NO812245L - Kopolymer av alfa-metylstyren og akrylonitril og gjenstand fremstilt av denne - Google Patents

Kopolymer av alfa-metylstyren og akrylonitril og gjenstand fremstilt av denne

Info

Publication number: NO812245L
Authority: NO; Norway
Prior art keywords: copolymer; polymerization; heat resistance; acrylonitrile; methylstyrene
Prior art date: 1980-07-01

Application number

NO812245A

Other languages

English (en)

Norwegian (no)

Inventor

Jan Tijssen

Jozef Lambertus Maria Van Loos

Original Assignee

Stamicarbon

Priority date (The priority date 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 date listed.)

1980-07-01

Filing date

1981-06-30

Publication date

1982-01-04

1981-06-30 Application filed by Stamicarbon filed Critical Stamicarbon

1982-01-04 Publication of NO812245L publication Critical patent/NO812245L/no

Links

NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 title claims description 18
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 title 1
229920001577 copolymer Polymers 0.000 claims description 45
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 17
239000000178 monomer Substances 0.000 claims description 15
239000000839 emulsion Substances 0.000 claims description 6
238000006116 polymerization reaction Methods 0.000 description 22
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
229920000642 polymer Polymers 0.000 description 12
238000003756 stirring Methods 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
150000001875 compounds Chemical class 0.000 description 9
238000000034 method Methods 0.000 description 8
239000000203 mixture Substances 0.000 description 8
235000019394 potassium persulphate Nutrition 0.000 description 8
239000003995 emulsifying agent Substances 0.000 description 7
239000003999 initiator Substances 0.000 description 7
239000000344 soap Substances 0.000 description 7
238000005452 bending Methods 0.000 description 6
230000008569 process Effects 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
239000004159 Potassium persulphate Substances 0.000 description 5
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 4
238000007720 emulsion polymerization reaction Methods 0.000 description 4
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
-1 hydrocarbon mercaptans Chemical class 0.000 description 3
239000004816 latex Substances 0.000 description 3
229920000126 latex Polymers 0.000 description 3
150000002898 organic sulfur compounds Chemical class 0.000 description 3
239000011347 resin Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 2
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical class SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
238000012662 bulk polymerization Methods 0.000 description 2
230000015271 coagulation Effects 0.000 description 2
238000005345 coagulation Methods 0.000 description 2
239000008367 deionised water Substances 0.000 description 2
229910021641 deionized water Inorganic materials 0.000 description 2
238000010528 free radical solution polymerization reaction Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000012429 reaction media Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000002904 solvent Substances 0.000 description 2
UUUYXCLERBDLEO-UHFFFAOYSA-N 1-hydroperoxy-1-methylcyclohexane Chemical compound OOC1(C)CCCCC1 UUUYXCLERBDLEO-UHFFFAOYSA-N 0.000 description 1
ZJCZFAAXZODMQT-UHFFFAOYSA-N 2-methylpentadecane-2-thiol Chemical group CCCCCCCCCCCCCC(C)(C)S ZJCZFAAXZODMQT-UHFFFAOYSA-N 0.000 description 1
FRQQKWGDKVGLFI-UHFFFAOYSA-N 2-methylundecane-2-thiol Chemical compound CCCCCCCCCC(C)(C)S FRQQKWGDKVGLFI-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
OCVLSHAVSIYKLI-UHFFFAOYSA-N 3h-1,3-thiazole-2-thione Chemical class SC1=NC=CS1 OCVLSHAVSIYKLI-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
239000004160 Ammonium persulphate Substances 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
239000006057 Non-nutritive feed additive Substances 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000012190 activator Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
235000019395 ammonium persulphate Nutrition 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
LTUFFQPUELZQBJ-UHFFFAOYSA-N cyclododeca-1,3-diene-1-thiol Chemical group SC1=CC=CCCCCCCCC1 LTUFFQPUELZQBJ-UHFFFAOYSA-N 0.000 description 1
XDQHLVSMADKFRH-UHFFFAOYSA-N cyclododecanethiol Chemical group SC1CCCCCCCCCCC1 XDQHLVSMADKFRH-UHFFFAOYSA-N 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000539 dimer Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000011552 falling film Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
229920000578 graft copolymer Polymers 0.000 description 1
230000036541 health Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-M hydrosulfide Chemical compound [SH-] RWSOTUBLDIXVET-UHFFFAOYSA-M 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000006872 improvement Effects 0.000 description 1
BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
238000004898 kneading Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910001463 metal phosphate Inorganic materials 0.000 description 1
SEXOVMIIVBKGGM-UHFFFAOYSA-N naphthalene-1-thiol Chemical compound C1=CC=C2C(S)=CC=CC2=C1 SEXOVMIIVBKGGM-UHFFFAOYSA-N 0.000 description 1
YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
ZVEZMVFBMOOHAT-UHFFFAOYSA-N nonane-1-thiol Chemical group CCCCCCCCCS ZVEZMVFBMOOHAT-UHFFFAOYSA-N 0.000 description 1
QJAOYSPHSNGHNC-UHFFFAOYSA-N octadecane-1-thiol Chemical group CCCCCCCCCCCCCCCCCCS QJAOYSPHSNGHNC-UHFFFAOYSA-N 0.000 description 1
KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical group CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000012966 redox initiator Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
229940048086 sodium pyrophosphate Drugs 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
238000010557 suspension polymerization reaction Methods 0.000 description 1
235000012976 tarts Nutrition 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
IPBROXKVGHZHJV-UHFFFAOYSA-N tridecane-1-thiol Chemical group CCCCCCCCCCCCCS IPBROXKVGHZHJV-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 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
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/12—Monomers containing a branched unsaturated aliphatic radical or a ring substituted by an alkyl radical

