GB867449A - Synthetic resins having anion-exchange properties - Google Patents
Synthetic resins having anion-exchange propertiesInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/12—Hydrolysis
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing 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.
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)
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)
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)
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 |
-
0
- NL NL113552D patent/NL113552C/xx active
-
1957
- 1957-12-02 DE DEF24526A patent/DE1054715B/en active Pending
-
1958
- 1958-12-02 GB GB3887758A patent/GB867449A/en not_active Expired
- 1958-12-02 FR FR780561A patent/FR1217732A/en not_active Expired
Cited By (10)
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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