JP2004160446A5 - - Google Patents
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- Publication number
- JP2004160446A5 JP2004160446A5 JP2003283890A JP2003283890A JP2004160446A5 JP 2004160446 A5 JP2004160446 A5 JP 2004160446A5 JP 2003283890 A JP2003283890 A JP 2003283890A JP 2003283890 A JP2003283890 A JP 2003283890A JP 2004160446 A5 JP2004160446 A5 JP 2004160446A5
- Authority
- JP
- Japan
- Prior art keywords
- ions
- ion
- water
- metal cyanide
- iii
- 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.)
- Pending
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- -1 halide ion Chemical group 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 239000003446 ligand Substances 0.000 description 8
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 150000002825 nitriles Chemical class 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical group [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical group [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 150000001450 anions Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-L Oxalate Chemical compound [O-]C(=O)C([O-])=O MUBZPKHOEPUJKR-UHFFFAOYSA-L 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- RKBAPHPQTADBIK-UHFFFAOYSA-N cobalt;hexacyanide Chemical compound [Co].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] RKBAPHPQTADBIK-UHFFFAOYSA-N 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical group OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 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
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10235130A DE10235130A1 (de) | 2002-08-01 | 2002-08-01 | Doppelmetallcyanid-Katalysatoren für die Herstellung von Polyetherpolyolen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004160446A JP2004160446A (ja) | 2004-06-10 |
| JP2004160446A5 true JP2004160446A5 (enExample) | 2006-09-14 |
Family
ID=30010550
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003283890A Pending JP2004160446A (ja) | 2002-08-01 | 2003-07-31 | ポリエーテルポリオールを製造するための複金属シアン化物触媒 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6852664B2 (enExample) |
| EP (1) | EP1386662A1 (enExample) |
| JP (1) | JP2004160446A (enExample) |
| KR (1) | KR101002887B1 (enExample) |
| CN (1) | CN1280336C (enExample) |
| BR (1) | BR0302487A (enExample) |
| CA (1) | CA2436394A1 (enExample) |
| DE (1) | DE10235130A1 (enExample) |
| MX (1) | MXPA03006798A (enExample) |
| PL (1) | PL361520A1 (enExample) |
| RU (1) | RU2003126303A (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004044034A1 (en) * | 2002-11-07 | 2004-05-27 | Dow Global Technologies, Inc. | Method for preparing metal cyanide catalysts using polymerizable complexing agents |
| US7300993B2 (en) * | 2004-06-03 | 2007-11-27 | Shell Oil Company | Process for the preparation of polyether polyols |
| KR101541188B1 (ko) | 2008-11-06 | 2015-08-03 | 삼성전자주식회사 | 폴리우레탄 발포체 조성물 및 이를 사용하여 제조된 폴리우레탄 발포체 |
| ES2728648T3 (es) * | 2011-04-04 | 2019-10-28 | Henkel Ag & Co Kgaa | Catalizador para la polimerización de un epóxido y para la copolimerización de epóxido con dióxido de carbono |
| KR101342899B1 (ko) | 2012-03-16 | 2013-12-18 | 부산대학교 산학협력단 | 새로운 유기 착화물제를 이용하여 합성한 이중금속 시안염 촉매 또는 다중금속 시안염 촉매를 이용한 에폭시계 단량체의 개환 중합에 의한 폴리올 제조 |
| EP2703426A1 (de) * | 2012-08-27 | 2014-03-05 | Bayer MaterialScience AG | Verfahren zur Herstellung von Polyethercarbonatpolyolen |
| CN103923309B (zh) * | 2014-03-27 | 2016-03-23 | 上海应用技术学院 | 一种双金属氰化物络合物催化剂的制备方法 |
| EP3694901A1 (en) | 2017-10-10 | 2020-08-19 | Stepan Company | Polymeric dispersants from aralkylated phenols |
| EP4509545A1 (en) | 2017-10-10 | 2025-02-19 | Stepan Company | Polymeric dispersants from phenyl glycidyl ether |
| PL3700956T3 (pl) * | 2017-10-27 | 2025-06-23 | Huntsman International Llc | Katalizatory do wytwarzania materiałów oksazolidynonowych |
| ES2941289T3 (es) * | 2018-12-21 | 2023-05-19 | Dow Global Technologies Llc | Proceso de polimerización de poliéter |
| US20220177403A1 (en) | 2019-03-08 | 2022-06-09 | Stepan Company | Reactive surfactants |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69125789T2 (de) | 1990-05-11 | 1997-08-14 | Asahi Glass Co Ltd | Verfahren zur herstellung einer polyoxyalkylenverbindungen |
| JP2653236B2 (ja) | 1990-10-05 | 1997-09-17 | 旭硝子株式会社 | ポリエーテル化合物の製造方法 |
| US5712216A (en) * | 1995-05-15 | 1998-01-27 | Arco Chemical Technology, L.P. | Highly active double metal cyanide complex catalysts |
| US5470813A (en) * | 1993-11-23 | 1995-11-28 | Arco Chemical Technology, L.P. | Double metal cyanide complex catalysts |
| US5482908A (en) * | 1994-09-08 | 1996-01-09 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| US5545601A (en) * | 1995-08-22 | 1996-08-13 | Arco Chemical Technology, L.P. | Polyether-containing double metal cyanide catalysts |
| US5627120A (en) * | 1996-04-19 | 1997-05-06 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| US6028230A (en) * | 1998-06-05 | 2000-02-22 | Arco Chemical Technology, L.P. | Epoxide polymerization process |
| MXPA02000305A (es) | 1999-07-09 | 2002-06-21 | Dow Chemical Co | Metodo para preparar catalizadores de cianuro metalicos utilizando acidos policarboxilicos. |
| KR20020030781A (ko) * | 1999-07-09 | 2002-04-25 | 그래햄 이. 테일러 | 작용화 개시제 상에서의 알킬렌 옥사이드의 중합방법 |
| DE19953546A1 (de) * | 1999-11-08 | 2001-05-10 | Bayer Ag | Doppelmetallcyanid-Katalysatoren für die Herstellung von Polyetherpolyolen |
| EP1146062B1 (en) * | 2000-04-12 | 2006-12-20 | Kaneka Corporation | Method of producing crosslinkable silyl group-containing polyoxyalkylene polymers |
-
2002
- 2002-08-01 DE DE10235130A patent/DE10235130A1/de not_active Withdrawn
-
2003
- 2003-07-22 EP EP03016466A patent/EP1386662A1/de not_active Withdrawn
- 2003-07-23 US US10/626,265 patent/US6852664B2/en not_active Expired - Fee Related
- 2003-07-30 BR BR0302487-3A patent/BR0302487A/pt not_active IP Right Cessation
- 2003-07-30 CA CA002436394A patent/CA2436394A1/en not_active Abandoned
- 2003-07-30 MX MXPA03006798A patent/MXPA03006798A/es unknown
- 2003-07-31 JP JP2003283890A patent/JP2004160446A/ja active Pending
- 2003-07-31 PL PL03361520A patent/PL361520A1/xx not_active Application Discontinuation
- 2003-07-31 KR KR1020030052960A patent/KR101002887B1/ko not_active Expired - Fee Related
- 2003-08-01 CN CNB031525237A patent/CN1280336C/zh not_active Expired - Fee Related
- 2003-08-29 RU RU2003126303/04A patent/RU2003126303A/ru not_active Application Discontinuation
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