CN102712751B - 具有改进的调整时间的湿固化配制品 - Google Patents
具有改进的调整时间的湿固化配制品 Download PDFInfo
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- CN102712751B CN102712751B CN201080048656.0A CN201080048656A CN102712751B CN 102712751 B CN102712751 B CN 102712751B CN 201080048656 A CN201080048656 A CN 201080048656A CN 102712751 B CN102712751 B CN 102712751B
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- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 229960001708 magnesium carbonate Drugs 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N mandelic acid Chemical compound OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
- 229960002510 mandelic acid Drugs 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- BLEJWUIEUACHKH-UHFFFAOYSA-N n-[[benzoyl(methyl)amino]-ethoxy-methylsilyl]-n-methylbenzamide Chemical compound C=1C=CC=CC=1C(=O)N(C)[Si](C)(OCC)N(C)C(=O)C1=CC=CC=C1 BLEJWUIEUACHKH-UHFFFAOYSA-N 0.000 description 1
- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
- NCCHARWOCKOHIH-UHFFFAOYSA-N n-methylbenzamide Chemical compound CNC(=O)C1=CC=CC=C1 NCCHARWOCKOHIH-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 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
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 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
- 239000012766 organic filler Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- HXTSPGYEPSIZKP-UHFFFAOYSA-N phenol;tin Chemical compound [Sn].OC1=CC=CC=C1 HXTSPGYEPSIZKP-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical group [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 description 1
- 239000001327 prunus amygdalus amara l. extract Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000790 scattering method Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 229950006389 thiodiglycol Drugs 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical compound [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- HXOGQBSDPSMHJK-UHFFFAOYSA-N triethoxy(6-methylheptyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCCCC(C)C HXOGQBSDPSMHJK-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229940089401 xylon Drugs 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide 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
- 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
- C08G65/04—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 only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/08—Saturated oxiranes
-
- 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
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
- C08F230/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
- C08F230/08—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
- C08F230/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
- C08F230/08—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
- C08F230/085—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon the monomer being a polymerisable silane, e.g. (meth)acryloyloxy trialkoxy silanes or vinyl trialkoxysilanes
-
- 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
- C09J171/00—Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
- C09J171/02—Polyalkylene oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Paints Or Removers (AREA)
- Polyethers (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009046268A DE102009046268A1 (de) | 2009-10-30 | 2009-10-30 | Zeitmodifizierte feuchtigkeitsaushärtende Formulierungen |
| DE102009046268.6 | 2009-10-30 | ||
| DE201010000705 DE102010000705A1 (de) | 2010-01-06 | 2010-01-06 | Zeitmodifiziert feuchtigkeitshärtende Formulierungen |
| DE102010000705.6 | 2010-01-06 | ||
| PCT/EP2010/066349 WO2011051385A2 (de) | 2009-10-30 | 2010-10-28 | Zeitmodifiziert feuchtigkeitsaushärtende formulierungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102712751A CN102712751A (zh) | 2012-10-03 |
| CN102712751B true CN102712751B (zh) | 2015-06-10 |
Family
ID=43737254
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201080048656.0A Expired - Fee Related CN102712751B (zh) | 2009-10-30 | 2010-10-28 | 具有改进的调整时间的湿固化配制品 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8592517B2 (enExample) |
