AU768857B2 - Dispersions of silyl-terminated polymers with a high solids content, their production and their use - Google Patents
Dispersions of silyl-terminated polymers with a high solids content, their production and their use Download PDFInfo
- Publication number
- AU768857B2 AU768857B2 AU18617/00A AU1861700A AU768857B2 AU 768857 B2 AU768857 B2 AU 768857B2 AU 18617/00 A AU18617/00 A AU 18617/00A AU 1861700 A AU1861700 A AU 1861700A AU 768857 B2 AU768857 B2 AU 768857B2
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- Prior art keywords
- polymer
- atoms
- radical
- polymer dispersion
- groups
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- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000002081 peroxide group Chemical group 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
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- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
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- 235000012015 potatoes Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000001424 substituent group Chemical group 0.000 description 1
- TYLSDQJYPYQCRK-UHFFFAOYSA-N sulfo 4-amino-4-oxobutanoate Chemical compound NC(=O)CCC(=O)OS(O)(=O)=O TYLSDQJYPYQCRK-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
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- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- VCDLLOVEJODESP-UHFFFAOYSA-L tin(2+);diphenoxide Chemical compound [Sn+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 VCDLLOVEJODESP-UHFFFAOYSA-L 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
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- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
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- 235000013311 vegetables Nutrition 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
-
- 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
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/71—Monoisocyanates or monoisothiocyanates
- C08G18/718—Monoisocyanates or monoisothiocyanates containing silicon
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09D201/10—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing hydrolysable silane groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/34—Filling pastes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J201/00—Adhesives based on unspecified macromolecular compounds
- C09J201/02—Adhesives based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09J201/10—Adhesives based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing hydrolysable silane groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1021—Polyurethanes or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/10—Polymers characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C08J2300/108—Polymers characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing hydrolysable silane groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Dispersion Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
- Silicon Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19858908 | 1998-12-11 | ||
| DE19858908 | 1998-12-11 | ||
| PCT/EP1999/009442 WO2000035981A1 (de) | 1998-12-11 | 1999-12-03 | Dispersionen silylterminierter polymere mit hohem feststoffgehalt, deren herstellung und verwendung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU1861700A AU1861700A (en) | 2000-07-03 |
| AU768857B2 true AU768857B2 (en) | 2004-01-08 |
Family
ID=7891874
