NO830537L - Organopolysiloksanblanding. - Google Patents
Organopolysiloksanblanding.Info
- Publication number
- NO830537L NO830537L NO830537A NO830537A NO830537L NO 830537 L NO830537 L NO 830537L NO 830537 A NO830537 A NO 830537A NO 830537 A NO830537 A NO 830537A NO 830537 L NO830537 L NO 830537L
- Authority
- NO
- Norway
- Prior art keywords
- group
- alkyl
- integer
- radicals
- silane
- Prior art date
Links
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 58
- 239000000203 mixture Substances 0.000 claims abstract description 173
- 239000003054 catalyst Substances 0.000 claims abstract description 58
- 238000009833 condensation Methods 0.000 claims abstract description 48
- 230000005494 condensation Effects 0.000 claims abstract description 48
- 238000000034 method Methods 0.000 claims abstract description 40
- 150000003606 tin compounds Chemical class 0.000 claims abstract description 9
- -1 alkoxy radicals Chemical class 0.000 claims description 131
- 229910000077 silane Inorganic materials 0.000 claims description 99
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 86
- 150000003254 radicals Chemical class 0.000 claims description 37
- 229920000642 polymer Polymers 0.000 claims description 31
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 27
- 150000001412 amines Chemical class 0.000 claims description 27
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 27
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 26
- 150000002357 guanidines Chemical class 0.000 claims description 26
- 239000000945 filler Substances 0.000 claims description 25
- 238000004132 cross linking Methods 0.000 claims description 22
- 230000000087 stabilizing effect Effects 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 18
- 125000003368 amide group Chemical group 0.000 claims description 17
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 17
- 239000004215 Carbon black (E152) Substances 0.000 claims description 15
- 229930195733 hydrocarbon Natural products 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 claims description 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- ZRALSGWEFCBTJO-UHFFFAOYSA-N anhydrous guanidine Natural products NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 12
- 239000000377 silicon dioxide Substances 0.000 claims description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 11
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 claims description 11
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 claims description 11
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 10
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- 239000003431 cross linking reagent Substances 0.000 claims description 7
- 229920001971 elastomer Polymers 0.000 claims description 7
- 239000000806 elastomer Substances 0.000 claims description 7
- ZUEIRGBMFHHKAC-UHFFFAOYSA-N 1,1,3,3-tetramethyl-2-(3-trimethoxysilylpropyl)guanidine Chemical compound CO[Si](OC)(OC)CCCN=C(N(C)C)N(C)C ZUEIRGBMFHHKAC-UHFFFAOYSA-N 0.000 claims description 6
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 claims description 6
- YTPNLBCMTSWLKJ-UHFFFAOYSA-N dimethoxy-methyl-prop-1-en-2-yloxysilane Chemical compound CO[Si](C)(OC)OC(C)=C YTPNLBCMTSWLKJ-UHFFFAOYSA-N 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 4
- ABQPZGFRMFRBBC-UHFFFAOYSA-N 2-butyl-1,1,3,3-tetramethylguanidine Chemical group CCCCN=C(N(C)C)N(C)C ABQPZGFRMFRBBC-UHFFFAOYSA-N 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 125000005265 dialkylamine group Chemical group 0.000 claims description 3
- ZWXYOPPJTRVTST-UHFFFAOYSA-N methyl-tris(prop-1-en-2-yloxy)silane Chemical group CC(=C)O[Si](C)(OC(C)=C)OC(C)=C ZWXYOPPJTRVTST-UHFFFAOYSA-N 0.000 claims description 3
- QREFMLYPZMSWJC-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]-n-methylacetamide Chemical group CO[Si](C)(OC)N(C)C(C)=O QREFMLYPZMSWJC-UHFFFAOYSA-N 0.000 claims description 3
- PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 2
- 125000005907 alkyl ester group Chemical group 0.000 claims 10
- 150000005215 alkyl ethers Chemical class 0.000 claims 10
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 1
- 150000001723 carbon free-radicals Chemical class 0.000 claims 1
- SDTDHTCWRNVNAJ-UHFFFAOYSA-L dimethyltin(2+);diacetate Chemical compound CC(=O)O[Sn](C)(C)OC(C)=O SDTDHTCWRNVNAJ-UHFFFAOYSA-L 0.000 claims 1
- BTQLZQAVGBUMOG-UHFFFAOYSA-N n-silylacetamide Chemical compound CC(=O)N[SiH3] BTQLZQAVGBUMOG-UHFFFAOYSA-N 0.000 claims 1
- 230000003014 reinforcing effect Effects 0.000 claims 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 20
