GB1306918A - Method of silylating organic vinylic polymers - Google Patents
Method of silylating organic vinylic polymersInfo
- Publication number
- GB1306918A GB1306918A GB3182971A GB3182971A GB1306918A GB 1306918 A GB1306918 A GB 1306918A GB 3182971 A GB3182971 A GB 3182971A GB 3182971 A GB3182971 A GB 3182971A GB 1306918 A GB1306918 A GB 1306918A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- free
- hydrocarbon
- styrene
- bulk
- 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
- 229920000642 polymer Polymers 0.000 title abstract 3
- 125000002348 vinylic group Chemical group 0.000 title 1
- -1 xenyl Chemical group 0.000 abstract 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- 150000002430 hydrocarbons Chemical group 0.000 abstract 4
- 150000003254 radicals Chemical class 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 abstract 2
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical class 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000012986 chain transfer agent Substances 0.000 abstract 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 abstract 1
- 125000004956 cyclohexylene group Chemical group 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 230000000977 initiatory effect Effects 0.000 abstract 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000004957 naphthylene group Chemical group 0.000 abstract 1
- 125000002347 octyl 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])[H] 0.000 abstract 1
- 150000003961 organosilicon compounds Chemical class 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 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 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 1
- 125000003944 tolyl group Chemical group 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 125000005023 xylyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Silicon Polymers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6689470A | 1970-08-25 | 1970-08-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1306918A true GB1306918A (en) | 1973-02-14 |
Family
ID=22072389
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3182971A Expired GB1306918A (en) | 1970-08-25 | 1971-07-07 | Method of silylating organic vinylic polymers |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3655633A (enExample) |
| JP (1) | JPS535353B1 (enExample) |
| BE (1) | BE771699A (enExample) |
| DE (1) | DE2142596C3 (enExample) |
| FR (1) | FR2105981A5 (enExample) |
| GB (1) | GB1306918A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7368515B2 (en) | 2002-07-25 | 2008-05-06 | Wacker Polymer Systems Gmbh & Co. Kg | Polyvinyl alcohols and polyvinyl acetals containing silane |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3870766A (en) * | 1971-06-18 | 1975-03-11 | Stauffer Chemical Co | Method of curing organic polymers and copolymers |
| US3884886A (en) * | 1973-01-15 | 1975-05-20 | Dow Corning | Cationic unsaturated amine-functional silane coupling agents |
| DE3003893A1 (de) * | 1980-02-02 | 1981-10-15 | Chemische Werke Hüls AG, 4370 Marl | Reaktive silylgruppen tragende homo- oder copolymere von 1,3-dienen, verfahren zu ihrer herstellung sowie deren verwendung |
| EP0042481B1 (de) * | 1980-06-19 | 1984-12-19 | Hüls Aktiengesellschaft | Homo- und Copolymere von 1,3-Dienen mit reaktiven Silylgruppen, Verfahren zu ihrer Herstellung sowie deren Verwendung |
| DE3504168A1 (de) * | 1985-02-07 | 1986-08-07 | Bayer Ag, 5090 Leverkusen | Verfahren zur quasi-ionischen polymerisation von polaren monomeren mit einer in (alpha)-stellung zur polaren gruppe befindlichen doppelbindung |
| US5079298A (en) * | 1985-06-11 | 1992-01-07 | Sunstar Giken Kabushiki Kaisha | Silicon-containing polymer having comb-shape structure |
| EP0217178A3 (en) * | 1985-09-24 | 1987-09-16 | Sunstar Giken Kabushiki Kaisha | Process for the production of telechelic vinyl polymer having alkoxysilyl group. |
| GB9700905D0 (en) * | 1997-01-17 | 1997-03-05 | Dow Corning | Reactive silicone/alkylenimine barrier coatings and applications thereof |
| BR9806759A (pt) | 1997-01-17 | 2000-03-14 | Eg Technology Partners | Composição, processo para a manufatura de um substrato tendo propriedades de barreira, e, recipiente de embalagem |
| JP2001516373A (ja) | 1997-01-17 | 2001-09-25 | イージー テクノロジー パートナーズ，エル．ピー． | シリコーン／多官能アクリレートバリヤコーティング |
| GB9700904D0 (en) * | 1997-01-17 | 1997-03-05 | Dow Corning | Reactive silicone/alkylenimine barrier laminating adhesives and applications thereof |
| GB9713279D0 (en) * | 1997-06-25 | 1997-08-27 | Dow Corning | Process for making silyl endblocked polymers |
| BR0115977A (pt) * | 2000-12-06 | 2003-12-30 | Pirelli | Processo para manufaturar, moldar e curar pneus para rodas de veìculo, e, pneu para uma roda de veìculo |
| EP1277766B1 (en) | 2001-07-20 | 2009-06-24 | Rohm And Haas Company | Polymer compound containing silicon ester moiety and composition therefrom |
| US6803406B2 (en) * | 2002-03-29 | 2004-10-12 | National Starch And Chemical Investmnet Holding Corporation | Electron donors, electron acceptors and adhesion promoters containing disulfide |
-
1970
- 1970-08-25 US US66894A patent/US3655633A/en not_active Expired - Lifetime
-
1971
- 1971-07-07 GB GB3182971A patent/GB1306918A/en not_active Expired
- 1971-07-20 JP JP5365671A patent/JPS535353B1/ja active Pending
- 1971-08-24 BE BE771699A patent/BE771699A/xx unknown
- 1971-08-24 FR FR7130711A patent/FR2105981A5/fr not_active Expired
- 1971-08-25 DE DE2142596A patent/DE2142596C3/de not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7368515B2 (en) | 2002-07-25 | 2008-05-06 | Wacker Polymer Systems Gmbh & Co. Kg | Polyvinyl alcohols and polyvinyl acetals containing silane |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2142596B2 (de) | 1980-06-26 |
| DE2142596A1 (de) | 1972-03-02 |
| US3655633A (en) | 1972-04-11 |
| JPS535353B1 (enExample) | 1978-02-25 |
| FR2105981A5 (enExample) | 1972-04-28 |
| BE771699A (fr) | 1972-02-24 |
| DE2142596C3 (de) | 1981-02-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |