CA2019459A1 - Agent pour rendre compatible une resine abs et une polyolefine; composition de resine thermoplastique a base de resine abs-polyolefine - Google Patents

Agent pour rendre compatible une resine abs et une polyolefine; composition de resine thermoplastique a base de resine abs-polyolefine

Info

Publication number: CA2019459A1
Authority: CA; Canada
Prior art keywords: polyolefin; agent; component; vinyl monomer; abs resin
Prior art date: 1989-06-29
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.): Abandoned

Application number

CA 2019459

Other languages

English (en)

Inventor

Youichirou Ezaki

Hiroshi Aibe

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Arakawa Chemical Industries Ltd

Original Assignee

Arakawa Chemical Industries Ltd

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.)

1989-06-29

Filing date

1990-06-20

Publication date

1990-12-29

1990-06-20 Application filed by Arakawa Chemical Industries Ltd filed Critical Arakawa Chemical Industries Ltd

1990-12-29 Publication of CA2019459A1 publication Critical patent/CA2019459A1/fr

Status Abandoned legal-status Critical Current

Links

229920000098 polyolefin Polymers 0.000 title claims abstract description 52
239000003795 chemical substances by application Substances 0.000 title claims abstract description 38
229920000122 acrylonitrile butadiene styrene Polymers 0.000 title claims abstract description 29
239000011342 resin composition Substances 0.000 title claims abstract description 23
229920005992 thermoplastic resin Polymers 0.000 title claims abstract description 22
239000000178 monomer Substances 0.000 claims abstract description 47
229920002554 vinyl polymer Polymers 0.000 claims abstract description 36
229920001577 copolymer Polymers 0.000 claims abstract description 31
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 25
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 13
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 11
229920005989 resin Polymers 0.000 claims abstract description 8
239000011347 resin Substances 0.000 claims abstract description 8
150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 7
-1 polypropylene Polymers 0.000 claims description 25
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 22
239000000203 mixture Substances 0.000 claims description 19
229920001155 polypropylene Polymers 0.000 claims description 17
239000004743 Polypropylene Substances 0.000 claims description 14
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 9
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 8
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 7
VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 claims description 3
229920000642 polymer Polymers 0.000 description 11
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 6
239000000243 solution Substances 0.000 description 6
239000000956 alloy Substances 0.000 description 5
229910045601 alloy Inorganic materials 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
239000004372 Polyvinyl alcohol Substances 0.000 description 3
150000001993 dienes Chemical class 0.000 description 3
229920000578 graft copolymer Polymers 0.000 description 3
229920002451 polyvinyl alcohol Polymers 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000008096 xylene Substances 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
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical class CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
150000003926 acrylamides Chemical class 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
229920003244 diene elastomer Polymers 0.000 description 2
238000007720 emulsion polymerization reaction Methods 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
230000001771 impaired effect Effects 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000002245 particle Substances 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
230000000379 polymerizing effect Effects 0.000 description 2
125000001453 quaternary ammonium group Chemical group 0.000 description 2
238000010992 reflux Methods 0.000 description 2
238000007127 saponification reaction Methods 0.000 description 2
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 2
238000010557 suspension polymerization reaction Methods 0.000 description 2
125000001302 tertiary amino group Chemical group 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
244000043261 Hevea brasiliensis Species 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
238000012662 bulk polymerization Methods 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
238000010559 graft polymerization reaction Methods 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
238000009863 impact test Methods 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
238000004898 kneading Methods 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
238000000465 moulding Methods 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229920005672 polyolefin resin Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
150000003384 small molecules Chemical class 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- 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
- C08L51/06—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 homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/12—Copolymers of styrene with unsaturated nitriles
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers

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)

CA 2019459 1989-06-29 1990-06-20 Agent pour rendre compatible une resine abs et une polyolefine; composition de resine thermoplastique a base de resine abs-polyolefine Abandoned CA2019459A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP169239/1989		1989-06-29
JP16923989A JPH0618954B2 (ja)	1989-06-29	1989-06-29	Ａｂｓ樹脂―ポリオレフィン用相溶化剤および該相溶化剤を含有してなる熱可塑性樹脂組成物

Publications (1)

