JP2002529436A5 - - Google Patents
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- Publication number
- JP2002529436A5 JP2002529436A5 JP2000580967A JP2000580967A JP2002529436A5 JP 2002529436 A5 JP2002529436 A5 JP 2002529436A5 JP 2000580967 A JP2000580967 A JP 2000580967A JP 2000580967 A JP2000580967 A JP 2000580967A JP 2002529436 A5 JP2002529436 A5 JP 2002529436A5
- Authority
- JP
- Japan
- Prior art keywords
- platinum
- reaction
- iridium
- weight
- reaction solvent
- 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.)
- Granted
Links
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 30
- 238000000034 method Methods 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 229910052697 platinum Inorganic materials 0.000 description 15
- 239000007810 chemical reaction solvent Substances 0.000 description 11
- 229910052741 iridium Inorganic materials 0.000 description 9
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 9
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 6
- 150000002367 halogens Chemical class 0.000 description 6
- 238000005810 carbonylation reaction Methods 0.000 description 5
- 229910052703 rhodium Inorganic materials 0.000 description 5
- 239000010948 rhodium Substances 0.000 description 5
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 5
- 230000006315 carbonylation Effects 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 150000004696 coordination complex Chemical class 0.000 description 3
- 238000006317 isomerization reaction Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 150000003057 platinum Chemical class 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical group IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002897 organic nitrogen compounds Chemical class 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR98/13954 | 1998-11-05 | ||
| FR9813954A FR2785606B1 (fr) | 1998-11-05 | 1998-11-05 | Preparation d'acide acetique et/ou d'acetate de methyle en presence d'iridium et de platine |
| PCT/FR1999/002652 WO2000027785A1 (fr) | 1998-11-05 | 1999-10-29 | Preparation d'acide acetique et/ou d'acetate de methyle en presence d'iridium et de platine |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002529436A JP2002529436A (ja) | 2002-09-10 |
| JP2002529436A5 true JP2002529436A5 (enExample) | 2006-01-05 |
| JP4066305B2 JP4066305B2 (ja) | 2008-03-26 |
Family
ID=9532421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000580967A Expired - Fee Related JP4066305B2 (ja) | 1998-11-05 | 1999-10-29 | イリジウム及びプラチナの存在下における酢酸及び／又は酢酸メチルの調製方法 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6916952B1 (enExample) |
| EP (1) | EP1127042B1 (enExample) |
| JP (1) | JP4066305B2 (enExample) |
| KR (1) | KR100687510B1 (enExample) |
| CN (1) | CN1216845C (enExample) |
| AT (1) | ATE245619T1 (enExample) |
| AU (1) | AU6348499A (enExample) |
| CA (1) | CA2348472C (enExample) |
| DE (1) | DE69909816T2 (enExample) |
| ES (1) | ES2205888T3 (enExample) |
| FR (1) | FR2785606B1 (enExample) |
| ID (1) | ID28477A (enExample) |
| MY (1) | MY121111A (enExample) |
| RU (1) | RU2220129C2 (enExample) |
| TW (1) | TW522146B (enExample) |
| UA (1) | UA68398C2 (enExample) |
| WO (1) | WO2000027785A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2820422B1 (fr) * | 2001-02-08 | 2003-04-25 | Acetex Chimie | Modification du systeme catalytique dans un procede industriel de fabrication d'acide acetique et/ou d'acetate de methyle |
| CA2496839A1 (en) | 2004-07-19 | 2006-01-19 | Woodland Chemical Systems Inc. | Process for producing ethanol from synthesis gas rich in carbon monoxide |
| AU2007235322A1 (en) * | 2006-04-05 | 2007-10-18 | Woodland Biofuels Inc. | System and method for converting biomass to ethanol via syngas |
| CN102442897B (zh) * | 2010-10-13 | 2014-05-28 | 中国石油化工股份有限公司 | 一种羰基化反应制备乙酸的方法 |
| CN102366724B (zh) * | 2011-12-01 | 2013-05-15 | 重庆大学 | 一种甲醇羰基化合成醋酸的催化剂体系及应用 |
| CN110642698A (zh) * | 2019-10-31 | 2020-01-03 | 江苏润普食品科技股份有限公司 | 山梨酸聚酯酸解制备山梨酸的生产方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE364254B (enExample) * | 1967-04-05 | 1974-02-18 | Monsanto Co | |
| ZA853339B (en) * | 1984-05-03 | 1985-12-24 | Celanese Corp | Methanol carbonylation process |
| FR2746795B1 (fr) * | 1996-03-27 | 1998-06-19 | Rhone Poulenc Chimie | Procede de preparation d'acide acetique et/ou d'acetate de methyle par isomerisation et carbonylation |
| FR2750985B1 (fr) * | 1996-07-10 | 1998-11-06 | Rhone Poulenc Chimie | Procede de preparation d'acide acetique et/ou d'acetate de methyle par carbonylation en presence d'iridium et de rhodium |
| US5900505A (en) * | 1997-02-04 | 1999-05-04 | Eastman Chemical Company | Heterogeneous vapor phase carbonylation process |
-
1998
- 1998-11-05 FR FR9813954A patent/FR2785606B1/fr not_active Expired - Fee Related
-
1999
- 1999-10-29 ES ES99950883T patent/ES2205888T3/es not_active Expired - Lifetime
- 1999-10-29 RU RU2001111864/04A patent/RU2220129C2/ru not_active IP Right Cessation
- 1999-10-29 JP JP2000580967A patent/JP4066305B2/ja not_active Expired - Fee Related
- 1999-10-29 AU AU63484/99A patent/AU6348499A/en not_active Abandoned
- 1999-10-29 EP EP99950883A patent/EP1127042B1/fr not_active Expired - Lifetime
- 1999-10-29 ID IDW00200100993A patent/ID28477A/id unknown
- 1999-10-29 KR KR1020017005479A patent/KR100687510B1/ko not_active Expired - Fee Related
- 1999-10-29 CN CN998128880A patent/CN1216845C/zh not_active Expired - Fee Related
- 1999-10-29 WO PCT/FR1999/002652 patent/WO2000027785A1/fr not_active Ceased
- 1999-10-29 CA CA002348472A patent/CA2348472C/en not_active Expired - Fee Related
- 1999-10-29 US US09/807,434 patent/US6916952B1/en not_active Expired - Lifetime
- 1999-10-29 DE DE69909816T patent/DE69909816T2/de not_active Expired - Lifetime
- 1999-10-29 UA UA2001053084A patent/UA68398C2/uk unknown
- 1999-10-29 AT AT99950883T patent/ATE245619T1/de not_active IP Right Cessation
- 1999-11-03 MY MYPI99004766A patent/MY121111A/en unknown
- 1999-11-05 TW TW088119347A patent/TW522146B/zh not_active IP Right Cessation
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