JP2002542940A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2002542940A5 JP2002542940A5 JP2000615369A JP2000615369A JP2002542940A5 JP 2002542940 A5 JP2002542940 A5 JP 2002542940A5 JP 2000615369 A JP2000615369 A JP 2000615369A JP 2000615369 A JP2000615369 A JP 2000615369A JP 2002542940 A5 JP2002542940 A5 JP 2002542940A5
- Authority
- JP
- Japan
- Prior art keywords
- manganese
- catalyst system
- palladium
- carbonylation catalyst
- cerium
- 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- Withdrawn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
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 32
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 20
- 230000006315 carbonylation Effects 0.000 description 19
- 238000005810 carbonylation reaction Methods 0.000 description 19
- 239000003054 catalyst Substances 0.000 description 19
- 238000000034 method Methods 0.000 description 15
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 13
- 229910052684 Cerium Inorganic materials 0.000 description 12
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 12
- 229910052763 palladium Inorganic materials 0.000 description 12
- 229910052742 iron Inorganic materials 0.000 description 10
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 8
- 229910052797 bismuth Inorganic materials 0.000 description 8
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 8
- 229910052802 copper Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 7
- 230000003197 catalytic effect Effects 0.000 description 7
- 229910052719 titanium Inorganic materials 0.000 description 7
- 239000010936 titanium Substances 0.000 description 7
- 229910052693 Europium Inorganic materials 0.000 description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
- -1 aromatic hydroxy compound Chemical class 0.000 description 6
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 6
- 229910052725 zinc Inorganic materials 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 5
- 229910052748 manganese Inorganic materials 0.000 description 5
- 239000011572 manganese Substances 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229910052769 Ytterbium Inorganic materials 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 239000011133 lead Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- SUHYKYPAFONDDV-UHFFFAOYSA-M bis(diethylamino)methylidene-diethylazanium;bromide Chemical compound [Br-].CCN(CC)C(N(CC)CC)=[N+](CC)CC SUHYKYPAFONDDV-UHFFFAOYSA-M 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- JKDRQYIYVJVOPF-FDGPNNRMSA-L palladium(ii) acetylacetonate Chemical group [Pd+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O JKDRQYIYVJVOPF-FDGPNNRMSA-L 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical group [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 2
- 229910052727 yttrium Inorganic materials 0.000 description 2
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/301,703 | 1999-04-29 | ||
| US09/301,703 US6197991B1 (en) | 1999-04-29 | 1999-04-29 | Method and catalyst system for producing |
| PCT/US2000/009643 WO2000066536A1 (en) | 1999-04-29 | 2000-04-11 | Method and catalyst system for producing aromatic carbonates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002542940A JP2002542940A (ja) | 2002-12-17 |
| JP2002542940A5 true JP2002542940A5 (enExample) | 2007-06-28 |
Family
ID=23164505
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000615369A Withdrawn JP2002542940A (ja) | 1999-04-29 | 2000-04-11 | 芳香族カーボネートを製造する方法及び触媒系 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US6197991B1 (enExample) |
| EP (1) | EP1189869A1 (enExample) |
| JP (1) | JP2002542940A (enExample) |
| KR (1) | KR20020006628A (enExample) |
