GB910799A - Plasticised polymers - Google Patents

Plasticised polymers

Info

Publication number
GB910799A
GB910799A GB2456460A GB2456460A GB910799A GB 910799 A GB910799 A GB 910799A GB 2456460 A GB2456460 A GB 2456460A GB 2456460 A GB2456460 A GB 2456460A GB 910799 A GB910799 A GB 910799A
Authority
GB
United Kingdom
Prior art keywords
methacrylate
acrylic
mixture
ethoxyethyl
ethyl acrylate
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
GB2456460A
Inventor
Edward George Gazzard
Dorothy Joyce Guest
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2456460A priority Critical patent/GB910799A/en
Publication of GB910799A publication Critical patent/GB910799A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/50Aqueous dispersion, e.g. containing polymers with a glass transition temperature (Tg) above 20°C
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/02Polyalkylene oxides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Aqueous dispersions of homopolymers or copolymers of acrylic or methacrylic esters are plasticized with an oxypropylene polymer containing a major proportion of the repeating unit of the formula -CH(CH3)CH2O-The polyoxypropylene chain may be terminated by alcoholic hydroxyl, ester, ether, amide, carboxyl, amine, mercapto, hydrazide or phosphate groups. Preferred polyoxypropylenes are polypropylene glycols 200-1500, but these may also be used products obtained by reacting polypropylene glycols with ethylene oxide, or vice versa, and by reacting propylene oxide with compounds such as saccharides or trimethylol propane. Acrylic and methacrylic esters specified are ethyl acrylate, methyl methacrylate, n-butyl methacrylate and ethoxyethyl methacrylate, which may be used in admixture with one another or with other monomers, e.g. vinyl esters, maleates and fumarates, styrene and acrylonitrile. The oxypropylene polymer is preferably incorporated in the acrylic or methacrylic ester at the time of its polymerization. In the examples: (1) a mixture of polypropylene glycol and n-butyl methacrylate is added gradually to a heated aqueous medium containing ammonium persulphate and Turkey Red Oil, (2) as in (1) but using a mixture of ethoxyethyl and methyl methacrylates, (3) as in (1) but using ethoxyethyl methacrylate, and (4) as in (1) but using a mixture of ethyl acrylate and methyl methacrylate.
GB2456460A 1960-07-14 1960-07-14 Plasticised polymers Expired GB910799A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2456460A GB910799A (en) 1960-07-14 1960-07-14 Plasticised polymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2456460A GB910799A (en) 1960-07-14 1960-07-14 Plasticised polymers

Publications (1)

Publication Number Publication Date
GB910799A true GB910799A (en) 1962-11-21

Family

ID=10213616

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2456460A Expired GB910799A (en) 1960-07-14 1960-07-14 Plasticised polymers

Country Status (1)

Country Link
GB (1) GB910799A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5599863A (en) * 1994-06-17 1997-02-04 Cyro Industries Gamma radiation sterilizable acrylic polymer

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5599863A (en) * 1994-06-17 1997-02-04 Cyro Industries Gamma radiation sterilizable acrylic polymer

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