JPS58180554A - 水分遮断下で貯蔵可能であり、かつ水分が侵入する際に室温で架橋してエラストマ−になるコンパウンド - Google Patents
水分遮断下で貯蔵可能であり、かつ水分が侵入する際に室温で架橋してエラストマ−になるコンパウンドInfo
- Publication number
- JPS58180554A JPS58180554A JP58051704A JP5170483A JPS58180554A JP S58180554 A JPS58180554 A JP S58180554A JP 58051704 A JP58051704 A JP 58051704A JP 5170483 A JP5170483 A JP 5170483A JP S58180554 A JPS58180554 A JP S58180554A
- Authority
- JP
- Japan
- Prior art keywords
- bonded
- groups
- silicon via
- silicon
- oxygen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229920001971 elastomer Polymers 0.000 title claims abstract description 28
- 239000000806 elastomer Substances 0.000 title claims abstract description 28
- 150000001875 compounds Chemical class 0.000 title claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 5
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 60
- 239000010703 silicon Substances 0.000 claims abstract description 59
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 32
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 32
- 239000001301 oxygen Substances 0.000 claims abstract description 31
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 28
- 125000003277 amino group Chemical group 0.000 claims abstract description 28
- 150000003377 silicon compounds Chemical class 0.000 claims abstract description 21
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 14
- 125000003544 oxime group Chemical group 0.000 claims abstract description 14
- 229910000077 silane Inorganic materials 0.000 claims abstract description 14
- 238000002156 mixing Methods 0.000 claims abstract description 8
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 7
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical group [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 18
- 230000007717 exclusion Effects 0.000 claims description 6
- 150000004756 silanes Chemical class 0.000 claims description 6
- 125000000962 organic group Chemical group 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 19
- 229920005645 diorganopolysiloxane polymer Polymers 0.000 abstract description 16
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 6
- 229930195733 hydrocarbon Natural products 0.000 abstract description 6
- 239000000047 product Substances 0.000 abstract description 4
- 125000004430 oxygen atom Chemical group O* 0.000 abstract description 3
- 229910052718 tin Inorganic materials 0.000 abstract description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 54
- 238000003860 storage Methods 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 14
- -1 siloxane units Chemical group 0.000 description 14
- 150000003606 tin compounds Chemical class 0.000 description 12
- 229910052782 aluminium Inorganic materials 0.000 description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 150000002430 hydrocarbons Chemical group 0.000 description 11
- 238000004132 cross linking Methods 0.000 description 10
- 238000009833 condensation Methods 0.000 description 9
- 230000005494 condensation Effects 0.000 description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
- 238000011049 filling Methods 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 239000000758 substrate Substances 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 239000002131 composite material Substances 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 230000007775 late Effects 0.000 description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- OGZPYBBKQGPQNU-DABLZPOSSA-N (e)-n-[bis[[(e)-butan-2-ylideneamino]oxy]-methylsilyl]oxybutan-2-imine Chemical compound CC\C(C)=N\O[Si](C)(O\N=C(/C)CC)O\N=C(/C)CC OGZPYBBKQGPQNU-DABLZPOSSA-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
- 241001102009 Loxa Species 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- LUZSPGQEISANPO-UHFFFAOYSA-N butyltin Chemical compound CCCC[Sn] LUZSPGQEISANPO-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 238000011017 operating method Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241000237518 Arion Species 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- JZUFKLXOESDKRF-UHFFFAOYSA-N Chlorothiazide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC2=C1NCNS2(=O)=O JZUFKLXOESDKRF-UHFFFAOYSA-N 0.000 description 1
- 101000952982 Conus striatus Conopressin-S Proteins 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001413 amino acids Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- VEZUQRBDRNJBJY-UHFFFAOYSA-N cyclohexanone-oximeFRProcd Natural products ON=C1CCCCC1 VEZUQRBDRNJBJY-UHFFFAOYSA-N 0.000 description 1
