CA1284849C - Compositions d'etancheite a auto-etalement, a base de silicone, et leur fabrication - Google Patents

Compositions d'etancheite a auto-etalement, a base de silicone, et leur fabrication

Info

Publication number: CA1284849C
Authority: CA; Canada
Prior art keywords: amine; composition; weight; acyloxy; polydiorganosiloxane
Prior art date: 1985-03-26
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.): Expired - Lifetime

Application number

CA000504145A

Other languages

English (en)

Inventor

Melvin D. Beers

John W. Dean

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

General Electric Co

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.)

1985-03-26

Filing date

1986-03-14

Publication date

1991-06-11

1986-03-14 Application filed by General Electric Co filed Critical General Electric Co

1991-06-11 Application granted granted Critical

1991-06-11 Publication of CA1284849C publication Critical patent/CA1284849C/fr

2008-06-11 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 87
238000000034 method Methods 0.000 title claims abstract description 29
239000004590 silicone sealant Substances 0.000 title abstract description 4
150000001412 amines Chemical class 0.000 claims abstract description 45
239000003054 catalyst Substances 0.000 claims abstract description 14
238000009833 condensation Methods 0.000 claims abstract description 14
230000005494 condensation Effects 0.000 claims abstract description 14
238000009877 rendering Methods 0.000 claims abstract description 8
-1 hydrocarbon radicals Chemical class 0.000 claims description 49
239000000945 filler Substances 0.000 claims description 24
150000003254 radicals Chemical class 0.000 claims description 23
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
239000004215 Carbon black (E152) Substances 0.000 claims description 18
229930195733 hydrocarbon Natural products 0.000 claims description 18
229910052751 metal Inorganic materials 0.000 claims description 14
239000002184 metal Substances 0.000 claims description 14
239000012763 reinforcing filler Substances 0.000 claims description 13
229910021485 fumed silica Inorganic materials 0.000 claims description 12
150000002430 hydrocarbons Chemical class 0.000 claims description 11
150000003335 secondary amines Chemical class 0.000 claims description 11
PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 5
150000002739 metals Chemical class 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 4
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 4
150000003141 primary amines Chemical class 0.000 claims description 4
229910052718 tin Inorganic materials 0.000 claims description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
125000000271 carboxylic acid salt group Chemical group 0.000 claims 2
125000004966 cyanoalkyl group Chemical group 0.000 claims 2
229910000077 silane Inorganic materials 0.000 claims 1
229920001296 polysiloxane Polymers 0.000 abstract description 20
150000003839 salts Chemical class 0.000 description 5
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000000565 sealant Substances 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
239000004614 Process Aid Substances 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
150000001734 carboxylic acid salts Chemical class 0.000 description 2
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
125000005386 organosiloxy group Chemical group 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
239000010703 silicon Substances 0.000 description 2
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
229910052770 Uranium Inorganic materials 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
OPARTXXEFXPWJL-UHFFFAOYSA-N [acetyloxy-bis[(2-methylpropan-2-yl)oxy]silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)(C)C)OC(C)(C)C OPARTXXEFXPWJL-UHFFFAOYSA-N 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
229910052787 antimony Inorganic materials 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
239000010425 asbestos Substances 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
229910052793 cadmium Inorganic materials 0.000 description 1
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
RPBPCPJJHKASGQ-UHFFFAOYSA-K chromium(3+);octanoate Chemical compound [Cr+3].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O RPBPCPJJHKASGQ-UHFFFAOYSA-K 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
238000010276 construction Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 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
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
QCWKNPBWGUZSTH-UHFFFAOYSA-L decanedioate;lead(2+) Chemical compound [Pb+2].[O-]C(=O)CCCCCCCCC([O-])=O QCWKNPBWGUZSTH-UHFFFAOYSA-L 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
239000004205 dimethyl polysiloxane Substances 0.000 description 1
229920005645 diorganopolysiloxane polymer Polymers 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
239000012530 fluid Substances 0.000 description 1
150000002357 guanidines Chemical class 0.000 description 1
125000006038 hexenyl group Chemical group 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
229940070765 laurate Drugs 0.000 description 1
239000011133 lead Substances 0.000 description 1
GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
239000000463 material Substances 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000005561 phenanthryl group Chemical group 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
230000009974 thixotropic effect Effects 0.000 description 1
239000011135 tin Substances 0.000 description 1
XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
229910001887 tin oxide Inorganic materials 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
229910052726 zirconium Inorganic materials 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
- C08K5/17—Amines; Quaternary ammonium compounds
- 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
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
- C07F7/14—Preparation thereof from optionally substituted halogenated silanes and hydrocarbons hydrosilylation reactions
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Sealing Material Composition (AREA)

CA000504145A 1985-03-26 1986-03-14 Compositions d'etancheite a auto-etalement, a base de silicone, et leur fabrication Expired - Lifetime CA1284849C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US71607385A	1985-03-26	1985-03-26
US716,073		1985-03-26

Publications (1)

Publication Number	Publication Date
CA1284849C true CA1284849C (fr)	1991-06-11

Family

ID=24876618

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000504145A Expired - Lifetime CA1284849C (fr)	1985-03-26	1986-03-14	Compositions d'etancheite a auto-etalement, a base de silicone, et leur fabrication

Country Status (6)