| CN (1) | CN1349494A (enExample) |
| AU (1) | AU4454500A (enExample) |
| BR (1) | BR0010149A (enExample) |
| WO (1) | WO2000066536A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6160155A (en) * | 1999-04-29 | 2000-12-12 | General Electric Company | Method and catalyst system for producing aromatic carbonates |
| US6114563A (en) * | 1999-04-29 | 2000-09-05 | General Electric Co. | Method and catalyst system for producing aromatic carbonates |
| EP1145763B1 (en) * | 1999-10-27 | 2012-07-04 | Idemitsu Kosan Co., Ltd. | Hydrotreating catalyst for hydrocarbon oil, carrier for the same and method for hydrotreating of hydrocarbon oil |
| US6245929B1 (en) * | 1999-12-20 | 2001-06-12 | General Electric Company | Catalyst composition and method for producing diaryl carbonates, using bisphosphines |
| US6207849B1 (en) * | 2000-01-31 | 2001-03-27 | General Electric Company | Method and catalyst system for producing aromatic carbonates |
| US6184409B1 (en) * | 2000-03-01 | 2001-02-06 | General Electric Company | Method and catalyst system for producing aromatic carbonates |
| US6384262B1 (en) | 2000-12-14 | 2002-05-07 | General Electric Company | Process for the production of diaryl carbonates |
| US6420589B1 (en) | 2000-12-14 | 2002-07-16 | General Electric Company | Process for the production of diaryl carbonates |
| US6521777B2 (en) * | 2000-12-14 | 2003-02-18 | General Electric Company | Process for the production of diaryl carbonates |
| EP1366014A1 (en) * | 2001-01-29 | 2003-12-03 | General Electric Company | Method and catalyst system for producing aromatic carbonates |
| US6440892B1 (en) | 2001-03-30 | 2002-08-27 | General Electric Company | Method and catalyst composition for producing aromatic carbonates |
| US6410774B1 (en) | 2001-03-30 | 2002-06-25 | General Electric Company | Method for recovery of catalyst components |
| US6506924B2 (en) | 2001-03-30 | 2003-01-14 | General Electric Company | Method for recovery of catalyst components |
| US6440893B1 (en) * | 2001-03-30 | 2002-08-27 | General Electric Company | Method and catalyst composition for producing aromatic carbonates |
| US6800779B2 (en) * | 2001-03-30 | 2004-10-05 | General Electric Company | Method for producing aromatic carbonates |
| DE60211884T2 (de) | 2001-04-30 | 2006-11-23 | Ciba Speciality Chemicals Holding Inc. | Verwendung von metallkomplexverbindungen als oxidationskatalysatoren |
| US6441215B1 (en) | 2001-06-06 | 2002-08-27 | General Electric Company | Method for reducing carbonate decomposition in reaction mixtures |
| US6903049B2 (en) * | 2002-02-25 | 2005-06-07 | General Electric Company | Method and catalyst composition for producing aromatic carbonates using activating solvents |
| US8822370B2 (en) * | 2011-05-16 | 2014-09-02 | Uop Llc | Substantially non-porous substrate supported noble metal-and lanthanide-containing catalysts |
Family Cites Families (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE736325C (de) | 1936-07-04 | 1943-06-11 | Seitz Werke Gmbh | Selbstverkaeufer |
| US4187242A (en) | 1976-10-12 | 1980-02-05 | General Electric Company | Catalytic aromatic carbonate process |
| US5142086A (en) | 1991-04-01 | 1992-08-25 | General Electric Company | Method for making organic carbonates |
| WO1993003000A1 (en) | 1991-07-29 | 1993-02-18 | General Electric Company | Method for making aromatic organic carbonates |
| JPH0641020A (ja) | 1992-06-01 | 1994-02-15 | Mitsubishi Gas Chem Co Inc | 芳香族炭酸エステルの製造方法 |
| JPH06239807A (ja) | 1992-07-31 | 1994-08-30 | Ube Ind Ltd | 炭酸エステルの製造法 |
| US5239106A (en) | 1992-08-17 | 1993-08-24 | General Electric Company | Method of recovering and purifying diphenylcarbonate from phenolic solutions thereof |
