GB785157A - Ion exchange resins and method of preparation thereof - Google Patents

Ion exchange resins and method of preparation thereof

Info

Publication number
GB785157A
GB785157A GB3186555A GB3186555A GB785157A GB 785157 A GB785157 A GB 785157A GB 3186555 A GB3186555 A GB 3186555A GB 3186555 A GB3186555 A GB 3186555A GB 785157 A GB785157 A GB 785157A
Authority
GB
United Kingdom
Prior art keywords
divinyl
vinyl
monovinyl
exchange resins
benzene
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
GB3186555A
Inventor
Irving Melvin Abrams
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.)
Chemical Process Co
Original Assignee
Chemical Process 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 Chemical Process Co filed Critical Chemical Process Co
Priority to GB3186555A priority Critical patent/GB785157A/en
Publication of GB785157A publication Critical patent/GB785157A/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
    • C08F293/00Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule

Landscapes

  • 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)

Abstract

Porous ion exchange resins are prepared by prepolymerizing a monovinyl aromatic monomer, mixing with an unpolymerized polyvinyl compound and copolymerizing the mixture to form a hard, water-insoluble matrix which is after-treated to introduce ion-exchange groups. Specified monovinyl monomers are styrene, vinyl toluene, vinyl xylene, vinyl naphthalene, ethyl vinyl benzene and vinyl chlorobenzene. Specified polyvinyl compounds are divinyl benzene, divinyl toluene, divinyl xylene, divinyl naphthalene, trivinyl benzene, divinyl chlorobenzene, diallyl phthalate, diallyl fumarate and divinyl acetylene. The monovinyl monomers may be prepolymerized by heating, preferably in an inert atmosphere, e.g. of carbon dioxide, nitrogen, helium, argon, methane and ethane, and optionally in the presence of a catalyst, e.g. benzoyl peroxide, lauroyl peroxide, tertiary-butyl hydroperoxide, methyl ethyl ketone peroxide, tertiary-butyl perbenzoate, aluminium chloride and sulphuric acid, and then cooling to stop further polymerization. The viscosity of the prepolymer may be adjusted by adding monomer or polymers of lower or higher viscosities. Alternatively completely prepolymerized monovinyl compounds may be dissolved in the monomers. The mixtures of prepolymers and polyvinyl compounds may be copolymerized by heating in bulk or preferably in aqueous dispersion in the presence of a suspending agent, e.g. polyvinyl alcohol, starch or gum arabic, and catalyst, e.g. organic peroxides such as benzoyl peroxide, inorganic peroxides, water-soluble perborates, persulphates and perchlorates, and ozone. The copolymers may be sulphonated, e.g. with sulphuric acid, nitrated or chlorinated, e.g. with phosphorus trichloride and chlorine; or chloromethylated, e.g. with methyl chloromethyl ether and anhydrous zinc chloride, and aminated, e.g. with dimethyl ethanolamine. In examples, anion exchange resins are used to decolorize diluted molasses.
GB3186555A 1955-11-08 1955-11-08 Ion exchange resins and method of preparation thereof Expired GB785157A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3186555A GB785157A (en) 1955-11-08 1955-11-08 Ion exchange resins and method of preparation thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3186555A GB785157A (en) 1955-11-08 1955-11-08 Ion exchange resins and method of preparation thereof

Publications (1)

Publication Number Publication Date
GB785157A true GB785157A (en) 1957-10-23

Family

ID=10329555

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3186555A Expired GB785157A (en) 1955-11-08 1955-11-08 Ion exchange resins and method of preparation thereof

Country Status (1)

Country Link
GB (1) GB785157A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2960480A (en) * 1957-03-13 1960-11-15 Nalco Chemical Co Production of haloalkylated resin particles
US3304272A (en) * 1957-11-20 1967-02-14 Ici Ltd Ion exchange materials prepared by absorbing styrene onto particulate polyethylene, introduction of ion exchange groups and shaping

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2960480A (en) * 1957-03-13 1960-11-15 Nalco Chemical Co Production of haloalkylated resin particles
US3304272A (en) * 1957-11-20 1967-02-14 Ici Ltd Ion exchange materials prepared by absorbing styrene onto particulate polyethylene, introduction of ion exchange groups and shaping

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