- WCRDXYSYPCEIAK-UHFFFAOYSA-N dibutylstannane Chemical compound CCCC[SnH2]CCCC WCRDXYSYPCEIAK-UHFFFAOYSA-N 0.000 description 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- JMANVNJQNLATNU-UHFFFAOYSA-N glycolonitrile Natural products N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000005358 mercaptoalkyl group Chemical group 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 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 1
- 238000003756 stirring Methods 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
- C08K5/57—Organo-tin compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Sealing Material Composition (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3212008.7 | 1982-03-31 | ||
| DE3212008A DE3212008A1 (de) | 1982-03-31 | 1982-03-31 | Unter ausschluss von wasser lagerfaehige, bei zutritt von wasser bei raumtemperatur zu elastomeren vernetzende massen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58180554A true JPS58180554A (ja) | 1983-10-22 |
| JPS6318975B2 JPS6318975B2 (enExample) | 1988-04-20 |
Family
ID=6159896
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58051704A Granted JPS58180554A (ja) | 1982-03-31 | 1983-03-29 | 水分遮断下で貯蔵可能であり、かつ水分が侵入する際に室温で架橋してエラストマ−になるコンパウンド |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4460761A (enExample) |
| EP (1) | EP0090409B1 (enExample) |
| JP (1) | JPS58180554A (enExample) |
| AT (1) | ATE20757T1 (enExample) |
| AU (1) | AU562779B2 (enExample) |
| CA (1) | CA1191650A (enExample) |
| DE (2) | DE3212008A1 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6134066A (ja) * | 1984-07-26 | 1986-02-18 | Kanegafuchi Chem Ind Co Ltd | 引張り特性の改善された組成物 |
| JP2001107023A (ja) * | 1999-07-30 | 2001-04-17 | Three Bond Co Ltd | 自動車用室温硬化性シール材組成物 |
| WO2007094186A1 (ja) * | 2006-02-17 | 2007-08-23 | Chugoku Marine Paints, Ltd. | 硬化性オルガノポリシロキサン組成物および防汚複合塗膜 |
| JP2008546882A (ja) * | 2005-06-24 | 2008-12-25 | ブルースター シリコーン フランス | 室温から加硫して自己粘着性エラストマーを形成するオルガノポリシロキサン組成物の使用 |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3336135A1 (de) * | 1983-10-05 | 1985-04-25 | Bayer Ag, 5090 Leverkusen | Rtv-siliconpasten |
| GB8401016D0 (en) * | 1984-01-14 | 1984-02-15 | Hagen Perennatorwerk | Organopolysiloxane compositions |
| DE3736654A1 (de) * | 1987-10-29 | 1989-05-11 | Bayer Ag | Unter abspaltung von oximen haertende 1 k rtv massen |
| DE4137698A1 (de) * | 1991-11-15 | 1993-05-19 | Wacker Chemie Gmbh | Zinnverbindung enthaltende massen als eine der beiden komponenten von bei raumtemperatur zu organopolysiloxanelastomeren vernetzenden zweikomponentensystemen |
| DE19620816A1 (de) * | 1996-05-23 | 1997-11-27 | Wacker Chemie Gmbh | Zu flammabweisende Elastomere vernetzbare Organopolysiloxanmassen |
| US6235832B1 (en) | 1998-12-21 | 2001-05-22 | Dow Corning Corporation | RTV silicone compositions with rapid development of green strength |
| DE102004047709A1 (de) * | 2004-09-30 | 2006-04-06 | Wacker Chemie Ag | Flaschenkorken mit reduzierter Trichloranisolfreisetzung und Verfahren zu seiner Herstellung |
| KR102256900B1 (ko) * | 2017-02-28 | 2021-05-31 | 와커 헤미 아게 | 엘라스토머를 제공하도록 가교 가능한 조성물의 제조 방법 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5236920A (en) * | 1975-09-19 | 1977-03-22 | Nippon Hoso Kyokai <Nhk> | Color framing unit for electronic editing |
| JPS53102956A (en) * | 1977-02-21 | 1978-09-07 | Toray Silicone Co Ltd | Room temperature moisture-setting organopolysiloxane composition |
| JPS57165453A (en) * | 1981-02-26 | 1982-10-12 | Gen Electric | Completly solvent-free binary system rtv silicone composition |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3186963A (en) * | 1960-09-05 | 1965-06-01 | Midland Silicones Ltd | Siloxane elastomers |
| GB1269644A (en) * | 1968-07-22 | 1972-04-06 | Midland Silicones Ltd | Organopolysiloxane compositions |
| DD83248A1 (de) * | 1969-08-06 | 1971-07-12 | Verfahren zur Herstellung von Härtern für Organopolysiloxane | |
| DE1964502C3 (de) * | 1969-12-23 | 1973-11-22 | Wacker Chemie Gmbh | Verbesserung der Haftfestigkeit von zu Elastomerer ?rtbaren Organopolysiloxanmassen |
| DE2259802B2 (de) * | 1972-12-06 | 1976-09-02 | Wacker-Chemie GmbH, 8000 München | Verfahren zum herstellen von plastischen, rueckprallelastizitaet aufweisenden massen aus organopolysiloxanen |
| US3957704A (en) * | 1974-12-19 | 1976-05-18 | General Electric Company | Cross-linking agents for room temperature vulcanizable silicone rubber compositions |
| DE2524000A1 (de) * | 1975-05-30 | 1976-12-16 | Wacker Chemie Gmbh | Silicium-zinn-verbindungen, verfahren zu ihrer herstellung und ihre verwendung zum herstellen von organopolysiloxanelastomeren |
| US4102860A (en) * | 1975-05-30 | 1978-07-25 | Wacker-Chemie Gmbh | Silicon-tin compounds as condensation catalysts in the preparation of organopolysiloxane elastomers |
| DE2737303C3 (de) * | 1977-08-18 | 1980-07-17 | Wacker-Chemie Gmbh, 8000 Muenchen | Unter Ausschluß von Wasser lagerfähige, bei Zutritt von Wasser bei Raumtemperatur zu Elastomeren vernetzende Formmassen |
-
1982
- 1982-03-31 DE DE3212008A patent/DE3212008A1/de not_active Withdrawn
-
1983
- 1983-02-14 US US06/466,255 patent/US4460761A/en not_active Expired - Lifetime
- 1983-03-02 AU AU11965/83A patent/AU562779B2/en not_active Ceased
- 1983-03-02 CA CA000422691A patent/CA1191650A/en not_active Expired
- 1983-03-29 JP JP58051704A patent/JPS58180554A/ja active Granted
- 1983-03-29 EP EP83103105A patent/EP0090409B1/de not_active Expired
- 1983-03-29 DE DE8383103105T patent/DE3364486D1/de not_active Expired
- 1983-03-29 AT AT83103105T patent/ATE20757T1/de not_active IP Right Cessation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5236920A (en) * | 1975-09-19 | 1977-03-22 | Nippon Hoso Kyokai <Nhk> | Color framing unit for electronic editing |
| JPS53102956A (en) * | 1977-02-21 | 1978-09-07 | Toray Silicone Co Ltd | Room temperature moisture-setting organopolysiloxane composition |
| JPS57165453A (en) * | 1981-02-26 | 1982-10-12 | Gen Electric | Completly solvent-free binary system rtv silicone composition |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6134066A (ja) * | 1984-07-26 | 1986-02-18 | Kanegafuchi Chem Ind Co Ltd | 引張り特性の改善された組成物 |
| JP2001107023A (ja) * | 1999-07-30 | 2001-04-17 | Three Bond Co Ltd | 自動車用室温硬化性シール材組成物 |
| JP2008546882A (ja) * | 2005-06-24 | 2008-12-25 | ブルースター シリコーン フランス | 室温から加硫して自己粘着性エラストマーを形成するオルガノポリシロキサン組成物の使用 |
| WO2007094186A1 (ja) * | 2006-02-17 | 2007-08-23 | Chugoku Marine Paints, Ltd. | 硬化性オルガノポリシロキサン組成物および防汚複合塗膜 |
Also Published As
| Publication number | Publication date |
|---|---|
| US4460761A (en) | 1984-07-17 |
| CA1191650A (en) | 1985-08-06 |
| AU1196583A (en) | 1983-10-06 |
| AU562779B2 (en) | 1987-06-18 |
| EP0090409B1 (de) | 1986-07-16 |
| DE3364486D1 (en) | 1986-08-21 |
| ATE20757T1 (de) | 1986-08-15 |
| EP0090409A2 (de) | 1983-10-05 |
| JPS6318975B2 (enExample) | 1988-04-20 |
| DE3212008A1 (de) | 1983-10-06 |
| EP0090409A3 (en) | 1984-05-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3542901A (en) | Organosilicon compositions | |
| US5597882A (en) | Tin compound-containing compositions as one of the two components of two component systems which crosslink at room temperature to give organopolysiloxane elastomers | |
| AU613696B2 (en) | Organopolysiloxane compositions which can be crosslinked to form elastomers with elimination of alcohols | |
| US7151150B2 (en) | Organopolysiloxane compositions and their use in low-modulus compositions which can be crosslinked at room temperature | |
| JPS6319537B2 (enExample) | ||
| US5304621A (en) | Organo(poly)siloxanes containing terminal siloxane units having organyloxy and hydrogen groups | |
| JP3419718B2 (ja) | Ｒｔｖ−１−アルコキシ組成物、その製造方法およびその使用 | |
| JPS58180554A (ja) | 水分遮断下で貯蔵可能であり、かつ水分が侵入する際に室温で架橋してエラストマ−になるコンパウンド | |
| JPS6112945B2 (enExample) | ||
| KR101914399B1 (ko) | 가교결합성 유기 폴리실록산 조성물 | |
| CZ20002367A3 (cs) | Organopolysiloxanové hmoty zesíťovatelné na elastomery za odštěpení alkoholů | |
| US4801673A (en) | Room temperature crosslinkable compositions | |
| US3647725A (en) | Room temperature vulcanizable silicone rubber stocks | |
| KR100753590B1 (ko) | 유기 규소 화합물을 기재로 한 가교결합형 생성물 | |
| EP0123915B1 (en) | A method for improving the adhesion of amine-containing organopolysiloxane composition | |
| US7491786B2 (en) | Crosslinkable compositions based on organosilicon compounds | |
| US11028268B2 (en) | Process for producing compositions crosslinkable to elastomers | |
| JP2001192558A (ja) | 架橋可能なオルガノポリシロキサン組成物及びこれを含有する成形体 | |
| KR102753036B1 (ko) | 오르가노실리콘 화합물을 기반으로 하는 가교성 조성물 | |
| KR20070046190A (ko) | 질소 함유 유기폴리실록산 및 가교성 재료에서의 그 용도 | |
| US6218498B1 (en) | Organosilicon compounds having urea groups, method for producing same and their utilization | |
| US7071278B2 (en) | Cross-linkable materials based on organosilicon compounds | |
| JP2574080B2 (ja) | 室温硬化性オルガノポリシロキサン組成物およびその硬化物 | |
| JP2582685B2 (ja) | 室温硬化性オルガノポリシロキサン組成物の製造方法 | |
| JP2669191B2 (ja) | 室温硬化性シリコーンゴム組成物及びその硬化物 |