GB980862A - Polymeric materials - Google Patents

Polymeric materials

Info

Publication number
GB980862A
GB980862A GB39263/61A GB3926361A GB980862A GB 980862 A GB980862 A GB 980862A GB 39263/61 A GB39263/61 A GB 39263/61A GB 3926361 A GB3926361 A GB 3926361A GB 980862 A GB980862 A GB 980862A
Authority
GB
United Kingdom
Prior art keywords
acrylic
acrylonitrile
heating
product
ester
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
GB39263/61A
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.)
VOLPATO Srl G
Original Assignee
VOLPATO Srl G
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 VOLPATO Srl G filed Critical VOLPATO Srl G
Publication of GB980862A publication Critical patent/GB980862A/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
    • 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
    • C08F20/62Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J39/00Cation exchange; Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
    • B01J39/08Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
    • B01J39/16Organic material
    • B01J39/18Macromolecular compounds
    • B01J39/20Macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
    • 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
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/14Methyl esters, e.g. methyl (meth)acrylate
    • 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
    • C08F220/42Nitriles
    • C08F220/44Acrylonitrile
    • 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
    • C08F8/00Chemical modification by after-treatment
    • 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
    • C08F8/00Chemical modification by after-treatment
    • C08F8/44Preparation of metal salts or ammonium salts
    • 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
    • C08F212/00Copolymers 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 an aromatic carbocyclic ring
    • C08F212/34Monomers containing two or more unsaturated aliphatic radicals
    • C08F212/36Divinylbenzene

Landscapes

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

Abstract

Cross-linked copolymers suitable for use as cation exchange resins are prepared by a process which comprises polymerizing in the presence of a polymerization catalyst a mixture comprising (1) acrylonitrile, (2) acrylic or methacrylic acid, an ester of acrylic or methacrylic acid, or a mixture of acrylic or methacrylic acid with an ester thereof and (3) commercially available divinyl benzene, saponifying the ester groups under mild conditions where the copolymers contain no carboxyl groups, heating the copolymers at 150 to 200 DEG C. to effect condensation of the carboxyl and nitrile groups, and if necessary saponifying under strong conditions to convert the nitrile and/or ester groups still present in the polymer to carboxyl groups. The catalyst may be benzoyl peroxide. Polymerization may be effected in aqueous suspension or in bulk, the product being ground or milled to the required granular size. Examples describe (I) the copolumerization of acrylonitrile, acrylic acid and divinyl benzene and (V) the heating of the product and saponification with hot concentrated sodium hydroxide solution; (II) the copolymerization of ethyl acrylate, acrylonitrile and divinylbenzene and (VI) the saponification of the ester groups with dilute sodium hydroxide solution and the heating of the product; and (III) the copolymerization of methyl acrylate, acrylonitrile, acrylic acid and divinylbenzene and (VII) the heating and saponification of the product. The saponified products are useful as cation exchange resins.
GB39263/61A 1960-11-03 1961-11-02 Polymeric materials Expired GB980862A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT1901160 1960-11-03

Publications (1)

Publication Number Publication Date
GB980862A true GB980862A (en) 1965-01-20

Family

ID=11153831

Family Applications (1)

Application Number Title Priority Date Filing Date
GB39263/61A Expired GB980862A (en) 1960-11-03 1961-11-02 Polymeric materials

Country Status (3)

Country Link
FR (1) FR1304499A (en)
GB (1) GB980862A (en)
NL (1) NL270884A (en)

Also Published As

Publication number Publication date
NL270884A (en)
FR1304499A (en) 1962-09-21

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