回収することと、
c.前記反応器流出物及びストリップガスを蒸発器へ送ることであって、前記ストリップガスが、一酸化炭素を含み、かつ再利用ストリップガス流及びメークアップストリップガス流から形成され、前記生成物アルデヒドが、前記蒸発器内で前記ストリップガス中に蒸発して、前記ストリップガス及び前記生成物アルデヒドを含む蒸気混合物、並びに前記配位子-ロジウム触媒を含む液体混合物を生じさせる、送ることと、
d.前記液体混合物を回収し、前記配位子-ロジウム触媒を前記反応ゾーンへ再利用することと、
e.前記蒸気混合物を回収し、前記蒸気混合物から前記生成物アルデヒドを分離して、生成物アルデヒド流及び工程(c)に戻すための前記再利用ストリップガス流を生成することと、
f.前記再利用ストリップガスの一部を、パージされたストリップガス流としてパージすることと、
g.前記パージされたストリップガス流を水素含有流と組み合わせて、水素及び一酸化炭素を含む再形成された合成ガス流を生成し、前記再形成された合成ガス流を工程(a)における前記反応ゾーンへフィードすることと、を含む、プロセス。 - 前記メークアップストリップガス流が、50~100mol%の一酸化炭素である、請求項1に記載のプロセス。
- 前記反応ゾーンに、前記再形成された合成ガス流及び新鮮な合成ガス流がフィードされる、請求項1又は2に記載のプロセス。
- 前記プロセスが、合成ガス流を前記水素含有流及び前記メークアップストリップガス流へ分離することを含む、請求項1~3のいずれか一項に記載のプロセス。
- 前記合成ガス流の前記水素含有流及び前記メークアップストリップガス流への前記分離が、膜分離ユニットを使用して行われる、請求項4に記載のプロセス。
- 前記メークアップストリップガス流中の一酸化炭素の濃度が、少なくとも95mol%である、請求項5に記載のプロセス。
- 前記合成ガス流中の水素対一酸化炭素のモル比が、0.5~2.0である、請求項4~6のいずれか一項に記載のプロセス。
- 前記再形成された合成ガス流中の水素対一酸化炭素のモル比が、前記合成ガス流中の水素対一酸化炭素のモル比と同等である、請求項4~7のいずれか一項に記載のプロセス。
- 前記蒸発器が、60~160℃の温度で作動される、請求項1~8のいずれか一項に記載のプロセス。
- 前記蒸発器が、0.1~2000kPaの圧力で作動される、請求項1~9のいずれか一項に記載のプロセス。
- 前記再形成された合成ガス流中の水素対一酸化炭素のモル比が、0.5~2.0である、請求項1~10のいずれか一項に記載のプロセス。
- 前記オレフィンがC2~C16オレフィンであり、前記アルデヒドがC3~C17アルデヒドである、請求項1~11のいずれか一項に記載のプロセス。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1907659.5 | 2019-05-30 | ||
GBGB1907659.5A GB201907659D0 (en) | 2019-05-30 | 2019-05-30 | Process |
PCT/GB2020/051301 WO2020240194A1 (en) | 2019-05-30 | 2020-05-29 | Process |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2022534671A true JP2022534671A (ja) | 2022-08-03 |
Family
ID=67385817
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2021565865A Pending JP2022534671A (ja) | 2019-05-30 | 2020-05-29 | プロセス |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP3976572B1 (ja) |
JP (1) | JP2022534671A (ja) |
KR (1) | KR20220016052A (ja) |
CN (1) | CN113784941A (ja) |
EA (1) | EA202192759A1 (ja) |
GB (2) | GB201907659D0 (ja) |
TW (1) | TW202112728A (ja) |
WO (1) | WO2020240194A1 (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2023114578A1 (en) | 2021-12-16 | 2023-06-22 | Dow Technology Investments Llc | Transition metal complex hydroformylation catalyst precuror compositions comprising such compounds, and hydroformylation processes |
WO2023114579A1 (en) | 2021-12-16 | 2023-06-22 | Dow Technology Investments Llc | Compounds, transition metal complex hydroformylation catalyst precuror compositions comprising such compounds, and hydroformylation processes |
KR102625989B1 (ko) | 2022-02-08 | 2024-01-18 | 광주과학기술원 | 신규 페난스롤린계 화합물, 이의 제조방법 및 이를 패시베이션층으로 포함하는 광전자 소자 |
GB202213997D0 (en) | 2022-09-26 | 2022-11-09 | Johnson Matthey Davy Technologies Ltd | Parallel zone hydroformylation reaction |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4148830A (en) | 1975-03-07 | 1979-04-10 | Union Carbide Corporation | Hydroformylation of olefins |