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU18617/00A Ceased AU768857B2 (en) | 1998-12-11 | 1999-12-03 | Dispersions of silyl-terminated polymers with a high solids content, their production and their use |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6790903B1 (enExample) |
| EP (1) | EP1151024B1 (enExample) |
| JP (1) | JP2002532589A (enExample) |
| KR (1) | KR100634073B1 (enExample) |
| CN (1) | CN1330667A (enExample) |
| AT (1) | ATE394437T1 (enExample) |
| AU (1) | AU768857B2 (enExample) |
| BR (1) | BR9916097A (enExample) |
| CA (1) | CA2354532A1 (enExample) |
| CZ (1) | CZ20012081A3 (enExample) |
| DE (2) | DE59914754D1 (enExample) |
| ES (1) | ES2306529T3 (enExample) |
| HU (1) | HU225361B1 (enExample) |
| ID (1) | ID30437A (enExample) |
| NO (1) | NO20012529L (enExample) |
| PL (1) | PL348046A1 (enExample) |
| RU (1) | RU2241728C2 (enExample) |
| TR (1) | TR200101608T2 (enExample) |
| WO (1) | WO2000035981A1 (enExample) |
| ZA (1) | ZA200104708B (enExample) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6314558B1 (en) * | 1996-08-27 | 2001-11-06 | Compuware Corporation | Byte code instrumentation |
| JP2002179753A (ja) * | 2000-12-13 | 2002-06-26 | Nippon Shiika Kk | 高耐候性ポリウレタン系一液型湿気硬化性組成物 |
| JP3887601B2 (ja) * | 2001-02-20 | 2007-02-28 | コンゾルテイウム フユール エレクトロケミツシエ インヅストリー ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | 高い硬化速度を有するイソシアネート不含の発泡性混合物 |
| US6713558B2 (en) * | 2001-07-13 | 2004-03-30 | Dow Corning Corporation | High solids emulsions of silylated elastomeric polymers |
| JP4800516B2 (ja) * | 2001-07-27 | 2011-10-26 | オート化学工業株式会社 | 硬化性組成物及びシーリング材組成物 |
| EP1421129B1 (de) * | 2001-08-28 | 2005-06-15 | Consortium für elektrochemische Industrie GmbH | Einkomponentige alkoxysilanterminierte polymere enthaltende schnell härtende abmischungen |
| DE10201703A1 (de) * | 2002-01-17 | 2003-08-07 | Consortium Elektrochem Ind | Alkoxysilanterminierte Polymere enthaltende vernetzbare Polymerabmischungen |
| DE10237270A1 (de) * | 2002-08-14 | 2004-03-04 | Consortium für elektrochemische Industrie GmbH | Silanvernetzbare Beschichtungsformulierungen |
| DE10317881A1 (de) * | 2003-04-17 | 2004-11-11 | Consortium für elektrochemische Industrie GmbH | Isocyanatfreie schäumbare Mischungen mit verbessertem Brandverhalten |
| US20040229046A1 (en) * | 2003-05-12 | 2004-11-18 | Tien-Chieh Chao | Aqueous vacuum-forming laminating adhesive composition containing polyether based plasticizers |
| DE10328844A1 (de) * | 2003-06-26 | 2005-02-03 | Consortium für elektrochemische Industrie GmbH | Alkoxysilanterminierte Prepolymere |
| US6989429B2 (en) * | 2003-10-02 | 2006-01-24 | Tremco Incorporated | Prepolymer compositions and sealants made therefrom |
| FR2863624B1 (fr) * | 2003-12-11 | 2007-02-09 | Bostik Findley | Compositions adhesives recticulables a l'humidite |
| US7238745B2 (en) * | 2003-12-15 | 2007-07-03 | Bayer Materialscience Llc | Aqueous polyurethane/urea dispersions containing alkoxysilane groups |
| DE10359704A1 (de) | 2003-12-18 | 2005-07-14 | Wacker-Chemie Gmbh | Dispersionen enthaltend Organopolysiloxan-Polyharnstoff-Copolymere |
| US7465778B2 (en) * | 2003-12-19 | 2008-12-16 | Bayer Materialscience Llc | Silante terminated polyurethane |
| CN1946815B (zh) * | 2004-01-08 | 2015-06-17 | 赫尔克里士公司 | 着色剂相容性涂料用合成增稠剂 |
| DE102004045358B4 (de) * | 2004-09-17 | 2009-11-26 | Kettenbach Gmbh & Co. Kg | Kondensationsvernetzendes Zweikomponenten-Dentalabformmaterial auf Basis von alkoxysilyl- und hydroxylsilylfunktionellen Polyethern |
| DE102004045214B4 (de) * | 2004-09-17 | 2010-01-28 | Kettenbach Gmbh & Co. Kg | Zweikomponenten-Dentalabformmaterial auf Basis von hydroxylfunktionellen Polyethern und Alkoxysilanen und/oder Kieselsäureestern |
