GB770322A - Improvements in cation-exchange resins - Google Patents

Improvements in cation-exchange resins

Info

Publication number
GB770322A
GB770322A GB24375/54A GB2437554A GB770322A GB 770322 A GB770322 A GB 770322A GB 24375/54 A GB24375/54 A GB 24375/54A GB 2437554 A GB2437554 A GB 2437554A GB 770322 A GB770322 A GB 770322A
Authority
GB
United Kingdom
Prior art keywords
cross
phenol
acetone
resorcinol
phenols
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
GB24375/54A
Inventor
Theodore Roger Ernest Kressman
Frank Laurence Tye
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.)
Permutit Co Ltd
Original Assignee
Permutit Co 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 Permutit Co Ltd filed Critical Permutit Co Ltd
Priority to GB24375/54A priority Critical patent/GB770322A/en
Priority to DEP14688A priority patent/DE1131020B/en
Publication of GB770322A publication Critical patent/GB770322A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14Polycondensates modified by chemical after-treatment
    • 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
    • B01J39/19Macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Cation exchange resins are made by introducing sulphonic acid groups into the benzene rings of a resin formed by reacting epichlorhydrin, a dihydric phenol and a phenol containing three or more hydroxy groups as a cross-linking agent. Specified dihydric phenols include resorcinol, catechol, hydroquinone and dihydric phenols derived from acetone or formaldehyde and phenols, e.g. diphenylol propane. The cross-linking agents specified are phloroglucinol, pyrocatechol and tetrahydric phenols derived from acetone and catechol, hydroquinone or resorcinol, e.g. bis-(2,4-dihydroxy phenyl)-dimethyl methane, whilst additional cross-linking agents, e.g. polyamines such as diethylene triamine, bifunctional compounds such as glyoxal, succinic acid, dichloromethyl ether, hexamethylene di-isocyanate and water soluble resins of the urea-, melamine- and phenol-formaldehyde types may be included. Sulphonic acid groups can be introduced into the cross-linked resin by sulphuric acid or oleum. In the example, a tetrahydric phenol prepared from resorcinol and acetone is mixed with diphenylol propane and epichlorhydrin and heated in caustic soda solution to solidification. The solid is dried, broken up and sulphonated with sulphuric acid.
GB24375/54A 1954-08-20 1954-08-20 Improvements in cation-exchange resins Expired GB770322A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB24375/54A GB770322A (en) 1954-08-20 1954-08-20 Improvements in cation-exchange resins
DEP14688A DE1131020B (en) 1954-08-20 1955-08-19 Process for the production of cation exchange resins based on epoxy compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB24375/54A GB770322A (en) 1954-08-20 1954-08-20 Improvements in cation-exchange resins

Publications (1)

Publication Number Publication Date
GB770322A true GB770322A (en) 1957-03-20

Family

ID=10210738

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24375/54A Expired GB770322A (en) 1954-08-20 1954-08-20 Improvements in cation-exchange resins

Country Status (2)

Country Link
DE (1) DE1131020B (en)
GB (1) GB770322A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1196160B (en) * 1961-12-22 1965-07-08 Bayer Ag Process for the production of anion exchange membranes, consisting of an anion exchange resin and a support fabric

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR839668A (en) * 1937-07-13 1939-04-07 Ig Farbenindustrie Ag Process for reducing the swelling of synthetic phenol resins
NL52346C (en) * 1938-08-23
US2469684A (en) * 1946-03-16 1949-05-10 American Cyanamid Co Anion active resins and processes of producing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1196160B (en) * 1961-12-22 1965-07-08 Bayer Ag Process for the production of anion exchange membranes, consisting of an anion exchange resin and a support fabric

Also Published As

Publication number Publication date
DE1131020B (en) 1962-06-07

Similar Documents

Publication Publication Date Title
GB762216A (en) Improvements in manufacture of resins
GB782072A (en) Manufacture of glycidyl ethers of phenols
GB770322A (en) Improvements in cation-exchange resins
GB675170A (en) Improvements in synthetic resins obtained by condensation of polyhydric phenols and epichlorhydrin
GB794634A (en) Improvements in or relating to phenol-formaldehyde resinous condensation products
GB791303A (en) Process for preparing compositions containing glycidyl ethers
GB907341A (en) Polyglycidyl ethers of polyphenols
GB932811A (en) Bis and polyphenols and production thereof
GB1116029A (en) Flame-retardant epoxy resins
GB949713A (en) Improvements in or relating to the production of curable phenol-formaldehyde resins
GB797438A (en) Improvements in the preparation of cation-exchange resins
GB1098528A (en) Polyepoxy ethers of polyhydric phenols and cured products obtained therefrom
GB966678A (en) Improvements in or relating to the manufacture of phenolic resins
GB740840A (en) Improvements in or relating to anion exchange resins
GB1163502A (en) Method for activating cycloaliphatic polyamines as curing agents for reaction with epoxide compounds
GB743345A (en) Improvements in or relating to the manufacture of resinous phenolic bodies
GB731270A (en) Improvements in or relating to the alkylation of phenols and naphthols
GB700708A (en) Process for the production of chemically resistant urea-formaldehyde resins
GB1013828A (en) Process for the preparation of water-insoluble condensation products
GB888658A (en) Curing epoxy resins
GB986711A (en) Improved lignin-extended phenolic resins
GB842714A (en) Process for the manufacture of insoluble ion-exchange synthetic resins
GB753268A (en) Process for the preparation of epoxy resins from novolac resins
Britton Synthetic Phenols for Resin Manufacture
GB789392A (en) Improvements in or relating to epoxide resins