GB861817A - Improvements in or relating to the polymerization of diallyl phthalate - Google Patents

Improvements in or relating to the polymerization of diallyl phthalate

Info

Publication number
GB861817A
GB861817A GB1114658A GB1114658A GB861817A GB 861817 A GB861817 A GB 861817A GB 1114658 A GB1114658 A GB 1114658A GB 1114658 A GB1114658 A GB 1114658A GB 861817 A GB861817 A GB 861817A
Authority
GB
United Kingdom
Prior art keywords
monomer
prepolymer
modifier
diallyl phthalate
weight
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
GB1114658A
Inventor
Charles Adam Heiberger
James Larue Thomas
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
Priority to GB1114658A priority Critical patent/GB861817A/en
Publication of GB861817A publication Critical patent/GB861817A/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

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)

Abstract

A solid diallyl phthalate prepolymer is prepared from diallyl phthalate by polymerizing at an elevated temperature, e.g. above 70 DEG C., a mixture containing diallyl phthalate monomer, water, an organic peroxide or organic hydroperoxide catalyst, and a polymerization modifier of the formula <FORM:0861817/IV (a)/1> where X is chlorine or a hydroxyl radical or any group which can be converted to a hydroxyl group under reaction conditions, R is a methyl and/or ethyl and/or propyl radical, m is 0 to 4, the total number of carbon atoms in the R substituents is less than 5, and n is 0 to (4 - m), the modifier comprising 1 to 50% by weight based on the monomer, the reaction being discontinued before substantial gelation occurs by lowering the temperature below the polymerization temperature, unreacted monomer being separated from the prepolymer formed, and solid prepolymer recovered. Optional dispersing-agents, e.g. animal glue, clay and sodium tripolyphosphate, may be employed for the reaction. When dimethyl benzyl chloride or dimethyl benzyl alcohol is used as polymerization modifier, optimum ratios by weight thereof to monomer are 1 : 3.5 and 1.4. Other modifiers specified are benzyl alcohol and methyl-, isopropyl-, o-chlor-, and p-chlor-benzyl alcohols. It is stated that the modifier apparently functions to control the chain length of the polymer; excess cross-linking does not occur and a prepolymer is obtained without gelation. The proportion of water may be from 2 to 600% by weight of monomer. Catalysts in a proportion of 0.1 to 10% by weight of monomer are exemplified by benzoyl, acetyl benzoyl and succinyl peroxides and t-butyl perbenzoate. Of the isomeric diallyl phthalates that may be employed, orthophthalates are preferred. The prepolymers can be moulded to acetone-soluble thermoplastic or thermoset products at moderate temperatures and pressures. Chopped fibres, magnesium oxide and wood flour may be incorporated in the cured prepolymer.
GB1114658A 1958-04-09 1958-04-09 Improvements in or relating to the polymerization of diallyl phthalate Expired GB861817A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1114658A GB861817A (en) 1958-04-09 1958-04-09 Improvements in or relating to the polymerization of diallyl phthalate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1114658A GB861817A (en) 1958-04-09 1958-04-09 Improvements in or relating to the polymerization of diallyl phthalate

Publications (1)

Publication Number Publication Date
GB861817A true GB861817A (en) 1961-03-01

Family

ID=9980879

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1114658A Expired GB861817A (en) 1958-04-09 1958-04-09 Improvements in or relating to the polymerization of diallyl phthalate

Country Status (1)

Country Link
GB (1) GB861817A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3339291A1 (en) * 1982-10-30 1984-05-03 Osaka Soda Co. Ltd., Osaka DIALLYLTEREPHTHALATE COPOLYMERES

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3339291A1 (en) * 1982-10-30 1984-05-03 Osaka Soda Co. Ltd., Osaka DIALLYLTEREPHTHALATE COPOLYMERES
FR2535327A1 (en) * 1982-10-30 1984-05-04 Osaka Soda Co Ltd COPOLYMER OF DIALLYL TEREPHTHALATE AND COMPOSITION COMPRISING SUCH A COPOLYMER

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