Publication Number	Publication Date
CA2019459A1 true CA2019459A1 (fr)	1990-12-29

Family

ID=15882821

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2019459 Abandoned CA2019459A1 (fr)	1989-06-29	1990-06-20	Agent pour rendre compatible une resine abs et une polyolefine; composition de resine thermoplastique a base de resine abs-polyolefine

Country Status (3)

Country	Link
JP (1)	JPH0618954B2 (fr)
CA (1)	CA2019459A1 (fr)
DE (1)	DE4020603A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN117683319A (zh) *	2024-02-02	2024-03-12	佛山市舍与得新材料科技有限公司	Pp-abs相容母粒、pp-abs合金及其制备方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4342605A1 (de) *	1993-12-14	1995-06-22	Buna Gmbh	Funktionalisierte Olefinhomo- und -copolymere

1989
- 1989-06-29 JP JP16923989A patent/JPH0618954B2/ja not_active Expired - Lifetime
1990
- 1990-06-20 CA CA 2019459 patent/CA2019459A1/fr not_active Abandoned
- 1990-06-28 DE DE19904020603 patent/DE4020603A1/de not_active Withdrawn

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN117683319A (zh) *	2024-02-02	2024-03-12	佛山市舍与得新材料科技有限公司	Pp-abs相容母粒、pp-abs合金及其制备方法
CN117683319B (zh) *	2024-02-02	2024-04-26	佛山市舍与得新材料科技有限公司	Pp-abs相容母粒、pp-abs合金及其制备方法

Also Published As

Publication number	Publication date
JPH0333141A (ja)	1991-02-13
JPH0618954B2 (ja)	1994-03-16
DE4020603A1 (de)	1991-01-03

Legal Events

Date	Code	Title	Description
1995-12-20	FZDE	Dead

Publication	Publication Date	Title
EP0114598A1 (fr)	1984-08-01	Masse de moulage thermoplastique
US4766175A (en)	1988-08-23	Blend comprising EPDM graft terpolymer and acrylate rubber
CS101191A2 (en)	1991-11-12	Mixtures containing polyketone polymer
JP3235411B2 (ja)	2001-12-04	ゴム変性熱可塑性樹脂およびその組成物
US5210135A (en)	1993-05-11	ABS moulding compounds with improved yield stress
CA2019459A1 (fr)	1990-12-29	Agent pour rendre compatible une resine abs et une polyolefine; composition de resine thermoplastique a base de resine abs-polyolefine
JP2524367B2 (ja)	1996-08-14	残存ブタジエン含量を低滅させたａｂｓ成形用組成物
JPH02240158A (ja)	1990-09-25	耐衝撃性に優れた熱可塑性樹脂組成物
JPH0613630B2 (ja)	1994-02-23	樹脂組成物
JPH0657049A (ja)	1994-03-01	相溶化剤およびそれを配合した熱可塑性樹脂組成物
JPH09176444A (ja)	1997-07-08	ポリアセタール樹脂組成物
JP2872779B2 (ja)	1999-03-24	熱可塑性樹脂組成物
JPH0336059B2 (fr)	1991-05-30
US5132370A (en)	1992-07-21	Method for preparing carboxylated styrenic resins
JP3086357B2 (ja)	2000-09-11	ポリアセタール樹脂組成物
CA2037978A1 (fr)	1991-12-16	Alliage de polyamide styrenique
JPH0333158A (ja)	1991-02-13	Ａｂｓ樹脂―ポリアミド用相溶化剤および該相溶化剤を含有してなる熱可塑樹脂組成物
JPH03255152A (ja)	1991-11-14	耐衝撃性に優れたポリアミド樹脂組成物
JPH05295047A (ja)	1993-11-09	グラフト重合体含有樹脂組成物の製法
JP3492435B2 (ja)	2004-02-03	熱可塑性樹脂組成物
EP0456179B1 (fr)	1995-08-02	Composition à résine thermoplastique
JPH05295044A (ja)	1993-11-09	グラフト重合体含有樹脂組成物
DE19610867A1 (de)	1997-09-25	Thermoplastische Polyamid-Formmassen
JPH06220273A (ja)	1994-08-09	熱可塑性樹脂組成物及び該組成物からなるシート又はフィルム状物
JPH0657047A (ja)	1994-03-01	熱可塑性樹脂組成物及び相溶化剤