GB1413383A - Cross-linked copolymers and their production - Google Patents

Cross-linked copolymers and their production

Info

Publication number
GB1413383A
GB1413383A GB2360075A GB2360075A GB1413383A GB 1413383 A GB1413383 A GB 1413383A GB 2360075 A GB2360075 A GB 2360075A GB 2360075 A GB2360075 A GB 2360075A GB 1413383 A GB1413383 A GB 1413383A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
glycol dimethacrylate
cross
copolymerized
residues
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
GB2360075A
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.)
Bayer AG
Original Assignee
Bayer AG
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
Priority claimed from DE2215539A external-priority patent/DE2215539C2/en
Application filed by Bayer AG filed Critical Bayer AG
Priority to GB2360075A priority Critical patent/GB1413383A/en
Publication of GB1413383A publication Critical patent/GB1413383A/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
    • C08F220/00Copolymers 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
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/26Esters containing oxygen in addition to the carboxy oxygen
    • 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
    • C08F222/00Copolymers 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 carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
    • C08F222/10Esters
    • C08F222/1006Esters of polyhydric alcohols or polyhydric phenols
    • C08F222/102Esters of polyhydric alcohols or polyhydric phenols of dialcohols, e.g. ethylene glycol di(meth)acrylate or 1,4-butanediol dimethacrylate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

1413383 Copolymers BAYER AG 29 March 1973 23600/75 Divided out of 1413381 Heading C3P A cross-linked copolymer comprising the following copolymerized residues (percentages being by weight of the cross-linked co-polymer): A: 0À1 to 50% of at least one α,#-olefinically unsaturated dicarboxylic acid anhydride having 4-9 carbon atoms; B: 99À9 to 50% of at least one di- and/or polyacrylate or methacrylate of a diol and/or a polyol, the said copolymer having a bulk volume of 1À4-30 ml./g. and a specific surface area of 0À1-500 m.<SP>2</SP>/g., and containing, after hydrolysis of the anhydride groups, 0À02 to 10 m.equiv. of acid per gram, is obtained by copolymerizing by precipitation or bead polymerization in a diluent inert to anhydride groups at 20-200‹ C. in the presence of a freeradical initiator, a mixture comprising 0À2 to 70 wt. per cent of component A and 99.9 to 30 wt. per cent of component B. Copolymerized residues A are preferably derived from at least one of maleic, itaconic, and citraconic anhydrides, and the polymerized residues B are preferably derived from di-acrylates and dimethacrylates of diols containing 2-4 carbon atoms, reaction products of 1 mole of diols having 2-4 carbon atoms with 1-20 moles of at least one C 2-4 alkylene oxide, and trimethylolpropane trimethacrylate. In the examples the following starting materials are copolymerized: tetraethylene glycol dimethacrylate; ethylene glycol dimethacrylate, diethylene glycol dimethacrylate and maleic anhydride using azoisobutyronitrile as initiator.
GB2360075A 1972-03-30 1973-03-29 Cross-linked copolymers and their production Expired GB1413383A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2360075A GB1413383A (en) 1972-03-30 1973-03-29 Cross-linked copolymers and their production

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2215539A DE2215539C2 (en) 1972-03-30 1972-03-30 New water-insoluble enzyme, in particular penicillin acylase or enzyme inhibitor preparations
GB2360075A GB1413383A (en) 1972-03-30 1973-03-29 Cross-linked copolymers and their production

Publications (1)

Publication Number Publication Date
GB1413383A true GB1413383A (en) 1975-11-12

Family

ID=10198289

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2360075A Expired GB1413383A (en) 1972-03-30 1973-03-29 Cross-linked copolymers and their production

Country Status (1)

Country Link
GB (1) GB1413383A (en)

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee