GB821229A - Method of manufacturing electrically conductive membranes - Google Patents

Method of manufacturing electrically conductive membranes

Info

Publication number
GB821229A
GB821229A GB35692/55A GB3569255A GB821229A GB 821229 A GB821229 A GB 821229A GB 35692/55 A GB35692/55 A GB 35692/55A GB 3569255 A GB3569255 A GB 3569255A GB 821229 A GB821229 A GB 821229A
Authority
GB
United Kingdom
Prior art keywords
ion
chloride
solvent
cast
styrene
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
GB35692/55A
Inventor
John Thacher Clarke
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.)
Suez WTS Systems USA Inc
Original Assignee
Ionics Inc
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 Ionics Inc filed Critical Ionics Inc
Priority to GB35692/55A priority Critical patent/GB821229A/en
Publication of GB821229A publication Critical patent/GB821229A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/20Manufacture of shaped structures of ion-exchange resins
    • C08J5/22Films, membranes or diaphragms
    • C08J5/2206Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
    • C08J5/2218Synthetic macromolecular compounds
    • C08J5/2268Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds, and by reactions not involving this type of bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2325/00Characterised by the use of homopolymers or copolymers 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; Derivatives of such polymers
    • C08J2325/02Homopolymers or copolymers of hydrocarbons
    • C08J2325/04Homopolymers or copolymers of styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2353/00Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
    • C08J2353/02Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers of vinyl aromatic monomers and conjugated dienes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (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)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

A solid electrolytically-conductive, selectively permeable, unfractured ion-exchange membrane of an insoluble, infusible, solid polymer in which the ion-exchange groups have a dissociation constant of at least 10-5 and an ion-exchange capacity of at least 0.3 milliequivalents per gram of solid material corrected for the solvent and reinforcing material content, in a gel form with an organic solvent is prepared (1) by dispersing the polymer forming material in at least 25% by weight on the total weight of organic solvent, (2) casting the dispersion as a membrane, (3) polymerizing and curing to the insoluble, infusible state in the presence of the solvent and under conditions preventive of the escape of the solvent, and (4) maintaining the solvent content of the structure. The polymers may be the addition type, e.g. copolymers of divinyl benzene, di-isopropenyl benzene and diallyl ether, and dimethacrylate esters of ethylene or tetraethylene glycols with acrylic or methacrylic acids and esters, maleic anhydride, styrene, styrene p-sulphonic acids or esters, p-chloromethyl styrene, p-dialkylamino styrene, dialkyl p-vinyl benzylamine, trialkyl p-vinyl benzyl ammonium salts, N-alkyl vinyl pyridinium salts, acrylonitrile, vinyl acetate and chloride, vinylidene chloride, and allyl alcohol; or the condensation type, e.g. condensates of aldehydes with phenol and substituted phenols, dihydroyybenzenes, phloroglucinol, aniline and substituted anilines, metaphenylene diamine, melamine, urea, guanidine and guanidine derivatives, polyhydic phenols and polyalkylene polyamines and of ketones with amines. The ion-exchange groups may be cation-permeable carboxylic or sulphonic ions with hydrogen or sodium associated therewith or anion permeable with mobile hydroxyl or chloride ions associated therewith, p, s- and t-amino or quaternary ammonium groups and not more than 4 milliequivalents or ion-exchange groups are incorporated for each mol. of cross-linking agent and not less than 1 equivalent of ion-exchange groups for each 10 mols. of monomer and may be present in the polymerizable components or incorporated after the gel is formed. Solvents mentioned are the lower aliphatic alcohols, saturated ethers, such as dioxane, saturated halogenated aliphatic liquids, such as ethylene chloride, ketones, or aromatic hydrocarbons such as toluene, and the dispersion of polymerizable components or partially polymerized components may be cast alone or with reinforcing material such as glass cloth, paper, polyvinylidene chloride screen, cellulose and polyvinyl chloride, battery paper, and polystyrene-coated glass fibre mat either admixed in the unpolymerized solution or present in the moulds or castings. The polymerizable components may be partially pre-polymerized before casting, and after polymerization the polymeric gel may be converted to an hydrous gel form by leaching repeatedly with water, or if the solvent is water-immiscible by an intermediate solvation with a mutually miscible liquid. Examples describe (1) the copolymerization of maleic anhydride and divinyl benzene with a 2-azo-bis (isobutyronitrile) catalyst in dioxane, by heating at 6.5 DEG C. when cast between two glass plates on glass cloth; (2) copolymerization of ethyl styrene and divinyl benzene with benzoyl peroxide in toluene cast as above, followed by sulphonation to ion-exchange resin; (3) condensation of a sulphonated mixture of resorcinol and phenol in methanol solution with paraformaldehyde; (4) condensation of diethylene triamine with resorcinol and paraformaldehyde and methanol; (5) copolymerization of a 2-vinyl pyridine quaternized with dimethyl sulphate, with divinyl benzene; (6) copolymerization of 2-vinyl pyridine and divinyl benzene in toluene with 2-azo-bis (isobutyronitrile) cast as above and quaternized with dimethyl sulphate in ethanol. The cast membranes are leached with water and equilibrated with sodium hydroxide, hydrochloric acid or sodium chloride. Specification 720,002 is referred to.
GB35692/55A 1955-12-13 1955-12-13 Method of manufacturing electrically conductive membranes Expired GB821229A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB35692/55A GB821229A (en) 1955-12-13 1955-12-13 Method of manufacturing electrically conductive membranes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB35692/55A GB821229A (en) 1955-12-13 1955-12-13 Method of manufacturing electrically conductive membranes

