JP2015507027A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015507027A5 JP2015507027A5 JP2014542789A JP2014542789A JP2015507027A5 JP 2015507027 A5 JP2015507027 A5 JP 2015507027A5 JP 2014542789 A JP2014542789 A JP 2014542789A JP 2014542789 A JP2014542789 A JP 2014542789A JP 2015507027 A5 JP2015507027 A5 JP 2015507027A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkoxysilane
- formula
- independently
- composition according
- 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
Links
- 239000000203 mixture Substances 0.000 claims 55
- 238000004519 manufacturing process Methods 0.000 claims 30
- 150000001336 alkenes Chemical group 0.000 claims 22
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 17
- -1 ethylhexenyl group Chemical group 0.000 claims 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 16
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 15
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 14
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 claims 11
- 125000004432 carbon atom Chemical group C* 0.000 claims 9
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 9
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 claims 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 8
- 239000003054 catalyst Substances 0.000 claims 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 7
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 7
- 230000004048 modification Effects 0.000 claims 7
- 238000012986 modification Methods 0.000 claims 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 7
- 125000002947 alkylene group Chemical group 0.000 claims 6
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 claims 6
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 claims 6
- 239000005977 Ethylene Substances 0.000 claims 5
- 238000009833 condensation Methods 0.000 claims 5
- 230000005494 condensation Effects 0.000 claims 5
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 5
- 239000002904 solvent Substances 0.000 claims 5
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 claims 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 5
- 238000005903 acid hydrolysis reaction Methods 0.000 claims 4
- XGZGKDQVCBHSGI-UHFFFAOYSA-N butyl(triethoxy)silane Chemical compound CCCC[Si](OCC)(OCC)OCC XGZGKDQVCBHSGI-UHFFFAOYSA-N 0.000 claims 4
- SXPLZNMUBFBFIA-UHFFFAOYSA-N butyl(trimethoxy)silane Chemical compound CCCC[Si](OC)(OC)OC SXPLZNMUBFBFIA-UHFFFAOYSA-N 0.000 claims 4
- 239000011248 coating agent Substances 0.000 claims 4
- 238000000576 coating method Methods 0.000 claims 4
- 125000003678 cyclohexadienyl group Chemical group C1(=CC=CCC1)* 0.000 claims 4
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims 4
- 125000000524 functional group Chemical group 0.000 claims 4
- 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 claims 4
- MSRJTTSHWYDFIU-UHFFFAOYSA-N octyltriethoxysilane Chemical compound CCCCCCCC[Si](OCC)(OCC)OCC MSRJTTSHWYDFIU-UHFFFAOYSA-N 0.000 claims 4
- 229920000642 polymer Polymers 0.000 claims 4
- WUMSTCDLAYQDNO-UHFFFAOYSA-N triethoxy(hexyl)silane Chemical compound CCCCCC[Si](OCC)(OCC)OCC WUMSTCDLAYQDNO-UHFFFAOYSA-N 0.000 claims 4
