JP4471492B2 - 触媒としての複数シアン化金属錯体 - Google Patents
触媒としての複数シアン化金属錯体 Download PDFInfo
- Publication number
- JP4471492B2 JP4471492B2 JP2000513857A JP2000513857A JP4471492B2 JP 4471492 B2 JP4471492 B2 JP 4471492B2 JP 2000513857 A JP2000513857 A JP 2000513857A JP 2000513857 A JP2000513857 A JP 2000513857A JP 4471492 B2 JP4471492 B2 JP 4471492B2
- Authority
- JP
- Japan
- Prior art keywords
- iii
- metal
- acetate
- complex
- metal cyanide
- 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 - Lifetime
Links
- 229910052751 metal Inorganic materials 0.000 title claims description 55
- 239000002184 metal Substances 0.000 title claims description 55
- 239000003054 catalyst Substances 0.000 title claims description 28
- 150000002825 nitriles Chemical class 0.000 title claims description 18
- 229920000570 polyether Polymers 0.000 claims description 26
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 24
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 23
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 22
- 229920005862 polyol Polymers 0.000 claims description 22
- 150000003077 polyols Chemical class 0.000 claims description 22
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 20
- 239000002253 acid Substances 0.000 claims description 19
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 238000002441 X-ray diffraction Methods 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 239000003446 ligand Substances 0.000 claims description 14
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical group [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 claims description 12
- 230000002378 acidificating effect Effects 0.000 claims description 12
- 150000002500 ions Chemical class 0.000 claims description 11
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 8
- 150000002576 ketones Chemical class 0.000 claims description 8
- 150000001299 aldehydes Chemical class 0.000 claims description 7
- 150000001408 amides Chemical class 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 150000001298 alcohols Chemical class 0.000 claims description 6
- 238000010586 diagram Methods 0.000 claims description 6
- 150000002170 ethers Chemical class 0.000 claims description 6
- -1 propionate anion Chemical class 0.000 claims description 6
- 150000003568 thioethers Chemical class 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 4
- 150000002009 diols Chemical class 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 12
- 239000007787 solid Substances 0.000 description 11
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical group [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 10
- 230000007935 neutral effect Effects 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 125000002947 alkylene group Chemical group 0.000 description 9
- 239000000725 suspension Substances 0.000 description 8
- 239000011701 zinc Substances 0.000 description 8
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000001308 synthesis method Methods 0.000 description 7
- 229910052725 zinc Inorganic materials 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 229910017052 cobalt Inorganic materials 0.000 description 5
- 239000010941 cobalt Substances 0.000 description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 5
- 239000012467 final product Substances 0.000 description 5
- 239000012299 nitrogen atmosphere Substances 0.000 description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- UOURRHZRLGCVDA-UHFFFAOYSA-D pentazinc;dicarbonate;hexahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Zn+2].[Zn+2].[Zn+2].[Zn+2].[Zn+2].[O-]C([O-])=O.[O-]C([O-])=O UOURRHZRLGCVDA-UHFFFAOYSA-D 0.000 description 4
- 230000008929 regeneration Effects 0.000 description 4
- 238000011069 regeneration method Methods 0.000 description 4
- 239000012266 salt solution Substances 0.000 description 4
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical group O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- NLTSCOZQKALPGZ-UHFFFAOYSA-N acetic acid;dihydrate Chemical compound O.O.CC(O)=O NLTSCOZQKALPGZ-UHFFFAOYSA-N 0.000 description 3
