GB853640A - Process for the production of cross-linked elastomers - Google Patents
Process for the production of cross-linked elastomersInfo
- Publication number
- GB853640A GB853640A GB344059A GB344059A GB853640A GB 853640 A GB853640 A GB 853640A GB 344059 A GB344059 A GB 344059A GB 344059 A GB344059 A GB 344059A GB 853640 A GB853640 A GB 853640A
- Authority
- GB
- United Kingdom
- Prior art keywords
- esters
- butyl
- vinyl
- acid
- monomer
- 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
- 229920001971 elastomer Polymers 0.000 title abstract 2
- 239000000806 elastomer Substances 0.000 title abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- 239000000178 monomer Substances 0.000 abstract 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- -1 dichlorobenzoyl Chemical group 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 abstract 2
- USVVENVKYJZFMW-ONEGZZNKSA-N (e)-carboxyiminocarbamic acid Chemical class OC(=O)\N=N\C(O)=O USVVENVKYJZFMW-ONEGZZNKSA-N 0.000 abstract 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 abstract 1
- WVAFEFUPWRPQSY-UHFFFAOYSA-N 1,2,3-tris(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1C=C WVAFEFUPWRPQSY-UHFFFAOYSA-N 0.000 abstract 1
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 abstract 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 abstract 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004641 Diallyl-phthalate Substances 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 150000002238 fumaric acids Chemical class 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229920005684 linear copolymer Polymers 0.000 abstract 1
- 150000002689 maleic acids Chemical class 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000005634 peroxydicarbonate group Chemical group 0.000 abstract 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 abstract 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 238000010526 radical polymerization reaction Methods 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 abstract 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 abstract 1
- SQAIGLXMIMWFEQ-UHFFFAOYSA-N tetrakis(prop-2-enyl) silicate Chemical compound C=CCO[Si](OCC=C)(OCC=C)OCC=C SQAIGLXMIMWFEQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
-
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
- C08F255/026—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms on to ethylene-vinylester copolymers
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF24942A DE1136485B (de) | 1958-01-30 | 1958-01-30 | Verfahren zur Herstellung von Elastomeren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB853640A true GB853640A (en) | 1960-11-09 |
Family
ID=7091423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB344059A Expired GB853640A (en) | 1958-01-30 | 1959-01-30 | Process for the production of cross-linked elastomers |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1136485B (enrdf_load_stackoverflow) |
| FR (1) | FR1225704A (enrdf_load_stackoverflow) |
| GB (1) | GB853640A (enrdf_load_stackoverflow) |
| IT (1) | IT602896A (enrdf_load_stackoverflow) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3257352A (en) * | 1960-08-11 | 1966-06-21 | Stamicarbon | Vulcanization of polyethylene with peroxides and compounds containing conjugated diene and carbonyl groups |
| DE1278689B (de) * | 1962-05-17 | 1968-09-26 | Bayer Ag | Verfahren zur Herstellung von gummielastischen Faeden |
| US3404112A (en) * | 1965-03-31 | 1968-10-01 | Air Reduction | Paper coating composition containing vinyl acetate-ethylene-triallyl cyanurate terpolymers and coated product formed therefrom |
| DE1285733B (de) * | 1961-04-24 | 1968-12-19 | Montedison Spa | Vulkanisierbare Formmassen auf der Grundlage von AEthylen-ª‡-Olefin-Mischpolymerisaten |
| US3493535A (en) * | 1962-06-01 | 1970-02-03 | Allied Chem | Polyethylene maleate diester graft copolymers containing certain filler material |
| US3531455A (en) * | 1967-04-28 | 1970-09-29 | Du Pont | Peroxide-cured chlorinated polyethylene |
| US3714296A (en) * | 1968-08-01 | 1973-01-30 | Denki Kagaku Kogyo Kk | Polychloroprene elastomer |
| US3951926A (en) * | 1974-08-05 | 1976-04-20 | Monsanto Company | Cross-linked ethylene-maleic anhydride interpolymers |
| US4104329A (en) * | 1977-06-10 | 1978-08-01 | Monsanto Company | Acrylate-modified ethylene-vinyl acetate polymer |