Country	Link
JP (1)	JPH0668103B2 (fr)
KR (1)	KR860007271A (fr)
CA (1)	CA1284849C (fr)
DE (1)	DE3609543A1 (fr)
FR (1)	FR2587351A1 (fr)
GB (1)	GB2174401B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1333307C (fr) *	1988-04-15	1994-11-29	John Earl Dietlein	Composition d'etancheite pour joints de dilatation de routes bitumees
US4889878A (en) *	1988-04-15	1989-12-26	Dow Corning Corporation	Flowable joint sealant for concrete highway
CA1337313C (fr) *	1988-04-15	1995-10-10	Dow Corning Corporation	Agent de scellement pour les routes, produisant une surface horizontale
WO2019002705A1 (fr) *	2017-06-29	2019-01-03	Elkem Silicones France Sas	Procédé de fabrication de moules en élastomère silicone

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB835790A (en) *	1957-07-12	1960-05-25	Rhone Poulenc Sa	Improvements in or relating to siloxane elastomers
GB849069A (en) *	1957-12-31	1960-09-21	Rhone Poulenc Sa	Organopolysiloxane compositions
GB856321A (en) *	1958-12-02	1960-12-14	Rhone Poulenc Sa	Improvements in or relating to siloxane elastomers
DE1167020B (de) *	1962-06-14	1964-04-02	Wacker Chemie Gmbh	Unter Ausschluss von Wasser lagerfaehige, bei Zutritt von Wasser bei Raumtemperatur zu Elastomeren haertende Formmassen auf Organopolysiloxangrundlage
JPS5594956A (en) *	1979-01-12	1980-07-18	Toshiba Silicone Co Ltd	Room temperature curable polysiloxane composition
US4304897A (en) *	1980-07-17	1981-12-08	General Electric Company	Room temperature vulcanizable silicone rubber compositions and process of making
DE3121984A1 (de) *	1981-06-03	1982-12-23	Wacker-Chemie GmbH, 8000 München	Zu elastomeren vernetzbare massen

1986
- 1986-03-14 CA CA000504145A patent/CA1284849C/fr not_active Expired - Lifetime
- 1986-03-21 DE DE19863609543 patent/DE3609543A1/de not_active Withdrawn
- 1986-03-21 GB GB8607073A patent/GB2174401B/en not_active Expired
- 1986-03-25 KR KR1019860002207A patent/KR860007271A/ko not_active Ceased
- 1986-03-26 JP JP61066122A patent/JPH0668103B2/ja not_active Expired - Lifetime
- 1986-03-26 FR FR8604365A patent/FR2587351A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
KR860007271A (ko)	1986-10-10
GB8607073D0 (en)	1986-04-30
DE3609543A1 (de)	1986-10-02
JPS61252286A (ja)	1986-11-10
GB2174401A (en)	1986-11-05
FR2587351A1 (fr)	1987-03-20
JPH0668103B2 (ja)	1994-08-31
GB2174401B (en)	1989-12-13

Legal Events

Date	Code	Title	Description
1995-12-11	MKLA	Lapsed

Publication	Publication Date	Title
US4672003A (en)	1987-06-09	RTV organopolysiloxane compositions and self-adhesive elastomers therefrom
US3334067A (en)	1967-08-01	Method of making one component room temperature curing siloxane rubbers
US4461867A (en)	1984-07-24	Composition for promoting adhesion of curable silicones to substrates
US4529752A (en)	1985-07-16	Solvent resistant vulcanizable silicone rubber composition
US4525400A (en)	1985-06-25	Composition for promoting adhesion of curable silicones to substrates
CA1233477A (fr)	1988-03-01	Compositions d'organopolysiloxane vulcanisables a la temperature de la piece
JP6215312B2 (ja)	2017-10-18	有機ケイ素化合物をベースとした架橋性組成物
JP2698268B2 (ja)	1998-01-19	改良された室温硬化性シリコ―ン組成物
EP0520717B1 (fr)	1996-09-11	Promoteurs d'adhésion pour compositions de silicone vulcanisables à température ambiante
EP0586240A2 (fr)	1994-03-09	Polydiorganosiloxane à groupes terminaux alkoxy et élastomères de silicone vulcanisables à température ambiante à partir de ceci
US4599374A (en)	1986-07-08	Solvent resistant vulcanizable silicone rubber compositions made with fluorosilicone hydride cross linking agents
US4894412A (en)	1990-01-16	Process for preparing self-crosslinkable aminosiloxane emulsion
US5034455A (en)	1991-07-23	Curable silicone caulk compositions
JP2000169587A (ja)	2000-06-20	Ｒｔｖ―１―アルコキシ材料、その製造方法およびその使用
US4554338A (en)	1985-11-19	Room temperature vulcanizable organopolysiloxane compositions and method for making
JPS6318625B2 (fr)	1988-04-19
AU735954B2 (en)	2001-07-19	Organopolysiloxane compositions crosslinkable with elimination of alcohols to give elastomers
DE4204306A1 (de)	1993-08-19	Organopolysiloxanzusammensetzung
CA1253655A (fr)	1989-05-09	Melanges stabilises a base de fluides de polysiloxane a fonction thio et de fluides d'organopolysiloxanes, methode pour les stabiliser
US4578492A (en)	1986-03-25	Non-corrosive silicone RTV compositions
US4230632A (en)	1980-10-28	Preparation of heat stable silicone fluids
CA1272335A (fr)	1990-07-31	Compositions d'organopolysiloxane moins corrosifs pour le cuivre
CA1284849C (fr)	1991-06-11	Compositions d'etancheite a auto-etalement, a base de silicone, et leur fabrication
EP0400786B1 (fr)	1995-09-20	Composition de polysiloxane à fonction acrylamide résistant à la chaleur
CA1246277A (fr)	1988-12-06	Compositions de caoutchouc de silicone rtv a un seul constituant, possedant de bonnes proprietes auto- adhesives avec les plastiques d'acrylate