| CN101170903A (zh) * | 2005-03-10 | 2008-04-30 | 巴斯福股份公司 | 含农药的聚合物水分散体的制备方法及其用途 |
| US20060205904A1 (en) * | 2005-03-11 | 2006-09-14 | St Clair David J | Oil gels of controlled distribution block copolymers and ester oils |
| DE102005023050A1 (de) * | 2005-05-13 | 2006-11-16 | Henkel Kgaa | Wässrige, lagerstabile Emulsion α-silyl terminierter Polymere, deren Herstellung und Verwendung |
| US7368174B2 (en) * | 2005-12-14 | 2008-05-06 | Lord Corporation | Aqueous dispersion coating composition having noise and/or friction abatement properties |
| CN1986644A (zh) * | 2005-12-21 | 2007-06-27 | 汉高股份两合公司 | 稳定的硅烷化聚合物乳液及其制备方法和应用 |
| EP1801138A1 (de) * | 2005-12-23 | 2007-06-27 | Sika Technology AG | Feuchtigkeitshärtende Heissschmelzklebstoffe umfassend mindestens ein silanfunktionelles Polyurethanprepolymer |
| US20080145655A1 (en) * | 2006-12-14 | 2008-06-19 | Ppg Industries Ohio, Inc. | Electrospinning Process |
| WO2009006277A1 (en) * | 2007-06-29 | 2009-01-08 | Hadfield Charles G | Method for producing topcoat additives |
| EP2011809A1 (de) * | 2007-07-03 | 2009-01-07 | Sika Technology AG | Polyurethanzusammensetzung enthaltend tertiäre Amine und Anhydridosilane |
| US7781513B2 (en) * | 2007-11-14 | 2010-08-24 | Momentive Performance Materials Inc. | Two-part moisture-curable resin composition and adhesive, sealant and coating compositions based thereon |
| US20090137711A1 (en) * | 2007-11-28 | 2009-05-28 | Georgeau Philip C | Moisture curable structural adhesive composition and method of applicatiion |
| ATE509972T1 (de) * | 2008-10-31 | 2011-06-15 | Sika Technology Ag | Organomethoxysilan enthaltende polyurethanzusammensetzung mit anisotropen materialeigenschaften |
| DE502008002637D1 (de) * | 2008-10-31 | 2011-03-31 | Sika Technology Ag | Alpha-Silan enthaltende Polyurethanzusammensetzung mit anisotropen Materialeigenschaften |
| DE102009027620A1 (de) | 2009-07-10 | 2011-01-13 | Evonik Röhm Gmbh | Copolymerisation von Silyl-funktionellen Komponenten in wässrigen Polymerisationssystemen |
| WO2011021589A1 (ja) * | 2009-08-17 | 2011-02-24 | 旭硝子株式会社 | 硬化性組成物 |
| US8709489B2 (en) * | 2009-09-30 | 2014-04-29 | Surmodics, Inc. | Emulsions containing arylboronic acids and medical articles made therefrom |
| DE102009047964A1 (de) * | 2009-10-01 | 2011-04-21 | Bayer Materialscience Ag | Hochfunktionelle Allophanat- und Silangruppen enthaltende Polyisocyanate |
| US20110178203A1 (en) * | 2009-10-19 | 2011-07-21 | Elmer's Products, Inc. | High strength glue formulation |
| WO2011057896A1 (de) | 2009-11-16 | 2011-05-19 | Saint-Gobain Isover | Kleb- und dichtstoffsystem |
| DE102009046739B4 (de) * | 2009-11-16 | 2020-03-05 | Saint-Gobain Isover G+H Ag | Zweikomponentiges Kleb- und Dichtstoffsystem |
| IN2015DN03074A (enExample) | 2012-10-09 | 2015-10-02 | Avery Dennison Corp | |
| DE102012221375A1 (de) * | 2012-11-22 | 2014-05-22 | Evonik Industries Ag | Feuchtigkeitshärtende Zusammensetzungen, Verfahren zu deren Herstellung und deren Verwendung |
| CA2975298C (en) | 2015-02-05 | 2020-03-10 | Pavel Janko | Label assemblies for adverse environments |
| US9328259B1 (en) * | 2015-02-09 | 2016-05-03 | Wacker Chemical Corporation | Elastomeric silicone emulsion for coating applications |
| US10709672B2 (en) | 2015-10-09 | 2020-07-14 | San-Ei Gen F.F.I., Inc. | Polyphenol-containing solid composition |
| RU2622411C1 (ru) * | 2016-04-11 | 2017-06-15 | Селезнев Антон Сергеевич | Гидрофобизирующая композиция |
| US10526511B2 (en) | 2016-12-22 | 2020-01-07 | Avery Dennison Corporation | Convertible pressure sensitive adhesives comprising urethane (meth)acrylate oligomers |
