JPS5984948A - 一成分有機ポリシロキサン組成物 - Google Patents
一成分有機ポリシロキサン組成物Info
- Publication number
- JPS5984948A JPS5984948A JP58140445A JP14044583A JPS5984948A JP S5984948 A JPS5984948 A JP S5984948A JP 58140445 A JP58140445 A JP 58140445A JP 14044583 A JP14044583 A JP 14044583A JP S5984948 A JPS5984948 A JP S5984948A
- Authority
- JP
- Japan
- Prior art keywords
- group
- titanium
- formula
- symbol
- carbon atoms
- 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 title claims abstract description 74
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 27
- -1 titanium ester Chemical class 0.000 claims abstract description 55
- 150000003608 titanium Chemical class 0.000 claims abstract description 43
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 39
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000010936 titanium Substances 0.000 claims abstract description 37
- 239000003054 catalyst Substances 0.000 claims abstract description 23
- 229920001971 elastomer Polymers 0.000 claims abstract description 16
- 239000000806 elastomer Substances 0.000 claims abstract description 15
- 150000003754 zirconium Chemical class 0.000 claims abstract description 13
- 238000003860 storage Methods 0.000 claims abstract description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 47
- 229920000642 polymer Polymers 0.000 claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 16
- 229910052726 zirconium Inorganic materials 0.000 claims description 15
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000000962 organic group Chemical group 0.000 claims description 10
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 10
- 125000004429 atom Chemical group 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 230000007062 hydrolysis Effects 0.000 claims description 8
- 238000006460 hydrolysis reaction Methods 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical group [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 101100237844 Mus musculus Mmp19 gene Proteins 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid group Chemical group C(CC(O)(C(=O)O)CC(=O)O)(=O)O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims 1
- 150000004756 silanes Chemical class 0.000 abstract description 14
- 125000004423 acyloxy group Chemical group 0.000 abstract description 6
- 238000004132 cross linking Methods 0.000 abstract 2
- 239000003431 cross linking reagent Substances 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 20
- 239000003795 chemical substances by application Substances 0.000 description 19
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- 239000006185 dispersion Substances 0.000 description 14
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 239000010408 film Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 9
- 150000002430 hydrocarbons Chemical group 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000000945 filler Substances 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000003085 diluting agent Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 6
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 5
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000013522 chelant Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229910000077 silane Inorganic materials 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- 239000004606 Fillers/Extenders Substances 0.000 description 4
