CA2056487A1 - Additifs servant a ameliorer le module faible de compositions a vulcanisation a la temperature de la piece - Google Patents

Additifs servant a ameliorer le module faible de compositions a vulcanisation a la temperature de la piece

Info

Publication number: CA2056487A1
Authority: CA; Canada
Prior art keywords: substrate; parts; composition according; docket; radicals
Prior art date: 1990-12-17
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.): Abandoned

Application number

CA 2056487

Other languages

English (en)

Inventor

Gary M. Lucas

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

General Electric Co

Original Assignee

Individual

Priority date (The priority date 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 date listed.)

1990-12-17

Filing date

1991-11-28

Publication date

1992-06-18

1991-11-28 Application filed by Individual filed Critical Individual

1992-06-18 Publication of CA2056487A1 publication Critical patent/CA2056487A1/fr

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 65
239000000654 additive Substances 0.000 title abstract description 3
239000003054 catalyst Substances 0.000 claims abstract description 20
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 16
229910000077 silane Inorganic materials 0.000 claims abstract description 15
229920001296 polysiloxane Polymers 0.000 claims abstract description 13
230000001737 promoting effect Effects 0.000 claims abstract description 10
238000009833 condensation Methods 0.000 claims abstract description 6
230000005494 condensation Effects 0.000 claims abstract description 6
239000000945 filler Substances 0.000 claims abstract description 6
-1 acryloxy Chemical group 0.000 claims description 40
239000004215 Carbon black (E152) Substances 0.000 claims description 33
229930195733 hydrocarbon Natural products 0.000 claims description 33
239000000758 substrate Substances 0.000 claims description 29
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 19
229920000642 polymer Polymers 0.000 claims description 16
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 10
125000000962 organic group Chemical group 0.000 claims description 10
229910052710 silicon Inorganic materials 0.000 claims description 10
239000000377 silicon dioxide Substances 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 7
239000011521 glass Substances 0.000 claims description 7
150000002430 hydrocarbons Chemical class 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000004093 cyano group Chemical group *C#N 0.000 claims description 6
229920002554 vinyl polymer Polymers 0.000 claims description 6
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 5
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
229910052782 aluminium Inorganic materials 0.000 claims description 5
125000003118 aryl group Chemical group 0.000 claims description 5
238000004132 cross linking Methods 0.000 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
229920000058 polyacrylate Polymers 0.000 claims description 5
229920000515 polycarbonate Polymers 0.000 claims description 5
229920000915 polyvinyl chloride Polymers 0.000 claims description 5
239000004800 polyvinyl chloride Substances 0.000 claims description 5
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
125000002252 acyl group Chemical group 0.000 claims description 3
125000004423 acyloxy group Chemical group 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
125000002993 cycloalkylene group Chemical group 0.000 claims description 3
229910021485 fumed silica Inorganic materials 0.000 claims description 3
125000001261 isocyanato group Chemical group *N=C=O 0.000 claims description 3
POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
150000002825 nitriles Chemical class 0.000 claims description 2
125000005504 styryl group Chemical group 0.000 claims description 2
239000004567 concrete Substances 0.000 claims 4
239000004417 polycarbonate Substances 0.000 claims 4
239000012763 reinforcing filler Substances 0.000 claims 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical group CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 claims 2
UYIOITAGWJIBKY-UHFFFAOYSA-N 3-(2-methyl-4-trimethoxysilylbut-3-en-2-yl)oxypropanenitrile Chemical compound CO[Si](OC)(OC)C=CC(C)(C)OCCC#N UYIOITAGWJIBKY-UHFFFAOYSA-N 0.000 claims 1
ITSZNKWGCBRYQB-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propanenitrile Chemical compound CCO[Si](C)(OCC)CCC#N ITSZNKWGCBRYQB-UHFFFAOYSA-N 0.000 claims 1
WKGYMMAZQLFVEB-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propanenitrile Chemical compound CO[Si](C)(OC)CCC#N WKGYMMAZQLFVEB-UHFFFAOYSA-N 0.000 claims 1
GBQYMXVQHATSCC-UHFFFAOYSA-N 3-triethoxysilylpropanenitrile Chemical compound CCO[Si](OCC)(OCC)CCC#N GBQYMXVQHATSCC-UHFFFAOYSA-N 0.000 claims 1
KVUMYOWDFZAGPN-UHFFFAOYSA-N 3-trimethoxysilylpropanenitrile Chemical compound CO[Si](OC)(OC)CCC#N KVUMYOWDFZAGPN-UHFFFAOYSA-N 0.000 claims 1
YSEVGVGBHWFTIF-UHFFFAOYSA-N 4-[dimethoxy(methyl)silyl]butanenitrile Chemical compound CO[Si](C)(OC)CCCC#N YSEVGVGBHWFTIF-UHFFFAOYSA-N 0.000 claims 1
VGIURMCNTDVGJM-UHFFFAOYSA-N 4-triethoxysilylbutanenitrile Chemical compound CCO[Si](OCC)(OCC)CCCC#N VGIURMCNTDVGJM-UHFFFAOYSA-N 0.000 claims 1
239000004593 Epoxy Substances 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
NDOGLIPWGGRQCO-UHFFFAOYSA-N hexane-2,4-dione Chemical compound CCC(=O)CC(C)=O NDOGLIPWGGRQCO-UHFFFAOYSA-N 0.000 claims 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 1
239000002516 radical scavenger Substances 0.000 claims 1
229920006395 saturated elastomer Polymers 0.000 claims 1
230000000996 additive effect Effects 0.000 abstract description 2
239000003431 cross linking reagent Substances 0.000 abstract 1
230000009977 dual effect Effects 0.000 abstract 1