- NMEPHPOFYLLFTK-UHFFFAOYSA-N trimethoxy(octyl)silane Chemical compound CCCCCCCC[Si](OC)(OC)OC NMEPHPOFYLLFTK-UHFFFAOYSA-N 0.000 claims 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 239000003377 acid catalyst Substances 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 239000000945 filler Substances 0.000 claims 3
- CZWLNMOIEMTDJY-UHFFFAOYSA-N hexyl(trimethoxy)silane Chemical compound CCCCCC[Si](OC)(OC)OC CZWLNMOIEMTDJY-UHFFFAOYSA-N 0.000 claims 3
- 230000007062 hydrolysis Effects 0.000 claims 3
- 238000006460 hydrolysis reaction Methods 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 claims 3
- 125000000913 palmityl 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])C([H])([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 claims 3
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 claims 3
- 125000005916 2-methylpentyl group Chemical group 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 125000005917 3-methylpentyl group Chemical group 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- 241000233855 Orchidaceae Species 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive effect Effects 0.000 claims 2
- RMCOJEZDSRZFOF-UHFFFAOYSA-N but-1-enyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=CCC RMCOJEZDSRZFOF-UHFFFAOYSA-N 0.000 claims 2
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- BAAAEEDPKUHLID-UHFFFAOYSA-N decyl(triethoxy)silane Chemical compound CCCCCCCCCC[Si](OCC)(OCC)OCC BAAAEEDPKUHLID-UHFFFAOYSA-N 0.000 claims 2
- KQAHMVLQCSALSX-UHFFFAOYSA-N decyl(trimethoxy)silane Chemical compound CCCCCCCCCC[Si](OC)(OC)OC KQAHMVLQCSALSX-UHFFFAOYSA-N 0.000 claims 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- YGUFXEJWPRRAEK-UHFFFAOYSA-N dodecyl(triethoxy)silane Chemical compound CCCCCCCCCCCC[Si](OCC)(OCC)OCC YGUFXEJWPRRAEK-UHFFFAOYSA-N 0.000 claims 2
- SCPWMSBAGXEGPW-UHFFFAOYSA-N dodecyl(trimethoxy)silane Chemical compound CCCCCCCCCCCC[Si](OC)(OC)OC SCPWMSBAGXEGPW-UHFFFAOYSA-N 0.000 claims 2
- 239000008151 electrolyte solution Substances 0.000 claims 2
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 claims 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000006038 hexenyl group Chemical group 0.000 claims 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 2
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 claims 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000005244 neohexyl group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000001400 nonyl 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])C([H])([H])[H] 0.000 claims 2
- 229960003493 octyltriethoxysilane Drugs 0.000 claims 2
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 claims 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims 2
- 239000011347 resin Substances 0.000 claims 2
- 229920005989 resin Polymers 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 claims 2
- JTSBPMJUIGOTAB-UHFFFAOYSA-N triethoxy(4-methylpentyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCC(C)C JTSBPMJUIGOTAB-UHFFFAOYSA-N 0.000 claims 2
- HXOGQBSDPSMHJK-UHFFFAOYSA-N triethoxy(6-methylheptyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCCCC(C)C HXOGQBSDPSMHJK-UHFFFAOYSA-N 0.000 claims 2
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 claims 2
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 claims 2