- 150000004756 silanes Chemical class 0.000 description 15
- 238000002156 mixing Methods 0.000 description 14
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 11
- 239000010936 titanium Substances 0.000 description 11
- 229910052719 titanium Inorganic materials 0.000 description 11
- 238000003860 storage Methods 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000013522 chelant Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 230000032683 aging Effects 0.000 description 8
- ZXDVQYBUEVYUCG-UHFFFAOYSA-N dibutyltin(2+);methanolate Chemical compound CCCC[Sn](OC)(OC)CCCC ZXDVQYBUEVYUCG-UHFFFAOYSA-N 0.000 description 7
- 230000009972 noncorrosive effect Effects 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 150000003335 secondary amines Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000004971 Cross linker Substances 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- GYQKYMDXABOCBE-UHFFFAOYSA-N chloro-dimethoxy-methylsilane Chemical compound CO[Si](C)(Cl)OC GYQKYMDXABOCBE-UHFFFAOYSA-N 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 3
- 235000013405 beer Nutrition 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000011067 equilibration Methods 0.000 description 3
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 3
- 229940093858 ethyl acetoacetate Drugs 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 230000005070 ripening Effects 0.000 description 3
- 239000000565 sealant Substances 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- NRQVEWMTFLREAZ-UHFFFAOYSA-N 1,1-dimethoxy-N-methylsilylmethanamine Chemical compound C[SiH2]NC(OC)OC NRQVEWMTFLREAZ-UHFFFAOYSA-N 0.000 description 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-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
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- JJLKTTCRRLHVGL-UHFFFAOYSA-L [acetyloxy(dibutyl)stannyl] acetate Chemical compound CC([O-])=O.CC([O-])=O.CCCC[Sn+2]CCCC JJLKTTCRRLHVGL-UHFFFAOYSA-L 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- 150000005840 aryl radicals Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- HXTZZFBBMWUFFG-UHFFFAOYSA-N n-[bis[acetyl(methyl)amino]-methylsilyl]-n-methylacetamide Chemical compound CC(=O)N(C)[Si](C)(N(C)C(C)=O)N(C)C(C)=O HXTZZFBBMWUFFG-UHFFFAOYSA-N 0.000 description 2
- LCUQPCZFCROAPF-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]-n-hexylhexan-1-amine Chemical compound CCCCCCN([Si](C)(OC)OC)CCCCCC LCUQPCZFCROAPF-UHFFFAOYSA-N 0.000 description 2
- ZWRBXRIQPXAXNU-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]propan-2-amine Chemical compound CO[Si](C)(OC)NC(C)C ZWRBXRIQPXAXNU-UHFFFAOYSA-N 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 229920005573 silicon-containing polymer Polymers 0.000 description 2
- 239000012974 tin catalyst Substances 0.000 description 2
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 2
- 150000003755 zirconium compounds Chemical class 0.000 description 2
- OVSGBKZKXUMMHS-VGKOASNMSA-L (z)-4-oxopent-2-en-2-olate;propan-2-olate;titanium(4+) Chemical compound [Ti+4].CC(C)[O-].CC(C)[O-].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O OVSGBKZKXUMMHS-VGKOASNMSA-L 0.000 description 1
- MPJJRYGVHNTASI-SUKNRPLKSA-L (z)-4-oxopent-2-en-2-olate;propane-1,3-diolate;titanium(4+) Chemical compound [Ti+4].[O-]CCC[O-].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O MPJJRYGVHNTASI-SUKNRPLKSA-L 0.000 description 1
- QMTFKWDCWOTPGJ-KVVVOXFISA-N (z)-octadec-9-enoic acid;tin Chemical compound [Sn].CCCCCCCC\C=C/CCCCCCCC(O)=O QMTFKWDCWOTPGJ-KVVVOXFISA-N 0.000 description 1
- BADAQYMNEFVLGH-UHFFFAOYSA-N 1,1,3-trimethyl-2-(3-silylpropyl)-3-(trimethoxymethyl)guanidine Chemical compound COC(N(C(=NCCC[SiH3])N(C)C)C)(OC)OC BADAQYMNEFVLGH-UHFFFAOYSA-N 0.000 description 1
- SOIOCWRKKDYODY-UHFFFAOYSA-N 1-[dimethoxy(methyl)silyl]-1,3,3-trimethylurea Chemical compound CO[Si](C)(OC)N(C)C(=O)N(C)C SOIOCWRKKDYODY-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- VSIKJPJINIDELZ-UHFFFAOYSA-N 2,2,4,4,6,6,8,8-octakis-phenyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound O1[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si]1(C=1C=CC=CC=1)C1=CC=CC=C1 VSIKJPJINIDELZ-UHFFFAOYSA-N 0.000 description 1
- ITLDOQCDKSCTPJ-UHFFFAOYSA-N 2,2-dimethoxy-N-methylsilylethanamine Chemical compound C[SiH2]NCC(OC)OC ITLDOQCDKSCTPJ-UHFFFAOYSA-N 0.000 description 1
- VIAWXLFFSHQNAO-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]butan-1-ol Chemical compound CCC(CO)N(CCO)CCO VIAWXLFFSHQNAO-UHFFFAOYSA-N 0.000 description 1