150000003254 radicals Chemical class 0.000 description 21
150000001875 compounds Chemical class 0.000 description 12
239000012530 fluid Substances 0.000 description 10
150000001412 amines Chemical class 0.000 description 8
238000010168 coupling process Methods 0.000 description 6
238000005859 coupling reaction Methods 0.000 description 6
150000002500 ions Chemical class 0.000 description 6
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
239000010703 silicon Substances 0.000 description 6
241000042812 Divales Species 0.000 description 5
239000002253 acid Substances 0.000 description 5
229920005645 diorganopolysiloxane polymer Polymers 0.000 description 5
239000003446 ligand Substances 0.000 description 5
238000002156 mixing Methods 0.000 description 5
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 5
229920002545 silicone oil Polymers 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
238000000034 method Methods 0.000 description 4
239000003921 oil Substances 0.000 description 4
244000116484 Inula helenium Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
150000005840 aryl radicals Chemical class 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229910052697 platinum Inorganic materials 0.000 description 3
UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-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
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
SJNALLRHIVGIBI-UHFFFAOYSA-N allyl cyanide Chemical compound C=CCC#N SJNALLRHIVGIBI-UHFFFAOYSA-N 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
239000003795 chemical substances by application Substances 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
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
UPCIBFUJJLCOQG-UHFFFAOYSA-L ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium;dibromide Chemical compound [Br-].[Br-].CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC UPCIBFUJJLCOQG-UHFFFAOYSA-L 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
WTEVQBCEXWBHNA-YFHOEESVSA-N neral Chemical compound CC(C)=CCC\C(C)=C/C=O WTEVQBCEXWBHNA-YFHOEESVSA-N 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
229920002631 room-temperature vulcanizate silicone Polymers 0.000 description 2
125000005372 silanol group Chemical group 0.000 description 2
238000003756 stirring Methods 0.000 description 2
PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 description 1
125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
241000357297 Atypichthys strigatus Species 0.000 description 1
239000007848 Bronsted acid Substances 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
241000040710 Chela Species 0.000 description 1
241001630921 Chlorida Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
102100024133 Coiled-coil domain-containing protein 50 Human genes 0.000 description 1
239000004971 Cross linker Substances 0.000 description 1
XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
241001397104 Dima Species 0.000 description 1
241001269524 Dura Species 0.000 description 1
MUQNGPZZQDCDFT-JNQJZLCISA-N Halcinonide Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CCl)[C@@]1(C)C[C@@H]2O MUQNGPZZQDCDFT-JNQJZLCISA-N 0.000 description 1
101000910772 Homo sapiens Coiled-coil domain-containing protein 50 Proteins 0.000 description 1
STECJAGHUSJQJN-USLFZFAMSA-N LSM-4015 Chemical compound C1([C@@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-USLFZFAMSA-N 0.000 description 1
241001274660 Modulus Species 0.000 description 1
101100001347 Mus musculus Akt1s1 gene Proteins 0.000 description 1
101100410811 Mus musculus Pxt1 gene Proteins 0.000 description 1
YFONKFDEZLYQDH-OPQQBVKSSA-N N-[(1R,2S)-2,6-dimethyindan-1-yl]-6-[(1R)-1-fluoroethyl]-1,3,5-triazine-2,4-diamine Chemical compound C[C@@H](F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-OPQQBVKSSA-N 0.000 description 1
208000034177 Self-improving collodion baby Diseases 0.000 description 1
241000613130 Tima Species 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
229920013624 Tylac Polymers 0.000 description 1
101000994673 Urodacus yaschenkoi Potassium channel toxin alpha-KTx 6.21 Proteins 0.000 description 1
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
YVPYQUNUQOZFHG-UHFFFAOYSA-N amidotrizoic acid Chemical compound CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C(O)=O)=C1I YVPYQUNUQOZFHG-UHFFFAOYSA-N 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
235000013405 beer Nutrition 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
210000005056 cell body Anatomy 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
WTEVQBCEXWBHNA-JXMROGBWSA-N citral A Natural products CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
230000008878 coupling Effects 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
230000005484 gravity Effects 0.000 description 1
229940028332 halog Drugs 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000007788 liquid Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
AMLJWLYRONUCKO-UHFFFAOYSA-N n-(6-amino-5-iodopyridin-2-yl)acetamide Chemical compound CC(=O)NC1=CC=C(I)C(N)=N1 AMLJWLYRONUCKO-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
239000003415 peat Substances 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
238000010791 quenching Methods 0.000 description 1
IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 description 1
239000000565 sealant Substances 0.000 description 1
208000003665 self-healing collodion baby Diseases 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000012974 tin catalyst Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
125000005389 trialkylsiloxy group Chemical group 0.000 description 1
125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
229910052726 zirconium Inorganic materials 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

