JP2007525559A5 - - Google Patents
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- Publication number
- JP2007525559A5 JP2007525559A5 JP2006520219A JP2006520219A JP2007525559A5 JP 2007525559 A5 JP2007525559 A5 JP 2007525559A5 JP 2006520219 A JP2006520219 A JP 2006520219A JP 2006520219 A JP2006520219 A JP 2006520219A JP 2007525559 A5 JP2007525559 A5 JP 2007525559A5
- Authority
- JP
- Japan
- Prior art keywords
- sio
- amino
- silicone resin
- functional silicone
- iii
- 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.)
- Granted
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- 229920002050 silicone resin Polymers 0.000 claims description 71
- 239000000203 mixture Substances 0.000 claims description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 24
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 18
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 15
- 239000000839 emulsion Substances 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 229910004283 SiO 4 Inorganic materials 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 6
- 101150065749 Churc1 gene Proteins 0.000 claims description 6
- 102100038239 Protein Churchill Human genes 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000000243 solution Substances 0.000 claims description 4
- 239000011550 stock solution Substances 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 239000011246 composite particle Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 2
- 239000003974 emollient agent Substances 0.000 claims 2
- 239000003755 preservative agent Substances 0.000 claims 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 claims 1
- 101100167062 Caenorhabditis elegans chch-3 gene Proteins 0.000 claims 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims 1
- 235000004866 D-panthenol Nutrition 0.000 claims 1
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 claims 1
- 239000011703 D-panthenol Substances 0.000 claims 1
- 239000004909 Moisturizer Substances 0.000 claims 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 claims 1
- 229930003268 Vitamin C Natural products 0.000 claims 1
- 229930003427 Vitamin E Natural products 0.000 claims 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims 1
- 150000003862 amino acid derivatives Chemical class 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 239000003093 cationic surfactant Substances 0.000 claims 1
- 229940106189 ceramide Drugs 0.000 claims 1
- 150000001783 ceramides Chemical class 0.000 claims 1
- 230000003750 conditioning effect Effects 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000002502 liposome Substances 0.000 claims 1
- 230000001333 moisturizer Effects 0.000 claims 1
- 239000002304 perfume Substances 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 229920005862 polyol Polymers 0.000 claims 1
- 150000003077 polyols Chemical class 0.000 claims 1
- 239000000565 sealant Substances 0.000 claims 1
- 239000000516 sunscreening agent Substances 0.000 claims 1
- 229930003231 vitamin Natural products 0.000 claims 1
- 239000011782 vitamin Substances 0.000 claims 1
- 235000013343 vitamin Nutrition 0.000 claims 1
- 229940088594 vitamin Drugs 0.000 claims 1
- 235000019155 vitamin A Nutrition 0.000 claims 1
- 239000011719 vitamin A Substances 0.000 claims 1
- 235000019154 vitamin C Nutrition 0.000 claims 1
- 239000011718 vitamin C Substances 0.000 claims 1
- 235000019165 vitamin E Nutrition 0.000 claims 1
- 229940046009 vitamin E Drugs 0.000 claims 1
- 239000011709 vitamin E Substances 0.000 claims 1
- 229940045997 vitamin a Drugs 0.000 claims 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 18
