NO753193L - - Google Patents
Info
- Publication number
- NO753193L NO753193L NO753193A NO753193A NO753193L NO 753193 L NO753193 L NO 753193L NO 753193 A NO753193 A NO 753193A NO 753193 A NO753193 A NO 753193A NO 753193 L NO753193 L NO 753193L
- Authority
- NO
- Norway
- Prior art keywords
- styrene
- acrylonitrile
- weight
- polymerization
- latex
- Prior art date
Links
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 58
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 23
- 238000006116 polymerization reaction Methods 0.000 claims description 17
- 229920001577 copolymer Polymers 0.000 claims description 16
- 229920000642 polymer Polymers 0.000 claims description 15
- 239000000178 monomer Substances 0.000 claims description 13
- 229920000126 latex Polymers 0.000 claims description 12
- 229920003244 diene elastomer Polymers 0.000 claims description 10
- 239000004816 latex Substances 0.000 claims description 10
- 150000001993 dienes Chemical class 0.000 claims description 8
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 6
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims description 5
- 239000000839 emulsion Substances 0.000 claims description 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
- 229910001882 dioxygen Inorganic materials 0.000 claims description 3
- 229920001519 homopolymer Polymers 0.000 claims description 3
- 239000000203 mixture Substances 0.000 description 13
- 238000007792 addition Methods 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000007334 copolymerization reaction Methods 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000000806 elastomer Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 150000003440 styrenes Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000003999 initiator Substances 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 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 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- -1 nonylphenyl Chemical group 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- HLOUDBQOEJSUPI-UHFFFAOYSA-N 1-ethenyl-2,3-dimethylbenzene Chemical class CC1=CC=CC(C=C)=C1C HLOUDBQOEJSUPI-UHFFFAOYSA-N 0.000 description 1
- QQHQTCGEZWTSEJ-UHFFFAOYSA-N 1-ethenyl-4-propan-2-ylbenzene Chemical class CC(C)C1=CC=C(C=C)C=C1 QQHQTCGEZWTSEJ-UHFFFAOYSA-N 0.000 description 1
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical class CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- CEBRPXLXYCFYGU-UHFFFAOYSA-N 3-methylbut-1-enylbenzene Chemical class CC(C)C=CC1=CC=CC=C1 CEBRPXLXYCFYGU-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 206010048010 Withdrawal syndrome Diseases 0.000 description 1
- 229920001893 acrylonitrile styrene Polymers 0.000 description 1
- 229910052783 alkali metal Chemical group 0.000 description 1
- 150000001340 alkali metals Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- SQHOHKQMTHROSF-UHFFFAOYSA-N but-1-en-2-ylbenzene Chemical compound CCC(=C)C1=CC=CC=C1 SQHOHKQMTHROSF-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical class C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000008542 thermal sensitivity Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
- C08F220/44—Acrylonitrile
-
- 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
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
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)
- Graft Or Block Polymers (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50776774A | 1974-09-20 | 1974-09-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO753193L true NO753193L (it) | 1976-03-23 |
Family
ID=24020053
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO753193A NO753193L (it) | 1974-09-20 | 1975-09-19 |
Country Status (17)
| Country | Link |
|---|---|
| JP (1) | JPS5156894A (it) |
| AR (1) | AR213393A1 (it) |
| AT (1) | AT340682B (it) |
| AU (1) | AU8421075A (it) |
| BE (1) | BE833635A (it) |
| BR (1) | BR7506070A (it) |
| CH (1) | CH617943A5 (it) |
| DE (1) | DE2538969A1 (it) |
| DK (1) | DK421675A (it) |
| FR (1) | FR2285405A1 (it) |
| GB (1) | GB1490821A (it) |
| IT (1) | IT1042565B (it) |
| LU (1) | LU73398A1 (it) |
| NL (1) | NL7511102A (it) |
| NO (1) | NO753193L (it) |
| SE (1) | SE7510549L (it) |
