JPH0668103B2 - 自己レベリング性シリコーンシーラント組成物およびその製法 - Google Patents

自己レベリング性シリコーンシーラント組成物およびその製法

Info

Publication number: JPH0668103B2
Authority: JP; Japan
Prior art keywords: amine; composition; terminated polydiorganosiloxane; amount; weight
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

JP61066122A

Other languages

English (en)

Japanese (ja)

Other versions

JPS61252286A (ja

Inventor

メルビン・デール・ビアーズ

ジヨン・ウイリアム・デイーン

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

1986-03-26

Publication date

1994-08-31

1986-03-26 Application filed by General Electric Co filed Critical General Electric Co

1986-11-10 Publication of JPS61252286A publication Critical patent/JPS61252286A/ja

1994-08-31 Publication of JPH0668103B2 publication Critical patent/JPH0668103B2/ja

2009-08-31 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims description 95
238000004519 manufacturing process Methods 0.000 title claims description 7
239000004590 silicone sealant Substances 0.000 title description 3
150000001412 amines Chemical class 0.000 claims description 45
238000000034 method Methods 0.000 claims description 26
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 25
239000000945 filler Substances 0.000 claims description 25
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims description 15
239000012763 reinforcing filler Substances 0.000 claims description 14
239000003054 catalyst Substances 0.000 claims description 13
238000009833 condensation Methods 0.000 claims description 13
230000005494 condensation Effects 0.000 claims description 13
229910021485 fumed silica Inorganic materials 0.000 claims description 13
229910052751 metal Inorganic materials 0.000 claims description 12
239000002184 metal Substances 0.000 claims description 12
150000003335 secondary amines Chemical class 0.000 claims description 11
125000004423 acyloxy group Chemical group 0.000 claims description 10
238000002156 mixing Methods 0.000 claims description 10
125000004966 cyanoalkyl group Chemical group 0.000 claims description 9
150000008282 halocarbons Chemical group 0.000 claims description 9
125000001183 hydrocarbyl group Chemical group 0.000 claims description 9
125000001931 aliphatic group Chemical group 0.000 claims description 8
239000000565 sealant Substances 0.000 claims description 8
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 6
239000011133 lead Substances 0.000 claims description 6
PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical group CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 4
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
150000007942 carboxylates Chemical group 0.000 claims description 4
229910052748 manganese Inorganic materials 0.000 claims description 4
239000011572 manganese Substances 0.000 claims description 4
150000003141 primary amines Chemical class 0.000 claims description 4
239000011135 tin Substances 0.000 claims description 4
229910052718 tin Inorganic materials 0.000 claims description 4
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
229910052793 cadmium Inorganic materials 0.000 claims description 2
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 2
229910052804 chromium Inorganic materials 0.000 claims description 2
239000011651 chromium Substances 0.000 claims description 2
229910017052 cobalt Inorganic materials 0.000 claims description 2
239000010941 cobalt Substances 0.000 claims description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
229910052742 iron Inorganic materials 0.000 claims description 2
150000002739 metals Chemical class 0.000 claims description 2
229910052759 nickel Inorganic materials 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
229910052725 zinc Inorganic materials 0.000 claims description 2
239000011701 zinc Substances 0.000 claims description 2
-1 polysiloxanes Polymers 0.000 description 20
229920001296 polysiloxane Polymers 0.000 description 18
239000006057 Non-nutritive feed additive Substances 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
125000005386 organosiloxy group Chemical group 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
229910052710 silicon Inorganic materials 0.000 description 3
239000010703 silicon 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
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-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
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 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
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
239000000654 additive Substances 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
229920005601 base polymer Polymers 0.000 description 2
239000012975 dibutyltin dilaurate Substances 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
229920005645 diorganopolysiloxane polymer Polymers 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
239000012530 fluid Substances 0.000 description 2
229920000435 poly(dimethylsiloxane) Polymers 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
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
SMSVUYQRWYTTLI-UHFFFAOYSA-L 2-ethylhexanoate;iron(2+) Chemical compound [Fe+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O SMSVUYQRWYTTLI-UHFFFAOYSA-L 0.000 description 1
KUQVFOOAIOMQOT-UHFFFAOYSA-N 2-methylpropyltin Chemical compound CC(C)C[Sn] KUQVFOOAIOMQOT-UHFFFAOYSA-N 0.000 description 1
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
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-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
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
TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
229910052787 antimony Inorganic materials 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
239000010425 asbestos Substances 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
239000011230 binding agent Substances 0.000 description 1
125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 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
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
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 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
125000006303 iodophenyl group Chemical group 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 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
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
GCHSKZYGFZYKBO-UHFFFAOYSA-N methoxycarbonyl(phenyl)tin Chemical compound COC(=O)[Sn]C1=CC=CC=C1 GCHSKZYGFZYKBO-UHFFFAOYSA-N 0.000 description 1
150000002762 monocarboxylic acid derivatives 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
125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 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
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
239000004014 plasticizer Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 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
150000003254 radicals Chemical class 0.000 description 1
238000009877 rendering Methods 0.000 description 1
238000000518 rheometry Methods 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
229920002631 room-temperature vulcanizate silicone Polymers 0.000 description 1
239000005060 rubber Substances 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
150000003512 tertiary amines Chemical class 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
125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 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
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
125000005023 xylyl group Chemical group 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)