- 239000002904 solvent Substances 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000008367 deionised water Substances 0.000 description 9
- 229910021641 deionized water Inorganic materials 0.000 description 9
- -1 polysiloxane Polymers 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 7
- 239000006227 byproduct Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000008096 xylene Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 4
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 4
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- GOCRPOKWZIVUQG-UHFFFAOYSA-N 3-(diethoxymethylsilyl)propan-1-amine Chemical compound CCOC(OCC)[SiH2]CCCN GOCRPOKWZIVUQG-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 238000010533 azeotropic distillation Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 229940120503 dihydroxyacetone Drugs 0.000 description 2
- CVQVSVBUMVSJES-UHFFFAOYSA-N dimethoxy-methyl-phenylsilane Chemical compound CO[Si](C)(OC)C1=CC=CC=C1 CVQVSVBUMVSJES-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- RSIHJDGMBDPTIM-UHFFFAOYSA-N ethoxy(trimethyl)silane Chemical compound CCO[Si](C)(C)C RSIHJDGMBDPTIM-UHFFFAOYSA-N 0.000 description 2
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 2
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 2
- MWRSABPHNREIIX-UHFFFAOYSA-N 9,9-dimethyldecan-1-ol Chemical class CC(C)(C)CCCCCCCCO MWRSABPHNREIIX-UHFFFAOYSA-N 0.000 description 1
- IMYZQPCYWPFTAG-UHFFFAOYSA-N Mecamylamine Chemical compound C1CC2C(C)(C)C(NC)(C)C1C2 IMYZQPCYWPFTAG-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- NINOVVRCHXVOKB-UHFFFAOYSA-N dialuminum;dioxido(dioxo)chromium Chemical compound [Al+3].[Al+3].[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O NINOVVRCHXVOKB-UHFFFAOYSA-N 0.000 description 1
- JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48769803P | 2003-07-16 | 2003-07-16 | |
| US60/487,698 | 2003-07-16 | ||
| PCT/US2004/021777 WO2005010076A2 (en) | 2003-07-16 | 2004-07-07 | Aminofunctional silicone resins and emulsions containing them |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007525559A JP2007525559A (ja) | 2007-09-06 |
| JP2007525559A5 true JP2007525559A5 (https=) | 2011-05-19 |
| JP4939215B2 JP4939215B2 (ja) | 2012-05-23 |
Family
ID=34102714
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006520219A Expired - Fee Related JP4939215B2 (ja) | 2003-07-16 | 2004-07-07 | アミノ官能性シリコーン樹脂とそれらを含むエマルジョン |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7501473B2 (https=) |
| EP (1) | EP1651703B1 (https=) |
| JP (1) | JP4939215B2 (https=) |
| CN (1) | CN100404589C (https=) |
| AT (1) | ATE371692T1 (https=) |
| DE (1) | DE602004008646T2 (https=) |
| WO (1) | WO2005010076A2 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004014217A1 (de) * | 2004-03-23 | 2005-10-13 | Wacker-Chemie Gmbh | Vernetzbare Massen auf der Basis von Organosiliciumverbindungen |
| US7705090B2 (en) * | 2004-08-20 | 2010-04-27 | Chevron Oronite Company Llc | Method for preparing polyolefins containing a high percentage of exo-olefin chain ends |
| CN101611098B (zh) * | 2006-12-20 | 2011-10-26 | 陶氏康宁公司 | 封端的异氰酸酯有机硅树脂 |
| CN101631813A (zh) | 2007-01-12 | 2010-01-20 | 陶氏康宁公司 | 含硅氧烷的组合物 |
| DE102009019329A1 (de) * | 2009-04-30 | 2010-11-18 | Ewald Dörken Ag | Bindemittel für die Beschichtung leitfähiger Oberflächen |
| WO2010127116A1 (en) * | 2009-04-30 | 2010-11-04 | Dow Global Technologies Inc. | Reactive inorganic clusters |
| EP2431421B1 (en) * | 2010-09-20 | 2013-11-06 | Wacker Chemie AG | Aqueous mixtures comprising aminoalkyl-containing polyorganosiloxanes and silicone resins |