| EP (1) | EP2493956B1 (enExample) |
| JP (1) | JP5684820B2 (enExample) |
| KR (1) | KR101768239B1 (enExample) |
| CN (1) | CN102712751B (enExample) |
| BR (1) | BR112012009910A2 (enExample) |
| ES (1) | ES2671187T3 (enExample) |
| PL (1) | PL2493956T3 (enExample) |
| PT (1) | PT2493956T (enExample) |
| WO (1) | WO2011051385A2 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010000881A1 (de) * | 2010-01-14 | 2011-07-21 | Henkel AG & Co. KGaA, 40589 | 1K- Kaschierklebstoff mit Silanvernetzung |
| DE102015204787A1 (de) * | 2015-03-17 | 2016-09-22 | Henkel Ag & Co. Kgaa | Härtbare Silikonzusammensetzungen |
| JP2016197560A (ja) * | 2015-04-06 | 2016-11-24 | 矢崎総業株式会社 | 自動車用電線及びそれを用いたワイヤーハーネス |
| DE102017219755A1 (de) * | 2017-11-07 | 2019-05-09 | Bona Gmbh Deutschland | Verwendung von Additiven zur Erhöhung der Zugscherfestigkeit und Zusammensetzung enthaltend ein silanfunktionalisiertes Präpolymer und Additive |
| CA3113952C (en) | 2018-09-24 | 2023-09-19 | Building Materials Investment Corporation | Roofing membranes with improved adhesive bonding strength |
| EP3763795A1 (de) | 2019-07-08 | 2021-01-13 | tesa SE | Feuchtigkeitsvernetzbare, dimensionsstabile polymermasse |
| US11339260B2 (en) | 2019-08-01 | 2022-05-24 | Covestro Llc | Pultrusion processes for producing fiber reinforced polyurethane compositions and polyurethane-forming reaction mixtures suitable for use in such processes |
| CN110591608B (zh) * | 2019-09-26 | 2021-04-23 | 厦门玻彩新材料有限公司 | 一种热固化量子点胶水、量子点膜及其制备方法 |
| CN112724919A (zh) * | 2020-12-25 | 2021-04-30 | 蚌埠高华电子股份有限公司 | 一种不易脱落的玻璃密封胶及加工工艺 |
| CN114479741B (zh) * | 2022-02-23 | 2023-03-31 | 广州市白云化工实业有限公司 | 一种低温可快速深层固化的单组分有机硅改性密封胶及其制备方法 |
| CN115433534B (zh) * | 2022-09-20 | 2024-02-13 | 江西博泓新材料科技有限公司 | 一种专用于汽车钣金的spu改性聚醚胶 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US3635906A (en) * | 1968-11-12 | 1972-01-18 | Du Pont | Preparation of polyurethanes using organo-tin catalyst and time-lapse modifier |
| US7351782B2 (en) * | 2002-10-02 | 2008-04-01 | Kaneka Corporation | One-part curable composition |
| WO2009103894A1 (fr) * | 2007-12-20 | 2009-08-27 | Bluestar Silicones France | Composition organopolysiloxanique vulcanisable a temperature ambiante en elastomere et nouveaux catalyseurs de polycondensation d'organopolysiloxanes |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2866774A (en) | 1953-09-23 | 1958-12-30 | Univ Notre Dame | Polyether polyurethane rubber |
| US3895149A (en) | 1973-07-05 | 1975-07-15 | Atlantic Richfield Co | Carpet backed with thixotropic polyurethane adhesive |
| DD108103A1 (enExample) | 1973-11-29 | 1974-09-05 | ||
| US4322327A (en) | 1979-10-19 | 1982-03-30 | Mitsubishi Petrochemical Co., Ltd. | Slow-curing water-curable urethane prepolymer composition |
| US4395528A (en) | 1981-03-02 | 1983-07-26 | M&T Chemicals Inc. | Catalyst composition and curable polymer compositions containing same |
| DE3213439A1 (de) | 1982-04-10 | 1983-10-20 | Chemiegesellschaft Gundernhausen mbH, 6101 Roßdorf | Verfahren und vorrichtung zur herstellung von teppichfliesen |
| US4871854A (en) | 1982-06-28 | 1989-10-03 | The United States Of America As Represented By The Secretary Of The Air Force | Cure catalyst for polyurethanes |
| US4611044A (en) | 1985-05-28 | 1986-09-09 | The Dow Chemical Company | Polyurethane carpet backing catalyzed with organoiron and organobismuth catalysts |
| JPH051225A (ja) | 1991-06-25 | 1993-01-08 | Kanegafuchi Chem Ind Co Ltd | 硬化性組成物 |
| EP0549210A3 (en) | 1991-12-24 | 1994-07-13 | Neste Oy | Crosslinkable polymeric conposition |
| US6001900A (en) | 1993-07-28 | 1999-12-14 | Elf Atochem North America, Inc. | Metal containing e-coat catalysts optionally with tin catalysts |
| US5474827A (en) | 1994-03-23 | 1995-12-12 | Minnesota Mining And Manufacturing Company | Retroreflective article and method of making the same |
| AU6801298A (en) | 1997-06-05 | 1998-12-10 | Rohm And Haas Company | Coating compositions having extended pot life and shortened cure time and combination of chemicals used therein |