- HDYOCGKYEWQGDZ-UHFFFAOYSA-N triethoxy(nonadecyl)silane Chemical compound CCCCCCCCCCCCCCCCCCC[Si](OCC)(OCC)OCC HDYOCGKYEWQGDZ-UHFFFAOYSA-N 0.000 claims 2
- BBWMWJONYVGXGQ-UHFFFAOYSA-N triethoxy(undecyl)silane Chemical compound CCCCCCCCCCC[Si](OCC)(OCC)OCC BBWMWJONYVGXGQ-UHFFFAOYSA-N 0.000 claims 2
- UWSYCPWEBZRZNJ-UHFFFAOYSA-N trimethoxy(2,4,4-trimethylpentyl)silane Chemical compound CO[Si](OC)(OC)CC(C)CC(C)(C)C UWSYCPWEBZRZNJ-UHFFFAOYSA-N 0.000 claims 2
- WYDMCUJHXCLUPN-UHFFFAOYSA-N trimethoxy(4-methylpentyl)silane Chemical compound CO[Si](OC)(OC)CCCC(C)C WYDMCUJHXCLUPN-UHFFFAOYSA-N 0.000 claims 2
- PPUHSHGIVZSPFO-UHFFFAOYSA-N trimethoxy(nonadecyl)silane Chemical compound CCCCCCCCCCCCCCCCCCC[Si](OC)(OC)OC PPUHSHGIVZSPFO-UHFFFAOYSA-N 0.000 claims 2
- LIJFLHYUSJKHKV-UHFFFAOYSA-N trimethoxy(undecyl)silane Chemical compound CCCCCCCCCCC[Si](OC)(OC)OC LIJFLHYUSJKHKV-UHFFFAOYSA-N 0.000 claims 2
- 125000002948 undecyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 claims 1
- 229910018557 Si O Inorganic materials 0.000 claims 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical group CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims 1
- 229920002522 Wood fibre Polymers 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 239000010405 anode material Substances 0.000 claims 1
- 239000002969 artificial stone Substances 0.000 claims 1
- XENHDKNZSONGFD-UHFFFAOYSA-N butan-2-yloxy-diethoxy-hex-1-enylsilane Chemical compound CCCCC=C[Si](OCC)(OCC)OC(C)CC XENHDKNZSONGFD-UHFFFAOYSA-N 0.000 claims 1
- 239000010406 cathode material Substances 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- DDJSWKLBKSLAAZ-UHFFFAOYSA-N cyclotetrasiloxane Chemical compound O1[SiH2]O[SiH2]O[SiH2]O[SiH2]1 DDJSWKLBKSLAAZ-UHFFFAOYSA-N 0.000 claims 1
- NFMVXENZMCVWMO-UHFFFAOYSA-N decyl-diethoxy-octan-2-yloxysilane Chemical compound CCCCCCCCCC[Si](OCC)(OCC)OC(C)CCCCCC NFMVXENZMCVWMO-UHFFFAOYSA-N 0.000 claims 1
- 239000002274 desiccant Substances 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 claims 1
- 239000000806 elastomer Substances 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 claims 1
- 239000000835 fiber Substances 0.000 claims 1
- 229920000578 graft copolymer Polymers 0.000 claims 1
- WRNFRRJFNJVKBT-UHFFFAOYSA-N hept-1-enyl(trimethoxy)silane Chemical compound CCCCCC=C[Si](OC)(OC)OC WRNFRRJFNJVKBT-UHFFFAOYSA-N 0.000 claims 1
- VRINOTYEGADLMW-UHFFFAOYSA-N heptyl(trimethoxy)silane Chemical compound CCCCCCC[Si](OC)(OC)OC VRINOTYEGADLMW-UHFFFAOYSA-N 0.000 claims 1
- XWHJQTQOUDOZGR-UHFFFAOYSA-N hex-1-enyl(trimethoxy)silane Chemical compound CCCCC=C[Si](OC)(OC)OC XWHJQTQOUDOZGR-UHFFFAOYSA-N 0.000 claims 1
- ZSVGBKYDNCPPPD-UHFFFAOYSA-N hex-1-enyl-dimethoxy-propoxysilane Chemical compound CCCCC=C[Si](OC)(OC)OCCC ZSVGBKYDNCPPPD-UHFFFAOYSA-N 0.000 claims 1
- RSKGMYDENCAJEN-UHFFFAOYSA-N hexadecyl(trimethoxy)silane Chemical compound CCCCCCCCCCCCCCCC[Si](OC)(OC)OC RSKGMYDENCAJEN-UHFFFAOYSA-N 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000003921 oil Substances 0.000 claims 1
- 150000001282 organosilanes Chemical class 0.000 claims 1
- 229910052697 platinum Inorganic materials 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 229920001296 polysiloxane Polymers 0.000 claims 1
- 239000011814 protection agent Substances 0.000 claims 1
- 239000003223 protective agent Substances 0.000 claims 1
