GB862180A - Improvements in and relating to ion exchange in non-aqueous media - Google Patents
Improvements in and relating to ion exchange in non-aqueous mediaInfo
- Publication number
- GB862180A GB862180A GB917/57A GB91757A GB862180A GB 862180 A GB862180 A GB 862180A GB 917/57 A GB917/57 A GB 917/57A GB 91757 A GB91757 A GB 91757A GB 862180 A GB862180 A GB 862180A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ion
- exchanger
- liquid
- ethyl
- cellulose
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J47/00—Ion-exchange processes in general; Apparatus therefor
- B01J47/015—Electron-exchangers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J47/00—Ion-exchange processes in general; Apparatus therefor
- B01J47/014—Ion-exchange processes in general; Apparatus therefor in which the adsorbent properties of the ion-exchanger are involved, e.g. recovery of proteins or other high-molecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
An ion-exchange reaction is characterized by the contacting of at least one ionizable substance in a substantially non-aqueous medium with an insoluble, open-chain high molecularweight polymer containing ion-exchange groups to effect an interchange of ions. This ion-exchanger may be a polysaccharide of vegetable, animal or bacterial origin, which can be either the structural or nutrient type, e.g. amylose, amylopectin, inulins, alpha cellulose, oxycellulose, xylans, pectins, algins, glycogens, chitins, mucopolysaccharides, chondroitin sulphuric acid, heparin hyaluronic acid; levans and dextrans. A preferred ion-exchanger can be derived from paper, cotton, wood pulp and cotton cloth and may be in the form of sheeting, belting, pressed solids or finely divided particles. These ion-exchange groups may be either cation exchanger, e.g. a carboxyl group, or anion exchanger, e.g. primary, secondary and tertiary amino groups or quaternary ammonium salts. The non-aqueous solvents exemplified are methylethyl ketone, methylisobutyl ketone, diethylketone, acetone, propionaldehyde, butyraldehyde, acetic, propionic, caproic, and pelargonic acids, acetic anhydride, ethyl, propyl and butyl ethers, methanol, ethanol, propanol, butanol, pentanol, hexanol, ethylene glycol, propylene glycol pentane, hexane, heptane, decane; heptene, octene, decene, tridecene, pentadecene; benzene, toluene, naphthalene, ethylene chloride, chloroform, carbon tetrachloride, nitroethylene, formamide, diethyl formamide, ethyl mercaptan, dimethylsulphoxide, liquid ammonia, liquid sulphur dioxide, liquid hydrogen fluoride, liquid nitrogen and liquid helium. Equimolar quantities of acetyl chloride are used in benzene to acetylate aniline and a diethylaminoethyl ether of cellulose exchanger is used to remove hydrogen chloride from the reaction. At completion, the exchanger is separated by filtration and the product by distillation. Similarly, N-acetylleucine ethyl ester is produced by acetylating with acetic anhydride, the leucine ethyl ester hydrochloride in anhydrous ethyl acetate in the presence of the diethylaminoethyl ether of cellulose. Iron salts are removed from commercial ethylene glycol normal butyl ether by passing through columns of carboxylmethylcellulose or a citrate ester of cellulose.ALSO:An ion-exchange reaction, characterized by the contacting of at least one ionizable substance in a substantially non-aqueous media with an insoluble, open-chain high molecular-weight polymer containing ion-exchange groups to effect an interchange of ions. This ion exchanger may be a polysaccharide of vegetable, animal or bacterial origin, which can be either the structural or nutrient type, e.g. amylose, amylopectin, inulins, alpha cellulose, oxycellulose, xylans, pectins, algins, glycogens, chitens, mucopolysaccharides, chondriotin sulphuric acid, heparin hyaluronic acid; levans and dextrans. A preferred ion-exchanger can be derived from paper, cotton, wood pulp and cotton cloth and may be in the form of sheeting, belting, pressed solids or finely divided particles. These ion-exchange groups may be either cation exchanger, e.g. a carboxyl group, or anion exchanger, e.g. primary, secondary and tertiary amino groups or quaternary ammonium salts. The non-aqueous solvents exemplified are methylethyl ketone, methylisobutyl ketone, diethyl ketone, acetone, propionaldehyde, butyraldehyde, acetic, propionic, caproic and pelargonic acids, acetic anhydride, ethyl, propyl and butyl ethers, methanol, ethanol, propanol, butanol, pentanol, hexanol, ethylene glycol, propylene glycol pentane, hexane, heptane, decane; heptene, octene, decene, tridecene, pentadecene; benzene, toluene, naphthalene, ethylene chloride, chloroform, carbon tetrachloride, nitroethylene, formamide, diethyl formamide, ethyl mercaptan, dimethylsulphoxide, liquid ammonia, liquid sulphur dioxide, liquid hydrogen fluoride, liquid nitrogen and liquid helium.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US862180XA | 1956-01-16 | 1956-01-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB862180A true GB862180A (en) | 1961-03-01 |
Family
ID=22197071
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB917/57A Expired GB862180A (en) | 1956-01-16 | 1957-01-09 | Improvements in and relating to ion exchange in non-aqueous media |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB862180A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101980962B (en) * | 2008-04-04 | 2012-11-28 | 巴斯夫欧洲公司 | Method for removing halogen from liquid ammonia |
-
1957
- 1957-01-09 GB GB917/57A patent/GB862180A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101980962B (en) * | 2008-04-04 | 2012-11-28 | 巴斯夫欧洲公司 | Method for removing halogen from liquid ammonia |
US8536376B2 (en) | 2008-04-04 | 2013-09-17 | Basf Se | Method for removing halogen from liquid ammonia |
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