- KTXWGMUMDPYXNN-UHFFFAOYSA-N 2-ethylhexan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCC(CC)C[O-].CCCCC(CC)C[O-].CCCCC(CC)C[O-].CCCCC(CC)C[O-] KTXWGMUMDPYXNN-UHFFFAOYSA-N 0.000 description 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- MKUWNMKVSHFQJR-UHFFFAOYSA-H COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O Chemical compound COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O MKUWNMKVSHFQJR-UHFFFAOYSA-H 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- SDPYGHWPYDANRI-UHFFFAOYSA-N N-ethenylsilyl-1,1-dimethoxymethanamine Chemical compound COC(N[SiH2]C=C)OC SDPYGHWPYDANRI-UHFFFAOYSA-N 0.000 description 1
- JLVYRZKAROXDAS-UHFFFAOYSA-N N-methyl-N-silylacetamide Chemical compound CN([SiH3])C(C)=O JLVYRZKAROXDAS-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- LHFURYICKMKJHJ-UHFFFAOYSA-L [benzoyloxy(dibutyl)stannyl] benzoate Chemical compound CCCC[Sn+2]CCCC.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 LHFURYICKMKJHJ-UHFFFAOYSA-L 0.000 description 1
- HAAANJSJNWKVMX-UHFFFAOYSA-L [butanoyloxy(dimethyl)stannyl] butanoate Chemical compound CCCC(=O)O[Sn](C)(C)OC(=O)CCC HAAANJSJNWKVMX-UHFFFAOYSA-L 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- HSULLSUSGAHAOJ-UHFFFAOYSA-N acetic acid;hexan-1-amine Chemical compound CC([O-])=O.CCCCCC[NH3+] HSULLSUSGAHAOJ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- FWYSSOIRLVHQNC-UHFFFAOYSA-M benzyl(trimethyl)azanium;acetate Chemical compound CC([O-])=O.C[N+](C)(C)CC1=CC=CC=C1 FWYSSOIRLVHQNC-UHFFFAOYSA-M 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- UBYDHPXTAIURJV-UHFFFAOYSA-N but-2-en-2-yloxy-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)OC(C)=CC UBYDHPXTAIURJV-UHFFFAOYSA-N 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LUZSPGQEISANPO-UHFFFAOYSA-N butyltin Chemical compound CCCC[Sn] LUZSPGQEISANPO-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- QAEKNCDIHIGLFI-UHFFFAOYSA-L cobalt(2+);2-ethylhexanoate Chemical compound [Co+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O QAEKNCDIHIGLFI-UHFFFAOYSA-L 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 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 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- OSXYHAQZDCICNX-UHFFFAOYSA-N dichloro(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](Cl)(Cl)C1=CC=CC=C1 OSXYHAQZDCICNX-UHFFFAOYSA-N 0.000 description 1
- YLJJAVFOBDSYAN-UHFFFAOYSA-N dichloro-ethenyl-methylsilane Chemical compound C[Si](Cl)(Cl)C=C YLJJAVFOBDSYAN-UHFFFAOYSA-N 0.000 description 1
- OQRBGEUZNWMSQN-UHFFFAOYSA-N dimethoxy-methyl-(1-phenylethenoxy)silane Chemical compound CO[Si](C)(OC)OC(=C)C1=CC=CC=C1 OQRBGEUZNWMSQN-UHFFFAOYSA-N 0.000 description 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 1
- LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 150000002084 enol ethers Chemical class 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052742 iron Inorganic materials 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
- RSQMHVALIQUOMV-UHFFFAOYSA-N isocyanato(dimethoxy)silane Chemical compound N(=C=O)[SiH](OC)OC RSQMHVALIQUOMV-UHFFFAOYSA-N 0.000 description 1
- MAMPQFAGGHUOQJ-UHFFFAOYSA-N isocyanato-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)N=C=O MAMPQFAGGHUOQJ-UHFFFAOYSA-N 0.000 description 1
- BUZRAOJSFRKWPD-UHFFFAOYSA-N isocyanatosilane Chemical class [SiH3]N=C=O BUZRAOJSFRKWPD-UHFFFAOYSA-N 0.000 description 1
- OFYZZNNWQRYKHA-UHFFFAOYSA-N isothiocyanato-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)N=C=S OFYZZNNWQRYKHA-UHFFFAOYSA-N 0.000 description 1
- 239000011499 joint compound Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- BCOLJLYGWZEIEA-UHFFFAOYSA-N methyl(trimethoxymethyl)silane Chemical compound C[SiH2]C(OC)(OC)OC BCOLJLYGWZEIEA-UHFFFAOYSA-N 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- SBSPZXNNGHZVCR-UHFFFAOYSA-N n-[[acetyl(methyl)amino]-methoxy-methylsilyl]-n-methylacetamide Chemical compound CC(=O)N(C)[Si](C)(OC)N(C)C(C)=O SBSPZXNNGHZVCR-UHFFFAOYSA-N 0.000 description 1
- NCWLQWGQNUJBNB-UHFFFAOYSA-N n-[bis[benzoyl(methyl)amino]-methylsilyl]-n-methylbenzamide Chemical compound C=1C=CC=CC=1C(=O)N(C)[Si](C)(N(C)C(=O)C=1C=CC=CC=1)N(C)C(=O)C1=CC=CC=C1 NCWLQWGQNUJBNB-UHFFFAOYSA-N 0.000 description 1
- PVRCBAPOFFYMJM-UHFFFAOYSA-N n-[ethyl(dimethoxy)silyl]-n-methylacetamide Chemical compound CC[Si](OC)(OC)N(C)C(C)=O PVRCBAPOFFYMJM-UHFFFAOYSA-N 0.000 description 1
- LHBDQZYSLUXAFT-UHFFFAOYSA-N n-ethyl-n-[ethyl(dimethoxy)silyl]propanamide Chemical compound CCC(=O)N(CC)[Si](CC)(OC)OC LHBDQZYSLUXAFT-UHFFFAOYSA-N 0.000 description 1
