DE102005023050A1 - Wässrige, lagerstabile Emulsion α-silyl terminierter Polymere, deren Herstellung und Verwendung - Google Patents
Wässrige, lagerstabile Emulsion α-silyl terminierter Polymere, deren Herstellung und Verwendung Download PDFInfo
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- DE102005023050A1 DE102005023050A1 DE102005023050A DE102005023050A DE102005023050A1 DE 102005023050 A1 DE102005023050 A1 DE 102005023050A1 DE 102005023050 A DE102005023050 A DE 102005023050A DE 102005023050 A DE102005023050 A DE 102005023050A DE 102005023050 A1 DE102005023050 A1 DE 102005023050A1
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- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
- DGAODIKUWGRDBO-UHFFFAOYSA-N butanethioic s-acid Chemical class CCCC(O)=S DGAODIKUWGRDBO-UHFFFAOYSA-N 0.000 description 1
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- 125000004181 carboxyalkyl group Chemical group 0.000 description 1
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- 238000004132 cross linking Methods 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
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- 235000019439 ethyl acetate Nutrition 0.000 description 1
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- 235000013312 flour Nutrition 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- VGWSECAZSRHNCT-UHFFFAOYSA-N hexadecyl octadecyl sulfate Chemical compound CCCCCCCCCCCCCCCCCCOS(=O)(=O)OCCCCCCCCCCCCCCCC VGWSECAZSRHNCT-UHFFFAOYSA-N 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 125000003010 ionic group Chemical group 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- BNQFLOSSLHYGLQ-UHFFFAOYSA-N n-[[dimethoxy(methyl)silyl]methyl]aniline Chemical compound CO[Si](C)(OC)CNC1=CC=CC=C1 BNQFLOSSLHYGLQ-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 229920002113 octoxynol Polymers 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
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
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- 239000003960 organic solvent Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 150000002972 pentoses Chemical group 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 229940031826 phenolate Drugs 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 239000007981 phosphate-citrate buffer Substances 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940057847 polyethylene glycol 600 Drugs 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
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- 150000003077 polyols Chemical class 0.000 description 1
- 229920003009 polyurethane dispersion Polymers 0.000 description 1
- 229920006316 polyvinylpyrrolidine Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
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- 150000003151 propanoic acid esters Chemical class 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
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- 150000003330 sebacic acids Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940100515 sorbitan Drugs 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
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- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-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
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
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- 239000004711 α-olefin 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
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4018—Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
-
- 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
- C08G18/285—Nitrogen containing compounds
- C08G18/2865—Compounds having only one primary or secondary amino group; Ammonia
-
- 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
- C08G18/28—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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
-
- 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
- C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
-
- 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
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Paints Or Removers (AREA)
- Sealing Material Composition (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005023050A DE102005023050A1 (de) | 2005-05-13 | 2005-05-13 | Wässrige, lagerstabile Emulsion α-silyl terminierter Polymere, deren Herstellung und Verwendung |
| PL06742857T PL1879936T3 (pl) | 2005-05-13 | 2006-05-10 | Wodne, stabilne podczas przechowywania emulsje polimerów zakończonych alfa-sililem, ich wytwarzanie i zastosowanie |
| CN2006800162635A CN101175784B (zh) | 2005-05-13 | 2006-05-10 | 贮存稳定的α-甲硅烷基封端的聚合物的水性乳液、所述乳液的制备及其用途 |
| CA002608210A CA2608210A1 (en) | 2005-05-13 | 2006-05-10 | Aqueous emulsion of .alpha.-silyl terminated polymers that is stable in storage, production of said emulsion and use of the latter |
| MX2007014033A MX2007014033A (es) | 2005-05-13 | 2006-05-10 | Emulsion acuosa de polimeros terminados en a-sililo, que es estable en almacenamiento, la produccion de la emulsion y el uso de esta ultima. |
| EP06742857.3A EP1879936B1 (de) | 2005-05-13 | 2006-05-10 | Wässrige, lagerstabile emulsion alpha-silyl terminierter polymere, deren herstellung und verwendung |
| BRPI0611444-0A BRPI0611444A2 (pt) | 2005-05-13 | 2006-05-10 | emulsão aquosa de polìmeros estável ao armazenamento, processo para a sua preparação e uso da mesma, polìmero terminado em alfa-silano, derivados de polioxialquileno terminados em alfa-silila, uso dos mesmos e colas, massas de vedação, composições de revestimento de superfìcies, ou massas moldadas poliméricas |
| PCT/EP2006/004372 WO2006122684A2 (de) | 2005-05-13 | 2006-05-10 | WÄSSRIGE, LAGERSTABILE EMULSION α-SILYL TERMINIERTER POLYMERE, DEREN HERSTELLUNG UND VERWENDUNG |
| JP2008510490A JP5117378B2 (ja) | 2005-05-13 | 2006-05-10 | 貯蔵安定性であるα−シリル末端ポリマーの水性エマルジョン、該エマルジョンの製造および該エマルジョンの使用 |
| US11/938,867 US7977445B2 (en) | 2005-05-13 | 2007-11-13 | Storage-stable aqueous emulsions of α-silyl terminated polymers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005023050A DE102005023050A1 (de) | 2005-05-13 | 2005-05-13 | Wässrige, lagerstabile Emulsion α-silyl terminierter Polymere, deren Herstellung und Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102005023050A1 true DE102005023050A1 (de) | 2006-11-16 |
Family
ID=36788851
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102005023050A Ceased DE102005023050A1 (de) | 2005-05-13 | 2005-05-13 | Wässrige, lagerstabile Emulsion α-silyl terminierter Polymere, deren Herstellung und Verwendung |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7977445B2 (https=) |
| EP (1) | EP1879936B1 (https=) |
| JP (1) | JP5117378B2 (https=) |
| CN (1) | CN101175784B (https=) |
| BR (1) | BRPI0611444A2 (https=) |
| CA (1) | CA2608210A1 (https=) |
| DE (1) | DE102005023050A1 (https=) |
| MX (1) | MX2007014033A (https=) |
| PL (1) | PL1879936T3 (https=) |