| DE202018006246U1 (de) * | 2017-09-19 | 2019-10-30 | The Sherwin-Williams Company | 1K-Beschichtung mit hoher Härte und hoher Schlagfestigkeit |
| RU2709528C1 (ru) * | 2019-02-01 | 2019-12-18 | Общество с ограниченной ответственностью "ПолиМикс Казань" | Способ получения водной полиуретановой дисперсии |
| CN110317068B (zh) * | 2019-07-19 | 2020-10-23 | 横店集团东磁股份有限公司 | 一种分散剂及其应用 |
| EP3808819A1 (de) | 2019-10-15 | 2021-04-21 | Clariant International Ltd | Helle reiskleiewachsoxidate mit einem hohen esteranteil |
| PL4045597T3 (pl) | 2019-10-15 | 2024-06-24 | Clariant International Ltd | Produkty utleniania wosku z otrębów ryżowych o niskich liczbach kwasowych |
| EP3808818A1 (de) | 2019-10-15 | 2021-04-21 | Clariant International Ltd | Teilverseifte reiskleiewachsoxidate |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5041494A (en) * | 1987-11-03 | 1991-08-20 | Bayer Aktiengesellschaft | Aqueous solutions or dispersions of polyurethanes, a process for their preparation and their use in coating compositions |
| EP0818496A2 (en) * | 1996-07-09 | 1998-01-14 | Dow Corning Corporation | Method for making aqueous emulsions of functionalized organic polymers |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE857364C (de) | 1948-10-23 | 1952-11-27 | Rohm & Haas | Verfahren zur Herstellung von Epoxyestern der OEl- und bzw. oder Linolsaeure |
| DE1768313B2 (de) | 1968-04-27 | 1977-05-18 | Henkel & Cie GmbH, 4000 Düsseldorf | Verfahren zur herstellung hoehermolekularer mehrwertiger alkohole |
| US3941733A (en) | 1975-01-02 | 1976-03-02 | Minnesota Mining And Manufacturing Company | Silanol-containing urethane dispersions |
| US4567228A (en) * | 1984-05-21 | 1986-01-28 | Ppg Industries, Inc. | Aqueous dispersion, internally silylated and dispersed polyurethane resins, and surfaces containing same |
| CA1248679A (en) | 1984-05-21 | 1989-01-10 | Peter C. Gaa | Aqueous dispersion, internally silylated and dispersed polyurethane resins, and process for producing same and surfaces containing same |
| JPS61141761A (ja) | 1984-12-12 | 1986-06-28 | Kanegafuchi Chem Ind Co Ltd | 硬化性組成物 |
| DE3637836A1 (de) | 1986-11-06 | 1988-05-19 | Wacker Chemie Gmbh | Waessrige silicondispersionen |
| US5162420A (en) * | 1989-07-31 | 1992-11-10 | Ppg Industries, Inc. | Aqueous compositions based on acid-functional acrylic silanol polymers |
| DE3939566A1 (de) | 1989-11-30 | 1991-06-06 | Henkel Kgaa | Steinschutzmittel, enthaltend alkoxysilangruppenterminierte polyurethane |
| DE4029505A1 (de) | 1990-09-18 | 1992-03-19 | Henkel Kgaa | Feuchtigkeitshaertende, alkoxysilanterminierte polyurethane |
| JP2980708B2 (ja) | 1991-02-08 | 1999-11-22 | キヤノン株式会社 | 光クロスバースイッチ |
| AU662511B2 (en) * | 1991-02-08 | 1995-09-07 | Sherwin-Williams Company, The | Silicon-containing, hydrophobically-modified polyurethane thickeners |
| DE4209325A1 (de) | 1992-03-23 | 1993-09-30 | Henkel Kgaa | Verfahren zur Herstellung verzweigter, silylierter Fettstoffe |
| DE4215648C2 (de) | 1992-05-13 | 1994-12-15 | Henkel Kgaa | Verwendung einer wäßrigen Dispersion oder Lösung eines Polyurethans |
| US5288359A (en) * | 1992-08-07 | 1994-02-22 | Minnestoa Mining And Manufacturing Company | Method for adhesively bonding close fitting components |
| DE4413562A1 (de) | 1994-04-19 | 1995-10-26 | Herberts Gmbh | Wäßrige Dispersion von Siloxanbrücken enthaltenden Polyurethanen, deren Herstellung und Verwendung in Überzugsmitteln |
| US5698628A (en) * | 1995-02-27 | 1997-12-16 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Resin composition suitable as water-based paint and process for forming coating films having excellent stain resistance |