| US5284964A (en) | 1992-08-17 | 1994-02-08 | General Electric Company | Method for making aromatic carbonates |
| US5231210A (en) | 1992-08-17 | 1993-07-27 | General Electric Company | Method for making aromatic carbonates |
| DE69309653T2 (de) | 1993-03-08 | 1997-09-11 | Mitsubishi Chem Corp | Verfahren zum Herstellen von aromatischem Carbonat |
| JPH06271506A (ja) | 1993-03-17 | 1994-09-27 | Mitsubishi Petrochem Co Ltd | 芳香族炭酸エステルの製造方法 |
| JPH06271509A (ja) | 1993-03-22 | 1994-09-27 | Mitsubishi Petrochem Co Ltd | 芳香族炭酸エステルの製造方法 |
| US5373083A (en) | 1993-06-17 | 1994-12-13 | General Electric Company | Thermoplastic resin and method using heterocyclic amine catalyst |
| JPH07145107A (ja) | 1993-11-08 | 1995-06-06 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造方法 |
| EP0663388B1 (en) | 1994-01-12 | 1998-03-11 | Mitsubishi Chemical Corporation | Method of producing an aromatic carbonate |
| JPH0892168A (ja) | 1994-09-21 | 1996-04-09 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造方法 |
| JPH0889810A (ja) | 1994-09-21 | 1996-04-09 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造方法 |
| JP3560077B2 (ja) | 1995-01-13 | 2004-09-02 | 三菱化学株式会社 | 芳香族炭酸エステルの製造法 |
| DE19512618A1 (de) * | 1995-04-05 | 1996-10-10 | Bayer Ag | Platinmetall enthaltende Träger-Katalysatoren und Verfahren zur Herstellung von Diarylcarbonaten |
| DE19512615A1 (de) | 1995-04-05 | 1996-10-10 | Bayer Ag | Platinmetall enthaltende Träger-Katalysatoren und Verfahren zur Herstellung von Diarylcarbonaten |
| DE19512616A1 (de) | 1995-04-05 | 1996-10-10 | Bayer Ag | Verfahren zur Herstellung von Diarylcarbonaten |
| JPH09110804A (ja) | 1995-10-16 | 1997-04-28 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造方法 |
| JP3719544B2 (ja) | 1996-03-26 | 2005-11-24 | 三菱化学株式会社 | 芳香族炭酸エステルの製造方法 |
| JP3719545B2 (ja) | 1996-04-05 | 2005-11-24 | 三菱化学株式会社 | 芳香族炭酸エステルの製造方法 |
| DE19614062A1 (de) * | 1996-04-09 | 1997-10-16 | Bayer Ag | Verfahren zur kontinuierlichen Herstellung von Diarylcarbonaten |
| JPH09278715A (ja) | 1996-04-16 | 1997-10-28 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造方法 |
| JPH09278716A (ja) | 1996-04-17 | 1997-10-28 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造方法 |
| DE19619949A1 (de) | 1996-05-17 | 1997-11-20 | Bayer Ag | Verfahren zur Herstellung von Diarylcarbonaten |
| JPH10158221A (ja) | 1996-12-03 | 1998-06-16 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造方法 |
| US5898079A (en) * | 1997-02-13 | 1999-04-27 | General Electric Company | Method for preparing diaryl carbonates employing hexaalkylguanidinium halides |
| US5760272A (en) | 1997-03-24 | 1998-06-02 | General Electric Company | Method for preparing diaryl carbonates with improved selectivity |
| JPH10316627A (ja) | 1997-05-16 | 1998-12-02 | Mitsubishi Chem Corp | 芳香族炭酸エステルの製造法 |
| CN1116930C (zh) * | 1997-08-04 | 2003-08-06 | 帝人株式会社 | 催化剂和芳香族碳酸酯的制造方法 |
| US6197091B1 (en) * | 1999-03-05 | 2001-03-06 | The Boc Group, Inc. | Ozone purification process |
| US6172254B1 (en) * | 1999-06-30 | 2001-01-09 | General Electric Company | Catalyst composition and method for producing diaryl carbonates using nitrile as promoter |
| US6215014B1 (en) * | 1999-08-27 | 2001-04-10 | General Electric Company | Catalyst composition and method for producing diaryl carbonates |
| US6114564A (en) * | 1999-08-27 | 2000-09-05 | General Electric Company | Catalyst composition and method for producing diaryl carbonates |
| US6180812B1 (en) * | 1999-08-27 | 2001-01-30 | General Electric Company | Catalyst composition and method for producing diaryl carbonates using amide as promoter |
| US6245929B1 (en) * | 1999-12-20 | 2001-06-12 | General Electric Company | Catalyst composition and method for producing diaryl carbonates, using bisphosphines |
