JPS6031848B2 - ハロゲン化ビニル重合体ならびにハロゲン化ビニル−オレフイン共重合体の製造方法 - Google Patents

ハロゲン化ビニル重合体ならびにハロゲン化ビニル−オレフイン共重合体の製造方法

Info

Publication number: JPS6031848B2
Authority: JP; Japan
Prior art keywords: polyolefin; weight; monomer; vinyl; polymer
Prior art date: 1976-11-30
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.): Expired

Application number

JP762277A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5369294A (en

Inventor

リ−・イ−・ウオ−カ−

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.)

Occidental Chemical Corp

Original Assignee

Occidental Chemical Corp

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.)

1976-11-30

Filing date

1977-01-25

Publication date

1985-07-24

1976-11-30 Priority claimed from US05/746,048 external-priority patent/US4067928A/en

1977-01-25 Application filed by Occidental Chemical Corp filed Critical Occidental Chemical Corp

1978-06-20 Publication of JPS5369294A publication Critical patent/JPS5369294A/ja

1985-07-24 Publication of JPS6031848B2 publication Critical patent/JPS6031848B2/ja

Status Expired legal-status Critical Current

Links

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238000005520 cutting process Methods 0.000 description 1
BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
150000001989 diazonium salts Chemical class 0.000 description 1
LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000005189 flocculation Methods 0.000 description 1
230000016615 flocculation Effects 0.000 description 1
238000009408 flooring Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 1
NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000010559 graft polymerization reaction Methods 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
KETWBQOXTBGBBN-UHFFFAOYSA-N hex-1-enylbenzene Chemical compound CCCCC=CC1=CC=CC=C1 KETWBQOXTBGBBN-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
GHXZPUGJZVBLGC-UHFFFAOYSA-N iodoethene Chemical compound IC=C GHXZPUGJZVBLGC-UHFFFAOYSA-N 0.000 description 1
230000001788 irregular Effects 0.000 description 1
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
238000011068 loading method 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
150000002688 maleic acid derivatives Chemical class 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
238000010128 melt processing Methods 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
NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 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
238000000465 moulding Methods 0.000 description 1
HULBECQFWZPEBI-ONNFQVAWSA-N octyl (e)-but-2-enoate Chemical compound CCCCCCCCOC(=O)\C=C\C HULBECQFWZPEBI-ONNFQVAWSA-N 0.000 description 1
NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
UIAMCVSNZQYIQS-KTKRTIGZSA-N oleonitrile Chemical compound CCCCCCCC\C=C/CCCCCCCC#N UIAMCVSNZQYIQS-KTKRTIGZSA-N 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
230000036961 partial effect Effects 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 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
150000002978 peroxides Chemical class 0.000 description 1
150000004965 peroxy acids 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
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
239000003505 polymerization initiator Substances 0.000 description 1
239000002954 polymerization reaction product Substances 0.000 description 1
229920006124 polyolefin elastomer Polymers 0.000 description 1
235000021395 porridge Nutrition 0.000 description 1
CAEWJEXPFKNBQL-UHFFFAOYSA-N prop-2-enyl carbonochloridate Chemical compound ClC(=O)OCC=C CAEWJEXPFKNBQL-UHFFFAOYSA-N 0.000 description 1
OTRMXXQNSIVZNR-UHFFFAOYSA-N prop-2-enyl nitrate Chemical compound [O-][N+](=O)OCC=C OTRMXXQNSIVZNR-UHFFFAOYSA-N 0.000 description 1
BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-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
238000007342 radical addition reaction Methods 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000009991 scouring Methods 0.000 description 1
238000007789 sealing Methods 0.000 description 1
DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
230000028327 secretion Effects 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000010959 steel Substances 0.000 description 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
239000000126 substance Substances 0.000 description 1
OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
238000010998 test method Methods 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
238000007039 two-step reaction Methods 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
150000008127 vinyl sulfides Chemical class 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F14/00—Homopolymers and 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
- C08F14/02—Monomers containing chlorine
- C08F14/04—Monomers containing two carbon atoms
- 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

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)

JP762277A 1976-11-30 1977-01-25 ハロゲン化ビニル重合体ならびにハロゲン化ビニル−オレフイン共重合体の製造方法 Expired JPS6031848B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US746048		1976-11-30
US05/746,048 US4067928A (en)	1975-01-15	1976-11-30	Method of preparing vinyl halide polymers and copolymers with polyolefins

Publications (2)

Publication Number	Publication Date
JPS5369294A JPS5369294A (en)	1978-06-20
JPS6031848B2 true JPS6031848B2 (ja)	1985-07-24

Family

ID=24999283

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP762277A Expired JPS6031848B2 (ja)	1976-11-30	1977-01-25	ハロゲン化ビニル重合体ならびにハロゲン化ビニル−オレフイン共重合体の製造方法

Country Status (11)