| US5686523A (en) * | 1995-05-26 | 1997-11-11 | Osi Specialties, Inc. | Aqueous curable silane/polymer compositions |
| US6313335B1 (en) * | 1997-11-25 | 2001-11-06 | 3M Innovative Properties | Room temperature curable silane terminated and stable waterborne polyurethane dispersions which contain fluorine and/or silicone and low surface energy coatings prepared therefrom |
| ATE252611T1 (de) * | 1998-04-27 | 2003-11-15 | Essex Specialty Prod | Verfahren zur fixierung eines fensters an einem substrat unter verwendung von einer silanfunktionellen klebstoffzusammensetzung |
-
1999
- 1999-12-03 CN CN99814308A patent/CN1330667A/zh active Pending
- 1999-12-03 ID IDW00200101505A patent/ID30437A/id unknown
- 1999-12-03 US US09/857,933 patent/US6790903B1/en not_active Expired - Lifetime
- 1999-12-03 AU AU18617/00A patent/AU768857B2/en not_active Ceased
- 1999-12-03 EP EP99962205A patent/EP1151024B1/de not_active Expired - Lifetime
- 1999-12-03 CA CA000000002A patent/CA2354532A1/en not_active Abandoned
- 1999-12-03 HU HU0104835A patent/HU225361B1/hu not_active IP Right Cessation
- 1999-12-03 RU RU2001119157/04A patent/RU2241728C2/ru not_active IP Right Cessation
- 1999-12-03 WO PCT/EP1999/009442 patent/WO2000035981A1/de not_active Ceased
- 1999-12-03 ES ES99962205T patent/ES2306529T3/es not_active Expired - Lifetime
- 1999-12-03 JP JP2000588236A patent/JP2002532589A/ja active Pending
- 1999-12-03 BR BR9916097-8A patent/BR9916097A/pt not_active Application Discontinuation
- 1999-12-03 PL PL99348046A patent/PL348046A1/xx unknown
- 1999-12-03 CZ CZ20012081A patent/CZ20012081A3/cs unknown
- 1999-12-03 KR KR1020017007206A patent/KR100634073B1/ko not_active Expired - Fee Related
- 1999-12-03 DE DE59914754T patent/DE59914754D1/de not_active Expired - Lifetime
- 1999-12-03 AT AT99962205T patent/ATE394437T1/de active
- 1999-12-03 TR TR2001/01608T patent/TR200101608T2/xx unknown
- 1999-12-04 DE DE19958525A patent/DE19958525A1/de not_active Withdrawn
-
2001
- 2001-05-23 NO NO20012529A patent/NO20012529L/no not_active Application Discontinuation
- 2001-06-08 ZA ZA200104708A patent/ZA200104708B/xx unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5041494A (en) * | 1987-11-03 | 1991-08-20 | Bayer Aktiengesellschaft | Aqueous solutions or dispersions of polyurethanes, a process for their preparation and their use in coating compositions |
| EP0818496A2 (en) * | 1996-07-09 | 1998-01-14 | Dow Corning Corporation | Method for making aqueous emulsions of functionalized organic polymers |
Also Published As
| Publication number | Publication date |
|---|---|
| NO20012529D0 (no) | 2001-05-23 |
| HUP0104835A2 (en) | 2002-06-29 |
| AU1861700A (en) | 2000-07-03 |
| KR100634073B1 (ko) | 2006-10-16 |
| ZA200104708B (en) | 2002-11-27 |
| CN1330667A (zh) | 2002-01-09 |
| BR9916097A (pt) | 2001-09-04 |
| HUP0104835A3 (en) | 2003-07-28 |
| WO2000035981A1 (de) | 2000-06-22 |
| EP1151024B1 (de) | 2008-05-07 |
| ID30437A (id) | 2001-12-06 |
| DE59914754D1 (de) | 2008-06-19 |
| TR200101608T2 (tr) | 2001-10-22 |
| ATE394437T1 (de) | 2008-05-15 |
| RU2241728C2 (ru) | 2004-12-10 |
| NO20012529L (no) | 2001-05-23 |
| HU225361B1 (en) | 2006-10-28 |
| ES2306529T3 (es) | 2008-11-01 |
| US6790903B1 (en) | 2004-09-14 |
| CZ20012081A3 (cs) | 2001-09-12 |
| CA2354532A1 (en) | 2000-06-22 |
| DE19958525A1 (de) | 2000-06-15 |
| JP2002532589A (ja) | 2002-10-02 |
| EP1151024A1 (de) | 2001-11-07 |
| KR20010080736A (ko) | 2001-08-22 |
| PL348046A1 (en) | 2002-05-06 |
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