- WZXSAXDNMYMUBG-UHFFFAOYSA-N n-methyl-n-trimethoxysilylacetamide Chemical compound CO[Si](OC)(OC)N(C)C(C)=O WZXSAXDNMYMUBG-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- IYMSIPPWHNIMGE-UHFFFAOYSA-N silylurea Chemical class NC(=O)N[SiH3] IYMSIPPWHNIMGE-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- XNDVYJMKIJRDPF-UHFFFAOYSA-N tetrakis(prop-1-en-2-yl) silicate Chemical compound CC(=C)O[Si](OC(C)=C)(OC(C)=C)OC(C)=C XNDVYJMKIJRDPF-UHFFFAOYSA-N 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- LSZKGNJKKQYFLR-UHFFFAOYSA-J tri(butanoyloxy)stannyl butanoate Chemical compound [Sn+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O LSZKGNJKKQYFLR-UHFFFAOYSA-J 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- CPRPKIMXLHBUGA-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC CPRPKIMXLHBUGA-UHFFFAOYSA-N 0.000 description 1
- SDDVFEDYRCTTKO-UHFFFAOYSA-N trimethyl prop-1-en-2-yl silicate Chemical compound CO[Si](OC)(OC)OC(C)=C SDDVFEDYRCTTKO-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
- C08K5/31—Guanidine; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/28—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen sulfur-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/60—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which all the silicon atoms are connected by linkages other than oxygen atoms
-
- 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)
- Cosmetics (AREA)
- Silicon Polymers (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/277,524 US4395526A (en) | 1981-06-26 | 1981-06-26 | One package, stable, moisture curable, polyalkoxy-terminated organopolysiloxane compositions and method for making |
Publications (1)
Publication Number | Publication Date |
---|---|
NO830537L true NO830537L (no) | 1983-02-17 |
Family
ID=23061241
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO830537A NO830537L (no) | 1981-06-26 | 1983-02-17 | Organopolysiloksanblanding. |
Country Status (13)
Country | Link |
---|---|
US (1) | US4395526A (es) |
EP (1) | EP0069256B1 (es) |
JP (1) | JPS58501040A (es) |
KR (1) | KR840000610A (es) |
AT (1) | ATE37038T1 (es) |
BR (1) | BR8207777A (es) |
CA (1) | CA1197035A (es) |
DE (1) | DE3278995D1 (es) |
DK (1) | DK93283A (es) |
ES (1) | ES513502A0 (es) |
NO (1) | NO830537L (es) |
WO (1) | WO1983000156A1 (es) |
ZA (1) | ZA824212B (es) |
Families Citing this family (92)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4517352A (en) * | 1981-06-26 | 1985-05-14 | General Electric Company | One package, stable, moisture curable, polyalkoxy-terminated _organopolysiloxane compositions and method for making |
US4539367A (en) * | 1982-02-17 | 1985-09-03 | General Electric Company | Low modulus one-component RTV compositions and processes |
US4528353A (en) * | 1982-02-17 | 1985-07-09 | General Electric Company | Adhesion promoters for one-component RTV silicone compositions |
US4472590A (en) * | 1982-02-17 | 1984-09-18 | General Electric Company | Silicone compounds |
US4513115A (en) * | 1982-02-17 | 1985-04-23 | General Electric Company | Low modulus one component RTV compositions processes |
US4483973A (en) * | 1982-02-17 | 1984-11-20 | General Electric Company | Adhesion promoters for one-component RTV silicone compositions |
US4720531A (en) * | 1982-09-29 | 1988-01-19 | General Electric Company | Novel scavengers for one-component RTV compositions |
US4839453A (en) * | 1982-09-29 | 1989-06-13 | General Electric Company | Novel Scavengers for one-component RTV compositions |
US4528324A (en) * | 1982-11-01 | 1985-07-09 | General Electric Company | Process for producing RTV silicone rubber compositions using a devolatilizing extruder |
ZA837448B (en) * | 1982-12-02 | 1984-05-30 | Gen Electric | Process for producing alkoxy-terminated polysiloxanes |
FR2537142A1 (fr) * | 1982-12-03 | 1984-06-08 | Gen Electric | Ethers de dialcoxysilylenol et leur procede de preparation |
US4593085A (en) * | 1982-12-13 | 1986-06-03 | General Electric Company | Alkoxy-functional one component RTV silicone rubber compositions |
US4508758A (en) * | 1982-12-27 | 1985-04-02 | At&T Technologies, Inc. | Encapsulated electronic circuit |
US4483972A (en) * | 1983-02-01 | 1984-11-20 | General Electric Company | Integrated cross-linkers and amine functional siloxane scavengers for RTV silicone rubber compositions |
US4503209A (en) * | 1983-02-07 | 1985-03-05 | General Electric Company | Acetamide scavengers for RTV silicone rubber compositions |
US4523001A (en) * | 1983-03-17 | 1985-06-11 | General Electric Company | Scavengers for one component alkoxy-functional RTV compositions |
