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GB1110033A - Methacrylate polymers - Google Patents

Methacrylate polymers

Info

Publication number
GB1110033A
GB1110033A GB34817/65A GB3481765A GB1110033A GB 1110033 A GB1110033 A GB 1110033A GB 34817/65 A GB34817/65 A GB 34817/65A GB 3481765 A GB3481765 A GB 3481765A GB 1110033 A GB1110033 A GB 1110033A
Authority
GB
United Kingdom
Prior art keywords
methacrylate
methylstyrene
acrylate
methyl
trimethyl
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
GB34817/65A
Inventor
Max Statman
William James Gammans
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak 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 Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of GB1110033A publication Critical patent/GB1110033A/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
    • C08F22/00Homopolymers 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 a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
    • C08F22/10Esters
    • C08F22/1006Esters of polyhydric alcohols or polyhydric phenols, e.g. ethylene glycol dimethacrylate

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

Copolymers are formed from 2,2,4-trimethylpentyl-1,3 -dimethacrylate (TMPD) and at least one other vinylidene or vinyl monomer. Specified comonomers are styrene, o-methylstyrene, m-methylstyrene, 2,4-dimethyl styrene, o-ethylstyrene, vinyl chloride, vinylidene chloride, acrylonitrile, 2,2,4-trimethyl-3-hydroxypentyl methacrylate and esters of formula <FORM:1110033/C3/1> wherein R1 is hydrogen or methyl and R is an alkyl group of 1 to 8 carbon atoms, an alicyclic group of 4 to 8 carbon atoms or an aryl or aralkyl group of 6 to 12 carbon atoms. For example R may be a cyclobutyl, cyclopentyl, phenyl, a -naphthyl or b -naphthyl group. The monomers are heated together to e.g. 40 DEG to 160 DEG C. The mixture may be cast into a film or mould either before heating or after partial reaction. In the latter case the copolymer may be cured by heating after casting. The monomer other than T.M.P.D. may be partially polymerized prior to addition of the T.M.P.D. In Example 1 a copolymer of T.M.P.D. and methyl methacrylate is prepared by polymerizing the latter to about 25% conversion and reacting the T.M.P.D. with the resulting syrup; in Example II 2,2,4 - trimethyl - 3 - hydroxypentyl methacrylate is also added to the methyl methacrylate syrup. In other examples terpolymers of T.M.P.D., (1) methyl methacrylate and (2) methyl acrylate, (3) ethyl acrylate, (4) n-butyl methacrylate, (5) n-butyl acrylate, (6) isobutyl acrylate, (7) 2-ethylhexyl methacrylate, (8) 2-ethylhexyl acrylate, (9) ethyl methacrylate and (10) isopropyl methacrylate are prepared. Copolymers of T.M.P.D. and (12) styrene, (13) o-methylstyrene, (14) m-methylstyrene, (15) 2,4-dimethylstyrene, (16) o-ethylstyrene, (17) vinyl chloride, (18) acrylonitrile and (19) vinylidene chloride are produced by reacting the monomers with t.-bu. hydroperoxide as catalyst. In Example 20 T.M.P.D. and 2,2,4-trimethyl-3-hydroxypentyl methacrylate are copolymerized using benzoyl peroxide as catalyst. In Examples 21 and 22 the comonomer is (21) cyclohexyl methacrylate and (22) a -phenylethyl methacrylate.
GB34817/65A 1964-08-13 1965-08-13 Methacrylate polymers Expired GB1110033A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US38947664A 1964-08-13 1964-08-13

Publications (1)

Publication Number Publication Date
GB1110033A true GB1110033A (en) 1968-04-18

Family

ID=23538421

Family Applications (1)

Application Number Title Priority Date Filing Date
GB34817/65A Expired GB1110033A (en) 1964-08-13 1965-08-13 Methacrylate polymers

Country Status (2)

Country Link
FR (1) FR1455276A (en)
GB (1) GB1110033A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5290602A (en) * 1992-10-19 1994-03-01 Union Carbide Chemicals & Plastics Technology Corporation Hindered-hydroxyl functional (meth) acrylate-containing copolymers particularly suitable for use in coating compositions which are sprayed with compressed fluids as viscosity reducing diluents
US5420341A (en) * 1992-10-19 1995-05-30 Union Carbide Chemicals & Plastics Hindered-hydroxyl functional (meth)acrylate compounds and processes for the preparation thereof
US5442023A (en) * 1994-06-30 1995-08-15 Union Carbide Chemicals & Plastics Technology Corporation Hindered-hydroxyl functional (meth)acrylate monomers containing di(meth)acrylates and compositions including same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5290602A (en) * 1992-10-19 1994-03-01 Union Carbide Chemicals & Plastics Technology Corporation Hindered-hydroxyl functional (meth) acrylate-containing copolymers particularly suitable for use in coating compositions which are sprayed with compressed fluids as viscosity reducing diluents
US5420341A (en) * 1992-10-19 1995-05-30 Union Carbide Chemicals & Plastics Hindered-hydroxyl functional (meth)acrylate compounds and processes for the preparation thereof
US5442023A (en) * 1994-06-30 1995-08-15 Union Carbide Chemicals & Plastics Technology Corporation Hindered-hydroxyl functional (meth)acrylate monomers containing di(meth)acrylates and compositions including same

Also Published As

Publication number Publication date
FR1455276A (en) 1966-04-01

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