Country	Link
JP (1)	JPS6031848B2 (fr)
BE (1)	BE850890A (fr)
BR (1)	BR7700207A (fr)
CA (1)	CA1111176A (fr)
DE (1)	DE2701680A1 (fr)
ES (1)	ES455205A1 (fr)
FR (1)	FR2372180A1 (fr)
GB (1)	GB1568632A (fr)
IT (1)	IT1084901B (fr)
NL (1)	NL7701001A (fr)
SU (1)	SU799672A3 (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT987193B (it) *	1972-05-08	1975-02-20	Hooker Chemical Corp	Procedimento di polimerizzazione di cloruro vinilico con polimeri e copolimeri olefinici e loro composizioni

1977
- 1977-01-07 GB GB446479A patent/GB1568632A/en not_active Expired
- 1977-01-12 BR BR7700207A patent/BR7700207A/pt unknown
- 1977-01-17 DE DE19772701680 patent/DE2701680A1/de not_active Ceased
- 1977-01-19 IT IT1942977A patent/IT1084901B/it active
- 1977-01-20 ES ES455205A patent/ES455205A1/es not_active Expired
- 1977-01-25 CA CA270,387A patent/CA1111176A/fr not_active Expired
- 1977-01-25 JP JP762277A patent/JPS6031848B2/ja not_active Expired
- 1977-01-26 SU SU772444853A patent/SU799672A3/ru active
- 1977-01-28 BE BE174499A patent/BE850890A/fr not_active IP Right Cessation
- 1977-01-28 FR FR7702429A patent/FR2372180A1/fr active Granted
- 1977-01-31 NL NL7701001A patent/NL7701001A/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
IT1084901B (it)	1985-05-28
FR2372180A1 (fr)	1978-06-23
SU799672A3 (ru)	1981-01-23
NL7701001A (nl)	1978-06-01
ES455205A1 (es)	1978-03-16
GB1568632A (en)	1980-06-04
JPS5369294A (en)	1978-06-20
FR2372180B1 (fr)	1983-08-19
DE2701680A1 (de)	1978-06-01
BE850890A (fr)	1977-07-28
BR7700207A (pt)	1978-06-06
CA1111176A (fr)	1981-10-20

Publication	Publication Date	Title
EP0301532A2 (fr)	1989-02-01	Agent épaississant de type acide acrylique sans solvant et procédé de leur préparation
US4806581A (en)	1989-02-21	Graft polymers of polymerizable monomers and olefin polymers
US4195137A (en)	1980-03-25	Method of preparing vinyl halide polymers and copolymers with polyolefins
JPS60108412A (ja)	1985-06-13	重合性モノマーとオレフインポリマーのグラフトポリマー
US4028329A (en)	1977-06-07	Process for the bulk polymerization of vinyl halide polymers showing reduced reactor scale formation
US4067928A (en)	1978-01-10	Method of preparing vinyl halide polymers and copolymers with polyolefins
JPH0470322B2 (fr)	1992-11-10
AU637523B2 (en)	1993-05-27	Preparation of an impact-resistant polyacrylate/vinyl chloride graft copolymer
US4137216A (en)	1979-01-30	Post bulk polymerization process for polyvinyl halide and composition thereof
JPS6031848B2 (ja)	1985-07-24	ハロゲン化ビニル重合体ならびにハロゲン化ビニル−オレフイン共重合体の製造方法
EP1420034B1 (fr)	2004-10-06	Procédé de récupération d'éthylène résiduel lors de la production de copolymères d'esters vinyliques-éthylène
CA1102046A (fr)	1981-05-26	Traduction non-disponible
CN109467633B (zh)	2022-04-08	一种氯乙烯-丙烯酸酯共聚物的制备方法
GB1568631A (en)	1980-06-04	Method of preparing vinyl or vinylidene halide polymer products
JPH0225923B2 (fr)	1990-06-06
US3666735A (en)	1972-05-30	Process for improving plasticizer absorption of polyvinyl halides
US4003962A (en)	1977-01-18	Method of preparing an easy processing polyvinyl halide by an in-process reaction
JP2910774B2 (ja)	1999-06-23	塩化ビニル樹脂の製造方法
JP3652832B2 (ja)	2005-05-25	塩素化塩化ビニル系樹脂の製造方法
JPS6291503A (ja)	1987-04-27	塩素化塩化ビニル系樹脂の製法
US3629369A (en)	1971-12-21	Process for the preparation of modified polyvinyl chloride with high impact resistance
JP3240196B2 (ja)	2001-12-17	ビニル系重合体の製造方法
JPH0469644B2 (fr)	1992-11-06
JPH05295008A (ja)	1993-11-09	塩化ビニル系単量体の懸濁重合方法
CA1109181A (fr)	1981-09-15	Methode de polymerisation d'halogenure vinylique avec des polymeres et des copolymeres olefiniques; composes a base de ces produits