US4472551A (en) * | 1983-04-01 | 1984-09-18 | General Electric Company | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions |
US4499230A (en) * | 1983-04-01 | 1985-02-12 | General Electric Company | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions containing a zeolite |
GB2138013A (en) * | 1983-04-01 | 1984-10-17 | Gen Electric | Cure accelerator for RTV composition |
US4477625A (en) * | 1983-04-01 | 1984-10-16 | General Electric Company | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions |
US4472564A (en) * | 1983-04-01 | 1984-09-18 | General Electric Company | Method for making an enoxy stabilized room temperature vulcanizable organopolysiloxane composition which resists color change upon aging |
US4489200A (en) * | 1983-04-11 | 1984-12-18 | General Electric Company | One-component RTV silicone rubber compositions with good self-bonding properties to acrylate plastics |
US4550056A (en) * | 1983-04-15 | 1985-10-29 | Union Carbide Corporation | Electrical cable containing cured elastomeric compositions |
US4526922A (en) * | 1983-04-15 | 1985-07-02 | Union Carbide Corporation | Organofunctional silane-siloxane oligomer coupling compositions, curable and cured elastomeric compositions containing same and novel electric cable containing said cured elastomeric compositions |
US4495331A (en) * | 1983-05-25 | 1985-01-22 | General Electric Company | Scavengers for RTV silicone rubber compositions |
DE3416851A1 (de) | 1983-05-25 | 1984-11-29 | General Electric Co., Schenectady, N.Y. | Durchscheinende und farblose, bei raumtemperatur vulkanisierbare zusammensetzungen |
US4783542A (en) * | 1983-05-25 | 1988-11-08 | General Electric Company | Silicone compounds |
US4495330A (en) * | 1983-05-25 | 1985-01-22 | General Electric Company | Crosslinkers for RTV compositions |
JPS6018544A (ja) * | 1983-07-11 | 1985-01-30 | Toshiba Silicone Co Ltd | 室温硬化性ポリオルガノシロキサン組成物 |
US4536540A (en) * | 1983-08-02 | 1985-08-20 | General Electric Company | Scavengers for ammonia in RTV compositions |
US4489191A (en) * | 1983-08-31 | 1984-12-18 | General Electric Company | Silane scavengers for hydroxy radicals containing silicon-hydrogen bonds |
US4499234A (en) * | 1983-10-14 | 1985-02-12 | General Electric Company | Non-corrosive silicone RTV compositions |
DE3379205D1 (en) * | 1983-10-18 | 1989-03-23 | Gen Electric | End-capping catalyst for forming alcoxy-functional one component rtv compositions |
EP0139064A1 (en) * | 1983-10-27 | 1985-05-02 | General Electric Company | Novel scavengers for one-component RTV compositions |
JPS60120756A (ja) * | 1983-11-30 | 1985-06-28 | ゼネラル・エレクトリツク・カンパニイ | オルガノポリシロキサン組成物 |
US4517337A (en) * | 1984-02-24 | 1985-05-14 | General Electric Company | Room temperature vulcanizable organopolysiloxane compositions and method for making |
US4563498A (en) * | 1984-07-05 | 1986-01-07 | General Electric Company | Curable silicone compositions and processes |
JPS6160771A (ja) * | 1984-08-31 | 1986-03-28 | Kanegafuchi Chem Ind Co Ltd | 粘着剤組成物 |
US4735979A (en) * | 1985-04-04 | 1988-04-05 | Loctite Corporation | Auto-adhering one-component RTV silicone sealant composition utilizing an adhesion promoter |
US4673750A (en) * | 1985-04-04 | 1987-06-16 | Loctite Corporation | Auto-adhering one-component RTV silicone sealant composition utilizing glycidoxyalkyl substituted alkoxy-oxime silane as an adhesion promoter |
US4680364A (en) * | 1985-06-18 | 1987-07-14 | General Electric Company | Room temperature vulcanizable silicone compositions having improved adhesion |
DE3523206A1 (de) * | 1985-06-28 | 1987-01-02 | Bayer Ag | Verfahren zur herstellung von poly(diorganosiloxanen) mit alkoxyendgruppen |
US4753993A (en) * | 1985-08-21 | 1988-06-28 | Union Carbide Corporation | Compositions based on thermoplastic polymers and metal carboxylate silanol condensation catalysts |
JPS62295958A (ja) * | 1986-06-13 | 1987-12-23 | Shin Etsu Chem Co Ltd | 室温硬化性オルガノシロキサン組成物 |
JP2565333B2 (ja) * | 1987-04-28 | 1996-12-18 | 東レ・ダウコーニング・シリコーン株式会社 | 電気・電子機器用室温硬化性オルガノポリシロキサン組成物 |
CA1327207C (en) * | 1987-08-27 | 1994-02-22 | Jeffrey Hayward Wengrovius | Polyalkoxysilyl-terminated polydiorganosiloxanes, methods for their preparation, and room temperature vulcanizable compositions containing them |
US4847400A (en) * | 1987-09-11 | 1989-07-11 | Dow Corning Corporation | Polyalkoxysilylalkylenedisilazanes and silylamines |
DE3801389A1 (de) * | 1988-01-19 | 1989-07-27 | Wacker Chemie Gmbh | Unter abspaltung von alkoholen zu elastomeren vernetzbare organopolysiloxanmassen |
US4954598A (en) * | 1988-10-13 | 1990-09-04 | Basf Corporation | Fast-cure polyurethane sealant composition containing silyl-substituted guanidine accelerators |