- 150000004703 alkoxides Chemical class 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 231100000252 nontoxic Toxicity 0.000 description 4
- 230000003000 nontoxic effect Effects 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 150000003961 organosilicon compounds Chemical class 0.000 description 4
- 239000012429 reaction media Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 125000003944 tolyl group Chemical group 0.000 description 4
- 125000005023 xylyl group Chemical group 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 235000008429 bread Nutrition 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 229920005645 diorganopolysiloxane polymer Polymers 0.000 description 3
- 239000012760 heat stabilizer Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 3
- 229940011051 isopropyl acetate Drugs 0.000 description 3
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 3
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 3
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 239000011135 tin Substances 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- NOKXNDKMAPFVBB-UHFFFAOYSA-N CC(C)[Ti] Chemical compound CC(C)[Ti] NOKXNDKMAPFVBB-UHFFFAOYSA-N 0.000 description 2
- DCERHCFNWRGHLK-UHFFFAOYSA-N C[Si](C)C Chemical compound C[Si](C)C DCERHCFNWRGHLK-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 241000237502 Ostreidae Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- CWZPGMMKDANPKU-UHFFFAOYSA-L butyl-di(dodecanoyloxy)tin Chemical group CCCC[Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O CWZPGMMKDANPKU-UHFFFAOYSA-L 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 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 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 235000020636 oyster Nutrition 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- QHUNJMXHQHHWQP-UHFFFAOYSA-N trimethylsilyl acetate Chemical compound CC(=O)O[Si](C)(C)C QHUNJMXHQHHWQP-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- MLRVZFYXUZQSRU-UHFFFAOYSA-N 1-chlorohexane Chemical compound CCCCCCCl MLRVZFYXUZQSRU-UHFFFAOYSA-N 0.000 description 1
- NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
- PTSLUOSUHFGQHV-UHFFFAOYSA-N 2-chloroheptane Chemical compound CCCCCC(C)Cl PTSLUOSUHFGQHV-UHFFFAOYSA-N 0.000 description 1
- YPIFGDQKSSMYHQ-UHFFFAOYSA-M 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC([O-])=O YPIFGDQKSSMYHQ-UHFFFAOYSA-M 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- 241001474374 Blennius Species 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- 125000006519 CCH3 Chemical group 0.000 description 1
- 241000283153 Cetacea Species 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 1
- 229920001875 Ebonite Polymers 0.000 description 1
- 241000218378 Magnolia Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- SZKKRCSOSQAJDE-UHFFFAOYSA-N Schradan Chemical group CN(C)P(=O)(N(C)C)OP(=O)(N(C)C)N(C)C SZKKRCSOSQAJDE-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QBLDFAIABQKINO-UHFFFAOYSA-N barium borate Chemical compound [Ba+2].[O-]B=O.[O-]B=O QBLDFAIABQKINO-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000005586 carbonic acid group Chemical group 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- DRVWBEJJZZTIGJ-UHFFFAOYSA-N cerium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Ce+3].[Ce+3] DRVWBEJJZZTIGJ-UHFFFAOYSA-N 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004966 cyanoalkyl group Chemical group 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000004188 dichlorophenyl group Chemical group 0.000 description 1
