NO793985L - Plastprodukt. - Google Patents

Plastprodukt.

Info

Publication number: NO793985L
Authority: NO; Norway
Prior art keywords: vinylidene chloride; mixture; latex; polyacrylate rubber; product
Prior art date: 1978-12-07

Application number

NO793985A

Other languages

English (en)

Norwegian (no)

Inventor

Owen Leroy Stafford

Original Assignee

Dow Chemical Co

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.)

1978-12-07

Filing date

1979-12-06

Publication date

1980-06-10

1979-12-06 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1980-06-10 Publication of NO793985L publication Critical patent/NO793985L/no

Links

239000004033 plastic Substances 0.000 title description 2
229920003023 plastic Polymers 0.000 title description 2
239000000203 mixture Substances 0.000 claims description 68
229920000126 latex Polymers 0.000 claims description 38
229920001577 copolymer Polymers 0.000 claims description 32
229920000058 polyacrylate Polymers 0.000 claims description 32
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 30
239000004816 latex Substances 0.000 claims description 30
229920001971 elastomer Polymers 0.000 claims description 29
239000000178 monomer Substances 0.000 claims description 29
239000005060 rubber Substances 0.000 claims description 29
238000007720 emulsion polymerization reaction Methods 0.000 claims description 14
239000000843 powder Substances 0.000 claims description 13
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical group CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
238000006116 polymerization reaction Methods 0.000 claims description 9
-1 alkyl hydrocarbon radical Chemical group 0.000 claims description 8
239000002245 particle Substances 0.000 claims description 8
239000004215 Carbon black (E152) Substances 0.000 claims description 7
229930195733 hydrocarbon Natural products 0.000 claims description 7
229920000642 polymer Polymers 0.000 claims description 7
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
150000001875 compounds Chemical class 0.000 claims description 3
238000001035 drying Methods 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
230000001112 coagulating effect Effects 0.000 claims 1
150000002500 ions Chemical class 0.000 claims 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
229920001485 poly(butyl acrylate) polymer Polymers 0.000 claims 1
239000000047 product Substances 0.000 description 31
239000007787 solid Substances 0.000 description 13
239000008367 deionised water Substances 0.000 description 10
239000003995 emulsifying agent Substances 0.000 description 10
238000002360 preparation method Methods 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000003054 catalyst Substances 0.000 description 7
LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 6
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
229910021641 deionized water Inorganic materials 0.000 description 6
239000000779 smoke Substances 0.000 description 6
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 6
239000000243 solution Substances 0.000 description 6
SOSQXPIKTBUEKF-UHFFFAOYSA-N 1,4-dihexoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound CCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCC SOSQXPIKTBUEKF-UHFFFAOYSA-N 0.000 description 4
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 4
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
239000003063 flame retardant Substances 0.000 description 4
229920002959 polymer blend Polymers 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
239000003431 cross linking reagent Substances 0.000 description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
125000005907 alkyl ester group Chemical group 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
238000009472 formulation Methods 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
239000002002 slurry Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical class C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
239000004971 Cross linker Substances 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
230000032683 aging Effects 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
229910000410 antimony oxide Inorganic materials 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000004891 communication Methods 0.000 description 1
238000000748 compression moulding Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
RZMWTGFSAMRLQH-UHFFFAOYSA-L disodium;2,2-dihexyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCC RZMWTGFSAMRLQH-UHFFFAOYSA-L 0.000 description 1
COHIUILBPQNABR-UHFFFAOYSA-N dodecyl phenylmethanesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)CC1=CC=CC=C1 COHIUILBPQNABR-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
125000005670 ethenylalkyl group Chemical group 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
239000011888 foil Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000000465 moulding Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
239000006069 physical mixture Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920005559 polyacrylic rubber Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000010557 suspension polymerization reaction Methods 0.000 description 1
229920001959 vinylidene polymer Polymers 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or 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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/08—Homopolymers or copolymers of vinylidene chloride
- 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
- C08F259/00—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00
- C08F259/02—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine
- C08F259/06—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine on to polymers of vinylidene chloride
- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds

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)
Compositions Of Macromolecular Compounds (AREA)
Containers Having Bodies Formed In One Piece (AREA)

NO793985A 1978-12-07 1979-12-06 Plastprodukt. NO793985L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/967,545 US4206105A (en)	1978-12-07	1978-12-07	Polyacrylate rubber-modified vinylidene chloride copolymer compositions

Publications (1)

Publication Number	Publication Date
NO793985L true NO793985L (no)	1980-06-10

Family

ID=25512955

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO793985A NO793985L (no)	1978-12-07	1979-12-06	Plastprodukt.

Country Status (8)

Country	Link
US (1)	US4206105A (fr)
EP (1)	EP0013087B1 (fr)
JP (1)	JPS5946983B2 (fr)
AU (1)	AU530521B2 (fr)
BR (1)	BR7907962A (fr)
CA (1)	CA1114087A (fr)
DE (1)	DE2967043D1 (fr)
NO (1)	NO793985L (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4340524A (en) *	1980-06-30	1982-07-20	Union Carbide Corporation	Water-resistant latex sealants
JPS5757741A (en) *	1980-09-26	1982-04-07	Badische Yuka Co Ltd	Aqueous dispersion of vinylidene chloride polymer
JPS5993646A (ja) *	1982-11-19	1984-05-30	東洋製罐株式会社	ラベル付プラスチツク容器
US4569964A (en) *	1983-10-27	1986-02-11	The Dow Chemical Company	Heat/light stable interpenetrating polymer network latexes
DE4027640A1 (de) *	1990-08-31	1992-03-05	Huels Chemische Werke Ag	Herstellung eines schlagzaehen polyacrylsaeureester-vinylchlorid- pfropfpolymerisats
CA2833603C (fr)	2011-05-04	2019-08-27	Michael Ray Leaman	Composition polymere amelioree pour sous-structures a base de ciment
CN103275653A (zh) *	2013-05-13	2013-09-04	浙江科冠聚合物有限公司	一种丙烯酸塑塑复合胶乳

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3206427A (en) *	1963-04-18	1965-09-14	Dow Chemical Co	Vinylidene chloride polymer compositions having improved low temperature properties
US3334156A (en) *	1964-04-22	1967-08-01	Gen Tire & Rubber Co	Graft polymers of vinyl chloride onto rubbery crosslinked acrylate backbones
NL130792C (fr) *	1964-06-04
NL129981C (fr) *	1966-03-26
US3424706A (en) *	1966-07-08	1969-01-28	Staley Mfg Co A E	Vinylidene chloride copolymerization in presence of preformed seed latex
LU56474A1 (fr) *	1967-07-12	1970-01-15	Du Pont	Procédé de préparation d'une composition de revêtement de copolymère de chlorure de vinylidène
US3567452A (en) *	1968-05-07	1971-03-02	Du Pont	Photographic element with polymeric film base
BE792492A (fr) *	1971-12-10	1973-06-08	Kanegafuchi Chemical Ind	Composition resineuse de la serie du chlorure de vinylidene amelioree
US3846828A (en) *	1973-04-04	1974-11-05	Dow Chemical Co	High solids content vinylidene chloride polymer dispersions in strongly hydrogen bonded dispersing media and process of preparation thereof
JPS5364297A (en) *	1976-11-19	1978-06-08	Kureha Chem Ind Co Ltd	Modified vinylidene chloride type polymer composition

1978
- 1978-12-07 US US05/967,545 patent/US4206105A/en not_active Expired - Lifetime
1979
- 1979-11-30 CA CA341,013A patent/CA1114087A/fr not_active Expired
- 1979-12-04 DE DE7979302784T patent/DE2967043D1/de not_active Expired
- 1979-12-04 EP EP79302784A patent/EP0013087B1/fr not_active Expired
- 1979-12-06 NO NO793985A patent/NO793985L/no unknown
- 1979-12-06 BR BR7907962A patent/BR7907962A/pt unknown
- 1979-12-06 AU AU53529/79A patent/AU530521B2/en not_active Ceased
- 1979-12-07 JP JP54159030A patent/JPS5946983B2/ja not_active Expired