| JP3903550B2 (ja) * | 1997-10-23 | 2007-04-11 | 旭硝子株式会社 | 室温硬化性組成物 |
| EP1146062B1 (en) * | 2000-04-12 | 2006-12-20 | Kaneka Corporation | Method of producing crosslinkable silyl group-containing polyoxyalkylene polymers |
| WO2001090224A1 (fr) * | 2000-05-24 | 2001-11-29 | Kaneka Corporation | Compositions durcissables et agent de compatibilite |
| US6579924B2 (en) * | 2000-12-12 | 2003-06-17 | Chem Link Inc. | Pitch pocket and sealant |
| WO2002098929A1 (en) * | 2001-05-31 | 2002-12-12 | Kaneka Corporation | Process for producing polymer having crosslinkable silyl group and curable composition |
| ATE496097T1 (de) * | 2002-10-02 | 2011-02-15 | Kaneka Corp | Härtbare zusammensetzung |
| EP1408062A1 (de) | 2002-10-08 | 2004-04-14 | Sika Technology AG | Bismutkatalysierte Polyurethanzusammensetzung |
| JP4101632B2 (ja) * | 2002-11-01 | 2008-06-18 | 株式会社カネカ | 硬化性組成物および復元性、クリープ性改善方法 |
| DE102004040386A1 (de) * | 2004-08-19 | 2006-03-02 | Heraeus Kulzer Gmbh | Zusammensetzungen auf Basis silanterminierter Polyether und deren Verwendung |
| DE102004043342A1 (de) | 2004-09-08 | 2006-03-09 | Bayer Materialscience Ag | Blockierte Polyurethan-Prepolymere als Klebstoffe |
| EP2546308B1 (en) * | 2004-11-10 | 2014-07-16 | Kaneka Corporation | Curable composition |
| US7781493B2 (en) * | 2005-06-20 | 2010-08-24 | Dow Global Technologies Inc. | Protective coating for window glass |
| US7834123B2 (en) | 2006-05-19 | 2010-11-16 | Henkel Ag & Co. Kgaa | Two component polyurethane adhesive |
| WO2008062866A1 (en) * | 2006-11-22 | 2008-05-29 | Kaneka Corporation | Curable composition and catalyst composition |
| DE102007039652A1 (de) * | 2006-12-05 | 2008-06-12 | Henkel Kgaa | Mittel zur Behandlung harter Oberflächen |
| US20090145067A1 (en) * | 2007-12-06 | 2009-06-11 | Tatley Ronald D | Composition, method of use, and structural barrier system |
| US8742050B2 (en) | 2008-03-28 | 2014-06-03 | Henkel US IP LLC | Two part hybrid adhesive |
| JP5822916B2 (ja) | 2010-05-17 | 2015-11-25 | ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング | 有機金属触媒用の非移行性ブロッキング剤を用いる、コントロールされた硬化性脂肪族積層用接着剤 |
-
2010
- 2010-10-28 EP EP10771440.4A patent/EP2493956B1/de active Active
- 2010-10-28 PL PL10771440T patent/PL2493956T3/pl unknown
- 2010-10-28 WO PCT/EP2010/066349 patent/WO2011051385A2/de not_active Ceased
- 2010-10-28 PT PT107714404T patent/PT2493956T/pt unknown
- 2010-10-28 BR BR112012009910A patent/BR112012009910A2/pt not_active Application Discontinuation
- 2010-10-28 CN CN201080048656.0A patent/CN102712751B/zh not_active Expired - Fee Related
- 2010-10-28 KR KR1020127010904A patent/KR101768239B1/ko not_active Expired - Fee Related
- 2010-10-28 JP JP2012535826A patent/JP5684820B2/ja not_active Expired - Fee Related
- 2010-10-28 ES ES10771440.4T patent/ES2671187T3/es active Active
-
2012
- 2012-04-30 US US13/460,129 patent/US8592517B2/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3635906A (en) * | 1968-11-12 | 1972-01-18 | Du Pont | Preparation of polyurethanes using organo-tin catalyst and time-lapse modifier |
| US7351782B2 (en) * | 2002-10-02 | 2008-04-01 | Kaneka Corporation | One-part curable composition |
| WO2009103894A1 (fr) * | 2007-12-20 | 2009-08-27 | Bluestar Silicones France | Composition organopolysiloxanique vulcanisable a temperature ambiante en elastomere et nouveaux catalyseurs de polycondensation d'organopolysiloxanes |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5684820B2 (ja) | 2015-03-18 |
| CN102712751A (zh) | 2012-10-03 |
| EP2493956B1 (de) | 2018-04-18 |
| KR101768239B1 (ko) | 2017-08-30 |
| WO2011051385A3 (de) | 2011-07-28 |
| KR20120102045A (ko) | 2012-09-17 |
| PL2493956T3 (pl) | 2018-09-28 |
| JP2013509475A (ja) | 2013-03-14 |
| EP2493956A2 (de) | 2012-09-05 |
| ES2671187T3 (es) | 2018-06-05 |
| BR112012009910A2 (pt) | 2016-03-08 |
| WO2011051385A2 (de) | 2011-05-05 |
| US8592517B2 (en) | 2013-11-26 |
| PT2493956T (pt) | 2018-05-30 |
| US20120277373A1 (en) | 2012-11-01 |
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