| WO (1) | WO2006122684A2 (https=) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011161011A1 (en) * | 2010-06-21 | 2011-12-29 | Huntsman International Llc | Alkoxysilane functionalized isocyanate based materials |
| WO2013045406A1 (de) * | 2011-09-29 | 2013-04-04 | Bayer Intellectual Property Gmbh | Schnellhärtende alkoxysilan-sprühschäume |
| CN119751894A (zh) * | 2024-12-17 | 2025-04-04 | 广州白云科技股份有限公司 | 硅烷改性聚醚-聚丁二烯、透明耐水解的硅烷改性聚醚密封胶及其制备方法 |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| DE102007000833A1 (de) | 2007-10-08 | 2009-04-09 | Wacker Chemie Ag | Silan-substituierte RAFT-Reagenzien und Silan-vernetzbare Polymere |
| KR20110036730A (ko) * | 2008-07-28 | 2011-04-08 | 아사히 가라스 가부시키가이샤 | 점착체, 점착 시트 및 그 용도 |
| JP2012500144A (ja) * | 2008-08-20 | 2012-01-05 | ヘンケル コーポレイション | モールドシーラーの調製方法、モールドシーラーアッセンブリおよびその組成物 |
| FR2940312B1 (fr) * | 2008-12-18 | 2011-02-25 | Bostik Sa | Composition adhesive pelable apres reticulation |
| WO2010110107A1 (ja) * | 2009-03-23 | 2010-09-30 | セメダイン株式会社 | 硬化性組成物 |
| DE102009022630A1 (de) | 2009-05-25 | 2010-12-02 | Evonik Goldschmidt Gmbh | Emulsionen auf Basis Silylgruppen tragender Hydroxylverbindungen |
| US8709489B2 (en) * | 2009-09-30 | 2014-04-29 | Surmodics, Inc. | Emulsions containing arylboronic acids and medical articles made therefrom |
| CN104822774A (zh) * | 2012-10-24 | 2015-08-05 | 墨尼克医疗用品有限公司 | 用于制备基于烷氧基硅烷的喷涂泡沫的多组分体系 |
| CN103406068B (zh) * | 2013-08-21 | 2015-01-07 | 齐齐哈尔大学 | 一种含酰胺键有机硅双子表面活性剂及其制备方法 |
| CN104861175B (zh) * | 2014-02-20 | 2019-03-19 | 瓦克化学（中国）有限公司 | 一种改性树脂水性分散液 |
| JP5904313B1 (ja) * | 2014-09-12 | 2016-04-13 | Dic株式会社 | 湿気硬化型ウレタン組成物及び被覆材 |
| US10030122B2 (en) | 2015-02-09 | 2018-07-24 | Wacker Chemical Corporation | Curable compositions |
| DE102015202278A1 (de) | 2015-02-09 | 2016-08-11 | Wacker Chemie Ag | Wässrige Dispersionen von Organosiliciumverbindungen |
| US9856173B2 (en) | 2015-02-09 | 2018-01-02 | Wacker Chemical Corporation | One component ready-to-use tile grout |
| US9328259B1 (en) * | 2015-02-09 | 2016-05-03 | Wacker Chemical Corporation | Elastomeric silicone emulsion for coating applications |
| US11236217B2 (en) | 2017-04-03 | 2022-02-01 | Continental Reifen Deutschland Gmbh | Modified resins and uses thereof |
| EP3609936B1 (en) | 2017-04-10 | 2023-10-11 | Continental Reifen Deutschland GmbH | Functionalized resin having a polar linker |
| ES2968401T3 (es) * | 2017-04-10 | 2024-05-09 | Synthomer Adhesive Tech Llc | Resina funcionalizada que tiene un ligador polar |
| ES2971873T3 (es) | 2017-04-10 | 2024-06-10 | Continental Reifen Deutschland Gmbh | Resina funcionalizada que tiene un conector polar |
| US10815320B2 (en) | 2017-04-10 | 2020-10-27 | Eastman Chemical Company | Functionalized resin having a polar linker |
| JP2018203892A (ja) * | 2017-06-06 | 2018-12-27 | 信越化学工業株式会社 | オルガノシリコーンエマルジョン組成物 |
| EP3533854B1 (en) | 2018-03-01 | 2022-05-04 | Momentive Performance Materials Inc. | Method of inhibiting water penetration into oil- and gas- producing formations |
| JP7429784B2 (ja) * | 2019-12-11 | 2024-02-08 | ワッカー ケミー アクチエンゲゼルシャフト | 塗装用途のためのシラン末端化ポリエーテルエマルジョン |
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| JPS596219A (ja) * | 1982-07-01 | 1984-01-13 | Kanegafuchi Chem Ind Co Ltd | 反応性エマルジヨン |
| DE3737245A1 (de) * | 1987-11-03 | 1989-05-18 | Bayer Ag | Waessrige loesungen oder dispersionen von polyurethanen, ein verfahren zu ihrer herstellung und ihre verwendung als beschichtungsmittel oder zur herstellung von beschichtungsmitteln |