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- PWEVMPIIOJUPRI-UHFFFAOYSA-N dimethyltin Chemical compound C[Sn]C PWEVMPIIOJUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011494 foam glass Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000001367 organochlorosilanes Chemical class 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 102220065682 rs77311724 Human genes 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000012749 thinning agent Substances 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 125000001874 trioxidanyl group Chemical group [*]OOO[H] 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/5406—Silicon-containing compounds containing elements other than oxygen or nitrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S528/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S528/901—Room temperature curable silicon-containing polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Paints Or Removers (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8213505 | 1982-07-30 | ||
| FR8213505A FR2531095B1 (fr) | 1982-07-30 | 1982-07-30 | Compositions organopolysiloxaniques monocomposantes comportant en tant que reticulants des silanes a groupements acyloxyle ou cetoniminoxyle et catalysees par des derives organiques du titane |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5984948A true JPS5984948A (ja) | 1984-05-16 |
| JPS6319539B2 JPS6319539B2 (OSRAM) | 1988-04-22 |
Family
ID=9276562
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58140445A Granted JPS5984948A (ja) | 1982-07-30 | 1983-07-30 | 一成分有機ポリシロキサン組成物 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4525565A (OSRAM) |
| EP (1) | EP0102268B1 (OSRAM) |
| JP (1) | JPS5984948A (OSRAM) |
| KR (1) | KR910000836B1 (OSRAM) |
| AT (1) | ATE24736T1 (OSRAM) |
| AU (1) | AU560439B2 (OSRAM) |
| BR (1) | BR8304060A (OSRAM) |
| CA (1) | CA1204242A (OSRAM) |
| DE (1) | DE3368946D1 (OSRAM) |
| ES (1) | ES524574A0 (OSRAM) |
| FR (1) | FR2531095B1 (OSRAM) |
| HK (1) | HK62990A (OSRAM) |
| PH (1) | PH21243A (OSRAM) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6026059A (ja) * | 1983-07-21 | 1985-02-08 | Toray Silicone Co Ltd | 室温硬化性オルガノポリシロキサン組成物 |
| JPH01121366A (ja) * | 1987-11-06 | 1989-05-15 | Toshiba Silicone Co Ltd | 室温硬化性ポリオルガノシロキサン組成物 |
| JPH02255768A (ja) * | 1989-03-29 | 1990-10-16 | Toshiba Silicone Co Ltd | 室温硬化性ポリオルガノシロキサン組成物 |
| JP2004231648A (ja) * | 2003-01-08 | 2004-08-19 | Nitto Kasei Co Ltd | ハフニウム化合物、該ハフニウム化合物からなる硬化触媒、該硬化触媒を含有する湿気硬化型オルガノポリシロキサン組成物 |
| JP2014070079A (ja) * | 2012-09-27 | 2014-04-21 | Shin Etsu Chem Co Ltd | オルガノポリシロキサン組成物 |
| CN109485672A (zh) * | 2017-09-11 | 2019-03-19 | 信越化学工业株式会社 | 有机钛化合物、湿气固化型组合物和成型体 |
| WO2019098112A1 (ja) * | 2017-11-14 | 2019-05-23 | 日東化成株式会社 | 有機重合体又はオルガノポリシロキサン用硬化触媒、湿気硬化型組成物、硬化物及びその製造方法 |
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4476155A (en) * | 1983-04-18 | 1984-10-09 | Dow Corning Corporation | High voltage insulators |
| GB8401016D0 (en) * | 1984-01-14 | 1984-02-15 | Hagen Perennatorwerk | Organopolysiloxane compositions |
| JPS6160771A (ja) * | 1984-08-31 | 1986-03-28 | Kanegafuchi Chem Ind Co Ltd | 粘着剤組成物 |
