GB678216A - Improvements in or relating to the polymerisation of vinyl-type compounds - Google Patents

Improvements in or relating to the polymerisation of vinyl-type compounds

Info

Publication number
GB678216A
GB678216A GB17852/49A GB1785249A GB678216A GB 678216 A GB678216 A GB 678216A GB 17852/49 A GB17852/49 A GB 17852/49A GB 1785249 A GB1785249 A GB 1785249A GB 678216 A GB678216 A GB 678216A
Authority
GB
United Kingdom
Prior art keywords
butyl
vinyl
methyl
allyl
sodium
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
GB17852/49A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB678216A publication Critical patent/GB678216A/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
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201Oxygen-containing compounds
    • B01J31/0209Esters of carboxylic or carbonic acids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201Oxygen-containing compounds
    • B01J31/0205Oxygen-containing compounds comprising carbonyl groups or oxygen-containing derivatives, e.g. acetals, ketals, cyclic peroxides
    • 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
    • C08F4/00Polymerisation catalysts
    • C08F4/28Oxygen or compounds releasing free oxygen
    • C08F4/32Organic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Polymerisation Methods In General (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Polymers and copolymers of ethylenically unsaturated monomers are made by polymerizing in the presence of catalysts consisting of the organic per-esters of non-aromatic carboxylic acids containing at least one tertiary alkyl percarboxylic acid ester group, the carbonyl group of which is linked to another carbonyl group either directly or via only one carbon atom. The polymerization may be carried out in bulk, solution or emulsion in the presence or absence of emulsifying agents, in acid, neutral, but preferably alkaline media, using heat and/or light, in a batchwise or continuous manner, under atmospheric, superatmospheric or subatmospheric pressure, in the absence of oxygen or in an atmosphere of the monomer. Before or during emulsion polymerization various ingredients may be added such as emulsion stabilizers, e.g. polysaccharides, gum arabic, soluble starch, dextrine, plasticizers, e.g. dioctyl phthalate, and glycerol monoleate, lubricants, dyes, pigments and fillers. Specified catalysts are t-butyl beta-keto perpropionate or pervalerate, t-amyl beta-keto, gamma-ethyl percaproate, t-butyl monoperoxalate, t-hexyl monopermalonate, t-hexyl, monopermethylmalonate, O,O - tert - butyl O-methyl or O-ethyl monoperoxalate, O,O-tertamyl O-butyl monopermalonate, t-butyl diperoxalate, t-amyl dipermalonate, t-hexyl dipermethylmalonate, t-butyl methyl diperoxalate, t-butyl butyl dipermalonate, di-tert-butyl diperoxalate, and di-tert-amyl dipermethyl-malonate, di-t-butyl dipermalonate, di-t-butyl diperoxalate, di-t-butyl monopermalonate, di-t-butyl dipermethylmalonate, t-butyl beta-keto perbutyrate and mixtures. Specified monomers are butadiene-1,3, 2,3-dimethylbutadiene-1,3, butadiene-3,4-carbonate, piperylene, isoprene, chloroprene, styrene, alpha-methyl styrene, dichlorostyrene, 4-methyl- and 4-butyl styrene, vinyl naphthalene, vinyl phenol, acrylic and alpha-alkyl acrylic acids, methyl or propyl acrylate, methyl or butyl methacrylate, vinylidene chloride or bromide, vinyl chloride or bromide, acrylonitrile and methacrylonitrile, vinyl acetate, chloracetate, benzoate, valerate, or caproate, divinyl succinate, divinyl adipate, vinyl allyl phthalate, vinyl methallyl pimelate, vinyl methyl glutarate, vinyl acrylate or crotonate or methacrylate, vinyl ethyl or butyl or allyl ether, vinyl butyl or ethyl ketone, allyl acetate, allyl butyrate, diallyl phthalate, diallyl adipate, diallyl succinate, allyl chloride, methallyl chloride, allyl acrylate, allyl crotonate, methallyl methacrylate, and diethyl fumarate or maleate. The emulsifying agent may be sodium or potassium myristate, laurate, palmitate, oleate, stearate, rosinate or hydroabietate, sodium lauryl sulphate, potassium stearyl sulphate, sodium lauryl sulphonate, potassium stearyl sulphonate, sodium cetyl sulphonate, sulphonated mineral oil and ammonium salt thereof, lauryl amine hydrochloride and stearyl amine hydrobromide. During emulsion a mildly alkaline condition may be maintained by the addition of compounds such as trisodium phosphate, sodium carbonate, sodium bicarbonate, tetrasodium pyrophosphate, disodium-hydrogen phosphate or calcium carbonate. Specification 612,331 is referred to.
GB17852/49A 1948-08-02 1949-07-06 Improvements in or relating to the polymerisation of vinyl-type compounds Expired GB678216A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US678216XA 1948-08-02 1948-08-02

Publications (1)

Publication Number Publication Date
GB678216A true GB678216A (en) 1952-08-27

Family

ID=22078634

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17852/49A Expired GB678216A (en) 1948-08-02 1949-07-06 Improvements in or relating to the polymerisation of vinyl-type compounds

Country Status (5)

Country Link
BE (1) BE490471A (en)
DE (1) DE912152C (en)
FR (1) FR991414A (en)
GB (1) GB678216A (en)
NL (1) NL71947C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3135723A (en) * 1960-08-19 1964-06-02 Baker Chem Co J T Process for copolymerizing alpha-methyl styrene and methyl methacrylate
US3341507A (en) * 1966-05-23 1967-09-12 Eastman Kodak Co Peroxydicarboxylic acid esters and polymerization processes employing same

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1072812B (en) * 1955-08-17 1960-01-07 Wacker-Chemie G.m.b.H., München PROCESS FOR HOMOPOLYMERIZATION OR MIXED POLYMERIZATION OF VINYL CHLORIDE IN Aqueous SUSPENSION
NL281167A (en) * 1961-07-20
DE1234989C2 (en) * 1962-12-14 1973-10-04 Eastman Kodak Co Process for the production of polymers from ethylenically unsaturated compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3135723A (en) * 1960-08-19 1964-06-02 Baker Chem Co J T Process for copolymerizing alpha-methyl styrene and methyl methacrylate
US3341507A (en) * 1966-05-23 1967-09-12 Eastman Kodak Co Peroxydicarboxylic acid esters and polymerization processes employing same

Also Published As

Publication number Publication date
FR991414A (en) 1951-10-05
NL71947C (en)
BE490471A (en) 1900-01-01
DE912152C (en) 1954-05-24

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