JP61066122A 1985-03-26 1986-03-26 自己レベリング性シリコーンシーラント組成物およびその製法 Expired - Lifetime JPH0668103B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US71607385A	1985-03-26	1985-03-26
US716073		1985-03-26

Publications (2)

Publication Number	Publication Date
JPS61252286A JPS61252286A (ja)	1986-11-10
JPH0668103B2 true JPH0668103B2 (ja)	1994-08-31

Family

ID=24876618

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61066122A Expired - Lifetime JPH0668103B2 (ja)	1985-03-26	1986-03-26	自己レベリング性シリコーンシーラント組成物およびその製法

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
CA1284849C (fr)	1991-06-11
JPS61252286A (ja)	1986-11-10
GB2174401A (en)	1986-11-05
FR2587351A1 (fr)	1987-03-20
GB2174401B (en)	1989-12-13

Publication	Publication Date	Title
JP2577150B2 (ja)	1997-01-29	改良された室温硬化性シリコーン組成物
CA1253276A (fr)	1989-04-25	Compositions durcissables de silicone, et procedes connexes
EP0069256B1 (fr)	1988-09-07	Compositions d'organopolysiloxanes stables, durcissables à l'humidité ayant des groupes alcoxy terminaux et leur procédé de préparation
US4461867A (en)	1984-07-24	Composition for promoting adhesion of curable silicones to substrates
EP0384183B1 (fr)	1995-08-02	Mélanges comprenant des polydiorganosiloxanes ayant des groupes silanols terminaux et procédés de préparation
US4525400A (en)	1985-06-25	Composition for promoting adhesion of curable silicones to substrates
US4489199A (en)	1984-12-18	Room temperature vulcanizable organopolysiloxane compositions
JPS60202152A (ja)	1985-10-12	室温加硫性オルガノポリシロキサン組成物及びその製造法
US4499234A (en)	1985-02-12	Non-corrosive silicone RTV compositions
US4599394A (en)	1986-07-08	Process for producing alkoxy-terminated polysiloxanes
US4304897A (en)	1981-12-08	Room temperature vulcanizable silicone rubber compositions and process of making
JPH0320148B2 (fr)	1991-03-18
US4554338A (en)	1985-11-19	Room temperature vulcanizable organopolysiloxane compositions and method for making
US4731411A (en)	1988-03-15	Process for producing alkoxy-terminated polysiloxanes
JPH0543803A (ja)	1993-02-23	低モジユラス１成分型ｒｔｖ組成物およびその製造方法
JPS6318625B2 (fr)	1988-04-19
US4895918A (en)	1990-01-23	Alkoxy-functional one-component RTV silicone rubber compositions
US4593085A (en)	1986-06-03	Alkoxy-functional one component RTV silicone rubber compositions
JPH04214764A (ja)	1992-08-05	室温硬化性オルガノポリシロキサン組成物
JPH0323107B2 (fr)	1991-03-28
CA1248264A (fr)	1989-01-03	Agents d'epuration pour compositions rtv a un seul constituant et a fonction alcoxy
JPH0561315B2 (fr)	1993-09-06
JPH0668103B2 (ja)	1994-08-31	自己レベリング性シリコーンシーラント組成物およびその製法
JPH0521940B2 (fr)	1993-03-26
US5011869A (en)	1991-04-30	Self-leveling silicone sealant compositions and methods for making same