| US4721511A (en) * | 1984-10-05 | 1988-01-26 | W. R. Grace & Co. | Leach resistant antimicrobial fabric |
| FR2603893B1 (fr) * | 1986-09-11 | 1988-12-09 | Rhone Poulenc Chimie | Composition diorganopolysiloxane durcissable en elastomere autoadherent |
| GB2208277B (en) * | 1987-07-30 | 1991-11-13 | Courtaulds Plc | Cellulosic fibre |
| JPH01136137U (OSRAM) * | 1988-02-29 | 1989-09-18 | ||
| US4956435A (en) * | 1989-03-22 | 1990-09-11 | Dow Corning Corporation | Neutral cure silicone sealants |
| FR2658828A1 (fr) * | 1990-02-27 | 1991-08-30 | Rhone Poulenc Chimie | Composition organopolysiloxane a fonction cetiminoxy durcissable en elastomere sans catalyseur organometallique. |
| GB9014564D0 (en) * | 1990-06-29 | 1990-08-22 | Courtaulds Coatings Holdings | Coating compositions |
| JP3110749B2 (ja) * | 1990-11-28 | 2000-11-20 | 東レ・ダウコーニング・シリコーン株式会社 | 室温硬化性オルガノポリシロキサン組成物 |
| US5266631A (en) * | 1991-06-13 | 1993-11-30 | Shin-Etsu Chemical Co., Ltd. | Process of producing room temperature curable organopolysiloxane composition |
| DE4139148A1 (de) * | 1991-11-28 | 1993-06-03 | Wacker Chemie Gmbh | Einkomponenten-rtv-massen |
| DE4210349A1 (de) * | 1992-03-30 | 1993-10-07 | Nuenchritz Chemie Gmbh | Verfahren zur Herstellung eines bei Raumtemperatur durch Kondensationsreaktionen vernetzenden Silikonkautschukes |
| US5424354A (en) * | 1993-12-28 | 1995-06-13 | Three Bond Co., Ltd. | Room temperature curable polyoganosiloxane composition |
| US5534588A (en) * | 1994-05-24 | 1996-07-09 | Alliedsignal Inc. | Room temperature vulcanizable silicone compositions employing phenyl substituted tris-functional ketoxime silanes |
| US6239048B1 (en) | 1994-12-28 | 2001-05-29 | Fibermark, Inc. | Light-activated antimicrobial and antiviral materials |
| US5908909A (en) * | 1995-06-08 | 1999-06-01 | Dow Corning S. A. | Organosiloxane compositions |
| EP0747443B1 (en) * | 1995-06-08 | 2007-08-01 | Dow Corning S.A. | Method of sealing joints with moisture curable organosiloxane compositions |
| GB9611291D0 (en) * | 1996-05-30 | 1996-07-31 | Dow Corning | Room temperature curable compositions |
| US5840794A (en) * | 1997-01-10 | 1998-11-24 | Dow Corning Corporation | Alkoxy functional sealants with rapid development of green strength |
| US5948854A (en) * | 1997-09-25 | 1999-09-07 | Dow Corning S.A. | Alkoxy-functional RTV compositions with increased green strength and increased storage stability |
| US6132664A (en) * | 1997-12-23 | 2000-10-17 | Dow Corning Corporation | Method of forming a seal in a confined configuration with an alkoxy-functional RTV composition |
| US6008284A (en) * | 1997-12-23 | 1999-12-28 | Dow Corning Corporation | Fast curing alkoxy-functional RTV compositions |
| US6562931B1 (en) * | 1999-10-29 | 2003-05-13 | Alliedsignal Inc. | Room temperature vulcanizable silicone compositions with improved adhesion to acrylic |
| DE19957336A1 (de) * | 1999-11-29 | 2001-07-12 | Wacker Chemie Gmbh | Vernetzbare Organopolysiloxanmassen |
| US6906147B2 (en) * | 2002-03-20 | 2005-06-14 | Cyclics Corporation | Catalytic systems |
| US7256241B2 (en) * | 2000-01-21 | 2007-08-14 | Cyclics Corporation | Methods for polymerizing macrocyclic polyester oligomers using catalyst promoters |
| US7750109B2 (en) | 2000-09-01 | 2010-07-06 | Cyclics Corporation | Use of a residual oligomer recyclate in the production of macrocyclic polyester oligomer |
