ZA200402798B - Process for the hydrogenation of acetone. - Google Patents
Process for the hydrogenation of acetone. Download PDFInfo
- Publication number
- ZA200402798B ZA200402798B ZA200402798A ZA200402798A ZA200402798B ZA 200402798 B ZA200402798 B ZA 200402798B ZA 200402798 A ZA200402798 A ZA 200402798A ZA 200402798 A ZA200402798 A ZA 200402798A ZA 200402798 B ZA200402798 B ZA 200402798B
- Authority
- ZA
- South Africa
- Prior art keywords
- reactor
- range
- anyone
- acetone
- hydrogenation
- Prior art date
Links
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 title claims abstract description 54
- 238000000034 method Methods 0.000 title claims abstract description 34
- 238000005984 hydrogenation reaction Methods 0.000 title claims abstract description 21
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000012530 fluid Substances 0.000 claims description 32
- 239000003054 catalyst Substances 0.000 claims description 22
- 239000007788 liquid Substances 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 17
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 239000007795 chemical reaction product Substances 0.000 claims description 8
- 239000000376 reactant Substances 0.000 claims description 7
- 230000003247 decreasing effect Effects 0.000 claims description 5
- 239000007789 gas Substances 0.000 description 9
- 239000001257 hydrogen Substances 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 5
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000012809 cooling fluid Substances 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 150000001728 carbonyl compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000110 cooling liquid Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- GXDVEXJTVGRLNW-UHFFFAOYSA-N [Cr].[Cu] Chemical compound [Cr].[Cu] GXDVEXJTVGRLNW-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
- C07C29/145—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones with hydrogen or hydrogen-containing gases
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Saccharide Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01309674 | 2001-11-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200402798B true ZA200402798B (en) | 2005-01-13 |
Family
ID=8182465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200402798A ZA200402798B (en) | 2001-11-16 | 2004-04-13 | Process for the hydrogenation of acetone. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6878851B2 (ru) |
| EP (1) | EP1444184B1 (ru) |
| JP (1) | JP4260016B2 (ru) |
| KR (1) | KR20040055808A (ru) |
| CN (1) | CN1296334C (ru) |
| AT (1) | ATE358660T1 (ru) |
| BR (1) | BR0214171A (ru) |
| DE (1) | DE60219341T2 (ru) |
| ES (1) | ES2283619T3 (ru) |
| MX (1) | MXPA04004554A (ru) |
| RU (1) | RU2288210C2 (ru) |
| TW (1) | TWI301480B (ru) |
| WO (1) | WO2003042142A1 (ru) |
| ZA (1) | ZA200402798B (ru) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7479576B1 (en) * | 2007-06-27 | 2009-01-20 | H R D Corporation | Method of hydrogenating aldehydes and ketones |
| CN103566836A (zh) * | 2013-11-25 | 2014-02-12 | 南京国昌化工科技有限公司 | 一种均温加氢反应器 |
| EP3483138A1 (en) * | 2017-11-09 | 2019-05-15 | Fundacion Tecnalia Research & Innovation | Method for continuous production of 2,3-butanediol |
| WO2024121714A1 (en) | 2022-12-06 | 2024-06-13 | Versalis S.P.A. | Process for preparing isopropanol in high yields and with a high degree of purity |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL59261C (ru) * | 1941-09-05 | |||
| GB8721964D0 (en) | 1987-09-18 | 1987-10-28 | Shell Int Research | Multitube reactor |
| JP2724001B2 (ja) * | 1989-01-17 | 1998-03-09 | 三井化学株式会社 | イソプロパノールの製造方法 |
| FR2656300B1 (fr) * | 1989-12-21 | 1993-06-11 | Inst Francais Du Petrole | Procede de production de phenol. |