CA 2056487 1990-12-17 1991-11-28 Additifs servant a ameliorer le module faible de compositions a vulcanisation a la temperature de la piece Abandoned CA2056487A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US62831590A	1990-12-17	1990-12-17
US628,315		1990-12-17

Publications (1)

Publication Number	Publication Date
CA2056487A1 true CA2056487A1 (fr)	1992-06-18

Family

ID=24518378

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2056487 Abandoned CA2056487A1 (fr)	1990-12-17	1991-11-28	Additifs servant a ameliorer le module faible de compositions a vulcanisation a la temperature de la piece

Country Status (2)

Country	Link
JP (1)	JPH04335066A (fr)
CA (1)	CA2056487A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0565309A1 (fr) *	1992-04-07	1993-10-13	General Electric Company	Compositions de silicone
DE102014222826A1 (de)	2014-11-07	2016-05-12	Wacker Chemie Ag	Vernetzbare Organopolysiloxanzusammensetzungen
EP3575373A4 (fr) *	2017-01-30	2020-12-09	Dow Toray Co., Ltd.	Agent de revêtement destiné à une structure en béton

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4221693A (en) *	1979-03-02	1980-09-09	Getson John C	Composition free of surface cure inhibition and method for preparing the same
US4780338A (en) *	1987-03-26	1988-10-25	General Electric Company	Solventless silicone coating composition
FR2634768A1 (fr) *	1988-07-29	1990-02-02	Rhone Poulenc Chimie	Procede de preparation de diorganopolysiloxanes a groupements terminaux alcoxy

1991
- 1991-11-28 CA CA 2056487 patent/CA2056487A1/fr not_active Abandoned
- 1991-12-11 JP JP35050191A patent/JPH04335066A/ja active Pending

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0565309A1 (fr) *	1992-04-07	1993-10-13	General Electric Company	Compositions de silicone
DE102014222826A1 (de)	2014-11-07	2016-05-12	Wacker Chemie Ag	Vernetzbare Organopolysiloxanzusammensetzungen
US10316149B2 (en)	2014-11-07	2019-06-11	Wacker Chemie Ag	Crosslinkable organopolysiloxane compositions
EP3575373A4 (fr) *	2017-01-30	2020-12-09	Dow Toray Co., Ltd.	Agent de revêtement destiné à une structure en béton

Also Published As

Publication number	Publication date
JPH04335066A (ja)	1992-11-24

Legal Events

Date	Code	Title	Description
1996-05-28	FZDE	Dead

Publication	Publication Date	Title
US4257936A (en)	1981-03-24	Self-bonding silicone compositions
CA2007660C (fr)	2000-09-05	Compositions formant des elastomeres
CA1197035A (fr)	1985-11-19	Compositions d'organopolysiloxanne avec terminaison polyalcoxy, sous forme d'un seul constituant, stables, et reticulables en presence d'humidite; methode de preparation
CA1195032A (fr)	1985-10-08	Agents ameliorant l'adherence pour compositions de silicone rtv a un seul constituant
US5175057A (en)	1992-12-29	Adhesion promoters for room temperature vulcanizable silicone compositions
CA2056525A1 (fr)	1992-06-18	Compositions a base de silicone, reticulables a la temperature de la piece
CA2056569A1 (fr)	1992-06-18	Compositions de silicone reticulables a la temperature de la piece
US5254657A (en)	1993-10-19	RTV silicone rubber compositions and cured products thereof
GB2144442A (en)	1985-03-06	Room temperature vulcanizable organopolysiloxane compositions
US5051467A (en)	1991-09-24	Silicone rubber compositions
CA2037653A1 (fr)	1991-09-20	Compositions simples d'organosiloxane stables au stockage
EP0566272A1 (fr)	1993-10-20	Composition durcissant rapidement à température ambiante
CA1242836A (fr)	1988-10-04	Polysiloxanes organiques vulcanisables a la temperature ambiante et methode de fabrication
NL8300604A (nl)	1983-09-16	Uit een pakket bestaande rtv-materialen met geringe modulus en werkwijzen ter bereiding hiervan.
JPH0563512B2 (fr)	1993-09-10
US5475076A (en)	1995-12-12	Organo(poly)siloxane compositions which can be cross-linked to give elastomers with elimination of alcohols
US5561184A (en)	1996-10-01	Room temperature curable silicone composition
US5959018A (en)	1999-09-28	RTV organopolysiloxane compositions
GB2137645A (en)	1984-10-10	A method for making an enoxy stabilized room temperature vulcanizable organopolysiloxane composition which resists color change upon aging
US5244938A (en)	1993-09-14	Room temperature curable organopolysiloxane composition
KR100224378B1 (ko)	1999-10-15	일 액형 열 경화성 오르가노폴리실록산 조성물
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