- 229910000077 silane Inorganic materials 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 claims 1
- 239000004590 silicone sealant Substances 0.000 claims 1
- 238000006557 surface reaction Methods 0.000 claims 1
- RSNQKPMXXVDJFG-UHFFFAOYSA-N tetrasiloxane Chemical compound [SiH3]O[SiH2]O[SiH2]O[SiH3] RSNQKPMXXVDJFG-UHFFFAOYSA-N 0.000 claims 1
- 239000004753 textile Substances 0.000 claims 1
- 229920001169 thermoplastic Polymers 0.000 claims 1
- 229920002397 thermoplastic olefin Polymers 0.000 claims 1
- 239000004416 thermosoftening plastic Substances 0.000 claims 1
- 238000005809 transesterification reaction Methods 0.000 claims 1
- OABRQVWBQLPFBN-UHFFFAOYSA-N triethoxy(hept-1-enyl)silane Chemical compound CCCCCC=C[Si](OCC)(OCC)OCC OABRQVWBQLPFBN-UHFFFAOYSA-N 0.000 claims 1
- SAWDTKLQESXBDN-UHFFFAOYSA-N triethoxy(heptyl)silane Chemical compound CCCCCCC[Si](OCC)(OCC)OCC SAWDTKLQESXBDN-UHFFFAOYSA-N 0.000 claims 1
- DVFZJTWMDGYBCD-UHFFFAOYSA-N triethoxy(hex-1-enyl)silane Chemical compound CCCCC=C[Si](OCC)(OCC)OCC DVFZJTWMDGYBCD-UHFFFAOYSA-N 0.000 claims 1
- OYGYKEULCAINCL-UHFFFAOYSA-N triethoxy(hexadecyl)silane Chemical compound CCCCCCCCCCCCCCCC[Si](OCC)(OCC)OCC OYGYKEULCAINCL-UHFFFAOYSA-N 0.000 claims 1
- AVAMIWASGKISLV-UHFFFAOYSA-N triethoxy(pent-1-enyl)silane Chemical compound CCCC=C[Si](OCC)(OCC)OCC AVAMIWASGKISLV-UHFFFAOYSA-N 0.000 claims 1
- UMFJXASDGBJDEB-UHFFFAOYSA-N triethoxy(prop-2-enyl)silane Chemical compound CCO[Si](CC=C)(OCC)OCC UMFJXASDGBJDEB-UHFFFAOYSA-N 0.000 claims 1
- BJDLPDPRMYAOCM-UHFFFAOYSA-N triethoxy(propan-2-yl)silane Chemical compound CCO[Si](OCC)(OCC)C(C)C BJDLPDPRMYAOCM-UHFFFAOYSA-N 0.000 claims 1
- ZYMHKOVQDOFPHH-UHFFFAOYSA-N trimethoxy(oct-1-enyl)silane Chemical compound CCCCCCC=C[Si](OC)(OC)OC ZYMHKOVQDOFPHH-UHFFFAOYSA-N 0.000 claims 1
- LFRDHGNFBLIJIY-UHFFFAOYSA-N trimethoxy(prop-2-enyl)silane Chemical compound CO[Si](OC)(OC)CC=C LFRDHGNFBLIJIY-UHFFFAOYSA-N 0.000 claims 1
- LGROXJWYRXANBB-UHFFFAOYSA-N trimethoxy(propan-2-yl)silane Chemical compound CO[Si](OC)(OC)C(C)C LGROXJWYRXANBB-UHFFFAOYSA-N 0.000 claims 1
- ZQTYRTSKQFQYPQ-UHFFFAOYSA-N trisiloxane Chemical compound [SiH3]O[SiH2]O[SiH3] ZQTYRTSKQFQYPQ-UHFFFAOYSA-N 0.000 claims 1
- 230000004580 weight loss Effects 0.000 claims 1
- 239000002023 wood Substances 0.000 claims 1
- 239000002025 wood fiber Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102011086862A DE102011086862A1 (de) | 2011-11-22 | 2011-11-22 | Zusammensetzung olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
| DE102011086862.3 | 2011-11-22 | ||
| PCT/EP2012/072975 WO2013076036A1 (de) | 2011-11-22 | 2012-11-19 | Zusammensetzung olefinisch funktionalisierter siloxanoligomere basierend auf alkoxysilanen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015507027A JP2015507027A (ja) | 2015-03-05 |
| JP2015507027A5 true JP2015507027A5 (enExample) | 2017-03-30 |
| JP6218741B2 JP6218741B2 (ja) | 2017-10-25 |
Family
ID=47428564
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014542789A Active JP6218741B2 (ja) | 2011-11-22 | 2012-11-19 | アルコキシシランベースのオレフィン官能化シロキサンオリゴマー組成物 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US9273186B2 (enExample) |
| EP (1) | EP2782953B1 (enExample) |
| JP (1) | JP6218741B2 (enExample) |