| ATE333483T1 (de) * | 2000-09-01 | 2006-08-15 | Cyclics Corp | Verfahren zur umsetzung von linearen polyestern in makrozyklischen oligoester-zusammensetzungen und makrozyklische oligoester |
| US7767781B2 (en) * | 2000-09-01 | 2010-08-03 | Cyclics Corporation | Preparation of low-acid polyalkylene terephthalate and preparation of macrocyclic polyester oligomer therefrom |
| ATE396184T1 (de) * | 2001-06-27 | 2008-06-15 | Cyclics Corp | Formgebende verarbeitung von makrozyklischen oligoestern |
| US7304123B2 (en) * | 2001-06-27 | 2007-12-04 | Cyclics Corporation | Processes for shaping macrocyclic oligoesters |
| US6787632B2 (en) * | 2001-10-09 | 2004-09-07 | Cyclics Corporation | Organo-titanate catalysts for preparing pure macrocyclic oligoesters |
| JP2003160587A (ja) * | 2001-11-28 | 2003-06-03 | Nitto Kasei Co Ltd | チタン化合物、該チタン化合物からなる硬化触媒、該硬化触媒を含有する湿気硬化型オルガノポリシロキサン組成物 |
| JP2004331914A (ja) * | 2003-05-12 | 2004-11-25 | Nitto Kasei Co Ltd | チタン化合物、該チタン化合物からなる硬化触媒、該硬化触媒を含有する湿気硬化型オルガノポリシロキサン組成物 |
| FR2880030B1 (fr) * | 2004-12-23 | 2007-02-16 | Rhodia Chimie Sa | Composition polyorganosiloxane monocomposante de polycondensation comprenant une charge |
| JP2009542848A (ja) * | 2006-07-07 | 2009-12-03 | ヘンケル コーポレイション | 低弾性率、耐湿性シリコーンｒｔｖ組成物およびこの製造方法 |
| US8404877B2 (en) * | 2007-06-22 | 2013-03-26 | General Electric Company | Metal oxide coatings |
| US7652157B2 (en) * | 2007-06-22 | 2010-01-26 | General Electric Company | Metal oxide coatings |
| US8624050B2 (en) * | 2007-06-22 | 2014-01-07 | General Electric Company | Solution process for transparent conductive oxide coatings |
| KR101565613B1 (ko) * | 2007-10-31 | 2015-11-03 | 제너럴 일렉트릭 캄파니 | 금속 산화물 코팅 |
| KR101443544B1 (ko) | 2007-12-20 | 2014-09-22 | 블루스타 실리콘즈 프랑스 에스에이에스 | 탄성중합체로의 실온 가황가능한 오르가노폴리실록산 화합물 및 신규 오르가노폴리실록산 중축합 촉매 |
| US9840640B2 (en) * | 2008-05-29 | 2017-12-12 | Bluestar Silicones France | Article having antifouling properties for aquatic and particularly sea use |
| DE102009000556A1 (de) | 2009-02-02 | 2010-08-05 | Wacker Chemie Ag | Alkoxyvernetzende Kautschukmischungen mit Niob- oder Tantal-Kondensationskatalysatoren |
| FR2946657A1 (fr) | 2009-06-12 | 2010-12-17 | Bluestar Silicones France | Procede d'etancheification et d'assemblage de composants d'un groupe moto-propulseur |
| FR2946656A1 (fr) | 2009-06-12 | 2010-12-17 | Bluestar Silicones France | Procede d'etancheification et d'assemblage de composants d'un groupe moto-propulseur |
| FR2946655A1 (fr) | 2009-06-15 | 2010-12-17 | Bluestar Silicones France | Procede d'enduction d'une composition silicone ne contenant pas d'etain sur un support souple. |
| FR2946654A1 (fr) | 2009-06-15 | 2010-12-17 | Bluestar Silicones France | Procede d'enduction d'une composition silicone ne contenant pas d'etain sur un support souple. |
| BR112012023235A2 (pt) | 2010-03-16 | 2016-05-17 | Bluestar Silicones France | composição de poliorganosiloxano x, elastômero obtido por reticulação, uso e processo para vedação e montagem de pelo menos um componente de um sistema de transmissão |
| ES2741431T3 (es) | 2011-09-16 | 2020-02-11 | Elkem Silicones France Sas | Procedimiento y composición útiles para la estanqueidad y el ensamblaje de componentes de un grupo moto-propulsor |
| DE102012206489A1 (de) * | 2012-04-19 | 2013-10-24 | Wacker Chemie Ag | Härterzusammensetzungen für kondensationsvernetzende RTV-2-Systeme |