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)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Adhesives Or Adhesive Processes (AREA)
Polymerisation Methods In General (AREA)
Compositions Of Macromolecular Compounds (AREA)
Battery Electrode And Active Subsutance (AREA)

NO812245A 1980-07-01 1981-06-30 Kopolymer av alfa-metylstyren og akrylonitril og gjenstand fremstilt av denne NO812245L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
NL8003798A NL8003798A (nl)	1980-07-01	1980-07-01	Copolymeer van alfa-methylstyreen en acrylonitril.

Publications (1)

Publication Number	Publication Date
NO812245L true NO812245L (no)	1982-01-04

Family

ID=19835541

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO812245A NO812245L (no)	1980-07-01	1981-06-30	Kopolymer av alfa-metylstyren og akrylonitril og gjenstand fremstilt av denne

Country Status (6)

Country	Link
EP (1)	EP0044101A3 (da)
JP (2)	JPS5744613A (da)
DK (1)	DK287181A (da)
ES (1)	ES8300803A1 (da)
NL (1)	NL8003798A (da)
NO (1)	NO812245L (da)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL8003799A (nl) *	1980-07-01	1982-02-01	Stamicarbon	Polymeercompositie.
DK397681A (da) *	1980-09-11	1982-03-12	Stamicarbon	Polymert materiale
JPS60243882A (ja) *	1984-05-18	1985-12-03	Denki Kagaku Kogyo Kk	テ−プカセツト
JPH08873B2 (ja) *	1985-08-14	1996-01-10	電気化学工業株式会社	熱可塑性樹脂組成物
JPS63139030A (ja) *	1986-11-28	1988-06-10	Sumitomo Electric Ind Ltd	光フアイバ母材の製造方法
JP2008291221A (ja) *	2007-04-26	2008-12-04	Dic Corp	乳化重合体水分散液の製造方法
JP5751605B2 (ja) *	2007-12-07	2015-07-22	日本エイアンドエル株式会社	重合体ラテックス、または重合体エマルジョンの製造方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3010936A (en) *	1958-08-07	1961-11-28	Borg Warner	Blend of graft copolymer of polybutadiene, styrene and acrylonitrile with interpolymer of alpha methyl styrene and acrylonitrile
US3268625A (en) *	1962-12-26	1966-08-23	Standard Oil Co	Bulk interpolymerization of monomeric mixture comprising acrylonitrile and alpha-alkyl styrene