- 150000002924 oxiranes Chemical class 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 2
- UFHGABBBZRPRJV-UHFFFAOYSA-N Hydroxysanguinarine Chemical class C12=CC=C3OCOC3=C2C(=O)N(C)C(C2=C3)=C1C=CC2=CC1=C3OCO1 UFHGABBBZRPRJV-UHFFFAOYSA-N 0.000 description 2
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- 239000011667 zinc carbonate Substances 0.000 description 2
- 229910000010 zinc carbonate Inorganic materials 0.000 description 2
- 235000004416 zinc carbonate Nutrition 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 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
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- SYSNUEKNSJHAGX-UHFFFAOYSA-N [Zn].N#C[Co](C#N)(C#N)(C#N)(C#N)C#N Chemical group [Zn].N#C[Co](C#N)(C#N)(C#N)(C#N)C#N SYSNUEKNSJHAGX-UHFFFAOYSA-N 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 230000007774 longterm Effects 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
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000013110 organic ligand Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 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
- 238000001228 spectrum Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 235000012976 tarts Nutrition 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 description 1
- XDWXRAYGALQIFG-UHFFFAOYSA-L zinc;propanoate Chemical compound [Zn+2].CCC([O-])=O.CCC([O-])=O XDWXRAYGALQIFG-UHFFFAOYSA-L 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/06—Cobalt compounds
-
- 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)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Toxicology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742978.5 | 1997-09-29 | ||
| DE19742978A DE19742978A1 (de) | 1997-09-29 | 1997-09-29 | Multimetallcyanidkomplexe als Katalysatoren |
| PCT/EP1998/006154 WO1999016775A1 (de) | 1997-09-29 | 1998-09-28 | Multimetallcyanidkomplexe als katalysatoren |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002500163A JP2002500163A (ja) | 2002-01-08 |
| JP2002500163A5 JP2002500163A5 (enExample) | 2006-01-05 |
| JP4471492B2 true JP4471492B2 (ja) | 2010-06-02 |
Family
ID=7843998
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000513857A Expired - Lifetime JP4471492B2 (ja) | 1997-09-29 | 1998-09-28 | 触媒としての複数シアン化金属錯体 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6303833B1 (enExample) |
| EP (1) | EP1021453B1 (enExample) |
| JP (1) | JP4471492B2 (enExample) |
| KR (1) | KR100563897B1 (enExample) |
| CN (1) | CN1221561C (enExample) |
| AR (1) | AR017166A1 (enExample) |
| AT (1) | ATE220684T1 (enExample) |
| CA (1) | CA2305668A1 (enExample) |
| DE (2) | DE19742978A1 (enExample) |
| ES (1) | ES2181291T3 (enExample) |
| WO (1) | WO1999016775A1 (enExample) |
Families Citing this family (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE50010642D1 (de) * | 1999-06-02 | 2005-08-04 | Basf Ag | Verfahren zur herstellung von polyetherpolyole unter verwendung von kristallinen multimetallcyanid-katalysatoren |
| US6613714B2 (en) * | 1999-06-02 | 2003-09-02 | Basf Aktiengesellschaft | Multimetal cyanide compounds, their preparation and their use |
| US6384183B1 (en) * | 1999-07-09 | 2002-05-07 | The Dow Chemical Company | Metal hexacyanocobaltate nitroferricyanide complexes |
| US6376645B1 (en) | 1999-07-09 | 2002-04-23 | The Dow Chemical Company | Complexing agent-modified hexacyanometallate hexanitrometallate catalysts |
| DE19957105A1 (de) * | 1999-11-26 | 2001-05-31 | Basf Ag | Verfahren zur Aufarbeitung von Polyetheralkoholen |
| DE10001779A1 (de) * | 2000-01-18 | 2001-07-19 | Basf Ag | Verfahren zur Herstellung von Polyetheralkoholen |
| DE10008635A1 (de) † | 2000-02-24 | 2001-09-06 | Basf Ag | Verfahren zur Herstellung von Polyetherpolyolen |
| DE10008629A1 (de) | 2000-02-24 | 2001-09-06 | Basf Ag | Verfahren zur Herstellung von Polyetherpolyolen in Gegenwart eines Multimetallcyanidkomplex-Katalysators |
| DE10008630A1 (de) * | 2000-02-24 | 2001-09-06 | Basf Ag | Verfahren zur Herstellung von Polyetherpolyolen in Gegenwart eines Multimetallcyanidkomplex-Katalysators |
