GB1588754A - Self-extinguishing silicone elastomerforming compositions and the silicone elastomers formed therefrom - Google Patents
Self-extinguishing silicone elastomerforming compositions and the silicone elastomers formed therefrom Download PDFInfo
- Publication number
- GB1588754A GB1588754A GB24996/77A GB2499677A GB1588754A GB 1588754 A GB1588754 A GB 1588754A GB 24996/77 A GB24996/77 A GB 24996/77A GB 2499677 A GB2499677 A GB 2499677A GB 1588754 A GB1588754 A GB 1588754A
- Authority
- GB
- United Kingdom
- Prior art keywords
- self
- component
- parts
- extinguishing
- weight
- 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.)
- Expired
Links
- 229920002379 silicone rubber Polymers 0.000 title claims description 33
- 239000000203 mixture Substances 0.000 title claims description 25
- 229920001296 polysiloxane Polymers 0.000 title claims description 18
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 21
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 15
- -1 triazole compound Chemical class 0.000 claims description 14
- 229910052697 platinum Inorganic materials 0.000 claims description 11
- 125000000962 organic group Chemical group 0.000 claims description 10
- 239000006229 carbon black Substances 0.000 claims description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 7
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 7
- 239000012964 benzotriazole Substances 0.000 claims description 7
- 239000004408 titanium dioxide Substances 0.000 claims description 7
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
- 229910021485 fumed silica Inorganic materials 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- HXQHRUJXQJEGER-UHFFFAOYSA-N 1-methylbenzotriazole Chemical compound C1=CC=C2N(C)N=NC2=C1 HXQHRUJXQJEGER-UHFFFAOYSA-N 0.000 claims 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 27
- 238000007792 addition Methods 0.000 description 8
- 235000019241 carbon black Nutrition 0.000 description 8
- 239000000945 filler Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 150000003058 platinum compounds Chemical class 0.000 description 4
- 239000010453 quartz Substances 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 3
- 150000001565 benzotriazoles Chemical class 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 150000000177 1,2,3-triazoles Chemical class 0.000 description 2
- 150000000178 1,2,4-triazoles Chemical class 0.000 description 2
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000001282 organosilanes Chemical class 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- WWNRKHUOXUIPKO-UHFFFAOYSA-N (1,4-dichlorocyclohexa-2,4-diene-1-carbonyl) 1,4-dichlorocyclohexa-2,4-diene-1-carboperoxoate Chemical compound C1=CC(Cl)=CCC1(Cl)C(=O)OOC(=O)C1(Cl)C=CC(Cl)=CC1 WWNRKHUOXUIPKO-UHFFFAOYSA-N 0.000 description 1
- WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
- QEASJVYPHMYPJM-UHFFFAOYSA-N 1,2-dihydrotriazol-5-one Chemical compound OC1=CNN=N1 QEASJVYPHMYPJM-UHFFFAOYSA-N 0.000 description 1
- ZHFSNPDZPPTJAU-UHFFFAOYSA-N 1,3-diphenyl-1,2,4-triazole Chemical compound C1=NC(C=2C=CC=CC=2)=NN1C1=CC=CC=C1 ZHFSNPDZPPTJAU-UHFFFAOYSA-N 0.000 description 1
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 1
- VRDSRXVCRBMZOD-UHFFFAOYSA-N 1-benzyltriazole Chemical compound C1=CN=NN1CC1=CC=CC=C1 VRDSRXVCRBMZOD-UHFFFAOYSA-N 0.000 description 1
- MWZDIEIXRBWPLG-UHFFFAOYSA-N 1-methyl-1,2,4-triazole Chemical compound CN1C=NC=N1 MWZDIEIXRBWPLG-UHFFFAOYSA-N 0.000 description 1