| JPH01318066A (ja) * | 1988-06-16 | 1989-12-22 | Toshiba Silicone Co Ltd | ポリエーテル水性エマルジョン組成物 |
| DE3939566A1 (de) * | 1989-11-30 | 1991-06-06 | Henkel Kgaa | Steinschutzmittel, enthaltend alkoxysilangruppenterminierte polyurethane |
| DE4019171A1 (de) * | 1990-06-15 | 1991-12-19 | Henkel Kgaa | Beschichtungsmittel |
| DE4029505A1 (de) * | 1990-09-18 | 1992-03-19 | Henkel Kgaa | Feuchtigkeitshaertende, alkoxysilanterminierte polyurethane |
| US5118752A (en) * | 1991-10-15 | 1992-06-02 | Ppg Industries, Inc. | Vinyl polymer latex systems |
| DE4215648C2 (de) * | 1992-05-13 | 1994-12-15 | Henkel Kgaa | Verwendung einer wäßrigen Dispersion oder Lösung eines Polyurethans |
| DE4242687B8 (de) * | 1992-12-17 | 2006-01-12 | Henkel Kgaa | Hydrophile Polyurethane |
| US5919860A (en) * | 1997-12-17 | 1999-07-06 | Bayer Corporation | Aqueous polyurethane/urea dispersions containing alkoxysilane groups |
| ATE394437T1 (de) * | 1998-12-11 | 2008-05-15 | Henkel Kgaa | Verwendung von dispersionen silylterminierter polymerer als dichtmassen |
| JP2002138251A (ja) * | 2000-11-01 | 2002-05-14 | Asahi Glass Co Ltd | 水性塗料用組成物 |
| ES2292747T5 (es) * | 2001-02-23 | 2014-04-10 | Henkel Ag & Co. Kgaa | Polímeros alcoxisililfuncionales mixtos |
| DE10237271A1 (de) * | 2002-08-14 | 2004-03-04 | Consortium für elektrochemische Industrie GmbH | Polymermassen auf Basis alkoxysilanterminierter Polymere mit regulierbarer Härtungsgeschwindigkeit |
-
2005
- 2005-05-13 DE DE102005023050A patent/DE102005023050A1/de not_active Ceased
-
2006
- 2006-05-10 EP EP06742857.3A patent/EP1879936B1/de not_active Not-in-force
- 2006-05-10 JP JP2008510490A patent/JP5117378B2/ja not_active Expired - Fee Related
- 2006-05-10 CN CN2006800162635A patent/CN101175784B/zh not_active Expired - Fee Related
- 2006-05-10 CA CA002608210A patent/CA2608210A1/en not_active Abandoned
- 2006-05-10 BR BRPI0611444-0A patent/BRPI0611444A2/pt not_active IP Right Cessation
- 2006-05-10 MX MX2007014033A patent/MX2007014033A/es active IP Right Grant
- 2006-05-10 PL PL06742857T patent/PL1879936T3/pl unknown
- 2006-05-10 WO PCT/EP2006/004372 patent/WO2006122684A2/de not_active Ceased
-
2007
- 2007-11-13 US US11/938,867 patent/US7977445B2/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011161011A1 (en) * | 2010-06-21 | 2011-12-29 | Huntsman International Llc | Alkoxysilane functionalized isocyanate based materials |
| WO2013045406A1 (de) * | 2011-09-29 | 2013-04-04 | Bayer Intellectual Property Gmbh | Schnellhärtende alkoxysilan-sprühschäume |
| US9579412B2 (en) | 2011-09-29 | 2017-02-28 | Covestro Deutschland Ag | Fast-curing alkoxysilane spray foams |
| CN119751894A (zh) * | 2024-12-17 | 2025-04-04 | 广州白云科技股份有限公司 | 硅烷改性聚醚-聚丁二烯、透明耐水解的硅烷改性聚醚密封胶及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006122684A2 (de) | 2006-11-23 |
| JP5117378B2 (ja) | 2013-01-16 |
| WO2006122684A3 (de) | 2007-03-15 |
| EP1879936B1 (de) | 2018-01-10 |
| EP1879936A2 (de) | 2008-01-23 |
| CN101175784A (zh) | 2008-05-07 |
| US7977445B2 (en) | 2011-07-12 |
| BRPI0611444A2 (pt) | 2010-09-08 |
| US20080125541A1 (en) | 2008-05-29 |
| JP2008540747A (ja) | 2008-11-20 |
| CA2608210A1 (en) | 2006-11-23 |
| CN101175784B (zh) | 2011-03-09 |
| PL1879936T3 (pl) | 2018-06-29 |
| MX2007014033A (es) | 2008-04-29 |
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Owner name: HENKEL AG & CO. KGAA, 40589 DUESSELDORF, DE |
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