| US6187942B1 (en) * | 2000-03-01 | 2001-02-13 | General Electric Company | Method and catalyst system for producing aromatic carbonates |
| US6215015B1 (en) * | 2000-04-17 | 2001-04-10 | General Electric Company | Catalyst composition and method for producing diaryl carbonates, using bisphosphines |
-
1999
- 1999-04-29 US US09/301,703 patent/US6197991B1/en not_active Expired - Lifetime
-
2000
- 2000-04-11 WO PCT/US2000/009643 patent/WO2000066536A1/en not_active Ceased
- 2000-04-11 JP JP2000615369A patent/JP2002542940A/ja not_active Withdrawn
- 2000-04-11 BR BR0010149-4A patent/BR0010149A/pt not_active IP Right Cessation
- 2000-04-11 KR KR1020017013706A patent/KR20020006628A/ko not_active Withdrawn
- 2000-04-11 CN CN00806916A patent/CN1349494A/zh active Pending
- 2000-04-11 EP EP00925926A patent/EP1189869A1/en not_active Withdrawn
- 2000-04-11 AU AU44545/00A patent/AU4454500A/en not_active Abandoned
-
2001
- 2001-02-05 US US09/777,818 patent/US6420587B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002542940A5 (enExample) | ||
| RU2214307C2 (ru) | Катализатор для винилацетата, содержащий металлический палладий, медь и золото, и его получение | |
| AU1814601A (en) | Catalyst composition and method for producing diaryl carbonates, using bisphosphines | |
| EP1380341A4 (en) | CATALYST FOR REFORMING HYDROCARBONS AND METHOD FOR THE PRODUCTION THEREOF, AND METHOD FOR REFORMING HYDROCARBONS USING THE CATALYST | |
| CA2225137A1 (en) | Iridium catalysed carbonylation process for the production of acetic acid | |
| CA2345011A1 (en) | Carbonylation of methanol in the presence of a rhodium/iridium/iodide ion catalytic system | |
| EP0842920A3 (en) | Process for the production of aromatic halogen-amino compounds | |
| ATE309975T1 (de) | Herstellung von diarylcarbonaten unter verwendung von amidpromotoren | |
| JP2003503472A5 (enExample) | ||
| CA2017425A1 (en) | Method for producing ibuprofen | |
| CA2304640A1 (en) | Vinyl acetate catalyst comprising metallic palladium and gold, and cupric acetate | |
| Griggs et al. | Photocatalytic dehydrogenation of propan-2-ol using rhodium based catalysts | |
| CA2537022A1 (en) | Purification catalyst for exhaust gas, production method therefor, and purification catalyst device for exhaust gas | |
| DE59509734D1 (de) | Palladium Katalysatoren mit sulfonierten Bisphoshinen als Liganden, Verfahren zu ihrer Herstellung und ihre Verwendung für Carbonylierungsreaktionen | |
| BR0010144A (pt) | Método e sistema catalisador para a produção de carbonatos aromáticos | |
| WO2002044122A3 (en) | Method and catalyst system for producing aromatic carbonates | |
| Camus et al. | Hydrogen transfer reactions from alcohols to α, β-unsaturated ketones:[Ir (3, 4, 7, 8-Me4-phen) COD] Cl, a very active catalyst precursor | |
| WO2001079149A3 (en) | Catalyst composition and method for producing diaryl carbonates, using bisphosphines | |
| Jenner et al. | Synthesis of aromatic acids via catalysed methyl formate-chloroarene reactions | |
| Kalinovskii et al. | Oxidative carbonylation of aromatic hydrocarbons in the system containing Pd or Rh compound, trifluoroacetic acid and its anhydride, and MnO2 or Mn2O3 | |
| RU2001111864A (ru) | Способ получения уксусной кислоты и/или метилацетата в присутствии иридия и платины | |
| Pt et al. | ASED-MO | |
| Markó | Transition metals in organic synthesis: Hydroformylation, reduction and oxidation: Annual survey covering the year 1981 | |
| TH44593A (th) | วิธีและระบบตัวเร่งปฏิกิริยาสำหรับผลิตแอโรเมทิค คาร์บอเนท | |
| Imanaka et al. | Kinetics and mechanism of the co-oligomerization of allyl chloride and acetylene catalyzed by palladium salts |