| US4410648A (en) | 1979-12-25 | 1983-10-18 | Dainichi-Nippon Cables, Ltd. | Flame retarding organic high polymer composition |
| EP0123801A1 (de) * | 1983-03-02 | 1984-11-07 | Siemens Aktiengesellschaft | Verfahren zur radikalischen Vernetzung organischer Polymerer |
| US4521558A (en) * | 1984-02-27 | 1985-06-04 | The Goodyear Tire & Rubber Company | Rubber-metal adhesion promoters |
| FR2558845A1 (fr) * | 1984-01-31 | 1985-08-02 | Atochem | Compositions adhesives a reticulation thermoreversible, leur procede de fabrication et leurs applications |
| US4968753A (en) * | 1987-01-14 | 1990-11-06 | Nippon Zeon Co., Ltd. | Acrylonitrile rubber with quinoline compound, organic peroxide, crosslinking agent |
| EP0756033A3 (en) * | 1995-07-27 | 1997-06-04 | Asahi Glass Co Ltd | Water and oil repellent composition, treatment method and copolymer |
| WO2004076507A3 (en) * | 2003-02-25 | 2004-10-28 | Dow Europ Gmbh | Reactive hot melt adhesive |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1181404B (de) * | 1962-10-11 | 1964-11-12 | Bayer Ag | Verfahren zum Vernetzen von AEthylen-Vinylester-Mischpolymerisaten |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2628214A (en) * | 1945-10-27 | 1953-02-10 | Du Pont | Curing of polyethylenes |
-
0
- IT IT602896D patent/IT602896A/it unknown
-
1958
- 1958-01-30 DE DEF24942A patent/DE1136485B/de active Pending
-
1959
- 1959-01-30 GB GB344059A patent/GB853640A/en not_active Expired
- 1959-01-30 FR FR785342A patent/FR1225704A/fr not_active Expired
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3257352A (en) * | 1960-08-11 | 1966-06-21 | Stamicarbon | Vulcanization of polyethylene with peroxides and compounds containing conjugated diene and carbonyl groups |
| DE1285733B (de) * | 1961-04-24 | 1968-12-19 | Montedison Spa | Vulkanisierbare Formmassen auf der Grundlage von AEthylen-ª‡-Olefin-Mischpolymerisaten |
| DE1278689B (de) * | 1962-05-17 | 1968-09-26 | Bayer Ag | Verfahren zur Herstellung von gummielastischen Faeden |
| US3493535A (en) * | 1962-06-01 | 1970-02-03 | Allied Chem | Polyethylene maleate diester graft copolymers containing certain filler material |
| US3404112A (en) * | 1965-03-31 | 1968-10-01 | Air Reduction | Paper coating composition containing vinyl acetate-ethylene-triallyl cyanurate terpolymers and coated product formed therefrom |
| US3531455A (en) * | 1967-04-28 | 1970-09-29 | Du Pont | Peroxide-cured chlorinated polyethylene |
| US3714296A (en) * | 1968-08-01 | 1973-01-30 | Denki Kagaku Kogyo Kk | Polychloroprene elastomer |
| US3951926A (en) * | 1974-08-05 | 1976-04-20 | Monsanto Company | Cross-linked ethylene-maleic anhydride interpolymers |
| US4104329A (en) * | 1977-06-10 | 1978-08-01 | Monsanto Company | Acrylate-modified ethylene-vinyl acetate polymer |
| US4410648A (en) | 1979-12-25 | 1983-10-18 | Dainichi-Nippon Cables, Ltd. | Flame retarding organic high polymer composition |
| EP0123801A1 (de) * | 1983-03-02 | 1984-11-07 | Siemens Aktiengesellschaft | Verfahren zur radikalischen Vernetzung organischer Polymerer |
| FR2558845A1 (fr) * | 1984-01-31 | 1985-08-02 | Atochem | Compositions adhesives a reticulation thermoreversible, leur procede de fabrication et leurs applications |
| EP0158540A1 (fr) * | 1984-01-31 | 1985-10-16 | Elf Atochem S.A. | Compositions adhesives à reticulation thermoreversible et leurs applications |
| US4521558A (en) * | 1984-02-27 | 1985-06-04 | The Goodyear Tire & Rubber Company | Rubber-metal adhesion promoters |
| US4968753A (en) * | 1987-01-14 | 1990-11-06 | Nippon Zeon Co., Ltd. | Acrylonitrile rubber with quinoline compound, organic peroxide, crosslinking agent |
| EP0756033A3 (en) * | 1995-07-27 | 1997-06-04 | Asahi Glass Co Ltd | Water and oil repellent composition, treatment method and copolymer |
| US5688309A (en) * | 1995-07-27 | 1997-11-18 | Asahi Glass Company Ltd. | Water and oil repellent composition, treating method therewith and copolymer |
| WO2004076507A3 (en) * | 2003-02-25 | 2004-10-28 | Dow Europ Gmbh | Reactive hot melt adhesive |
| US7271202B2 (en) | 2003-02-25 | 2007-09-18 | Dow Global Technologies Inc. | Reactive hot melt adhesive |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1136485B (de) | 1962-09-13 |
| IT602896A (enrdf_load_stackoverflow) | |
| FR1225704A (fr) | 1960-07-04 |
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