| ZA (1) | ZA755276B (it) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3449472A (en) * | 1966-10-21 | 1969-06-10 | Eastman Kodak Co | Continuous equilibrium process for preparing biphase plastics |
| BE757564A (fr) * | 1969-11-06 | 1971-04-15 | Standard Oil Co | Procede de copolymerisation nitrile olefinique/styrene |
-
1975
- 1975-08-18 ZA ZA00755276A patent/ZA755276B/xx unknown
- 1975-08-22 AU AU84210/75A patent/AU8421075A/en not_active Expired
- 1975-09-02 DE DE19752538969 patent/DE2538969A1/de not_active Withdrawn
- 1975-09-08 AT AT691075A patent/AT340682B/de not_active IP Right Cessation
- 1975-09-09 AR AR260307A patent/AR213393A1/es active
- 1975-09-12 FR FR7528078A patent/FR2285405A1/fr active Granted
- 1975-09-15 IT IT27253/75A patent/IT1042565B/it active
- 1975-09-15 LU LU73398A patent/LU73398A1/xx unknown
- 1975-09-17 GB GB38183/75A patent/GB1490821A/en not_active Expired
- 1975-09-17 JP JP50112507A patent/JPS5156894A/ja active Pending
- 1975-09-19 SE SE7510549A patent/SE7510549L/xx unknown
- 1975-09-19 BE BE160220A patent/BE833635A/xx unknown
- 1975-09-19 NL NL7511102A patent/NL7511102A/xx not_active Application Discontinuation
- 1975-09-19 DK DK421675A patent/DK421675A/da unknown
- 1975-09-19 BR BR7506070*A patent/BR7506070A/pt unknown
- 1975-09-19 CH CH1216475A patent/CH617943A5/de not_active IP Right Cessation
- 1975-09-19 NO NO753193A patent/NO753193L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA755276B (en) | 1976-07-28 |
| AR213393A1 (es) | 1979-01-31 |
| IT1042565B (it) | 1980-01-30 |
| FR2285405A1 (fr) | 1976-04-16 |
| AU8421075A (en) | 1977-02-24 |
| CH617943A5 (en) | 1980-06-30 |
| AT340682B (de) | 1977-12-27 |
| DE2538969A1 (de) | 1976-04-01 |
| ATA691075A (de) | 1977-04-15 |
| JPS5156894A (en) | 1976-05-18 |
| FR2285405B1 (it) | 1979-01-05 |
| DK421675A (da) | 1976-03-21 |
| BR7506070A (pt) | 1976-08-03 |
| NL7511102A (nl) | 1976-03-23 |
| LU73398A1 (it) | 1977-05-11 |
| GB1490821A (en) | 1977-11-02 |
| BE833635A (fr) | 1976-01-16 |
| SE7510549L (sv) | 1976-03-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR0178368B1 (ko) | 내충격성 비닐 방향족(공) 중합체의 연속 벌크형 제조방법 | |
| US4567232A (en) | Continuous preparation of rubber-modified polymers of vinyl-aromatics | |
| JPS63118346A (ja) | 耐衝撃ポリスチレンの連続的製造方法 | |
| GB1576772A (en) | Manufacture of styrene polymers which have been modified to improve their impact strength | |
| EP0021488A1 (en) | Improved impact polymers and their preparation | |
| US3337650A (en) | Process for preparing graft polymers having high impact strength | |
| KR0161974B1 (ko) | 개선된 특성을 갖는 모노비닐리덴 방향족 중합체 및 이의 제조방법 | |
| US4097555A (en) | Transparent polymeric polyblend | |
| NO754132L (it) | ||
| NO753193L (it) | ||
| Hayes | Polymeric chain transfer reactions. Polymerization of some vinyl monomers in the presence of vinyl polymers | |
| EP0014574A2 (en) | Process for the production of graft polymer, the polymer so produced and polystyrene compositions containing it as an impact modifier | |
| Sari et al. | The effect of styrene monomer in the graft copolymerization of acrylonitrile onto deproteinized natural rubber | |
| US4972032A (en) | Process for preparing copolymers of alpha-methylstyrene and acrylonitrile | |
| US5286792A (en) | ABS with novel morphology | |
| WO1991013118A1 (en) | A process for the preparation of impact resistant and high gloss thermoplastic resin | |
| US4143100A (en) | Graft copolymers containing polyoxazoline and polyoxazine, and the preparation thereof | |
| US3629370A (en) | Process for the production of thermoplastic-elastic moulding compositions of high impact and notched impact strength | |
| US5166261A (en) | High gloss ABS made by continuous process | |
| US3859388A (en) | Preparation of nitrile polymers with aralkyl mercaptans as polymerization modifiers | |
| EP0474618A2 (en) | High-gloss ABS made by continuous process | |
| US3265677A (en) | Process for regulating molecular weight in polymerization of vinylidene monomers using 1-methylcyclohexene-1 as regulator | |
| US2917496A (en) | Copolymer of a fluoro-butadiene and an acrylic comonomer and process of making same | |
| NO300596B1 (no) | Fremgangsmåte for kontinuerlig fremstilling av vinylaromatiske blokk-kopolymerer | |
| DK149128B (da) | Fremgangsmaade til fremstilling af podede copolymere ved podningspolymerisation i masse |