- JWAWEQBUZOGIBZ-UHFFFAOYSA-N 1-methyltriazole Chemical compound CN1C=CN=N1 JWAWEQBUZOGIBZ-UHFFFAOYSA-N 0.000 description 1
- WFYLHMAYBQLBEM-UHFFFAOYSA-N 1-phenyl-1,2,4-triazolidine-3,5-dione Chemical compound O=C1NC(=O)NN1C1=CC=CC=C1 WFYLHMAYBQLBEM-UHFFFAOYSA-N 0.000 description 1
- LJVQHXICFCZRJN-UHFFFAOYSA-N 1h-1,2,4-triazole-5-carboxylic acid Chemical compound OC(=O)C1=NC=NN1 LJVQHXICFCZRJN-UHFFFAOYSA-N 0.000 description 1
- SYOANZBNGDEJFH-UHFFFAOYSA-N 2,5-dihydro-1h-triazole Chemical compound C1NNN=C1 SYOANZBNGDEJFH-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- GFNZYOVVRMWTOF-UHFFFAOYSA-N 2-methyltriazole-4-carboxylic acid Chemical compound CN1N=CC(C(O)=O)=N1 GFNZYOVVRMWTOF-UHFFFAOYSA-N 0.000 description 1
- FMCSQSRRTBWAFT-UHFFFAOYSA-N 2-phenyl-1h-1,2,4-triazol-3-one Chemical compound O=C1N=CNN1C1=CC=CC=C1 FMCSQSRRTBWAFT-UHFFFAOYSA-N 0.000 description 1
- XJRLKUOFBZMRBR-UHFFFAOYSA-N 2-phenylbenzotriazole Chemical compound C1=CC=CC=C1N1N=C2C=CC=CC2=N1 XJRLKUOFBZMRBR-UHFFFAOYSA-N 0.000 description 1
- MOLKLIYWXFEEJM-UHFFFAOYSA-N 2h-triazole-4-carbaldehyde Chemical compound O=CC1=CNN=N1 MOLKLIYWXFEEJM-UHFFFAOYSA-N 0.000 description 1
- UVQSQWZYJWNHSU-UHFFFAOYSA-N 2h-triazole-4-carbonitrile Chemical compound N#CC1=CNN=N1 UVQSQWZYJWNHSU-UHFFFAOYSA-N 0.000 description 1
- UKKDZCUPSSYZKY-UHFFFAOYSA-N 4,5-diphenyltriazol-1-amine Chemical compound NN1N=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 UKKDZCUPSSYZKY-UHFFFAOYSA-N 0.000 description 1
- CEASQVCZPCGKPJ-UHFFFAOYSA-N 4-methyl-2-phenyltriazole Chemical compound N1=C(C)C=NN1C1=CC=CC=C1 CEASQVCZPCGKPJ-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 206010073306 Exposure to radiation Diseases 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- RJYXQRMOMGXGPO-UHFFFAOYSA-N OC(=O)CN1N=NC=C1O Chemical compound OC(=O)CN1N=NC=C1O RJYXQRMOMGXGPO-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- DLEZVOPJBSAAGW-UHFFFAOYSA-N methyl benzotriazole-1-carboxylate Chemical compound C1=CC=C2N(C(=O)OC)N=NC2=C1 DLEZVOPJBSAAGW-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 125000005375 organosiloxane group Chemical group 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
- 238000011417 postcuring Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- MPSUGQWRVNRJEE-UHFFFAOYSA-N triazol-1-amine Chemical compound NN1C=CN=N1 MPSUGQWRVNRJEE-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- 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
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
-
- 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
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6932976A JPS52152450A (en) | 1976-06-15 | 1976-06-15 | Self-extinguishing silicone elastomer compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1588754A true GB1588754A (en) | 1981-04-29 |
Family
ID=13399390
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB24996/77A Expired GB1588754A (en) | 1976-06-15 | 1977-06-15 | Self-extinguishing silicone elastomerforming compositions and the silicone elastomers formed therefrom |
Country Status (11)
| Country | Link |
|---|---|
| JP (1) | JPS52152450A (cg-RX-API-DMAC7.html) |
| AT (1) | AT364869B (cg-RX-API-DMAC7.html) |
| AU (1) | AU509769B2 (cg-RX-API-DMAC7.html) |
| BE (1) | BE855705A (cg-RX-API-DMAC7.html) |
| CA (1) | CA1086441A (cg-RX-API-DMAC7.html) |