US4950462A (en) | 1987-09-30 | 1990-08-21 | Babcock-Hitachi Kabushiki Kaisha | Process for absorbing CO |
US5001274A (en) * | 1989-06-23 | 1991-03-19 | Union Carbide Chemicals And Plastics Company Inc. | Hydroformylation process |
US5382417A (en) | 1990-01-03 | 1995-01-17 | Herr Haase, Inc. | Process for removal of selected component gases from multi-component gas streams |
US5087763A (en) | 1990-11-09 | 1992-02-11 | Union Carbide Chemicals & Plastics Technology Corporation | Hydroformylation process |
US5648553A (en) * | 1994-12-09 | 1997-07-15 | Mitsubishi Chemical Corporation | Method for producing aldehydes |
DE10031520A1 (de) * | 2000-06-28 | 2002-01-10 | Basf Ag | Verfahren zur Hydroformylierung von Olefinen mit 2 bis 8 Kohlenstoffatomen |
DE10048301A1 (de) | 2000-09-29 | 2002-04-11 | Oxeno Olefinchemie Gmbh | Stabilisierung von Rhodiumkatalysatoren für die Hydroformylierung von Olefinen |
KR100732894B1 (ko) * | 2001-03-08 | 2007-06-27 | 미쓰비시 가가꾸 가부시키가이샤 | 알데히드의 제조 방법 |
WO2010003073A1 (en) * | 2008-07-03 | 2010-01-07 | Dow Technology Investments Llc | Process of controlling heavies in a recycle catalyst stream |
RU2561171C1 (ru) * | 2014-09-12 | 2015-08-27 | Открытое акционерное общество "Нефтяная компания "Роснефть" | Способ непрерывного двухступенчатого гидроформилирования олефинов с3, с4 и технологическая установка для его осуществления |
MY184826A (en) * | 2014-12-04 | 2021-04-24 | Dow Technology Investments Llc | Hydroformylation process |
-
2019
- 2019-05-30 GB GBGB1907659.5A patent/GB201907659D0/en not_active Ceased
-
2020
- 2020-05-28 TW TW109117848A patent/TW202112728A/zh unknown
- 2020-05-29 EA EA202192759A patent/EA202192759A1/ru unknown
- 2020-05-29 JP JP2021565865A patent/JP2022534671A/ja active Pending
- 2020-05-29 CN CN202080032920.5A patent/CN113784941A/zh active Pending
- 2020-05-29 KR KR1020217036347A patent/KR20220016052A/ko unknown
- 2020-05-29 GB GB2008069.3A patent/GB2586327B/en active Active
- 2020-05-29 EP EP20732269.4A patent/EP3976572B1/en active Active
- 2020-05-29 WO PCT/GB2020/051301 patent/WO2020240194A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
GB202008069D0 (en) | 2020-07-15 |
EP3976572B1 (en) | 2024-05-01 |
TW202112728A (zh) | 2021-04-01 |
GB2586327A (en) | 2021-02-17 |
GB2586327B (en) | 2021-09-08 |
CN113784941A (zh) | 2021-12-10 |
EA202192759A1 (ru) | 2022-02-15 |
WO2020240194A1 (en) | 2020-12-03 |
GB201907659D0 (en) | 2019-07-17 |
KR20220016052A (ko) | 2022-02-08 |
US20220185757A1 (en) | 2022-06-16 |
EP3976572A1 (en) | 2022-04-06 |
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