Publications (1)

Publication Number Publication Date
GB821229A true GB821229A (en) 1959-10-07

Family

ID=10380512

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35692/55A Expired GB821229A (en) 1955-12-13 1955-12-13 Method of manufacturing electrically conductive membranes

Country Status (1)

Country Link
GB (1) GB821229A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2884253A1 (en) * 2005-04-08 2006-10-13 Univ Lille Sciences Tech FUNCTIONALIZABLE MONOLITHIC MATERIALS
WO2009086226A2 (en) * 2007-12-21 2009-07-09 E. I. Du Pont De Nemours And Company Papers containing floc derived from diamino diphenyl sulfone
EP2407582A1 (en) * 2010-07-15 2012-01-18 Abbott Laboratories Vascular Enterprises Limited Method and electrolytic solution for electropolishing stents made of high strength medical alloys
KR101249271B1 (en) * 2005-04-06 2013-04-02 다우 코닝 코포레이션 Organosiloxane compositions
US8647496B2 (en) 2009-01-16 2014-02-11 Abbott Laboratories Vascular Enterprises Limited Method, apparatus, and electrolytic solution for electropolishing metallic stents

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101249271B1 (en) * 2005-04-06 2013-04-02 다우 코닝 코포레이션 Organosiloxane compositions
FR2884253A1 (en) * 2005-04-08 2006-10-13 Univ Lille Sciences Tech FUNCTIONALIZABLE MONOLITHIC MATERIALS
WO2006108943A1 (en) * 2005-04-08 2006-10-19 Universite Des Sciences Et Technologies De Lille Monolithic functionalisable materials
JP2008539281A (en) * 2005-04-08 2008-11-13 ユニヴェルシテ デ シヤーンス エ テクノロジ ドゥ リール Monolith functionalizable material
KR101013317B1 (en) * 2005-04-08 2011-02-09 위니베르시떼 데 시앙스 에 테크놀로지 드 릴레 Monolithic functionalisable materials
CN101171075B (en) * 2005-04-08 2012-06-20 里尔科学技术大学 Monolithic functionalisable materials
WO2009086226A2 (en) * 2007-12-21 2009-07-09 E. I. Du Pont De Nemours And Company Papers containing floc derived from diamino diphenyl sulfone
WO2009086226A3 (en) * 2007-12-21 2009-08-27 E. I. Du Pont De Nemours And Company Papers containing floc derived from diamino diphenyl sulfone
KR101538190B1 (en) * 2007-12-21 2015-07-20 이 아이 듀폰 디 네모아 앤드 캄파니 Papers containing floc derived from diamino diphenyl sulfone
US8647496B2 (en) 2009-01-16 2014-02-11 Abbott Laboratories Vascular Enterprises Limited Method, apparatus, and electrolytic solution for electropolishing metallic stents
US9255341B2 (en) 2009-01-16 2016-02-09 Abbott Laboratories Vascular Enterprises Limited Method, apparatus, and electrolytic solution for electropolishing metallic stents
EP2407582A1 (en) * 2010-07-15 2012-01-18 Abbott Laboratories Vascular Enterprises Limited Method and electrolytic solution for electropolishing stents made of high strength medical alloys

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