GB720506A - Improvements in or relating to interpolymers - Google Patents

Improvements in or relating to interpolymers

Info

Publication number
GB720506A
GB720506A GB12718/52A GB1271852A GB720506A GB 720506 A GB720506 A GB 720506A GB 12718/52 A GB12718/52 A GB 12718/52A GB 1271852 A GB1271852 A GB 1271852A GB 720506 A GB720506 A GB 720506A
Authority
GB
United Kingdom
Prior art keywords
hydroxy
ester
butyl
per cent
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
GB12718/52A
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.)
Goodrich Corp
Original Assignee
BF Goodrich 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 BF Goodrich Corp filed Critical BF Goodrich Corp
Publication of GB720506A publication Critical patent/GB720506A/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
    • C08F214/00Copolymers 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
    • C08F214/02Monomers containing chlorine
    • C08F214/04Monomers containing two carbon atoms
    • C08F214/06Vinyl chloride

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

Interpolymers are prepared by polymerizing a mixture of monomeric materials comprising from 35 to 90 per cent by weight of vinyl chloride, from 5 to 65 per cent by weight of an alkyl ester of acrylic acid and from 0.2 to 25 per cent by weight of an ester of the formula <FORM:0720506/IV (a)/1> wherein X is an ester linkage and R is a divalent saturated aliphatic radical, or from 0.2 to 25 per cent by weight of a hydroxy-alkyl ester of acrylic acid, said mixture containing at least 90 per cent by weight of said alkyl ester of acrylic acid, said vinyl chloride and said ester of given formula or said hydroxy-alkyl ester of acrylic acid, the polymerization being carried out under acidic conditions when an ester of the above formula is used. The alkyl acrylate may be methyl, ethyl, propyl, n-butyl, n-amyl, n-hexyl, n-heptyl, isohexyl, n-heptyl, isoheptyl, capryl, n-octyl, 2-ethylhexyl, 6-methyl-heptyl, n-nonyl, 3,5,5-trimethylhexyl, n-decyl or lauryl acrylate. The ester of the given formula may be the monovinyl ester of malonic, chloro- or bromo-malonic, hydroxy-malonic, dihydroxy-malonic, isosuccinic, ethyl malonic; succinic, malic, bromo-succinic, tartaric, ethyl succinic, citramalic, acetoxy-succinic, glutaric, alpha-hydroxy - glutaric, adipic, pimelic, suberic, azelaic, sebacic, brassylic or thapsic acid, or may be acryloxyacetic acid, beta-acryloxy propionic acid or 4-carboxy-butyl acrylate. The hydroxy-alkyl ester of acrylic acid may be 2-hydroxyethyl, 1-chloro-2-hydroxyethyl, 3-hydroxy - propyl, glyceryl, 2 - methoxy - 3 - hydroxy - propyl, 2 - hydroxy - butyl, 3 - hydroxy - butyl, 3,4 - dihydroxy - butyl, 2 - methoxy, 3,4 - dihydroxy - butyl, 5 - hydroxy - amyl, 6 - hydroxy - hexyl, 2 - ethyl - 6 - hydroxy - hexyl, 7 - hydroxy - heptyl, 1 - methyl - 7 - hydroxy - heptyl, 8 - hydroxy - octyl, 3,5,5 - trimethyl - 6 - hydroxy - hexyl or 10 - hydroxy - decyl acrylate. Other monomers such as vinylidene chloride, vinyl acetate, vinyl benzoate, diethyl fumarate, acrylonitrile, styrene and methyl or ethyl acrylate may be utilized to the extent of 10 per cent by weight of the monomer mixture. Polymerization may be effected in an aqueous medium at pH 4.0 to 7.0. Emulsifiers referred to are the hymolal sulphates and sulphonates, such as the sodium salt of a sulphonated paraffin oil, salts of organic bases containing long carbon chains and polyether alcohols. Granular polymers may be obtained by polymerizing in an aqueous medium containing a colloidal suspension agent such as gelatin, bentonite clay, polyvinyl alcohol, polyacrylic acid and water-soluble phenolaldehyde and urea-aldehyde condensation products. The reaction may be catalysed by actinic radiation, or a peroxygen compound such as hydrogen, benzoyl, o,o1-dichlorobenzoyl, caproyl, caprylyl, and polygonyl peroxides, cumene, tertiary butyl and 1-hydroxy-cyclohexyl hydroperoxides, tertiary butyl diperphthalate, tertiary butyl perbenzoate, sodium, potassium and ammonium persulphates, sodium peracetate and sodium percarbonate. The interpolymers of the invention are suitable for the production of films, sheets and coatings.
GB12718/52A 1951-05-22 1952-05-20 Improvements in or relating to interpolymers Expired GB720506A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US720506XA 1951-05-22 1951-05-22

Publications (1)

Publication Number Publication Date
GB720506A true GB720506A (en) 1954-12-22

Family

ID=22105255

Family Applications (1)

Application Number Title Priority Date Filing Date
GB12718/52A Expired GB720506A (en) 1951-05-22 1952-05-20 Improvements in or relating to interpolymers

Country Status (1)

Country Link
GB (1) GB720506A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5380786A (en) * 1988-09-09 1995-01-10 The Geon Company Polyvinyl chloride blends having improved physical properties including low temperature brittleness

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5380786A (en) * 1988-09-09 1995-01-10 The Geon Company Polyvinyl chloride blends having improved physical properties including low temperature brittleness

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