Also Published As

Publication number	Publication date
EP0013087B1 (fr)	1984-06-06
US4206105A (en)	1980-06-03
JPS5946983B2 (ja)	1984-11-16
DE2967043D1 (en)	1984-07-12
JPS5598240A (en)	1980-07-26
BR7907962A (pt)	1980-07-22
EP0013087A1 (fr)	1980-07-09
AU5352979A (en)	1980-06-12
CA1114087A (fr)	1981-12-08
AU530521B2 (en)	1983-07-21

Publication	Publication Date	Title
JP2007327073A (ja)	2007-12-20	アクリロニトリルおよびオレフィン性不飽和モノマーから調製される高ニトリルマルチポリマーの製造方法
US3652726A (en)	1972-03-28	Thermoplastic compositions
US3268623A (en)	1966-08-23	Rigid polyvinyl chloride compositions having improved physical properties
KR102661730B1 (ko)	2024-04-29	용융 강도 및 선명성 공정 조제로서 아크릴 코폴리머를 함유하는 열가소성 조성물
NO793985L (no)	1980-06-10	Plastprodukt.
US4065613A (en)	1977-12-27	Alternating copolymers of alkyl acrylate/ethylene/branching agents
CN106854256B (zh)	2020-07-24	一种可熔融加工改性聚乙烯醇及其制备方法
US3322858A (en)	1967-05-30	Multicomponent blends containing graft copolymer of vinyl chloride onto ethylene-vinyl acetate copolymer
EP0741150B1 (fr)	1999-02-17	Procédé de préparation d'une polymère d'acrylonitrile, de méthacrylonitrile et de monomères insaturés oléfiniquement
US3962371A (en)	1976-06-08	Weather-resistant thermoplasts
US3639512A (en)	1972-02-01	Process for preparing an impact resistant vinyl chloride resin composition
US3544661A (en)	1970-12-01	Cross-linkable internally plasticized vinyl chloride compositions
CA2138762A1 (fr)	1994-01-20	Procede permettant de modifier la viscosite des copolymeres d'ethylene et des acides carboxyliques insatures
EP0118631A1 (fr)	1984-09-19	Procédé de production de polymères de chlorure de vinyle
US4141936A (en)	1979-02-27	High impact strength polymer triblends
US3158665A (en)	1964-11-24	Binary polyblends of styrene/acrylonitrile copolymer and chlorosulfonated ethylene polymer
Kolawole et al.	1982	Environmental degradation of some polymer blends. Blends of polystyrene with acrylonitrile butadiene styrene, poly (vinyl chloride), and polybutadiene and blends of polybutadiene with poly (vinyl chloride)
JPS5923565B2 (ja)	1984-06-02	アクリル酸エステル、ビニルエステルおよび不飽和ニトリルからなるタ−ポリマ−の製造法
US5883187A (en)	1999-03-16	Polymer composition with improved toughness
US3297792A (en)	1967-01-10	Blends of (1) graft copolymer of vinyl chloride onto chlorinated polyolefin, (2) diene-nitrile rubber and (3) ethylenevinyl acetate copolymer
Schellenberg et al.	1989	Preparation and properties of graft copolymers of vinyl chloride on atactic polypropylene
JPS5817546B2 (ja)	1983-04-07	塩化ビニル系樹脂組成物
US2524023A (en)	1950-09-26	Vinylidene chloride-butadiene-methyl methacrylate interpolymers
JPS6031513A (ja)	1985-02-18	塩化ビニルグラフト共重合樹脂の製造方法
JPS582311A (ja)	1983-01-07	改良された塩化ビニル共重合体の製造方法