| US9512294B2 (en) | 2012-12-20 | 2016-12-06 | Bluestar Silicones France Sas | Organopolysiloxane composition suitable for vulcanisation into an elastomer at room temperature and new organopolysiloxane polycondensation catalysts |
| FR3000090A1 (fr) | 2012-12-20 | 2014-06-27 | Bluestar Silicones France | Procede et compositions utiles pour l'etancheification et l'assemblage de composants d'un groupe moto-propulseur |
| JP6023897B2 (ja) | 2012-12-20 | 2016-11-09 | ブルースター・シリコーンズ・フランス・エスアエス | 室温におけるエラストマーへの加硫に適したオルガノポリシロキサン組成物及び新規のオルガノポリシロキサン重縮合触媒 |
| FR2999980A1 (fr) | 2012-12-20 | 2014-06-27 | Bluestar Silicones France | Article presentant des proprietes antisalissures et destine a etre utilise dans des applications aquatiques en particulier marines |
| US9464197B2 (en) | 2012-12-20 | 2016-10-11 | Bluestar Silicones France Sas | Article with antifouling properties, intended for aquatic uses and, in particular, for marine uses |
| FR3014107A1 (fr) | 2013-12-03 | 2015-06-05 | Bluestar Silicones France | Article presentant des proprietes antisalissures et destine a etre utilise dans des applications aquatiques en particulier marines |
| FR3014106B1 (fr) | 2013-12-03 | 2017-03-10 | Bluestar Silicones France | Composition silicone durcissable en presence d'eau ou d'humidite de l'air |
| FR3020067A1 (fr) | 2014-04-18 | 2015-10-23 | Bluestar Silicones France | Procede d'enduction d'un composition silicone sur un support souple |
| CN105111747B (zh) * | 2015-10-12 | 2018-06-19 | 山东大学 | 一种自催化的脱酮肟型室温硫化硅橡胶及其制备方法 |
| FR3052457B1 (fr) * | 2016-06-14 | 2018-06-22 | Bostik Sa | Compositions adhesives a base de polymeres silyles reticulables |
| EP3532559B1 (en) | 2016-10-31 | 2021-05-26 | Wacker Chemie AG | One-part room-temperature curable compositions on basis of organosilicon compounds and titanium curing catalysts |
| BR112019013971A2 (pt) * | 2017-01-17 | 2020-04-28 | Akzo Nobel Coatings Int Bv | composição de revestimento de liberação de incrustação líquida não aquosa para controlar bioincrustantes aquosos em objetos produzidos pelo homem, substrato, processo para controlar bioincrustação aquática de um objeto produzido pelo homem e uso da composição de revestimento de liberação de incrustação |
| EP3392313A1 (de) | 2017-04-21 | 2018-10-24 | Nitrochemie Aschau GmbH | Härtbare silikonkautschukmassen |
| EP3875541B1 (de) | 2020-03-03 | 2024-08-14 | PolyU GmbH | Zusammensetzung und verfahren zur herstellung von silikonmassen und deren verwendung |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4943377A (OSRAM) * | 1972-07-14 | 1974-04-24 | ||
| JPS5634226A (en) * | 1979-08-29 | 1981-04-06 | Toshiba Corp | Electric valve unit |
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| CA700572A (en) * | 1964-12-22 | Wacker-Chemie Gmbh | Silicone elastomer | |
| NL290275A (OSRAM) * | 1962-03-26 | 1900-01-01 | ||
| NL287586A (OSRAM) * | 1962-05-17 | |||
| US3409573A (en) * | 1964-02-05 | 1968-11-05 | Rhone Poulenc Sa | Process for the preparation of vulcanized polysiloxane composition |
| DE2007002C3 (de) * | 1970-02-16 | 1974-02-14 | Wacker-Chemie Gmbh, 8000 Muenchen | Verbesserung der Standfestigkeit von bei Raumtemperatur zu Elastomeren härtenden Organopolysiloxanmassen |
| GB1401804A (en) * | 1972-02-25 | 1975-07-30 | Ici Ltd | Elastomer-forming compositions |