| US5495055A (en) * | 1994-08-12 | 1996-02-27 | Arco Chemical Technology, L.P. | Acetone hydrogenation using a supported ruthenium catalyst |
| DE19721898A1 (de) * | 1997-05-26 | 1998-12-03 | Degussa | Geformter, aktivierter Metall-Festbettkatalysator |
| DE10008924A1 (de) * | 2000-02-25 | 2001-09-06 | Phenolchemie Gmbh & Co Kg | Verfahren zur Herstellung von Phenol |
| AU2002240870A1 (en) * | 2000-12-23 | 2002-07-08 | Degussa Ag | Method for producing alcohols by hydrogenating carbonyl compounds |
| TWI266762B (en) * | 2001-11-16 | 2006-11-21 | Shell Int Research | Process for the preparation of isopropanol |
-
2002
- 2002-11-11 TW TW091133011A patent/TWI301480B/zh not_active IP Right Cessation
- 2002-11-12 CN CNB028227271A patent/CN1296334C/zh not_active Expired - Fee Related
- 2002-11-12 WO PCT/EP2002/012641 patent/WO2003042142A1/en active IP Right Grant
- 2002-11-12 DE DE60219341T patent/DE60219341T2/de not_active Expired - Lifetime
- 2002-11-12 ES ES02787656T patent/ES2283619T3/es not_active Expired - Lifetime
- 2002-11-12 BR BR0214171-0A patent/BR0214171A/pt not_active Application Discontinuation
- 2002-11-12 EP EP02787656A patent/EP1444184B1/en not_active Expired - Lifetime
- 2002-11-12 JP JP2003543981A patent/JP4260016B2/ja not_active Expired - Fee Related
- 2002-11-12 RU RU2004118067/04A patent/RU2288210C2/ru not_active IP Right Cessation
- 2002-11-12 AT AT02787656T patent/ATE358660T1/de not_active IP Right Cessation
- 2002-11-12 KR KR10-2004-7007473A patent/KR20040055808A/ko not_active Application Discontinuation
- 2002-11-12 MX MXPA04004554A patent/MXPA04004554A/es active IP Right Grant
- 2002-11-14 US US10/294,782 patent/US6878851B2/en not_active Expired - Fee Related
-
2004
- 2004-04-13 ZA ZA200402798A patent/ZA200402798B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA04004554A (es) | 2004-08-13 |
| ATE358660T1 (de) | 2007-04-15 |
| CN1296334C (zh) | 2007-01-24 |
| WO2003042142A8 (en) | 2004-05-27 |
| BR0214171A (pt) | 2004-09-28 |
| CN1589250A (zh) | 2005-03-02 |
| RU2288210C2 (ru) | 2006-11-27 |
| US6878851B2 (en) | 2005-04-12 |
| EP1444184B1 (en) | 2007-04-04 |
| KR20040055808A (ko) | 2004-06-26 |
| ES2283619T3 (es) | 2007-11-01 |
| TW200407283A (en) | 2004-05-16 |
| DE60219341D1 (de) | 2007-05-16 |
| EP1444184A1 (en) | 2004-08-11 |
| JP2005509015A (ja) | 2005-04-07 |
| WO2003042142A1 (en) | 2003-05-22 |
| DE60219341T2 (de) | 2007-12-13 |
| TWI301480B (en) | 2008-10-01 |
| RU2004118067A (ru) | 2006-01-10 |
| JP4260016B2 (ja) | 2009-04-30 |
| US20030130546A1 (en) | 2003-07-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0319208B1 (en) | Process for hydrogenating | |
| EP0300018B1 (en) | Hydrogenation process | |
| EP0379323B1 (en) | Preparation of isopropanol | |
| US7740829B2 (en) | Synthesis gas production and use | |
| WO2004092063A1 (en) | Process to prepare synthesis gas | |
| AU2008339360B2 (en) | Method of regulating temperature in reaction vessel, reactor, and process for producing dimethyl ether | |
| JPS5919931B2 (ja) | ジアセトキシブテンの水素化方法 | |
| JPH01503454A (ja) | 不飽和有機化合物の水素化方法 | |
| US6878851B2 (en) | Process for the hydrogenation of acetone | |
| US20050228059A1 (en) | Process for the preparation of hydrocarbons | |
| EA024857B1 (ru) | Газожидкостный реактор и способ осуществления реакции в системе газ/жидкость | |
| JP2834495B2 (ja) | イソプロパノールの製造方法及び装置 | |
| CN114040905A (zh) | 使用锥形逐级反应器合成二烷基醚的强化方法 | |
| WO1994012274A1 (en) | Reactor and process for highly exothermic or endothermic reactions | |
| JP2024511854A (ja) | エタノールとアセトアルデヒドとの混合物から１，３－ブタジエンを生産するための断熱的に実施されるプロセス | |
| JP2000053597A (ja) | シクロペンテンの製造方法 | |
| WO2024089647A1 (en) | Process configuration for production of isopropyl alcohol | |
| JP2002003484A (ja) | 無水コハク酸の製造方法 | |
| JP2002030045A (ja) | ジアリールアミン類の連続製造方法および装置 |