NO830432L - Fremgangsmaate ved fremstilling av podede styrenpolymerer - Google Patents
Fremgangsmaate ved fremstilling av podede styrenpolymererInfo
- Publication number
- NO830432L NO830432L NO830432A NO830432A NO830432L NO 830432 L NO830432 L NO 830432L NO 830432 A NO830432 A NO 830432A NO 830432 A NO830432 A NO 830432A NO 830432 L NO830432 L NO 830432L
- Authority
- NO
- Norway
- Prior art keywords
- styrene
- weight
- rubbery
- viscosity
- parts
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 17
- 229920000642 polymer Polymers 0.000 title claims description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 53
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 17
- 229920006132 styrene block copolymer Polymers 0.000 claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
- 229920001897 terpolymer Polymers 0.000 claims description 26
- 229920001971 elastomer Polymers 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 10
- 239000005060 rubber Substances 0.000 claims description 10
- 239000012074 organic phase Substances 0.000 claims description 8
- 239000000725 suspension Substances 0.000 claims description 7
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 3
- 229920001038 ethylene copolymer Polymers 0.000 claims description 2
- 230000032683 aging Effects 0.000 abstract description 5
- 229920001577 copolymer Polymers 0.000 abstract description 5
- 229920002943 EPDM rubber Polymers 0.000 abstract 1
- 229920000578 graft copolymer Polymers 0.000 description 14
- 239000002245 particle Substances 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- 229920001400 block copolymer Polymers 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 238000009826 distribution Methods 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 4
- -1 ethylene, propylene Chemical group 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- ODBCKCWTWALFKM-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhex-3-yne Chemical compound CC(C)(C)OOC(C)(C)C#CC(C)(C)OOC(C)(C)C ODBCKCWTWALFKM-UHFFFAOYSA-N 0.000 description 3
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- 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 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 2
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-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
- NNKVOMXOJAYJEN-UHFFFAOYSA-N 3-ethylbicyclo[2.2.1]hept-2-ene Chemical compound C1CC2C(CC)=CC1C2 NNKVOMXOJAYJEN-UHFFFAOYSA-N 0.000 description 1
- MVKNKYUEMVWBOK-UHFFFAOYSA-N 3-propan-2-ylidene-1,2,7,7a-tetrahydroindene Chemical compound C1C=CC=C2C(=C(C)C)CCC21 MVKNKYUEMVWBOK-UHFFFAOYSA-N 0.000 description 1
- UFERIGCCDYCZLN-UHFFFAOYSA-N 3a,4,7,7a-tetrahydro-1h-indene Chemical compound C1C=CCC2CC=CC21 UFERIGCCDYCZLN-UHFFFAOYSA-N 0.000 description 1
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 1
- UWAQOKCAUJGLQO-UHFFFAOYSA-N 5-hex-5-enylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCCC=C)CC1C=C2 UWAQOKCAUJGLQO-UHFFFAOYSA-N 0.000 description 1
- WTQBISBWKRKLIJ-UHFFFAOYSA-N 5-methylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C)CC1C=C2 WTQBISBWKRKLIJ-UHFFFAOYSA-N 0.000 description 1
- UAKPCRIFCXQISY-UHFFFAOYSA-N 5-prop-2-enylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CC=C)CC1C=C2 UAKPCRIFCXQISY-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 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
- 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
- C08F255/06—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 ethene-propene-diene terpolymers
-
- 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
- C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Polymerisation Methods In General (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Prostheses (AREA)
- Multicomponent Fibers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8202138A FR2521150B1 (fr) | 1982-02-10 | 1982-02-10 | Procede de preparation de polymeres greffes de styrene |
Publications (1)
Publication Number | Publication Date |
---|---|
NO830432L true NO830432L (no) | 1983-08-11 |
Family
ID=9270840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO830432A NO830432L (no) | 1982-02-10 | 1983-02-09 | Fremgangsmaate ved fremstilling av podede styrenpolymerer |
Country Status (9)
Country | Link |
---|---|
US (1) | US4469847A (da) |
EP (1) | EP0086123B1 (da) |
JP (1) | JPS58154713A (da) |
AT (1) | ATE19092T1 (da) |
CA (1) | CA1189216A (da) |
DE (1) | DE3362839D1 (da) |
DK (1) | DK55883A (da) |
FR (1) | FR2521150B1 (da) |
NO (1) | NO830432L (da) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2574802B1 (fr) * | 1984-12-19 | 1987-01-09 | Charbonnages Ste Chimique | Procede de preparation de polystyrene choc stable au vieillissement |
DE3785852T2 (de) * | 1986-11-20 | 1993-11-04 | Litovitz Theodore A | Verfahren zur chromatographischen trennung von metallionen. |
GB9020579D0 (en) * | 1990-09-20 | 1990-10-31 | Shell Int Research | Process for manufacture of poly(vinyl substituted aromatic)compounds and epdm rubber containing polymer compositions |
WO1999054402A1 (en) * | 1998-04-20 | 1999-10-28 | Nova Chemicals (International) S.A. | Process for the preparation of a polyvinylarene composition and polyvinylarene compositions |
US6664208B1 (en) * | 1999-09-07 | 2003-12-16 | Sumitomo Chemical Company, Limited | Modified aluminum oxy compound, polymerization catalyst and process for producing olefin polymer and alkenyl aromatic hydrocarbon polymer |
CN111247177A (zh) * | 2017-10-20 | 2020-06-05 | 株式会社普利司通 | 多元共聚物、橡胶组合物、交联橡胶组合物、橡胶制品和轮胎 |
CN111116828B (zh) * | 2019-11-29 | 2022-12-09 | 东莞海丽化学材料有限公司 | 一种尼龙用三元乙丙共聚物增韧材料及其制备方法、尼龙材料 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE627652A (da) * | 1962-01-29 | |||
US3536784A (en) * | 1968-11-04 | 1970-10-27 | Koppers Co Inc | Process for preparing abs polymers |
US3639521A (en) * | 1969-04-23 | 1972-02-01 | Phillips Petroleum Co | Polar compound adjuvants for improved block polymers prepared with primary hydrocarbyllithium initiators |
US4051197A (en) * | 1975-11-10 | 1977-09-27 | Phillips Petroleum Company | Blend of radial block copolymers having high impact strength |
US4277575A (en) * | 1979-10-02 | 1981-07-07 | General Electric Company | Impact modifier for thermoplastic compositions |
LU82375A1 (fr) * | 1980-04-18 | 1981-12-02 | Montefina Sa | Compositions de resine styrenique resistant aux intemperies et procede pour les preparer |
-
1982
- 1982-02-10 FR FR8202138A patent/FR2521150B1/fr not_active Expired
-
1983
- 1983-01-12 CA CA000419295A patent/CA1189216A/en not_active Expired
- 1983-01-18 EP EP83400113A patent/EP0086123B1/fr not_active Expired
- 1983-01-18 AT AT83400113T patent/ATE19092T1/de active
- 1983-01-18 DE DE8383400113T patent/DE3362839D1/de not_active Expired
- 1983-02-09 NO NO830432A patent/NO830432L/no unknown
- 1983-02-09 US US06/465,143 patent/US4469847A/en not_active Expired - Fee Related
- 1983-02-09 JP JP58020536A patent/JPS58154713A/ja active Granted
- 1983-02-09 DK DK55883A patent/DK55883A/da not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JPS58154713A (ja) | 1983-09-14 |
DK55883A (da) | 1983-08-11 |
DE3362839D1 (en) | 1986-05-15 |
US4469847A (en) | 1984-09-04 |
DK55883D0 (da) | 1983-02-09 |
FR2521150A1 (fr) | 1983-08-12 |
ATE19092T1 (de) | 1986-04-15 |
JPS6336608B2 (da) | 1988-07-21 |
EP0086123B1 (fr) | 1986-04-09 |
EP0086123A1 (fr) | 1983-08-17 |
CA1189216A (en) | 1985-06-18 |
FR2521150B1 (fr) | 1985-11-15 |
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