| AU2001255735A1 (en) * | 2000-04-28 | 2001-11-12 | Synuthane International, Inc. | Double metal cyanide catalysts containing polyglycol ether complexing agents |
| US6388048B1 (en) * | 2000-05-19 | 2002-05-14 | The Dow Chemical Company | Complexing agent-modified trimetal cyanide catalyst |
| DE10137628A1 (de) * | 2001-08-03 | 2003-02-27 | Basf Ag | Verfahren zur Herstellung von Polyurethan-Weichschaumstoffen |
| DE10143195A1 (de) * | 2001-09-04 | 2003-03-20 | Basf Ag | Integriertes Verfahren zur Herstellung von Polyurethan-Schäumen |
| CN1258507C (zh) | 2002-04-26 | 2006-06-07 | 巴斯福股份公司 | C10链烷醇烷氧基化物混合物及其应用 |
| BR0309548B1 (pt) | 2002-04-26 | 2013-11-12 | Mistura de alcoxilato, processo para a preparação da mesma, agente de lavagem ou de limpeza, e, uso do mesmo | |
| US6764978B2 (en) * | 2002-08-28 | 2004-07-20 | Basf Aktiengesellschaft | Multimetal cyanide compounds |
| US6855658B1 (en) * | 2003-08-26 | 2005-02-15 | Bayer Antwerp, N.V. | Hydroxide containing double metal cyanide (DMC) catalysts |
| DE10341724A1 (de) * | 2003-09-10 | 2005-04-21 | Basf Ag | In Alkalien stabile Alkoxylate |
| DE10341725A1 (de) * | 2003-09-10 | 2005-04-21 | Basf Ag | Festes wasserfreies Kompositmaterial |
| DE10348420A1 (de) * | 2003-10-14 | 2005-05-25 | Basf Ag | C10-Alkanolalkoxylat-Gemische und ihre Verwendung - Neue schaumarme Netzer |
| AU2005321515B2 (en) | 2004-12-24 | 2010-08-19 | Basf Aktiengesellschaft | Use of non-ionic surfactants in the production of metals |
| US7671228B2 (en) * | 2005-03-29 | 2010-03-02 | Basf Corporation | Method of forming a polyethercarbonate polyol using a CO2-philic compound or substituent |
| US7268204B2 (en) * | 2005-03-29 | 2007-09-11 | Basf Corporation | Complex of a multimetal cyanide compound and methods of forming polyethercarbonate polyols |
| US20060223973A1 (en) * | 2005-03-29 | 2006-10-05 | Basf Corporation | Method of forming a polyethercarbonate polyol |
| US20080021191A1 (en) * | 2006-07-20 | 2008-01-24 | Reese Jack R | High water content tolerant process for the production of polyethers |
| US7977501B2 (en) | 2006-07-24 | 2011-07-12 | Bayer Materialscience Llc | Polyether carbonate polyols made via double metal cyanide (DMC) catalysis |
| DE102007019457A1 (de) | 2007-04-25 | 2008-10-30 | Basf Se | Maschinengeschirrspülmittel mit ausgezeichneter Klarspülleistung |
| DE102007019458A1 (de) | 2007-04-25 | 2008-10-30 | Basf Se | Phosphatfreies Maschinengeschirrspülmittel mit ausgezeichneter Klarspülleistung |
| 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 |
| WO2010072769A1 (de) | 2008-12-23 | 2010-07-01 | Basf Se | Verfahren zur herstellung von polyether-blockcopolymeren |
| EP2408841B1 (de) | 2009-03-17 | 2014-11-19 | Basf Se | POLYURETHANFORMKÖRPER MIT VERBESSERTER WEITERREIßFESTIGKEIT UND VERBESSERTEM DAUERBIEGEVERHALTEN |
| EP2459618B1 (de) | 2009-07-29 | 2014-04-23 | Basf Se | Verfahren zur herstellung von polyetherolen aus alkylenoxiden |
| JP2013501702A (ja) | 2009-08-13 | 2013-01-17 | ビーエーエスエフ ソシエタス・ヨーロピア | 多金属シアニド化合物の製造方法 |
| MX2012003697A (es) | 2009-09-30 | 2012-04-19 | Basf Se | Polimeros alcoxilados. |
| MX2012003976A (es) | 2009-10-14 | 2012-05-08 | Basf Se | Proceso para la extraccion terciaria de petroleo usando mezclas de surfactantes. |
| CN102712840A (zh) | 2009-10-14 | 2012-10-03 | 巴斯夫欧洲公司 | 使用表面活性剂混合物的三次矿物油开采方法 |
| US8853136B2 (en) | 2009-10-14 | 2014-10-07 | Basf Se | Process for tertiary mineral oil production using surfactant mixtures |
| US8584750B2 (en) | 2009-10-14 | 2013-11-19 | Basf Se | Process for tertiary mineral oil production using surfactant mixtures |
| EP2490805B1 (en) * | 2009-10-19 | 2019-05-01 | Basf Se | Conditioning of double metal cyanide catalysts |
| SG181448A1 (en) | 2010-01-15 | 2012-08-30 | Basf Se | "process for the dmc-catalyzed preparation of polyols" |
| US20110218295A1 (en) * | 2010-03-02 | 2011-09-08 | Basf Se | Anionic associative rheology modifiers |
| US8673275B2 (en) | 2010-03-02 | 2014-03-18 | Basf Se | Block copolymers and their use |
| ES2544283T3 (es) | 2010-03-02 | 2015-08-28 | Basf Se | Copolímeros de bloque y su uso |
| WO2011160296A1 (en) | 2010-06-23 | 2011-12-29 | Basf Se | Modified double metal cyanide catalyst |
| DE102010039090A1 (de) | 2010-08-09 | 2012-02-09 | Basf Se | Verfahren zur Herstellung von Polyetheralkoholen |
| WO2012098177A1 (de) | 2011-01-21 | 2012-07-26 | Basf Se | Verwendung von talgfettalkoholethoxylaten in der maschinellen geschirrreinigung |
| KR102220786B1 (ko) * | 2013-07-18 | 2021-03-02 | 에스케이이노베이션 주식회사 | 이중금속 시아나이드(dmc) 촉매 및 이를 통해 제조된 에폭사이드/이산화탄소 공중합체 |
| EP3138865A1 (de) | 2015-09-07 | 2017-03-08 | Basf Se | Verfahren zur herstellung von polyetherpolyolen |
| US9562135B1 (en) | 2015-12-21 | 2017-02-07 | Covestro Llc | Polyether carbonates by DMC catalysis |
| MX2020000504A (es) | 2017-07-14 | 2020-02-26 | Basf Se | Tensioactivo biodegradable. |
| 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 |
| WO2020084046A1 (de) | 2018-10-26 | 2020-04-30 | Basf Se | Verfahren zur herstellung von propylenoxy-haltigen hydrophob assoziierenden monomeren mittels dmc-katalyse |
| WO2020084033A1 (de) | 2018-10-26 | 2020-04-30 | Basf Se | Hydrophob assoziierende copolymere für die tertiäre erdölförderung umfassend monomere mit propylenoxy-einheiten |
| 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 |
| WO2024081701A1 (en) | 2022-10-14 | 2024-04-18 | Basf Se | Leaching aids and methods of preparation and use thereof |
| WO2024137042A1 (en) | 2022-12-23 | 2024-06-27 | Basf Se | Compositions for leaching metal-sulfide-containing materials and methods of preparation and use thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5158922A (en) * | 1992-02-04 | 1992-10-27 | Arco Chemical Technology, L.P. | Process for preparing metal cyanide complex catalyst |
| US5470813A (en) | 1993-11-23 | 1995-11-28 | Arco Chemical Technology, L.P. | Double metal cyanide complex catalysts |
| US5712216A (en) | 1995-05-15 | 1998-01-27 | Arco Chemical Technology, L.P. | Highly active double metal cyanide complex catalysts |
| US5426081A (en) * | 1993-12-23 | 1995-06-20 | Arco Chemical Technology, L.P. | Polyurethane foam-supported double metal cyanide catalysts for polyol synthesis |
| US5627122A (en) * | 1995-07-24 | 1997-05-06 | Arco Chemical Technology, L.P. | Highly active double metal cyanide complex catalysts |
| DE19709031A1 (de) | 1997-03-06 | 1998-09-10 | Basf Ag | Verfahren zur Herstellung von Doppelmetallcyanidkatalysatoren |
-
1997
- 1997-09-29 DE DE19742978A patent/DE19742978A1/de not_active Withdrawn
-
1998
- 1998-09-28 ES ES98954291T patent/ES2181291T3/es not_active Expired - Lifetime
- 1998-09-28 CN CNB988095912A patent/CN1221561C/zh not_active Expired - Fee Related
- 1998-09-28 AT AT98954291T patent/ATE220684T1/de not_active IP Right Cessation
- 1998-09-28 KR KR1020007003299A patent/KR100563897B1/ko not_active Expired - Fee Related
- 1998-09-28 CA CA002305668A patent/CA2305668A1/en not_active Abandoned
- 1998-09-28 JP JP2000513857A patent/JP4471492B2/ja not_active Expired - Lifetime
- 1998-09-28 EP EP98954291A patent/EP1021453B1/de not_active Expired - Lifetime
- 1998-09-28 DE DE59804828T patent/DE59804828D1/de not_active Expired - Lifetime
- 1998-09-28 WO PCT/EP1998/006154 patent/WO1999016775A1/de not_active Ceased
- 1998-09-28 US US09/509,515 patent/US6303833B1/en not_active Expired - Lifetime
- 1998-09-29 AR ARP980104847A patent/AR017166A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO1999016775A1 (de) | 1999-04-08 |
| CN1221561C (zh) | 2005-10-05 |
| ATE220684T1 (de) | 2002-08-15 |
| AR017166A1 (es) | 2001-08-22 |
| EP1021453A1 (de) | 2000-07-26 |
| CA2305668A1 (en) | 1999-04-08 |
| ES2181291T3 (es) | 2003-02-16 |
| JP2002500163A (ja) | 2002-01-08 |
| CN1275986A (zh) | 2000-12-06 |
| KR20010015642A (ko) | 2001-02-26 |
| EP1021453B1 (de) | 2002-07-17 |
| US6303833B1 (en) | 2001-10-16 |
| KR100563897B1 (ko) | 2006-03-24 |
| DE19742978A1 (de) | 1999-04-01 |
| DE59804828D1 (de) | 2002-08-22 |
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