GB767821A - Improvements in and relating to ion-exchange resins - Google Patents

Improvements in and relating to ion-exchange resins

Info

Publication number
GB767821A
GB767821A GB1612953A GB1612953A GB767821A GB 767821 A GB767821 A GB 767821A GB 1612953 A GB1612953 A GB 1612953A GB 1612953 A GB1612953 A GB 1612953A GB 767821 A GB767821 A GB 767821A
Authority
GB
United Kingdom
Prior art keywords
groups
acid
copolymer
derivative
amine
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
GB1612953A
Inventor
Douglas Knight Hale
Stanley Lewis Sheldon Thomas
Kenneth Welch Pepper
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.)
National Research Development Corp UK
Original Assignee
National Research Development Corp UK
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 National Research Development Corp UK filed Critical National Research Development Corp UK
Priority to GB1612953A priority Critical patent/GB767821A/en
Publication of GB767821A publication Critical patent/GB767821A/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
    • 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
    • C08F2800/00Copolymer characterised by the proportions of the comonomers expressed
    • C08F2800/20Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
    • 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
    • C08F2810/00Chemical modification of a polymer
    • C08F2810/20Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently

Landscapes

  • Chemical & Material Sciences (AREA)
  • General 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

An insoluble ion-exchange resin derived from a copolymer of an aromatic monovinyl hydrocarbon, e.g. styrene, and an aromatic divinyl hydrocarbon, e.g. divinyl benzene, contains both organic acid groups and basic nitrogen groups attached to the same resin matrix. The organic acid group is preferably derived from acetic or diacetyl acetic acid. The resin may be produced by (1) condensing an amine derivative of the copolymer with a halogenated organic acid, e.g. chloracetic acid, or salt thereof to give a product containing imino groups, or (2) condensing such a copolymer containing reactive halogen groups with an acid containing imino groups, e.g. imino-diacetic acid, or with a derivative thereof, e.g. the dinitrile of iminodiacetic acid, followed by hydrolysis to liberate the acid groups, which results in a product containing t-amine groups. The halogen groups may be introduced into the copolymer as described in Specifications 654,706, 670,348 and 679,850-3, and for use in method (1) a resin containing halo-alkyl groups thus produced may then be aminated by reacting with (a) ammonia, an arylamine, an alkylamine, e.g. methylamine, ethylene diamine or a poly-primary amine, or (b) potassium phthalimide or a monophthalimido derivative of a diprimary amine, such as ethylene diamine, followed by hydrolysing off the phthalic acid structure. Additional basic nitrogen groups may then be introduced into the aminated copolymer by condensation with ethylene or polyethylene imine. The products serve either as cation- or anion-exchange resins and when the acidic and basic groups are separated by one or two carbon atoms they will form complexes with particular metallic ions, e.g. those of copper, nickel, cobalt, chromium or manganese. In examples, the copolymer of styrene and divinyl benzene is produced by heating with benzoyl peroxide catalyst in aqueous suspension using a cellulose derivative as stabilizer.
GB1612953A 1953-06-11 1953-06-11 Improvements in and relating to ion-exchange resins Expired GB767821A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1612953A GB767821A (en) 1953-06-11 1953-06-11 Improvements in and relating to ion-exchange resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1612953A GB767821A (en) 1953-06-11 1953-06-11 Improvements in and relating to ion-exchange resins

Publications (1)

Publication Number Publication Date
GB767821A true GB767821A (en) 1957-02-06

Family

ID=10071703

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1612953A Expired GB767821A (en) 1953-06-11 1953-06-11 Improvements in and relating to ion-exchange resins

Country Status (1)

Country Link
GB (1) GB767821A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1054715B (en) * 1957-12-02 1959-04-09 Bayer Ag Process for the production of synthetic resins with anion-exchange properties
DE1168080B (en) * 1964-04-16 Bayer Ag Process for the production of finely divided, insoluble plastics with anion-exchanging properties
US3277023A (en) * 1962-09-13 1966-10-04 Dow Chemical Co Method for making exchange resins from anilinium exchange resins
US3969284A (en) * 1973-05-24 1976-07-13 Owens-Illinois, Inc. Amino acid derivatives of chloromethylated polymers and methods of making the same
US3970603A (en) * 1973-05-24 1976-07-20 Owens-Illinois, Inc. Amino acid derivatives of chloromethylated polymers and methods of making the same
US3985715A (en) * 1973-05-24 1976-10-12 Owens-Illinois, Inc. Oxazolidone derivatives of chloromethylated polymers and methods of making the same
US10577480B2 (en) 2015-06-22 2020-03-03 Mitsubishi Chemical Corporation Iminodiacetate chelating resin and manufacturing method therefor

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1168080B (en) * 1964-04-16 Bayer Ag Process for the production of finely divided, insoluble plastics with anion-exchanging properties
DE1054715B (en) * 1957-12-02 1959-04-09 Bayer Ag Process for the production of synthetic resins with anion-exchange properties
US3277023A (en) * 1962-09-13 1966-10-04 Dow Chemical Co Method for making exchange resins from anilinium exchange resins
US3969284A (en) * 1973-05-24 1976-07-13 Owens-Illinois, Inc. Amino acid derivatives of chloromethylated polymers and methods of making the same
US3970603A (en) * 1973-05-24 1976-07-20 Owens-Illinois, Inc. Amino acid derivatives of chloromethylated polymers and methods of making the same
US3985715A (en) * 1973-05-24 1976-10-12 Owens-Illinois, Inc. Oxazolidone derivatives of chloromethylated polymers and methods of making the same
US10577480B2 (en) 2015-06-22 2020-03-03 Mitsubishi Chemical Corporation Iminodiacetate chelating resin and manufacturing method therefor

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