GB874576A - Process for the production of spheroidally shaped polymer particles - Google Patents

Process for the production of spheroidally shaped polymer particles

Info

Publication number
GB874576A
GB874576A GB37456/59A GB3745659A GB874576A GB 874576 A GB874576 A GB 874576A GB 37456/59 A GB37456/59 A GB 37456/59A GB 3745659 A GB3745659 A GB 3745659A GB 874576 A GB874576 A GB 874576A
Authority
GB
United Kingdom
Prior art keywords
polymer
vinyl
monomers
polymerization
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
GB37456/59A
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.)
Dow Chemical Co
Original Assignee
Dow Chemical 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 Dow Chemical Co filed Critical Dow Chemical Co
Publication of GB874576A publication Critical patent/GB874576A/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
    • C08F257/00Macromolecular compounds obtained by polymerising monomers on to polymers of aromatic monomers as defined in group C08F12/00
    • C08F257/02Macromolecular compounds obtained by polymerising monomers on to polymers of aromatic monomers as defined in group C08F12/00 on to polymers of styrene or alkyl-substituted styrenes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J39/00Cation exchange; Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
    • B01J39/08Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
    • B01J39/16Organic material
    • B01J39/18Macromolecular compounds
    • B01J39/20Macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
    • 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
    • C08F2/00Processes of polymerisation
    • C08F2/12Polymerisation in non-solvents
    • C08F2/16Aqueous medium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Spheroidal solid polymer particles, e.g. beads, are made by the suspension polymerization of ethylenically unsaturated water-insoluble monomers in aqueous medium in the presence of a colloidally dispersed water-swollen but waterinsoluble sulphonated vinylidene aromatic polymer, e.g. homopolymers of styrene, alpha- and ar-methyl styrenes, ar-dimethyl, -ethyl and -chlorostyrenes, isopropenyl toluenes and vinyl naphthalenes and copolymers of such compounds with each other or with other compounds such as isobutylene, butadiene, acrylonitrile and C1-C12 alkyl acrylates and methacrylates. The sulphonated polymer may be used in free acid or salt form. The polymerizable monomer may be one of the above-mentioned monomers, N-vinyl carbazole, vinylidene chloride or divinyl benzene which may be polymerized alone or in admixture with one another, e.g. a mixture of styrene and divinyl benzene. Polymerization may be initiated by compounds such as benzoyl, di-tertbutyl and cumyl peroxides and azobisisobutyronitrile. The aqueous medium may contain a polymerization inhibitor, e.g. potassium di-chromate, to prevent the formation of colloidal polymer, and may have an alkaline or acid pH, e.g. pH6. The monomeric material may contain 1%-15% of a volatile organic liquid, e.g. C4-C7 hydrocarbon, to provide products which may be expanded by heating to a temperature above the boiling point of the liquid and above the softening point of the polymer. The Specification describes also the sulphonation of an m-vinyl toluene-p-vinyl toluene copolymer with sulphuric acid and the conversion of the resulting product to ammonium salt form. Specifications 775,409 and 784,028 are referred to.ALSO:Foamed polymeric material is made by the suspension polymerization of a mixture ethylenically unsaturated water-insoluble monomeric material and 1 to 15% of a volatile organic liquid in which the resulting polymer is only sparingly soluble, the polymerization being carried out in an aqueous medium containing a colloidally dispersed water-swollen but water-insoluble vinylidene aromatic polymer (see Group IV(a)) to yield spheroidal polymer particles which are expanded by heating to a temperature above the boiling point of the liquid and above the softening point of the polymer. Monomers specified are styrene, ar-methyl and-ethyl stirenes, ar-dimethylstyrenes, isopropenyltoluenes, ar-methoxystyrenes, ar-chlorostyrenes, vinyl naphthalenes, C1-C12 alkyl and cycloalkyl acrylates and lower aklyl substituted acrylates, which may be polymerized alone or in admixture with one another or with other monomers, e.g. isobutylene, butadiene, acrylontrile, N-vinyl carbazole, vinylidene chloride and divinyl benzene. Volatile organic liquids specified are butane, pentane, neopentane, hexane, cyclohexane and low-boiling petroleum ether. Example (3) describes the use of pentane to produce an expanded styrenedivinyl benzene copolymer. Specifications 775,409 and 784,028 are referred to.
GB37456/59A 1958-11-06 1959-11-04 Process for the production of spheroidally shaped polymer particles Expired GB874576A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US874576XA 1958-11-06 1958-11-06

Publications (1)

Publication Number Publication Date
GB874576A true GB874576A (en) 1961-08-10

Family

ID=22205297

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37456/59A Expired GB874576A (en) 1958-11-06 1959-11-04 Process for the production of spheroidally shaped polymer particles

Country Status (5)

Country Link
BE (1) BE584231A (en)
DE (1) DE1150527B (en)
FR (1) FR1246365A (en)
GB (1) GB874576A (en)
NL (1) NL245047A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3468833A (en) * 1967-03-10 1969-09-23 Gen Tire & Rubber Co Process for the preparation of large-particle-size latices
EP0148548A1 (en) * 1984-01-12 1985-07-17 Arco Chemical Technology, Inc. Vinyl aromatic suspension polymerization
EP2889085A1 (en) * 2013-12-26 2015-07-01 Dionex Corporation Ion exchange foams to remove ions from samples
US10921298B2 (en) 2014-12-30 2021-02-16 Dionex Corporation Vial cap and method for removing matrix components from a liquid sample

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1013977A (en) * 1944-01-24 1952-08-06 Ig Farbenindustrie Ag Process for the preparation of polymerization products
US2932629A (en) * 1955-03-28 1960-04-12 Dow Chemical Co Quiescent suspension polymerization

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3468833A (en) * 1967-03-10 1969-09-23 Gen Tire & Rubber Co Process for the preparation of large-particle-size latices
EP0148548A1 (en) * 1984-01-12 1985-07-17 Arco Chemical Technology, Inc. Vinyl aromatic suspension polymerization
EP2889085A1 (en) * 2013-12-26 2015-07-01 Dionex Corporation Ion exchange foams to remove ions from samples
US20150182875A1 (en) * 2013-12-26 2015-07-02 Dionex Corporation Ion exchange foams to remove ions from samples
US9592458B2 (en) 2013-12-26 2017-03-14 Dionex Corporation Ion exchange foams to remove ions from samples
US20170136465A1 (en) * 2013-12-26 2017-05-18 Dionex Corporation Ion exchange foams to remove ions from samples
CN104741101B (en) * 2013-12-26 2018-02-09 戴安公司 For removing the ion exchange foam of ion from sample
US10076756B2 (en) 2013-12-26 2018-09-18 Dionex Corporation Ion exchange foams to remove ions from samples
CN108043374B (en) * 2013-12-26 2020-10-30 戴安公司 Ion exchange foam for removing ions from a sample
US10921298B2 (en) 2014-12-30 2021-02-16 Dionex Corporation Vial cap and method for removing matrix components from a liquid sample
US12038422B2 (en) 2014-12-30 2024-07-16 Dionex Corporation Vial cap and method for removing matrix components from a liquid sample

Also Published As

Publication number Publication date
FR1246365A (en) 1960-11-18
BE584231A (en)
NL245047A (en)
DE1150527B (en) 1963-06-20

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