| DE (1) | DE2726567A1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES459810A1 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2355050A1 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1588754A (cg-RX-API-DMAC7.html) |
| IT (1) | IT1080897B (cg-RX-API-DMAC7.html) |
| MX (1) | MX143343A (cg-RX-API-DMAC7.html) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0801111A1 (en) * | 1996-04-10 | 1997-10-15 | Dow Corning Toray Silicone Company, Limited | Heat-curable silicone rubber composition and method for the preparation thereof |
| EP0808874A1 (en) * | 1996-05-24 | 1997-11-26 | Dow Corning Toray Silicone Company Ltd. | Liquid silicone rubber composition |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1591754A (en) * | 1977-03-31 | 1981-06-24 | Dow Corning Ltd | Organosiloxane elastomers |
| JPS5416567A (en) * | 1977-07-08 | 1979-02-07 | Toray Silicone Co Ltd | Room temperature curing silicone rubber composition |
| JPS5643349A (en) * | 1979-09-14 | 1981-04-22 | Toray Silicone Co Ltd | Flame retardant silicone rubber composition |
| JPS601895B2 (ja) * | 1980-03-28 | 1985-01-18 | ト−レ・シリコ−ン株式会社 | 難燃性シリコ−ンゴム組成物 |
| DE3713267C3 (de) * | 1987-04-18 | 1998-10-01 | Minnesota Mining & Mfg | Flammwidrige Silikonkautschuk-Masse und ihre Verwendung |
| JPS63180110U (cg-RX-API-DMAC7.html) * | 1987-05-12 | 1988-11-21 | ||
| JPH01116671A (ja) * | 1987-10-30 | 1989-05-09 | Shin Etsu Chem Co Ltd | 定着ロール |
| DE3831478A1 (de) * | 1988-09-16 | 1990-03-29 | Wacker Chemie Gmbh | Zu schwerbrennbaren und/oder kriechstromfesten sowie lichtbogenbestaendigen organopolysiloxanelastomeren vernetzbare massen |
| US5204395A (en) * | 1991-12-11 | 1993-04-20 | General Electric Company | Flame retardant polyphenylene ether compositions |
-
1976
- 1976-06-15 JP JP6932976A patent/JPS52152450A/ja active Granted
-
1977
- 1977-06-13 CA CA280,376A patent/CA1086441A/en not_active Expired
- 1977-06-13 DE DE19772726567 patent/DE2726567A1/de not_active Withdrawn
- 1977-06-14 AT AT0417577A patent/AT364869B/de not_active IP Right Cessation
- 1977-06-15 MX MX169477A patent/MX143343A/es unknown
- 1977-06-15 AU AU26095/77A patent/AU509769B2/en not_active Expired
- 1977-06-15 ES ES459810A patent/ES459810A1/es not_active Expired
- 1977-06-15 IT IT24691/77A patent/IT1080897B/it active
- 1977-06-15 BE BE178457A patent/BE855705A/xx not_active IP Right Cessation
- 1977-06-15 GB GB24996/77A patent/GB1588754A/en not_active Expired
- 1977-06-15 FR FR7718317A patent/FR2355050A1/fr active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0801111A1 (en) * | 1996-04-10 | 1997-10-15 | Dow Corning Toray Silicone Company, Limited | Heat-curable silicone rubber composition and method for the preparation thereof |
| EP0808874A1 (en) * | 1996-05-24 | 1997-11-26 | Dow Corning Toray Silicone Company Ltd. | Liquid silicone rubber composition |
Also Published As
| Publication number | Publication date |
|---|---|
| ES459810A1 (es) | 1978-11-16 |
| CA1086441A (en) | 1980-09-23 |
| FR2355050A1 (fr) | 1978-01-13 |
| DE2726567A1 (de) | 1977-12-29 |
| BE855705A (fr) | 1977-12-15 |
| AT364869B (de) | 1981-11-25 |
| JPS5316019B2 (cg-RX-API-DMAC7.html) | 1978-05-29 |
| ATA417577A (de) | 1981-04-15 |
| IT1080897B (it) | 1985-05-16 |
| FR2355050B1 (cg-RX-API-DMAC7.html) | 1981-11-20 |
| JPS52152450A (en) | 1977-12-17 |
| MX143343A (es) | 1981-04-15 |
| AU2609577A (en) | 1978-12-21 |
| AU509769B2 (en) | 1980-05-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PE20 | Patent expired after termination of 20 years |
Effective date: 19970614 |