US5097053A (en) * | 1988-10-13 | 1992-03-17 | Basf Corporation | Fast-cure polyurethane sealant composition containing silyl-substituted guanidine accelerators |
FR2638752B1 (fr) * | 1988-11-04 | 1992-07-24 | Rhone Poulenc Chimie | Procede de preparation de diorganopolysiloxanes a groupements terminaux alcoxy |
US5213899A (en) * | 1990-12-17 | 1993-05-25 | General Electric Company | Room temperature vulcanizable silicone compositions |
CA2056569A1 (en) * | 1990-12-17 | 1992-06-18 | Gary M. Lucas | Room temperature vulcanizable silicone compositions |
JPH04359058A (ja) * | 1991-06-03 | 1992-12-11 | Shin Etsu Chem Co Ltd | 室温硬化性オルガノポリシロキサン組成物の製造方法 |
DE4207212A1 (de) * | 1992-03-06 | 1993-09-09 | Bayer Ag | Verfahren zur herstellung von organyloxy-endgestoppten polysiloxanen |
US5453126A (en) * | 1992-03-30 | 1995-09-26 | Jmk International, Inc. | Flexible, heat-resistant reflective coatings, coated elastomeric components and methods |
JP3500168B2 (ja) * | 1992-07-02 | 2004-02-23 | ジーイー東芝シリコーン株式会社 | 室温硬化性ポリオルガノシロキサン組成物 |
DE4223468A1 (de) * | 1992-07-16 | 1994-01-20 | Wacker Chemie Gmbh | Stabilisierung von Organosiloxanen mit SiOC-gebundenen Resten |
US5446075A (en) * | 1993-04-01 | 1995-08-29 | Jmk International, Inc. | Monitor putty |
US5502144A (en) * | 1994-07-15 | 1996-03-26 | University Of Cincinnati | Composition and method for preparing silicone elastomers |
US6114438A (en) * | 1995-09-08 | 2000-09-05 | Dow Corning Corporation | Oil resistant silicone sealants |
DE19533915A1 (de) * | 1995-09-13 | 1997-03-20 | Bayer Ag | Verfahren zur Herstellung von Poly(diorganosiloxanen) mit Diorganyloxyorganylsilyl- oder Triorganylsilyl-Endgruppen, vernetzbare Mischungen, enthaltend Poly(diorganosiloxane) mit Diorganyloxyorganylsilyl- oder Triorganyloxysilyl-Endgruppen und deren Verwendung |
DE19536410A1 (de) * | 1995-09-29 | 1997-04-03 | Wacker Chemie Gmbh | Unter Abspaltung von Alkoholen zu Elastomeren vernetzbare Organopolysiloxanmassen |
US5962559A (en) * | 1997-09-30 | 1999-10-05 | General Electric Company | Neutral cure one component room temperature vulcanizable silicone compositions |
US6235832B1 (en) | 1998-12-21 | 2001-05-22 | Dow Corning Corporation | RTV silicone compositions with rapid development of green strength |
DE10103421A1 (de) * | 2001-01-26 | 2002-08-14 | Ge Bayer Silicones Gmbh & Co | Polyorganosiloxan-Zusammensetzung |
DE10121514A1 (de) | 2001-05-03 | 2002-11-14 | Wacker Chemie Gmbh | Unter Abspaltung von Alkoholen aus Alkoxysilylendgruppen zu Elastomeren vernetzbare Massen |
JP2003119387A (ja) * | 2001-10-10 | 2003-04-23 | Shin Etsu Chem Co Ltd | 室温硬化性オルガノポリシロキサン組成物 |
DE10218490B4 (de) * | 2002-04-25 | 2007-09-13 | Wacker Chemie Ag | Unter Abspaltung von Alkoholen aus Alkoxysilylendgruppen zu Elastomeren vernetzbare Massen |
JP4101632B2 (ja) * | 2002-11-01 | 2008-06-18 | 株式会社カネカ | 硬化性組成物および復元性、クリープ性改善方法 |
FR2856695B1 (fr) * | 2003-06-27 | 2005-09-16 | Rhodia Chimie Sa | Composition polyorganosiloxane monocomposante reticulant en elastomere silicone |
US20050288415A1 (en) * | 2004-06-23 | 2005-12-29 | Beers Melvin D | Highly elastomeric and paintable silicone compositions |
FR2880030B1 (fr) * | 2004-12-23 | 2007-02-16 | Rhodia Chimie Sa | Composition polyorganosiloxane monocomposante de polycondensation comprenant une charge |
US7605203B2 (en) * | 2005-05-26 | 2009-10-20 | Tremco Incorporated | Polymer compositions and adhesives, coatings, and sealants made therefrom |
WO2007037484A1 (ja) * | 2005-09-30 | 2007-04-05 | Kaneka Corporation | 硬化性組成物 |
US8076439B2 (en) * | 2005-09-30 | 2011-12-13 | Kaneka Corporation | Curable composition |
JP5226315B2 (ja) * | 2005-09-30 | 2013-07-03 | 株式会社カネカ | 硬化性組成物 |
FR2946656A1 (fr) * | 2009-06-12 | 2010-12-17 | Bluestar Silicones France | Procede d'etancheification et d'assemblage de composants d'un groupe moto-propulseur |
FR2946657A1 (fr) * | 2009-06-12 | 2010-12-17 | Bluestar Silicones France | Procede d'etancheification et d'assemblage de composants d'un groupe moto-propulseur |
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. |
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. |
FR2946981A1 (fr) * | 2009-06-19 | 2010-12-24 | Bluestar Silicones France | Composition silicone reticulable par deshydrogenocondensation en presence d'un catalyseur metallique |
WO2010146254A1 (fr) * | 2009-06-19 | 2010-12-23 | Bluestar Silicones France | Composition silicone reticulable par deshydrogenocondensation en presence d'un catalyseur non mettalique |
