GB1085920A - Stabilised compositions of alkyl vinyl pyridines - Google Patents

Stabilised compositions of alkyl vinyl pyridines

Info

Publication number
GB1085920A
GB1085920A GB53064/64A GB5306464A GB1085920A GB 1085920 A GB1085920 A GB 1085920A GB 53064/64 A GB53064/64 A GB 53064/64A GB 5306464 A GB5306464 A GB 5306464A GB 1085920 A GB1085920 A GB 1085920A
Authority
GB
United Kingdom
Prior art keywords
alkyl
methyl
acrylonitrile
alkyl group
stabilized
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
GB53064/64A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB1085920A publication Critical patent/GB1085920A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • 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
    • C08F2/00Processes of polymerisation
    • C08F2/38Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
    • 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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/08Anhydrides
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/38Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising unsaturated nitriles as the major constituent

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Pyridine Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Artificial Filaments (AREA)

Abstract

Polymers of improved colour are made by the polymerization or co-polymerization of a C1- 5 alkylvinyl pyridine which is stabilized by the addition thereto of a mixture of (A) 1,2-dihydroxy-4-t-butyl benzene and (B) one or more of acrylonitrile or an alkyl acrylate of the formula <FORM:1085920/C3/1> where R is hydrogen or a methyl group and R1 is an alkyl group, provided that when R1 represents an alkyl group of 2 or more carbon atoms, the amount of alkyl acrylate is at most 0.5% by wt. based on alkylvinylpyridine. Example 29 describes the preparation of a copolymer of acrylonitrile, methyl acrylate and stabilized 2-methyl-5-vinyl pyridine, using hydrogen peroxide as catalyst and 1-thio-glycerol as an activator.ALSO:C1- 5 monoalkyl vinyl pyridines are stabilized by addition of a mixture comprising (A) 1,2-dihydroxy-4-t.-butyl benzene and (B) one or more of acrylonitrile and alkyl acrylates of the formula <FORM:1085920/C2/1> where R is hydrogen or a methyl group and R1 is an alkyl group, with the proviso that when R1 represents an alkyl group of 2 or more carbon atoms, the amount of alkyl acrylate in the composition is at most 0.5% by weight based on alkyl vinyl pyridine. When component (B) is acrylonitrile the mixture may also contain vinyl acetate. Examples relate to the stabilization of 2-methyl-5-vinyl pyridine.
GB53064/64A 1963-12-31 1964-12-31 Stabilised compositions of alkyl vinyl pyridines Expired GB1085920A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US334937A US3255160A (en) 1963-12-31 1963-12-31 Stabilization of alkyl vinyl pyridines using tertiary butyl catechol and subsequent copolymerization of the alkyl vinyl pyridines with acrylonitrile or acrylate derivatives

Publications (1)

Publication Number Publication Date
GB1085920A true GB1085920A (en) 1967-10-04

Family

ID=23309525

Family Applications (1)

Application Number Title Priority Date Filing Date
GB53064/64A Expired GB1085920A (en) 1963-12-31 1964-12-31 Stabilised compositions of alkyl vinyl pyridines

Country Status (3)

Country Link
US (1) US3255160A (en)
GB (1) GB1085920A (en)
NL (1) NL6415274A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3043672A (en) * 1956-08-22 1962-07-10 Ethyl Corp Substituted catechol antioxidants
NL271517A (en) * 1960-11-17

Also Published As

Publication number Publication date
US3255160A (en) 1966-06-07
NL6415274A (en) 1965-07-02

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