| DE2413850C3 (de) * | 1974-03-22 | 1979-01-11 | Bayer Ag, 5090 Leverkusen | Bei Zutritt von Wasser oder Wasserdampf zu transparenten Elastomeren vernetzbare Polysüoxanforrrurtasse |
| ZA792758B (en) * | 1978-07-25 | 1981-02-25 | Gen Electric | Low modulus room temperature vulcanizable silicone rubber compositions |
| US4273698A (en) * | 1979-02-28 | 1981-06-16 | General Electric Company | Self-bonding room temperature vulcanizable silicone rubber compositions |
-
1982
- 1982-07-30 FR FR8213505A patent/FR2531095B1/fr not_active Expired
-
1983
- 1983-07-22 AT AT83401508T patent/ATE24736T1/de not_active IP Right Cessation
- 1983-07-22 EP EP83401508A patent/EP0102268B1/fr not_active Expired
- 1983-07-22 DE DE8383401508T patent/DE3368946D1/de not_active Expired
- 1983-07-27 AU AU17322/83A patent/AU560439B2/en not_active Ceased
- 1983-07-27 PH PH29301A patent/PH21243A/en unknown
- 1983-07-29 CA CA000433540A patent/CA1204242A/fr not_active Expired
- 1983-07-29 US US06/518,488 patent/US4525565A/en not_active Expired - Lifetime
- 1983-07-29 ES ES524574A patent/ES524574A0/es active Granted
- 1983-07-29 BR BR8304060A patent/BR8304060A/pt not_active IP Right Cessation
- 1983-07-30 KR KR1019830003580A patent/KR910000836B1/ko not_active Expired
- 1983-07-30 JP JP58140445A patent/JPS5984948A/ja active Granted
-
1990
- 1990-08-09 HK HK629/90A patent/HK62990A/xx not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4943377A (OSRAM) * | 1972-07-14 | 1974-04-24 | ||
| JPS5634226A (en) * | 1979-08-29 | 1981-04-06 | Toshiba Corp | Electric valve unit |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6026059A (ja) * | 1983-07-21 | 1985-02-08 | Toray Silicone Co Ltd | 室温硬化性オルガノポリシロキサン組成物 |
| JPH01121366A (ja) * | 1987-11-06 | 1989-05-15 | Toshiba Silicone Co Ltd | 室温硬化性ポリオルガノシロキサン組成物 |
| JPH02255768A (ja) * | 1989-03-29 | 1990-10-16 | Toshiba Silicone Co Ltd | 室温硬化性ポリオルガノシロキサン組成物 |
| JP2004231648A (ja) * | 2003-01-08 | 2004-08-19 | Nitto Kasei Co Ltd | ハフニウム化合物、該ハフニウム化合物からなる硬化触媒、該硬化触媒を含有する湿気硬化型オルガノポリシロキサン組成物 |
| JP2014070079A (ja) * | 2012-09-27 | 2014-04-21 | Shin Etsu Chem Co Ltd | オルガノポリシロキサン組成物 |
| CN109485672A (zh) * | 2017-09-11 | 2019-03-19 | 信越化学工业株式会社 | 有机钛化合物、湿气固化型组合物和成型体 |
| CN109485672B (zh) * | 2017-09-11 | 2023-09-26 | 信越化学工业株式会社 | 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 |
| WO2019098112A1 (ja) * | 2017-11-14 | 2019-05-23 | 日東化成株式会社 | 有機重合体又はオルガノポリシロキサン用硬化触媒、湿気硬化型組成物、硬化物及びその製造方法 |
| JPWO2019098112A1 (ja) * | 2017-11-14 | 2020-11-19 | 日東化成株式会社 | 有機重合体又はオルガノポリシロキサン用硬化触媒、湿気硬化型組成物、硬化物及びその製造方法 |
| US11466157B2 (en) | 2017-11-14 | 2022-10-11 | Nitto Kasei Co., Ltd. | Curing catalyst for organic polymer or organopolysiloxane, moisturecurable composition, cured product, and production method therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| KR910000836B1 (ko) | 1991-02-11 |
| ES8404704A1 (es) | 1984-05-01 |
| JPS6319539B2 (OSRAM) | 1988-04-22 |
| EP0102268A1 (fr) | 1984-03-07 |
| KR840005476A (ko) | 1984-11-14 |
| FR2531095A1 (fr) | 1984-02-03 |
| EP0102268B1 (fr) | 1987-01-07 |
| ES524574A0 (es) | 1984-05-01 |
| FR2531095B1 (fr) | 1987-08-14 |
| HK62990A (en) | 1990-08-17 |
| US4525565A (en) | 1985-06-25 |
| CA1204242A (fr) | 1986-05-06 |
| ATE24736T1 (de) | 1987-01-15 |
| PH21243A (en) | 1987-08-31 |
| DE3368946D1 (en) | 1987-02-12 |
| BR8304060A (pt) | 1984-03-07 |
| AU560439B2 (en) | 1987-04-09 |
| AU1732283A (en) | 1984-02-02 |
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