US8455562B2 (en) * | 2009-06-19 | 2013-06-04 | Bluestar Silicones France Sas | Silicone composition suitable for cross-linking by dehydrogenative condensation in the presence of a non-metal catalyst |
US8889801B2 (en) * | 2009-10-28 | 2014-11-18 | Momentive Performance Materials, Inc. | Surface protective coating and methods of use thereof |
DE102013216777A1 (de) | 2013-08-23 | 2015-02-26 | Evonik Industries Ag | Bei Raumtemperatur härtbare Silikonharz-Zusammensetzungen |
DE102014214408A1 (de) * | 2014-07-23 | 2016-01-28 | Wacker Chemie Ag | Härtbare Organopolysiloxanzusammensetzungen |
CN110997266B (zh) * | 2017-06-29 | 2022-04-26 | 埃肯有机硅法国简易股份公司 | 有机硅弹性体制模具的制造方法 |
EP3712215B1 (en) * | 2017-11-14 | 2021-10-27 | Nitto Kasei Co., Ltd. | Curing catalyst for organic polymer or organopolysiloxane, moisture-curable composition, cured product, and production method therefor |
CN112358201B (zh) * | 2020-11-11 | 2022-07-22 | 贵州理工学院 | 一种玄武岩纤维浸润剂增强改性方法 |
CN115895587A (zh) * | 2022-12-28 | 2023-04-04 | 广州市白云化工实业有限公司 | 一种快速薄层消粘的醇型硅酮密封胶及其制备方法 |
WO2024166696A1 (ja) * | 2023-02-08 | 2024-08-15 | 株式会社カネカ | 硬化性組成物、及びその製造方法 |
Family Cites Families (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3296161A (en) * | 1967-01-03 | Curable organopolysiloxane | ||
US3127363A (en) * | 1955-08-05 | 1964-03-31 | Process for the manufacture of elasto- | |
LU35994A1 (fr) * | 1957-07-12 | 1958-06-17 | Rhone Poulenc Sa | Procédé de fabrication d'elastomères à base de diorgano-polysiloxanes et produits ainsi obtenus. |
US3065194A (en) * | 1959-07-16 | 1962-11-20 | Wacker Chemie Gmbh | Method of preparing silicone rubber compositions |
FR1262450A (fr) | 1960-07-15 | 1961-05-26 | Wacker Chemie Gmbh | Procédé de préparation de masses de caoutchouc de silicone durcissables à froid |
US3170894A (en) * | 1960-09-26 | 1965-02-23 | Dow Corning | Silicon-bonded polyhydrocarbonoxy organopolysiloxanes and one-component room temperature cured compositions containing said organopolysiloxanes and condensation catalysts |
US3122522A (en) * | 1961-10-16 | 1964-02-25 | Dow Corning | One-component room temperature curing system employing new silicone intermediates |
BE623603A (es) | 1961-10-16 | |||
US3296195A (en) * | 1963-12-20 | 1967-01-03 | Gen Electric | Curable composition |
DE1224039B (de) * | 1964-02-06 | 1966-09-01 | Bayer Ag | Unter Ausschluss von Wasser lagerfaehige, plastische Organopolysiloxanformmassen |
US3294739A (en) * | 1964-11-19 | 1966-12-27 | Dow Corning | Method of making one component room temperature curing siloxane rubbers |
GB1154724A (en) * | 1965-08-11 | 1969-06-11 | Midland Silicones Ltd | Improvements in or relating to Organopolysiloxanes |
US3471434A (en) * | 1965-12-27 | 1969-10-07 | Stauffer Chemical Co | Room temperature curing organopolysiloxane elastomers |
US3334067A (en) * | 1966-04-08 | 1967-08-01 | Dow Corning | Method of making one component room temperature curing siloxane rubbers |
US3438930A (en) * | 1967-05-01 | 1969-04-15 | Gen Electric | Alkoxyhydroxy-terminated polydiorganosiloxanes curable at room temperature |
US3560442A (en) * | 1967-10-20 | 1971-02-02 | Bayer Ag | Organo - polysiloxane compositions convertible into elastomers at room temperature |
US3542901A (en) * | 1968-06-26 | 1970-11-24 | Midland Silicones Ltd | Organosilicon compositions |
US3549590A (en) * | 1968-07-17 | 1970-12-22 | Gen Electric | Aminoalkoxyalkenyl-polysiloxanes |
US3622529A (en) * | 1969-03-14 | 1971-11-23 | Gen Electric | Rtv silicone composition containing an imidatosilane |
US3665026A (en) * | 1969-03-14 | 1972-05-23 | Gen Electric | Imidatosilanes |
US3796686A (en) * | 1969-09-11 | 1974-03-12 | Bayer Ag | Organopolysiloxane compositions convertible into elastomers at room temperature |
US3896079A (en) * | 1969-11-12 | 1975-07-22 | Rhone Poulenc Sa | Iminoxyorganosilanes |
BE759621A (fr) | 1969-12-01 | 1971-06-01 | Dow Corning | Copolymeres sequences d'organosiloxanes non corrosifs, vulcanisables a la temperature ambiante |
US3647917A (en) * | 1970-04-06 | 1972-03-07 | Dow Corning | Room temperature vulcanizable silicone rubber with unprimed adhesion |
US3839386A (en) * | 1970-12-30 | 1974-10-01 | Stauffer Chemical Co | Oximo endblocked disiloxanes and process therefor |
US3689454A (en) * | 1971-01-06 | 1972-09-05 | Gen Electric | Curable compositions |
US3779986A (en) * | 1971-01-06 | 1973-12-18 | Gen Electric | Curable compositions |
US3829529A (en) * | 1971-12-30 | 1974-08-13 | Stauffer Chemical Co | Room-temperature curing organopolysiloxanes |
US3826782A (en) * | 1972-07-10 | 1974-07-30 | Stauffer Chemical Co | Room temperature curable organopolysiloxanes |