| KR (1) | KR101827045B1 (enExample) |
| CN (1) | CN104053701B (enExample) |
| BR (1) | BR112014012199B1 (enExample) |
| CA (1) | CA2856452C (enExample) |
| DE (2) | DE102011086862A1 (enExample) |
| ES (1) | ES2689771T3 (enExample) |
| IN (1) | IN2014CN04468A (enExample) |
| MA (1) | MA35736B1 (enExample) |
| MX (1) | MX366013B (enExample) |
| MY (1) | MY170918A (enExample) |
| PL (1) | PL2782953T3 (enExample) |
| PT (1) | PT2782953T (enExample) |
| RU (1) | RU2613325C2 (enExample) |
| SI (1) | SI2782953T1 (enExample) |
| TR (1) | TR201815256T4 (enExample) |
| WO (1) | WO2013076036A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102011086863A1 (de) | 2011-11-22 | 2013-05-23 | Evonik Degussa Gmbh | Besonders VOC-arme Gemische olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
| DE102011086865A1 (de) | 2011-11-22 | 2013-05-23 | Evonik Degussa Gmbh | Chloridarme Zusammensetzungen olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
| JP5855552B2 (ja) * | 2012-10-15 | 2016-02-09 | 信越化学工業株式会社 | ポリオルガノシロキサンの製造方法 |
| DE102013216504A1 (de) | 2013-08-21 | 2015-02-26 | Evonik Industries Ag | Zinn-freie Katalysator-haltige Zusammensetzung für einen Monosil-Prozess mit optimierter Prozesscharakteristik |
| DE102013216502A1 (de) | 2013-08-21 | 2015-02-26 | Evonik Industries Ag | Zinn-freie Zusammensetzung für die Vernetzung von thermoplastischen Polyolefinen |
| DE102015109125A1 (de) | 2014-07-04 | 2016-01-07 | Fischerwerke Gmbh & Co. Kg | Epoxidbasiertes Befestigungskunstmörtelsystem mit Siloxanoligomeren |
| DE102014111651A1 (de) * | 2014-08-12 | 2016-02-18 | Fischerwerke Gmbh & Co. Kg | Radikalisch härtbare Kunstharzmasse mit Siloxanoligomerzusätzen |
| DE102015111484A1 (de) | 2014-09-17 | 2016-03-17 | Fischerwerke Gmbh & Co. Kg | Härterzusammensetzung für additionspolymerisationsbasierte Befestigungskunstmörtelsysteme, dessen Verwendung und Herstellung |
| DE102015113352A1 (de) | 2014-09-23 | 2016-03-24 | Fischerwerke Gmbh & Co. Kg | Befestigungssysteme mit feinteiligen Füllstoffen |
| DE112016000366T5 (de) | 2015-01-15 | 2017-09-28 | Dionex Corporation | Chromatographisches Material mit verbesserter pH-Stabilität, Verfahren zu dessen Herstellung und dessen Verwendungen |
| US10294251B2 (en) | 2016-06-10 | 2019-05-21 | Momentive Performance Materials Inc. | Process for preparing alkoxysilanes |
| BR112020027084A2 (pt) | 2018-07-11 | 2021-03-30 | Evonik Operations Gmbh | Composição que compreende pelo menos um micro-organismo e processo para produção de produtos de construção |
| JP7492454B2 (ja) * | 2018-08-09 | 2024-05-29 | 日星電気株式会社 | 絶縁電線、及びその製造方法 |
| WO2020064619A1 (en) | 2018-09-24 | 2020-04-02 | Evonik Operations Gmbh | Use of trialkoxysilane-based compounds for lubricants |
| JP6959950B2 (ja) | 2019-03-04 | 2021-11-05 | 信越化学工業株式会社 | 非硬化型熱伝導性シリコーン組成物 |
| EP3708569B1 (de) * | 2019-03-11 | 2024-06-12 | Evonik Operations GmbH | Ein voc freies, wässriges und lagerstabiles n-vinylbenzylaminalkyl-funktionelles siloxanol und verfahren zu dessen herstellung |
| EP4073142B1 (en) * | 2019-12-11 | 2023-06-14 | Wacker Chemie AG | Silane terminated polyether emulsions for coating applications |
| CN114774007A (zh) * | 2022-06-17 | 2022-07-22 | 宁波长阳科技股份有限公司 | 一种高耐水太阳能电池封装用eva胶膜及其制备方法 |
