GB959514A - New cation exchange resins - Google Patents

New cation exchange resins

Info

Publication number
GB959514A
GB959514A GB17068/62A GB1706862A GB959514A GB 959514 A GB959514 A GB 959514A GB 17068/62 A GB17068/62 A GB 17068/62A GB 1706862 A GB1706862 A GB 1706862A GB 959514 A GB959514 A GB 959514A
Authority
GB
United Kingdom
Prior art keywords
vinyl
acid
benzene
styrene
divinyl
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
GB17068/62A
Inventor
Reinhard Bachmann
Ulrich Krauss
Hans Reuter
Gerhard Schwachula
Dieter Warnecke
Wilhelm Wehlend
Friedrich Wolf
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.)
Filmfabrik Wolfen VEB
Original Assignee
Filmfabrik Wolfen VEB
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 Filmfabrik Wolfen VEB filed Critical Filmfabrik Wolfen VEB
Priority to GB17068/62A priority Critical patent/GB959514A/en
Priority to FR896290A priority patent/FR1321798A/en
Publication of GB959514A publication Critical patent/GB959514A/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
    • 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
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • 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
    • 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
    • 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

Abstract

Substantially abrasion-resistant cation exchange resins are prepared by sulphonating copolymers obtained by polymerizing one or more monovinyl aromatic compounds with one or more polyvinyl compounds and with vinyl or epoxy-group containing polymerizable polar compounds, the latter being present in amounts of 0.001 to 0.2 mol. per mol. of monovinyl aromatic compound or compounds, the polar compounds being different from the monovinyl and polyvinyl compounds. Monovinyl and polyvinyl compounds mentioned are styrene, vinyl-toluene, vinyl-ethyl-benzene, vinylanisole and divinyl-benzene, divinyl-ethyl-benzene, trivinyl-benzene, divinyl-acetylene, butadiene and divinyl ketone. Polar compounds mentioned are acrylic and methacrylic acids and their derivatives, especially acrylo- and methacrylo-nitriles, methylvinyl ketone and its homologues, vinyl halides, vinyl-benzene halides, methyl-vinyl ether and its homologues, vinylsulphonic acid and its derivatives, styrene-sulphonic acids and their derivatives, vinyl pyridine and its homologues, esters of vinyl alcohol such as vinyl acetate and propionate, maleic acid and its derivatives, styrene oxide, vinyl-toluene-oxide, ethyl-styrene oxide, ethylene and propylene oxides and epichlorohydrin. In the examples copolymers are produced from styrene and divinyl benzene with one of the following: methylmethacrylate, epichlorohydrin, methylvinylketone, acrylonitrile, methacrylic acid, maleic anhydride, propyl ester of styrene-sulphonic acid, ethyl acrylate, vinyl-sulphonic acid, vinyl pyridine, vinyl chloride or styrene oxide, in an aqueous suspension containing magnesium silicate, hydroxy-apatite, methyl-cellulose or magnesium hydroxide, the catalyst being diacetyl, dibenzoyl or dilauroyl peroxide or azo-bis-isobutyric acid nitrile. The copolymers which may first be swelled with a chlorinated hydrocarbon are sulphonated with sulphuric acid monohydrate, oleum, chlorosulphonic acid, oleum and chlorosulphonic acid or liquid sulphur trioxide.
GB17068/62A 1962-05-03 1962-05-03 New cation exchange resins Expired GB959514A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB17068/62A GB959514A (en) 1962-05-03 1962-05-03 New cation exchange resins
FR896290A FR1321798A (en) 1962-05-03 1962-05-03 Process for preparing copolymers containing sulfonic acid groups capable of exchanging ions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB17068/62A GB959514A (en) 1962-05-03 1962-05-03 New cation exchange resins

Publications (1)

Publication Number Publication Date
GB959514A true GB959514A (en) 1964-06-03

Family

ID=10088690

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17068/62A Expired GB959514A (en) 1962-05-03 1962-05-03 New cation exchange resins

Country Status (1)

Country Link
GB (1) GB959514A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2203438A (en) * 1987-04-06 1988-10-19 Asahi Chemical Ind Photosensitive and heat-sensitive polymers, process for producing the same and process for recording information using the same
WO2013101584A1 (en) * 2011-12-28 2013-07-04 Rohm And Haas Company Process for preparing a strong acid catalyst
US9968920B2 (en) 2011-12-28 2018-05-15 Rohm And Haas Company Strong acid catalyst composition
CN111957346A (en) * 2020-08-17 2020-11-20 丹东明珠特种树脂有限公司 Etherification catalyst for preparing methyl tert-butyl ether from methanol-tert-butyl alcohol and preparation method thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2203438A (en) * 1987-04-06 1988-10-19 Asahi Chemical Ind Photosensitive and heat-sensitive polymers, process for producing the same and process for recording information using the same
GB2203438B (en) * 1987-04-06 1991-12-11 Asahi Chemical Ind Photosensitive and heat-sensitive polymers, process for producing the same and process for recording information using the same
WO2013101584A1 (en) * 2011-12-28 2013-07-04 Rohm And Haas Company Process for preparing a strong acid catalyst
CN103974771A (en) * 2011-12-28 2014-08-06 罗门哈斯公司 Process for preparing a strong acid catalyst
CN103974771B (en) * 2011-12-28 2016-11-23 罗门哈斯公司 The method preparing strong acid catalyst
US9968920B2 (en) 2011-12-28 2018-05-15 Rohm And Haas Company Strong acid catalyst composition
CN111957346A (en) * 2020-08-17 2020-11-20 丹东明珠特种树脂有限公司 Etherification catalyst for preparing methyl tert-butyl ether from methanol-tert-butyl alcohol and preparation method thereof

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