JPS5139673B2 (es) * | 1972-07-14 | 1976-10-29 | ||
NL7311581A (es) * | 1972-08-29 | 1974-03-04 | ||
US3983265A (en) * | 1973-05-11 | 1976-09-28 | Rhone-Poulenc S.A. | Method of coating a substrate with curable organopolysiloxane compositions |
FR2228814B1 (es) * | 1973-05-11 | 1975-11-21 | Rhone Poulenc Ind | |
JPS5138693A (en) * | 1974-09-30 | 1976-03-31 | Tohoku Denki Koji Kk | Kasenzagyoji notarumi boshihonarabinisochi |
US4248993A (en) * | 1977-06-29 | 1981-02-03 | Shin-Etsu Chemical Co. Ltd. | Room temperature curable organopolysiloxane |
JPS5411953A (en) * | 1977-06-29 | 1979-01-29 | Shin Etsu Chem Co Ltd | Cold-curable organopolysiloxane composition |
US4257932A (en) * | 1978-06-27 | 1981-03-24 | General Electric Company | Curable compositions and process |
JPS5846153B2 (ja) * | 1978-07-27 | 1983-10-14 | ナトコペイント株式会社 | 被覆用樹脂組成物 |
JPS5543119A (en) * | 1978-09-20 | 1980-03-26 | Sws Silicones Corp | Titanium ester contained vulcanizable organopolysiloxane composition and its manufacture |
US4267297A (en) * | 1979-10-19 | 1981-05-12 | Toray Silicone Company, Ltd. | Room temperature curable silicone resins |
-
1981
- 1981-06-26 US US06/277,524 patent/US4395526A/en not_active Expired - Lifetime
-
1982
- 1982-06-09 JP JP57502288A patent/JPS58501040A/ja active Granted
- 1982-06-09 BR BR8207777A patent/BR8207777A/pt unknown
- 1982-06-09 WO PCT/US1982/000787 patent/WO1983000156A1/en active Application Filing
- 1982-06-11 CA CA000404949A patent/CA1197035A/en not_active Expired
- 1982-06-15 ZA ZA824212A patent/ZA824212B/xx unknown
- 1982-06-17 AT AT82105311T patent/ATE37038T1/de not_active IP Right Cessation
- 1982-06-17 DE DE8282105311T patent/DE3278995D1/de not_active Expired
- 1982-06-17 EP EP82105311A patent/EP0069256B1/en not_active Expired
- 1982-06-25 ES ES513502A patent/ES513502A0/es active Granted
- 1982-06-25 KR KR1019820002843A patent/KR840000610A/ko unknown
-
1983
- 1983-02-17 NO NO830537A patent/NO830537L/no unknown
- 1983-02-25 DK DK93283A patent/DK93283A/da not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
ES8307854A1 (es) | 1983-08-01 |
ZA824212B (en) | 1983-04-27 |
JPS6365229B2 (es) | 1988-12-15 |
BR8207777A (pt) | 1983-06-21 |
WO1983000156A1 (en) | 1983-01-20 |
DK93283D0 (da) | 1983-02-25 |
CA1197035A (en) | 1985-11-19 |
EP0069256A3 (en) | 1983-06-08 |
DE3278995D1 (en) | 1988-10-13 |
EP0069256B1 (en) | 1988-09-07 |
US4395526A (en) | 1983-07-26 |
KR840000610A (ko) | 1984-02-25 |
EP0069256A2 (en) | 1983-01-12 |
DK93283A (da) | 1983-02-25 |
ES513502A0 (es) | 1983-08-01 |
JPS58501040A (ja) | 1983-06-30 |
ATE37038T1 (de) | 1988-09-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO830537L (no) | Organopolysiloksanblanding. | |
KR100194303B1 (ko) | 개선된 실온 경화성 실리콘 조성물 | |
US4472551A (en) | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions | |
US3542901A (en) | Organosilicon compositions | |
US4513115A (en) | Low modulus one component RTV compositions processes | |
US4477625A (en) | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions | |
EP0384183A2 (en) | Mixtures comprising silanol-terminated polydiorganosiloxane and processes | |
US4472564A (en) | Method for making an enoxy stabilized room temperature vulcanizable organopolysiloxane composition which resists color change upon aging | |
US4731411A (en) | Process for producing alkoxy-terminated polysiloxanes | |
JPH0543803A (ja) | 低モジユラス1成分型rtv組成物およびその製造方法 | |
US4499230A (en) | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions containing a zeolite | |
US4424157A (en) | Silicon containing lactams | |
US4895918A (en) | Alkoxy-functional one-component RTV silicone rubber compositions | |
US4467063A (en) | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions | |
US4517352A (en) | One package, stable, moisture curable, polyalkoxy-terminated _organopolysiloxane compositions and method for making | |
US4593085A (en) | Alkoxy-functional one component RTV silicone rubber compositions | |
US4539367A (en) | Low modulus one-component RTV compositions and processes | |
US4499229A (en) | One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions | |
US4670532A (en) | Alkoxy-functional one-component RTV silicone rubber compositions | |
US4503209A (en) | Acetamide scavengers for RTV silicone rubber compositions | |
CA1248264A (en) | Scavengers for one component alkoxy-functional rtv compositions | |
US4755578A (en) | Alkoxy-functional one-component RTV silicone rubber compositions | |
GB2138013A (en) | Cure accelerator for RTV composition | |
JPH038657B2 (es) | ||
JPH0455225B2 (es) |