JP4121602B2 - 二種金属シアン化物触媒の製造方法 - Google Patents
二種金属シアン化物触媒の製造方法 Download PDFInfo
- Publication number
- JP4121602B2 JP4121602B2 JP04805698A JP4805698A JP4121602B2 JP 4121602 B2 JP4121602 B2 JP 4121602B2 JP 04805698 A JP04805698 A JP 04805698A JP 4805698 A JP4805698 A JP 4805698A JP 4121602 B2 JP4121602 B2 JP 4121602B2
- Authority
- JP
- Japan
- Prior art keywords
- iii
- ligand
- catalyst
- water
- suspension
- 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.)
- Expired - Fee Related
Links
- 239000003054 catalyst Substances 0.000 title claims description 37
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 238000000034 method Methods 0.000 claims description 26
- 229920000570 polyether Polymers 0.000 claims description 19
- 239000000243 solution Substances 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 18
- 239000003446 ligand Substances 0.000 claims description 15
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 13
- 150000001298 alcohols Chemical class 0.000 claims description 12
- 239000000725 suspension Substances 0.000 claims description 11
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 150000002170 ethers Chemical class 0.000 claims description 6
- 150000002576 ketones Chemical class 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 150000002825 nitriles Chemical class 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 239000004246 zinc acetate Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 150000001299 aldehydes Chemical class 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 229910021645 metal ion Inorganic materials 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- 239000007900 aqueous suspension Substances 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- 230000003197 catalytic effect Effects 0.000 claims description 2
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 claims 2
- 239000013110 organic ligand Substances 0.000 claims 2
- 229910002651 NO3 Inorganic materials 0.000 claims 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 19
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 16
- 150000003839 salts Chemical class 0.000 description 16
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- 239000007787 solid Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 11
- 229910052700 potassium Inorganic materials 0.000 description 11
- 239000011591 potassium Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 8
- 229910052725 zinc Inorganic materials 0.000 description 8
- 239000011701 zinc Substances 0.000 description 8
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 8
- 125000005842 heteroatom Chemical group 0.000 description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 7
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000012299 nitrogen atmosphere Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 239000011592 zinc chloride Substances 0.000 description 4
- 235000005074 zinc chloride Nutrition 0.000 description 4
- 238000000862 absorption spectrum Methods 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 150000003818 basic metals Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 239000002244 precipitate 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
- 239000012266 salt solution Substances 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4866—Polyethers having a low unsaturation value
-
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
- B01J27/26—Cyanides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2642—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds characterised by the catalyst used
- C08G65/2645—Metals or compounds thereof, e.g. salts
- C08G65/2663—Metal cyanide catalysts, i.e. DMC's
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Toxicology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
- Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19709031A DE19709031A1 (de) | 1997-03-06 | 1997-03-06 | Verfahren zur Herstellung von Doppelmetallcyanidkatalysatoren |
| DE19709031.1 | 1997-03-06 | ||
| US09/035,601 US6303533B1 (en) | 1997-03-06 | 1998-03-05 | Process for preparing two-metal cyanide catalysts |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPH10277398A JPH10277398A (ja) | 1998-10-20 |
| JPH10277398A5 JPH10277398A5 (enExample) | 2005-09-02 |
| JP4121602B2 true JP4121602B2 (ja) | 2008-07-23 |
Family
ID=26034540
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP04805698A Expired - Fee Related JP4121602B2 (ja) | 1997-03-06 | 1998-02-27 | 二種金属シアン化物触媒の製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6303533B1 (enExample) |
| EP (1) | EP0862947B2 (enExample) |
| JP (1) | JP4121602B2 (enExample) |
| CA (1) | CA2228651A1 (enExample) |
| DE (2) | DE19709031A1 (enExample) |
| ES (1) | ES2198610T5 (enExample) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19742978A1 (de) | 1997-09-29 | 1999-04-01 | Basf Ag | Multimetallcyanidkomplexe als Katalysatoren |
| US6051680A (en) * | 1998-06-08 | 2000-04-18 | Arco Chemical Technology, L.P. | Silylated double metal cyanide complex catalysts |
| DE19917897A1 (de) † | 1999-04-20 | 2000-10-26 | Basf Ag | Verfahren zur Herstellung von Polyurethanen |
| DE19919267A1 (de) | 1999-04-28 | 2000-11-02 | Bayer Ag | Kristallisierende Polyetherpolyole, ein Verfahren zu deren Herstellung sowie deren Verwendung |
| ES2244446T3 (es) * | 1999-06-02 | 2005-12-16 | Basf Aktiengesellschaft | Procedimiento para la preparacion de polieterpolioles con empleo de catalizadores cristalinos de cianuros polimetalicos. |
| US6800583B2 (en) * | 1999-06-02 | 2004-10-05 | Basf Aktiengesellschaft | Suspension of multimetal cyanide compounds, their preparation and their use |
| US6613714B2 (en) * | 1999-06-02 | 2003-09-02 | Basf Aktiengesellschaft | Multimetal cyanide compounds, their preparation and their use |
| JP2003504461A (ja) * | 1999-07-09 | 2003-02-04 | ザ ダウ ケミカル カンパニー | スルホン化合物またはスルホキシド化合物で錯化された金属触媒 |
| US6376645B1 (en) * | 1999-07-09 | 2002-04-23 | The Dow Chemical Company | Complexing agent-modified hexacyanometallate hexanitrometallate catalysts |
| US6358877B1 (en) | 1999-09-10 | 2002-03-19 | The Dow Chemical Company | Metal catalysts complexed with sulfone or sulfoxide compounds |
| DE19949091A1 (de) | 1999-10-12 | 2001-04-26 | Basf Ag | Polyester-Polyetherblockcopolymere |
| US6429166B1 (en) * | 2000-05-19 | 2002-08-06 | Dow Global Technologies Inc. | Method for preparing metal cyanide catalyst/polyol initiator slurries |
| US6436867B1 (en) * | 2000-08-01 | 2002-08-20 | Basf Corporation | One-step synthesis of double metal cyanides |
| DE10137628A1 (de) * | 2001-08-03 | 2003-02-27 | Basf Ag | Verfahren zur Herstellung von Polyurethan-Weichschaumstoffen |
| DE10141122A1 (de) * | 2001-08-22 | 2003-03-13 | Basf Ag | Verfahren zur Erhöhung der katalytischen Aktivität von Multimetallcyanidverbindungen |
| US6696383B1 (en) * | 2002-09-20 | 2004-02-24 | Bayer Polymers Llc | Double-metal cyanide catalysts which can be used to prepare polyols and the processes related thereto |
| US6806348B2 (en) * | 2003-02-11 | 2004-10-19 | Basf Corporation | Process for removing and regenerating a double metal cyanide (DMC) catalyst from a polymer polyol |
| CN1867609A (zh) * | 2003-03-07 | 2006-11-22 | 陶氏环球技术公司 | 制备聚醚多元醇的连续方法和设备 |
| US6855658B1 (en) | 2003-08-26 | 2005-02-15 | Bayer Antwerp, N.V. | Hydroxide containing double metal cyanide (DMC) catalysts |
| DE102004013408A1 (de) | 2004-03-18 | 2005-10-06 | Basf Ag | Polyetheralkohole und Verfahren zur Herstellung von Polyetheralkoholen zur Polyurethansynthese |