1980
- 1980-07-01 NL NL8003798A patent/NL8003798A/nl not_active Application Discontinuation
1981
- 1981-06-19 EP EP81200694A patent/EP0044101A3/en not_active Withdrawn
- 1981-06-29 DK DK287181A patent/DK287181A/da not_active Application Discontinuation
- 1981-06-30 ES ES503549A patent/ES8300803A1/es not_active Expired
- 1981-06-30 NO NO812245A patent/NO812245L/no unknown
- 1981-07-01 JP JP56101392A patent/JPS5744613A/ja active Pending
- 1981-07-01 JP JP56101393A patent/JPS5740511A/ja active Pending

Also Published As

Publication number	Publication date
ES503549A0 (es)	1982-11-01
NL8003798A (nl)	1982-02-01
EP0044101A2 (en)	1982-01-20
ES8300803A1 (es)	1982-11-01
JPS5740511A (en)	1982-03-06
DK287181A (da)	1982-01-02
EP0044101A3 (en)	1982-02-03
JPS5744613A (en)	1982-03-13

Publication	Publication Date	Title
US20030018125A1 (en)	2003-01-23	Process for preparing thermoplastic resin having superior heat-stability
US10066041B2 (en)	2018-09-04	Thermoplastic resin, method of preparing the same and thermoplastic resin composition including the same
US4703090A (en)	1987-10-27	Method for the preparation of graft copolymers by emulsion copolymerization
EP0043613B1 (en)	1984-05-16	Polymer composition and object prepared therefrom
NO155731B (no)	1987-02-09	Polymerblanding basert paa polykarbonat og en podekopolymer og anvendelse derav ved fremstilling av formede gjenstander.
EP0044101A2 (en)	1982-01-20	Copolymer of alpha-methylstyrene and acrylonitrile, and object prepared therefrom
KR20070037988A (ko)	2007-04-09	잔류 단량체 함량이 낮은 그라프트 고무 라텍스의 제조방법
DE2614674A1 (de)	1976-10-21	Herstellung von acrylnitril-copolymerisaten
FI73705C (fi)	1987-11-09	Polymerkomposition baserad pao abs-plast och en kopolymer av -metylstyren och akrylnitril.
KR100441799B1 (ko)	2004-07-27	고무강화 열가소성 수지의 제조방법
EP0041703A1 (en)	1981-12-16	Process for preparing copolymers
KR100540507B1 (ko)	2006-01-11	백색도 및 열안정성이 우수한 ａｂｓ 수지 조성물의제조방법
KR100518891B1 (ko)	2005-09-30	저온응력백화성이 저감된 열가소성 수지 조성물
US3594453A (en)	1971-07-20	Method of producing alpha-methylstyrene resin
NO158509B (no)	1988-06-13	Fremgangsmaate ved fremstilling av kopolymer.
US4871802A (en)	1989-10-03	Process for the preparation of a thermoplastic with high monomer conversion
US3691261A (en)	1972-09-12	Graft copolymer with an alkyl acrylate and ethylthiaethyl metharylate backbone
KR102068651B1 (ko)	2020-01-21	공액디엔 고무질 중합체의 제조방법
KR100348751B1 (ko)	2002-08-13	내충격성 및 열안정성이 우수한 열가소성 난연성아크릴로니트릴/부타디엔/스티렌 수지조성물 및 그제조방법
NO823799L (no)	1983-05-16	Polymerblanding.
EP0094135B1 (en)	1986-04-16	Process for the preparation of a thermoplastic moulding composition with low surface gloss
US3662026A (en)	1972-05-09	Process for preparing graft copolymers containing n,n-di(beta-hydroxyethyl) glycine salts
KR20010057253A (ko)	2001-07-04	난연성 ａｂｓ수지에 있어서 내충격성 및 유동성이 우수한그라프트 공중합체의 제조방법
NL8102415A (nl)	1982-12-16	Werkwijze voor het bereiden van een copolymeer.
KR0179187B1 (ko)	1999-05-15	색 안정성이 우수한 열가소성 수지 조성물의 제조방법