| EP4424764A1 (de) | 2023-02-28 | 2024-09-04 | Evonik Operations GmbH | Zusammensetzung und deren verwendung als fugenmasse |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2120423T3 (es) * | 1991-06-08 | 1998-11-01 | Huels Chemische Werke Ag | Mezclas de oligomeros de siloxano en forma de cadena y ciclicos, procedimiento para su fabricacion, asi como su uso. |
| DE19639782A1 (de) | 1996-09-27 | 1998-04-02 | Huels Chemische Werke Ag | Glycidether-, Acryl- und/oder Methacryl-funktionelle Organopolysiloxan-haltige Zusammensetzungen auf Wasser-Basis, Verfahren zu deren Herstellung sowie deren Verwendung |
| JPH10251516A (ja) * | 1997-03-14 | 1998-09-22 | Chisso Corp | シランオリゴマー組成物 |
| JPH10298289A (ja) | 1997-04-25 | 1998-11-10 | Mitsubishi Chem Corp | シロキサンポリマーの製造方法 |
| US6140445A (en) * | 1998-04-17 | 2000-10-31 | Crompton Corporation | Silane functional oligomer |
| DE10056343A1 (de) | 2000-11-14 | 2002-05-16 | Degussa | Kontinuierliches Verfahren zur Herstellung von Organoalkoxysiloxanen |
| DE10056344A1 (de) * | 2000-11-14 | 2002-05-16 | Degussa | n-Propylethoxysiloxane, Verfahren zu deren Herstellung und deren Verwendung |
| DE10142555A1 (de) | 2001-08-30 | 2003-03-20 | Degussa | Mittel für die Verbesserung der Scorch-Bedingungen bei der Herstellung gepfropfter und/oder vernetzter Polymere sowie gefüllter Kunststoffe |
| EP1331238A3 (de) * | 2002-01-23 | 2004-01-14 | Degussa AG | Gemisch kettenförmiger und cyclischer Siloxanoligomerer, dessen Herstellung und dessen Verwendung |
| JP4489381B2 (ja) | 2002-07-16 | 2010-06-23 | 宇部日東化成株式会社 | オルガノシロキサン系オリゴマーおよびその製造方法 |
| DE102004037043A1 (de) | 2004-07-29 | 2006-03-23 | Degussa Ag | Blockkondensate organofunktioneller Siloxane, deren Herstellung, Verwendung sowie deren Eigenschaften |
| DE102004049427A1 (de) | 2004-10-08 | 2006-04-13 | Degussa Ag | Polyetherfunktionelle Siloxane, polyethersiloxanhaltige Zusammensetzungen, Verfahren zu deren Herstellung und deren Verwendung |
| DE102005004871A1 (de) | 2005-02-03 | 2006-08-10 | Degussa Ag | Hochviskose wässrige Emulsionen von funktionellen Alkoxysilanen, deren kondensierten Oligomeren, Organopolysiloxanen, deren Herstellung und Verwendung zur Oerflächenbehandlung von anorganischen Materialien |
| DE102005004872A1 (de) | 2005-02-03 | 2006-08-10 | Degussa Ag | Wässrige Emulsionen von funktionellen Alkoxysilanen und deren kondensierten Oligomeren, deren Herstellung und Verwendung zur Oberflächenbehandlung |
| CN100343311C (zh) | 2005-06-16 | 2007-10-17 | 南京市化学工业研究设计院有限公司 | 一种乙烯基三甲氧基硅烷低聚物的制备方法 |
| PL1982964T3 (pl) | 2007-04-20 | 2019-08-30 | Evonik Degussa Gmbh | Mieszanina zawierająca związek krzemoorganiczny i jej zastosowanie |
| DE102008041920A1 (de) | 2008-09-09 | 2010-03-11 | Evonik Degussa Gmbh | Neue Katalysatoren für die Vernetzung von funktionellen Silanen oder funktionellen Siloxanen, insbesondere mit Substraten |
| DE102008041918A1 (de) | 2008-09-09 | 2010-03-11 | Evonik Degussa Gmbh | Silanolkondensationskatalysatoren zur Vernetzung von gefüllten und ungefüllten Polymer-Compounds |
| RU2387677C1 (ru) * | 2008-12-15 | 2010-04-27 | Государственное образовательное учреждение высшего профессионального образования "Московский государственный текстильный университет имени А.Н. Косыгина" | Олиго(алкилен)алкоксисилоксаны для модификации волокнистых материалов и способ их получения |
| DE102011086865A1 (de) | 2011-11-22 | 2013-05-23 | Evonik Degussa Gmbh | Chloridarme Zusammensetzungen olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
| DE102011086863A1 (de) | 2011-11-22 | 2013-05-23 | Evonik Degussa Gmbh | Besonders VOC-arme Gemische olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
-
2011
- 2011-11-22 DE DE102011086862A patent/DE102011086862A1/de not_active Ceased
- 2011-11-22 DE DE202011110267U patent/DE202011110267U1/de not_active Expired - Lifetime
-
2012
- 2012-11-19 MY MYPI2014001463A patent/MY170918A/en unknown
- 2012-11-19 KR KR1020147016672A patent/KR101827045B1/ko active Active
- 2012-11-19 CA CA2856452A patent/CA2856452C/en active Active
- 2012-11-19 BR BR112014012199-0A patent/BR112014012199B1/pt active IP Right Grant
- 2012-11-19 IN IN4468CHN2014 patent/IN2014CN04468A/en unknown
- 2012-11-19 PL PL12805606T patent/PL2782953T3/pl unknown
- 2012-11-19 EP EP12805606.6A patent/EP2782953B1/de active Active
- 2012-11-19 CN CN201280067739.3A patent/CN104053701B/zh active Active
- 2012-11-19 PT PT12805606T patent/PT2782953T/pt unknown
- 2012-11-19 WO PCT/EP2012/072975 patent/WO2013076036A1/de not_active Ceased
- 2012-11-19 MX MX2014006142A patent/MX366013B/es active IP Right Grant
- 2012-11-19 TR TR2018/15256T patent/TR201815256T4/tr unknown
- 2012-11-19 JP JP2014542789A patent/JP6218741B2/ja active Active
- 2012-11-19 SI SI201231388T patent/SI2782953T1/sl unknown
- 2012-11-19 ES ES12805606.6T patent/ES2689771T3/es active Active
- 2012-11-19 US US14/360,127 patent/US9273186B2/en active Active
- 2012-11-19 RU RU2014125140A patent/RU2613325C2/ru active
-
2014
- 2014-06-13 MA MA37134A patent/MA35736B1/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015507027A5 (enExample) | ||
| JP6218741B2 (ja) | アルコキシシランベースのオレフィン官能化シロキサンオリゴマー組成物 | |
| JP5940165B2 (ja) | アルコキシシランをベースとする、ｖｏｃ含分が非常に低いオレフィン官能化シロキサンオリゴマー混合物 | |
| CN106459586B (zh) | 室温固化性有机聚硅氧烷组合物和为该室温固化性有机聚硅氧烷组合物的固化物的成型物 | |
| KR102619534B1 (ko) | 실온 경화성 조성물, 실링재, 및 물품 | |
| TW201124477A (en) | Polysiloxane composition and cured article thereof | |
| JP2007231173A5 (enExample) | ||
| WO2005108496A1 (ja) | ケイ素含有硬化性組成物、及びこれを熱硬化させた硬化物 | |
| JP6099661B2 (ja) | 塩化物含分が低く、アルコキシシランをベースとする、オレフィン官能化シロキサンオリゴマーの組成物 | |
| WO2016160806A1 (en) | High refractive index solvent free silicone nanocomposites | |
| CN103619913A (zh) | 含膦酸酯催化剂的可缩合反应固化的有机硅有机嵌段共聚物组合物及所述组合物的制备和使用方法 | |
| JP2008531809A (ja) | 周囲温度において湿分の存在下で硬化してエラストマーになるオルガノポリシロキサン組成物 | |
| CN105778100B (zh) | 一种有机硅增粘剂及其制备方法和一种加成型硅橡胶组合物 | |
| WO2022009759A1 (ja) | 二成分型室温速硬化性オルガノポリシロキサン組成物、該組成物の硬化物及び物品 | |
| CN109485672B (zh) | 固化催化剂、湿气固化型室温固化性有机聚硅氧烷组合物和成型体 | |
| CN104053699B (zh) | 基于烷氧基硅烷的烯烃官能化的硅氧烷低聚物的低氯组合物 | |
| DE102011086866A1 (de) | Verfahren zur Herstellung von im Wesentlichen chlorfreien Zusammensetzungen olefinisch funktionalisierter Siloxanoligomere | |
| HK1201866B (en) | Composition of olefinically functionalsied siloxane oligomers based on alkoxy silanes | |
| HK1201865B (en) | Mixtures, particularly low in volatile organic compounds (voc), of olefinically functionalized siloxane oligomers based on alkoxy silanes | |
| HK1201864B (en) | Low chloride compositions of olefinically functionalised siloxane oligomers based on alkoxysilanes |