GB863573A - Improved polymerization process - Google Patents

Improved polymerization process

Info

Publication number
GB863573A
GB863573A GB90257D GB90257D GB863573A GB 863573 A GB863573 A GB 863573A GB 90257 D GB90257 D GB 90257D GB 90257 D GB90257 D GB 90257D GB 863573 A GB863573 A GB 863573A
Authority
GB
United Kingdom
Prior art keywords
amount
isopropanol
weight
diluent
diallyl
Prior art date
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
GB90257D
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.)
FMC Corp
Original Assignee
FMC Corp
Food Machinery and 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.)
Filing date
Publication date
Application filed by FMC Corp, Food Machinery and Chemical Corp filed Critical FMC Corp
Publication of GB863573A publication Critical patent/GB863573A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F18/00Homopolymers 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 an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
    • C08F18/02Esters of monocarboxylic acids
    • C08F18/04Vinyl esters
    • C08F18/08Vinyl acetate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F36/20Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds unconjugated
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/28Oxygen or compounds releasing free oxygen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polymerization Catalysts (AREA)
  • Polyamides (AREA)
  • Polymerisation Methods In General (AREA)

Abstract

863,573. Polymerizing dicarboxylic acid esters. FOOD MACHINERY & CHEMICAL CORPORATION. April 1, 1957 [April 2, 1956], No. 9202/57. Class 2(6). A fusible polymer, capable of further polymerization, is made by polymerizing a diallyl or dimethallyl ester of a dicarboxylic acid in the presence of hydrogen peroxide and an organic diluent. The diluent, which may be methanol, ethanol, isopropanol, benzene, toluene, xylene, ethylbenzene or isopropylbenzene, may be used in amount of 5 to 50% by weight of the ester and diluent. Water in amount up to 1% by weight can be tolerated in the reaction mixture, and an organic peroxide may also be added to the reaction mixture preferably in amount not greater than the amount of the H 2 O 2 . Polymerization proceeds at 85‹ to 200‹C. under atmospheric pressure, though other pressures may be used. The H 2 O 2 , generally as a 30% aqueous solution, is used in amount of 0À08 to 5À0% by weight of the monomer. In Examples (1, 3 to 7) diallyl phthalate, isopropanol and aqueous H 2 O 2 were charged into a reactor, agitated and heated to'reflux (104‹-108‹C.) for about 10 hours; the batch was then cooled, mixed with isopropanol and the polymer which precipitated at 0‹C. was separated by filtration; (2) dimethallylphthalate was similarly polymerized. Other esters specified are diallyl-isophthalate, -maleate, -itaconate, -adipate and -dithioglycollate and dimethallylorthophthalate, -azelate and -tetrachlorophthalate. Specifications 572,858 and 687,295 are referred to.
GB90257D 1956-04-02 1957-04-01 Improved polymerization process Expired GB863573A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US57536256A 1956-04-02 1956-04-02

Publications (1)

Publication Number Publication Date
GB863573A true GB863573A (en) 1961-03-22

Family

ID=24300010

Family Applications (1)

Application Number Title Priority Date Filing Date
GB90257D Expired GB863573A (en) 1956-04-02 1957-04-01 Improved polymerization process

Country Status (6)

Country Link
BE (1) BE556317A (en)
CH (1) CH363807A (en)
DE (1) DE1097143B (en)
FR (1) FR1173460A (en)
GB (1) GB863573A (en)
NL (2) NL101284C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0154136A1 (en) * 1984-01-27 1985-09-11 Mitsubishi Rayon Co., Ltd. Plastic lens and method of manufacturing thereof
GB2173808A (en) * 1985-04-03 1986-10-22 Ppg Industries Inc Free radical initiated polymerization of polymerizable ethylenically unsaturated monomer component in the presence of hydrogen peroxide
EP0308652A2 (en) * 1987-08-24 1989-03-29 Showa Denko Kabushiki Kaisha Diallyl terephthalate prepolymer and process for producing same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0154136A1 (en) * 1984-01-27 1985-09-11 Mitsubishi Rayon Co., Ltd. Plastic lens and method of manufacturing thereof
GB2173808A (en) * 1985-04-03 1986-10-22 Ppg Industries Inc Free radical initiated polymerization of polymerizable ethylenically unsaturated monomer component in the presence of hydrogen peroxide
GB2173808B (en) * 1985-04-03 1989-06-28 Ppg Industries Inc Free radical initiated polymerization of polymerizable ethylenically unsaturated monomer component in the presence of hydrogen peroxide
EP0308652A2 (en) * 1987-08-24 1989-03-29 Showa Denko Kabushiki Kaisha Diallyl terephthalate prepolymer and process for producing same
EP0308652A3 (en) * 1987-08-24 1990-05-09 Showa Denko Kabushiki Kaisha Diallyl terephthalate prepolymer and process for producing same

Also Published As

Publication number Publication date
FR1173460A (en) 1959-02-25
DE1097143B (en) 1961-01-12
NL101284C (en)
BE556317A (en)
CH363807A (en) 1962-08-15
NL215929A (en)

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