| CN102040842B (zh) * | 2010-10-28 | 2012-12-26 | 华南理工大学 | 自催化交联型有机硅-环氧复合材料及其制备方法 |
| WO2013082112A1 (en) | 2011-11-29 | 2013-06-06 | Dow Corning Corporation | Aminofunctional silicone emulsions |
| US8987180B2 (en) | 2012-12-18 | 2015-03-24 | Kimberly-Clark Worldwide, Inc. | Wet wipes including silicone reactive amino containing dimethicone copolyols |
| CN103333339B (zh) * | 2013-06-04 | 2016-08-10 | 黄山市强力化工有限公司 | 一种羟基封端苯基氨基聚醚改性硅油 |
| CN109071820B (zh) * | 2016-05-10 | 2021-08-17 | 美国陶氏有机硅公司 | 具有氨基官能封端基团的有机硅嵌段共聚物及其制备和使用方法 |
| EP3580277B1 (en) * | 2017-05-27 | 2021-02-17 | Wacker Chemie AG | Oil-in-water microemulsions and the preparation thereof |
| CN108342085A (zh) * | 2018-03-21 | 2018-07-31 | 东莞市正安有机硅科技有限公司 | 一种耐高温的硅混炼胶及其制备方法 |
| KR102756395B1 (ko) | 2018-07-19 | 2025-01-16 | 다우 글로벌 테크놀로지스 엘엘씨 | 내후성 및 내구성 코팅 조성물 |
| US11932775B2 (en) | 2018-07-19 | 2024-03-19 | Dow Global Technologies Llc | Weatherable and durable coating compositions |
| EP4139379A4 (en) * | 2020-04-21 | 2024-08-28 | Energizer Auto, Inc. | WATER-BASED SILICONE COMBINATION SURFACE MODIFICATION COMPOSITIONS AND METHODS OF USE THEREOF |
| WO2025254798A1 (en) | 2024-06-04 | 2025-12-11 | Dow Global Technologies Llc | Aldehyde – amine curable polyorganosiloxane composition and methods for the preparation and use thereof |
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| JPS52147657A (en) | 1976-06-02 | 1977-12-08 | Toray Silicone Co Ltd | Curable organopolysiloxane compositions |
| US4125510A (en) | 1977-03-01 | 1978-11-14 | Dow Corning Corporation | Method of improving crack resistance of siloxane molding compositions |
| DE2730744A1 (de) | 1977-07-07 | 1979-05-03 | Bayer Ag | Mit polyurethan modifizierte organopolysiloxan-massen |
| US4234697A (en) | 1979-01-18 | 1980-11-18 | Dow Corning Corporation | Method of preparing cross-linked polydiorganosiloxane using organic isocyanates and products prepared therefrom |
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| EP0620242B1 (en) | 1993-04-15 | 1998-08-19 | Dow Corning Toray Silicone Company, Limited | Epoxy group-containing silicone resin and compositions based thereon |
| US5804616A (en) | 1993-05-19 | 1998-09-08 | Ameron International Corporation | Epoxy-polysiloxane polymer composition |
| JP3095330B2 (ja) | 1993-11-10 | 2000-10-03 | 信越化学工業株式会社 | 皮膜形成組成物 |
| JP3147677B2 (ja) | 1994-09-30 | 2001-03-19 | 株式会社村田製作所 | 液状エポキシ樹脂組成物 |
| DE19680435T1 (de) | 1995-05-09 | 1997-06-05 | Dainippon Ink & Chemicals | Härtbare Harzzusammensetzung |
| DE19638125A1 (de) | 1996-09-18 | 1998-03-19 | Wacker Chemie Gmbh | Aminogruppen aufweisende Organosiliciumverbindungen, deren Herstellung und Verwendung |
| JP4420548B2 (ja) * | 2000-09-28 | 2010-02-24 | 旭化成ケミカルズ株式会社 | ポリフェニレンエーテル系樹脂組成物 |
| WO2005010115A1 (en) * | 2003-07-16 | 2005-02-03 | Dow Corning Corporation | Coating compositions comprising epoxy resins and aminofunctional silicone resins |
| CN100572420C (zh) * | 2003-07-16 | 2009-12-23 | 陶氏康宁公司 | 含有氨基官能的有机硅树脂的涂料组合物 |
-
2004
- 2004-07-07 EP EP04756739A patent/EP1651703B1/en not_active Expired - Lifetime
- 2004-07-07 JP JP2006520219A patent/JP4939215B2/ja not_active Expired - Fee Related
- 2004-07-07 AT AT04756739T patent/ATE371692T1/de not_active IP Right Cessation
- 2004-07-07 WO PCT/US2004/021777 patent/WO2005010076A2/en not_active Ceased
- 2004-07-07 CN CNB2004800203481A patent/CN100404589C/zh not_active Expired - Fee Related
- 2004-07-07 DE DE602004008646T patent/DE602004008646T2/de not_active Expired - Lifetime
- 2004-07-07 US US10/564,610 patent/US7501473B2/en not_active Expired - Lifetime
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