GB863064A - Improvements in and relating to ion exchange in polyphase solvent media - Google Patents

Improvements in and relating to ion exchange in polyphase solvent media

Info

Publication number
GB863064A
GB863064A GB919/57A GB91957A GB863064A GB 863064 A GB863064 A GB 863064A GB 919/57 A GB919/57 A GB 919/57A GB 91957 A GB91957 A GB 91957A GB 863064 A GB863064 A GB 863064A
Authority
GB
United Kingdom
Prior art keywords
chloride
cellulose
acids
ethyl
ion exchange
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
GB919/57A
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.)
Armour and Co
Original Assignee
Armour and Co
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 Armour and Co filed Critical Armour and Co
Publication of GB863064A publication Critical patent/GB863064A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J47/00Ion-exchange processes in general; Apparatus therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J47/00Ion-exchange processes in general; Apparatus therefor
    • B01J47/015Electron-exchangers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

An ion exchange reaction, comprising the step of treating at least one ionizable substance and an insoluble, open-chain high molecular-weight polymer containing ion exchange groups in a polyphase solvent medium comprising an aqueous phase and a water-immiscible phase to effect an interchange of ions. This insoluble ion exchanger may be amylose, amylopectin, inulins, alpha cellulose, oxycellulose, xylans, pectins, algins, glycogens, chitins, 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 acidic (cation exchanger) e.g. a carboxyl group, or basic (anion exchanger), e.g. primary, secondary and tertiary amino groups or quaternary ammonium salts. The non-aqueous solvents may be methylethyl ketone, methylisobutyl ketone, diethyl ketone, methylamyl ketons, butanal, pentanal, hexanal, heptanal, valeric, capric, caproic, caprylic and pelargonic acids, ethyl acetate, ethyl proprionate, ethyl, propyl and butyl ethers, pentanol, hexanol, heptanol, octanol, nonanol, methane, ethane, propane, butane, pentane, hexane, heptane, decane, ethene, butene, octene, decene, tridecene, pentadecene, benzene, toluene, naphthalene, ethylenechloride, chloroform, carbon tetrachloride, nitrohexane, nitroheptane, nitrodecane, caprylamide, octylamine, ethyl-mercaptan, dimethylsulfoxide, thioesters, liquid ammonia, liquid sulphur dioxide, liquid hydrogen fluoride, liquid nitrogen and liquid helium. Quaternary ammonium compounds are adsorbed on or eluted from such high molecular weight polymers containing cation exchange groups. These quaternary ammonium compounds can be halide or hydroxide derivatives in which the quaternary component is alkyltrimethyl ammonium. The alkyl group (or groups) of these quaternary ammonium compounds can contain from 8 to 22 carbon atoms and can be saturated or unsaturated. Dimethyldidodecyl ammonium chloride, trimethyldidecyl ammonium chloride, dimethyldioctadecylammonium chloride, trimethyloctadecylammonium chloride, dodecyldimethylbenzyl-ammonium chloride, octadecyldimethybenzylammonium chloride, (p - diiso butylphenoxethoxy) ethylbenzyldimethylammonium chloride, trimethyloctylammonium-chloride, dimethyldodecylbenzylammonium chloride and methyltrioctadecylammonium chloride, trimethyl "coco" ammonium chloride, dimethyldi "tallow" ammonium chloride and trimethyl "soya" ammonium chloride, are examples of such quaternary ammonium compounds. Specifically exemplified are the separation of trimethyloctadecyl ammonium hydroxide, chloride, acetate or stearate in chloroform using a cellulose citrate, carboxymethyl cellulose or cellulose phosphate. Also exemplified are the use of butanol or ethyl acetate acidified with hyrochloric acid and substantially saturated with water as eluants for the quaternary compound. Antipyrine and copper ions can be eluted with chloroform and xylene together with hydrochloric acid and 8-hydroxyquinoline respectively. Dicarboxylic acids containing from 4 to 8 carbon atoms may be selectively eluted from the citrate ester of cellulose buffered with water at pH 5,4 with an amount of butanol in chloroform as the eluant the acids of greater chain length being desorbed prior to those of shorter chain length. Monocarboxylic acids (e.g. fatty acids) may be selectively eluted from the free base form of dimethylaminoethyl ether of cellulose substantially saturated by water, by increasing the amount of n-butyl ether in Skelly B (petroleum ether fraction) the longer chain length acids are desorbed from the cellulose exchange prior to removal of acids of shorter chain length. Specifications 862,180 and 862,181 are referred to.ALSO:An ion exchange reaction, comprising the step of treating at least one ionizable substance and an insoluble, open-chain high molecular-weight polymer containing ion exchange groups in a polyphase solvent medium comprising an aqueous phase and a water-immiscible phase to effect an interchange of ions. This insoluble ion exchanger may be amylose, amylopectin, inulins, alpha cellulose, oxycellulose, xylans, pectins, algins, glycogens, chitins, 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 acidic (cation exchanger) e.g. a carboxyl group, or basic (anion exchanger), e.g. primary, secondary and tertiary amino groups or quaternary ammonium salts. The non-aqueous solvents may be methylethyl ketone, methylisobutyl ketone, diethyl ketone, methylamyl ketone, butanal, pentanal, hexanal, heptanal, valeric, capric, caproic, caprylic and pelargonic acids, ethyl acetate, ethyl propionate, ethyl, propyl and butyl ethers, pentanol, hexanol, heptanol, octanol, nonanol, methane, ethane, propane, butane, pentane, hexane, heptane, decane, ethene, butene, octene, decene, tridecene, pentadecene, benzene, toluene, naphthalene, ethylene chloride, chloroform, carbon tetrachloride, nitrohexane, nitroheptane, nitrodecane, caprylamide, octylamine, ethyl-mercaptan, dimethylsulfoxide, thioesters, liquid ammonia, liquid sulphur dioxide, liquid hydrogen fluoride, liquid nitrogen and liquid helium.
GB919/57A 1956-01-16 1957-01-09 Improvements in and relating to ion exchange in polyphase solvent media Expired GB863064A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US863064XA 1956-01-16 1956-01-16

Publications (1)

Publication Number Publication Date
GB863064A true GB863064A (en) 1961-03-15

Family

ID=22197693

Family Applications (1)

Application Number Title Priority Date Filing Date
GB919/57A Expired GB863064A (en) 1956-01-16 1957-01-09 Improvements in and relating to ion exchange in polyphase solvent media

Country Status (1)

Country Link
GB (1) GB863064A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2455617A1 (en) * 1979-05-03 1980-11-28 Le I Textilnoi REACTIVE POROUS MATERIAL LOADED WITH OPEN CELLS AND PREPARATION METHOD THEREOF

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2455617A1 (en) * 1979-05-03 1980-11-28 Le I Textilnoi REACTIVE POROUS MATERIAL LOADED WITH OPEN CELLS AND PREPARATION METHOD THEREOF

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