| EP1983010A3 (de) | 2007-04-19 | 2009-07-29 | Basf Se | Verfahren zur Herstellung von Polyurethanen |
| EP2003156A1 (de) | 2007-04-19 | 2008-12-17 | Basf Se | Urethangruppen und Isocyanatgruppen enthaltende Prepolymere |
| DE102008042715A1 (de) | 2007-10-12 | 2009-04-16 | Basf Se | Polyetherpolyole |
| PT2238195E (pt) | 2008-01-29 | 2015-04-02 | Basf Se | Método para a produção de poliéter álcoois |
| CN101684184A (zh) | 2008-09-27 | 2010-03-31 | 巴斯夫欧洲公司 | 可通过使用可再生的原料获得的聚氨酯鞋底 |
| DE102009045651A1 (de) | 2008-10-17 | 2010-04-29 | Basf Se | Textilien und Verfahren zu ihrer Herstellung |
| BR112012000634A2 (pt) | 2009-07-10 | 2016-02-10 | Basf Se | processo para a produção de polióis, poliol, uso de polióis, e, processo para a produção de poliuretanos |
| WO2011085772A1 (en) | 2010-01-15 | 2011-07-21 | Basf Se | "process for the dmc-catalyzed preparation of polyols" |
| DE102010039090A1 (de) | 2010-08-09 | 2012-02-09 | Basf Se | Verfahren zur Herstellung von Polyetheralkoholen |
| CN105189719B (zh) | 2013-03-11 | 2018-05-29 | 巴斯夫欧洲公司 | 聚烷氧基化物在润滑剂组合物中的用途 |
| AU2014267528B2 (en) | 2013-05-17 | 2017-05-18 | Basf Se | The use of polytetrahydrofuranes in lubricating oil compositions |
| KR102220786B1 (ko) * | 2013-07-18 | 2021-03-02 | 에스케이이노베이션 주식회사 | 이중금속 시아나이드(dmc) 촉매 및 이를 통해 제조된 에폭사이드/이산화탄소 공중합체 |
| US20150113867A1 (en) | 2013-10-24 | 2015-04-30 | Basf Se | Use of an alkoxylated polytetrahydrofuran to reduce fuel consumption |
| WO2015113850A1 (en) | 2014-01-28 | 2015-08-06 | Basf Se | The use of alkoxylated polyethylene glycols in lubricating oil compositions |
| EP3146028B1 (en) | 2014-05-22 | 2018-07-11 | Basf Se | Lubricant compositions containing beta-glucans |
| EP3029087A1 (de) | 2014-12-05 | 2016-06-08 | Evonik Degussa GmbH | Verfahren zur Herstellung von niedrigviskosen Polyethersiloxanen |
| US9562135B1 (en) | 2015-12-21 | 2017-02-07 | Covestro Llc | Polyether carbonates by DMC catalysis |
| EP3315591A1 (en) | 2016-10-28 | 2018-05-02 | Basf Se | Energy efficient lubricant compositions |
| PL3700956T3 (pl) | 2017-10-27 | 2025-06-23 | Huntsman International Llc | Katalizatory do wytwarzania materiałów oksazolidynonowych |
| US10479862B2 (en) | 2017-12-07 | 2019-11-19 | Covestro Llc | Amine based polymer polyol stabilizers |
| US10526484B2 (en) | 2017-12-20 | 2020-01-07 | Covestro Llc | Dithiocarbonate containing polyols as polymer polyol stabilizers |
| ES2941289T3 (es) * | 2018-12-21 | 2023-05-19 | Dow Global Technologies Llc | Proceso de polimerización de poliéter |
| US11566145B2 (en) | 2019-03-14 | 2023-01-31 | Covestro Llc | Polyurethane coating compositions and their use as gel coats |
| US10544158B1 (en) | 2019-03-14 | 2020-01-28 | Covestro Llc | Process for producing polycyclic polyether polyols |
| KR102717144B1 (ko) * | 2021-07-15 | 2024-10-11 | 아주대학교산학협력단 | 하이드로젠 헥사시아노코발테이트와 아연 카복실레이트의 조합으로 제조된 더블메탈시아나이드 촉매 및 이를 이용한 프로필렌 옥사이드 중합 |
| CN116376001A (zh) * | 2023-04-10 | 2023-07-04 | 浙江皇马科技股份有限公司 | 一种改性双金属氰化物合成宽分子量分布脂肪醇聚醚的方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD148957A1 (de) * | 1980-01-31 | 1981-06-17 | Gerhard Behrendt | Verfahren zur herstellung von hochmolekularen polyetheralkoholen |
| US4764567A (en) | 1986-11-20 | 1988-08-16 | Basf Corporation | Process for the preparation of polyoxyalkylene block polyethers having enhanced properties |
| CA2138063C (en) * | 1993-12-23 | 2007-02-20 | Bi Le-Khac | Polyurethane foam-supported double metal cyanide catalysts for polyol synthesis |
| US5482908A (en) * | 1994-09-08 | 1996-01-09 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| US5627122A (en) | 1995-07-24 | 1997-05-06 | Arco Chemical Technology, L.P. | Highly active double metal cyanide complex catalysts |
| US5639705A (en) * | 1996-01-19 | 1997-06-17 | Arco Chemical Technology, L.P. | Double metal cyanide catalysts and methods for making them |
-
1997
- 1997-03-06 DE DE19709031A patent/DE19709031A1/de not_active Withdrawn
-
1998
- 1998-02-17 EP EP98102671A patent/EP0862947B2/de not_active Expired - Lifetime
- 1998-02-17 DE DE59808009T patent/DE59808009D1/de not_active Expired - Lifetime
- 1998-02-17 ES ES98102671T patent/ES2198610T5/es not_active Expired - Lifetime
- 1998-02-27 JP JP04805698A patent/JP4121602B2/ja not_active Expired - Fee Related
- 1998-03-05 CA CA002228651A patent/CA2228651A1/en not_active Abandoned
- 1998-03-05 US US09/035,601 patent/US6303533B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE19709031A1 (de) | 1998-09-10 |
| ES2198610T3 (es) | 2004-02-01 |
| ES2198610T5 (es) | 2008-02-16 |
| EP0862947B1 (de) | 2003-04-23 |
| US6303533B1 (en) | 2001-10-16 |
| EP0862947B2 (de) | 2007-09-05 |
| DE59808009D1 (de) | 2003-05-28 |
| EP0862947A1 (de) | 1998-09-09 |
| JPH10277398A (ja) | 1998-10-20 |
| CA2228651A1 (en) | 1998-09-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4121602B2 (ja) | 二種金属シアン化物触媒の製造方法 | |
| JP4471492B2 (ja) | 触媒としての複数シアン化金属錯体 | |
| US5789626A (en) | Highly active double metal cyanide catalysts | |
| KR100355336B1 (ko) | 고활성이중금속시안나이드촉매 | |
| JP4043061B2 (ja) | 改良されたポリエーテル含有二重金属シアン化物触媒並びにその製法および用途 | |
| ES2199712T3 (es) | Nuevos catalizadores de cianuro bimetalico para la fabricacion de polioleteres. | |
| CA2179946A1 (en) | Highly active double metal cyanide complex catalysts | |
| JPH0480933B2 (enExample) | ||
| US6596842B2 (en) | Polymerizing alkylene oxide with sound or radiation treated DMC | |
| HUP0103774A2 (hu) | Kettős fém-cianid katalizátorok poliéter-poliolok előállítására | |
| US6624286B2 (en) | Double-metal cyanide catalysts containing polyester for preparing polyether polyols | |
| KR100589580B1 (ko) | 폴리에테르 폴리올의 제조에 사용되는 이중 금속시아나이드 촉매 | |
| CA2306386C (en) | Double metal cyanide catalysts containing polyester for preparing polyether polyols | |
| KR20010101746A (ko) | 폴리에테르 폴리올의 제조 방법 | |
| HU223381B1 (hu) | Kettős fémcianid-katalizátorok alkalmazása poliéter-poliolok előállítására | |
| JP2005509051A (ja) | 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 | |
| CN1326614C (zh) | 用零价金属制备金属氰化物催化剂的方法 | |
| JP2005501947A (ja) | 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 | |
| US6358877B1 (en) | Metal catalysts complexed with sulfone or sulfoxide compounds | |
| RU2237515C2 (ru) | Двойной металлцианидный катализатор, способ его получения и способ получения полиэфирполиолов | |
| MXPA98001797A (en) | Process for the preparation of two-metal cyanide catalysts | |
| MXPA00003563A (en) | Crystalline double metal cyanide catalysts for producing polyether polyols | |
| MXPA00003447A (en) | Double metal cyanide catalysts containing polyester for preparing polyether polyoles | |
| JP2003504461A (ja) | スルホン化合物またはスルホキシド化合物で錯化された金属触媒 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20050225 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20050225 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20061219 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20061221 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070301 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20070828 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20071126 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20080401 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20080430 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110509 Year of fee payment: 3 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| LAPS | Cancellation because of no payment of annual fees |