GB867449A - Synthetic resins having anion-exchange properties - Google Patents

Synthetic resins having anion-exchange properties

Info

Publication number
GB867449A
GB867449A GB3887758A GB3887758A GB867449A GB 867449 A GB867449 A GB 867449A GB 3887758 A GB3887758 A GB 3887758A GB 3887758 A GB3887758 A GB 3887758A GB 867449 A GB867449 A GB 867449A
Authority
GB
United Kingdom
Prior art keywords
acid
chloromethyl
benzene
diglycolic
imide
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
GB3887758A
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
Application filed by Bayer AG filed Critical Bayer AG
Publication of GB867449A publication Critical patent/GB867449A/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
    • C08F8/12Hydrolysis
    • 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
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups

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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Water-insoluble anion-exchange resins are prepared by condensing (1) a benzene-insoluble vinyl-aromatic polymer cross-linked with up to 30% (calculated on the monomer) of a polyethylenically unsaturated cross-linking agent with (2) a N-(halogenoalkyl)-imide in the presence of a swelling agent and a Friedel-Crafts catalyst, and then saponifying. Copolymers of styrene, substituted styrenes, and vinyl naphthalene with divinyl benzene toluene, ethyl benzene, and vinylether, and trivinyl benzene, ethylene glycol dimethacrylate or diacrylate, dialkyl maleate, or a polyester of e.g. ethylene glycol and maleic acid, which may have a gel or sponge structure are used with for example N-chloromethyl succinimide, phthalimide, a diglycolic acidimide, and N-bromomethyl phthalimide. Friedel-Crafts catalysts mentioned are, stearic chloride, zinc bromide and chloride, and aluminium chloride and concentrated sulphuric acid, and the swelling agents may be ethylene dichloride or dibromide, methylene chloride, carbon tetrachloride, tetrachorethane, trichloro- or tribromoethylene, 1, 1, 2-trichlorethane, pentachloroethane, dichloro-, trichloro, tetrachloro- and pentachloropropanes and 1, 2, 3, 3-tetrachloropropylene. The reaction takes place at elevated temperatures and the imidoalkyl intermediate is separated and saponified by alkaline or acid hydrolysis or by conversion with hydrazine and subsequent acid hydrolysis. The products after isolation and purification are alkylated, with for example alkyl halides, dialkyl sulphates, alkylene oxides, halohydrins, polyhalogen compounds, or epihalohydrins, or a mixture of formaldehyde and formic acid. Secondary, tertiary or quaternary amino derivatives or mixtures thereof may be obtained. Examples describe the reaction of pearl copolymers of styrene, divinyl benzene and ethyl styrene with N-(chloromethyl)-phthalimide, chloromethyl-diglycolic acid imide, N-(chloromethyl)-succinimide and the saponification of the products to yield anion exchange resins. Specifications 654,706, 679,851, 679,852, 700,470, 714,366 and 779,994 are referred to.ALSO:Hydroxy methyl-digylcolic acid imide is prepared by heating diglycolic acid imide in an aqueous formaldehyde solution (40% by vol) and concentrating in vacuum at 40-45 DEG C. The diglycolic acid imide is distilled from diglycolic acid neutralised with ammonia. Specifications 654,706, 679,851, 679,852, 700,470, 714,366 and 779,994 are referred to.
GB3887758A 1957-12-02 1958-12-02 Synthetic resins having anion-exchange properties Expired GB867449A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF24526A DE1054715B (en) 1957-12-02 1957-12-02 Process for the production of synthetic resins with anion-exchange properties

Publications (1)

Publication Number Publication Date
GB867449A true GB867449A (en) 1961-05-10

Family

ID=7091264

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3887758A Expired GB867449A (en) 1957-12-02 1958-12-02 Synthetic resins having anion-exchange properties

Country Status (4)

Country Link
DE (1) DE1054715B (en)
FR (1) FR1217732A (en)
GB (1) GB867449A (en)
NL (1) NL113552C (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996025440A1 (en) * 1995-02-16 1996-08-22 British Technology Group Limited Polymeric compounds
US5851518A (en) * 1993-02-17 1998-12-22 British Technology Group Limited Polymeric compositions
US6417318B1 (en) 2000-02-10 2002-07-09 Bayer Aktiengesellschaft Process for the removal of dissolved oxygen from phenol
CN111100254A (en) * 2018-10-25 2020-05-05 中国石油化工股份有限公司 Strong alkaline carbon nano tube composite ion exchange resin material and preparation method thereof
US20210115170A1 (en) * 2018-06-14 2021-04-22 Lanxess Deutschland Gmbh Method for producing amido-methylated vinyl-aromatic bead polymers

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3437631A1 (en) * 1984-10-13 1986-04-24 Agfa-Gevaert Ag, 5090 Leverkusen TREATMENT OF USED DEVELOPERS
DE4328075A1 (en) * 1993-08-20 1995-02-23 Bayer Ag Process for the preparation of weakly basic anion exchangers and suitable reagents
NZ332116A (en) * 1996-05-03 2000-06-23 Warner Lambert Co Rapid purification of synthetic intermediates and products by polymer supported quench reagents
DE19714582A1 (en) 1997-04-09 1998-10-15 Bayer Ag Process for the production of strongly basic anion exchangers with ethylene oxide

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL73179C (en) * 1947-07-05
US2591573A (en) * 1947-07-05 1952-04-01 Rohm & Haas Resinous insoluble reaction products of tertiary amines with haloalkylated vinyl aromatic hydrocarbon copolymers
GB660815A (en) * 1947-11-24 1951-11-14 Erik Johan Von Heidenstam Improvements in vertical sliding shuttering
GB767821A (en) * 1953-06-11 1957-02-06 Nat Res Dev Improvements in and relating to ion-exchange resins

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5851518A (en) * 1993-02-17 1998-12-22 British Technology Group Limited Polymeric compositions
US5880208A (en) * 1993-02-17 1999-03-09 Btg International Limited Polymer compounds
US6132706A (en) * 1993-02-17 2000-10-17 Btg International Limited Methods of medical treatment for excess phosphate using guanidino-containing polymers
WO1996025440A1 (en) * 1995-02-16 1996-08-22 British Technology Group Limited Polymeric compounds
AU709065B2 (en) * 1995-02-16 1999-08-19 British Technology Group Limited Therapeutic use of polystyrene polymers containing guanidino or biguanidino groups
US5968499A (en) * 1995-02-16 1999-10-19 Btg International Limited Polymeric compounds
US6417318B1 (en) 2000-02-10 2002-07-09 Bayer Aktiengesellschaft Process for the removal of dissolved oxygen from phenol
US20210115170A1 (en) * 2018-06-14 2021-04-22 Lanxess Deutschland Gmbh Method for producing amido-methylated vinyl-aromatic bead polymers
US11981766B2 (en) * 2018-06-14 2024-05-14 Lanxess Deutschland Gmbh Method for producing amido-methylated vinyl-aromatic bead polymers
CN111100254A (en) * 2018-10-25 2020-05-05 中国石油化工股份有限公司 Strong alkaline carbon nano tube composite ion exchange resin material and preparation method thereof

Also Published As

Publication number Publication date
NL113552C (en)
DE1054715B (en) 1959-04-09
FR1217732A (en) 1960-05-05

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