GB678943A - Method of polymerisation and products produced thereby - Google Patents

Method of polymerisation and products produced thereby

Info

Publication number
GB678943A
GB678943A GB2988849A GB2988849A GB678943A GB 678943 A GB678943 A GB 678943A GB 2988849 A GB2988849 A GB 2988849A GB 2988849 A GB2988849 A GB 2988849A GB 678943 A GB678943 A GB 678943A
Authority
GB
United Kingdom
Prior art keywords
alpha
butyl
methyl
methallyl
ethyl
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
GB2988849A
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 GB678943A publication Critical patent/GB678943A/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
    • 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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/62Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
    • 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
    • C08F291/00Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00

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

Polymers of at least one compound containing in the molecule the grouping <FORM:0678943/IV (a)/1> where Z is a halogen atom or an alkyl radical, are made by polymerizing, e.g. in solution or aqueous emulsion, by heating for between 4 and 10 minutes to a temperature of at least 90 DEG C. but below the decomposition temperature of the compound, then cooling within ten minutes to a temperature between -10 DEG C. and 25 DEG C. and completing the polymerization, preferably in the dark, at this lower temperature. The polymerizable mixture may contain initially another polymerizable unsaturated compound, or the compound may be added at any later stage, e.g. when the polymerization of the compounds originally present is substantially complete. Plasticizers, e.g. dioctyl phthalate, emulsion stabilizers, dyes, lubricants and pigments may also be added before or during the polymerization. The polymerization may be effected in batch, continuously or semi-continuously, in the presence of catalysts, and preferably in the absence of light and molecular oxygen, e.g. the oxygen in the reaction vessel being replaced by nitrogen, methane or carbon dioxide. Specified compounds containing the above grouping are methacrylonitrile, methyl methacrylate, 4-ethyl - 4 - pentoate, amyl - 4 - butyl - 4 - pento-ate, 4 - butyl - 4 - pentenenitrile, 5 - isopropyl-5 - hexenenitrile, 4 - isobutyl - 4 - pentenamide, 4 - amyl - 4 - pentenamide, 3 - methyl - 3-butene - 2 - one, 4 - isopropyl - 4 - pentene - 3-one, 2 - chloropropene - 1, 2 - methylbutene - 1, 2 - ethylbutene - 1, alpha - chlorostyrene, methallyl chloride, methallyl acetate, ethallyl benzoate, alpha - chloroallylcaproate, dimethallyl phthalate, 3 - methallyl - cyclohexanone, alpha - chloro - 4 - ethylstyrene, alpha - chloroacrylonitrile, butyl - 4 - chloro - 4 - pentenoate, ethyl alpha - bromoacrylate, alpha - methyl - 4-methoxystyrene, butyl alpha-chloroacrylate, 2-bromo - 1 - heptene - 3 - one, 4 - methallylbenzonitrile, 4 - chloro - 4 - pentenamide, 4-butyl - 4 - pentene - 2 - one, 4 - iodo - 4 - pentenamide, 3 - fluoro - 3 - butenenitrile, 3 - chloro-3 - butenenitrile, 5 - isopropyl - 5 - hexenenitrile, 3 - alpha - chlorovinyl - 1 - carbethoxycyclohexane, 4 - methallyl - 1 - acetoxy - benzene, 4 - carbamyl - 2 - butyl - 1 - butene, alphamethyl - vinylcyclopentane, beta - chloroallylbenzene, 4 - carboxy - 2 - chloro - 1 - pentene, 4 - methallyl - benzamide, 3 - alpha - methyl vinylcyclohexanamide, 2 - methallyl - cyclohexanecarboxamide, 7 - ethallyl - 2 - naphthamide, 7 - ethallyl - 2 - naphthonitrile, 2-alpha - ethylvinylcyclohexanenitrile, 4 - ethallyl - 2 - cyclopentanenitrile, 3 - methallylcyclopentanone, 3 - ethallyl - 1 - acetylbenzene, butyl - 2 - methyl - 2, propenoate, ethyl - 3-methyl - 3, butenoate, isobutyl - 4 - ethyl pentenoate, 2 - methyl - 2 - propenenitrile, 3-ethyl - 3 - butenenitrile, 2 - methallyl - 1-carboethoxybenzene, 3 - ethallyl - 2 - naphthamide, 5 - isopropyl - 5 - hexenenitrile, 2-methyl - 2 - propenamide, 3 - ethyl - 3 - butenamide, 3 - butyl - 3 - butenamide, 2 - methallylbenzonitrile, 3 - ethyl - butene - 2 - one, 2-methallylcyclohexanone - 5 - amyl - 5 - pentene-2 - one, 5 - ethyl - 5 - pentene - 4 - one, and mixtures. The other polymerizable compound may be styrene, alpha methyl styrene, dichlorostyrene, vinyl naphthalene, vinyl phenol, acrylic acid, alpha-substituted acrylic acids, acrylonitrile, methacrylonitrile, methyl and propyl acrylate, methyl and butyl methacrylate, vinylidene chloride and bromide, vinyl chloride, bromide or fluoride, vinyl acetate, chloroacetate, benzoate and valerate, divinyl adipate, divinyl succinate, vinyl allyl phthalate, vinyl methallyl pimelate, diallyl phthalate, allyl acetate and diallyl succinate. In solution the solvents may be water, cyclohexanone, cyclohexane, butane and hexane. In aqueous emulsion the emulsifying agent may be ammonium, sodium and potassium myristates, laurates, palmitates, oleates, stearates, rosinates, and hydrobietates, sodium lauryl and potassium stearyl sulphates, sodium lauryl and potassium stearyl sulphonates, sodium cetyl sulphonate, sulphonated mineral oils, lauryl amine hydrochloride and stearyl amine hydrobromide. Specified catalysts are benzoyl or acetyl or hydrogen or t-butyl or sodium or succinyl peroxide, persulphuric acid, peracetic acid, perphthalic acid, potassium persulphate, t-butyl perbutyrate, and di-t-butyl dipermalonate.
GB2988849A 1948-11-22 1949-11-22 Method of polymerisation and products produced thereby Expired GB678943A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US1000243XA 1948-11-22 1948-11-22

Publications (1)

Publication Number Publication Date
GB678943A true GB678943A (en) 1952-09-10

Family

ID=26748379

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2988849A Expired GB678943A (en) 1948-11-22 1949-11-22 Method of polymerisation and products produced thereby

Country Status (4)

Country Link
DE (1) DE829222C (en)
FR (1) FR1000243A (en)
GB (1) GB678943A (en)
NL (1) NL73429C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2840447A (en) * 1954-04-28 1958-06-24 Du Pont Process for preparing filaments from dispersions containing graft polymers obtained from ethylenically unsaturated monomers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2840447A (en) * 1954-04-28 1958-06-24 Du Pont Process for preparing filaments from dispersions containing graft polymers obtained from ethylenically unsaturated monomers

Also Published As

Publication number Publication date
DE829222C (en) 1952-01-24
FR1000243A (en) 1952-02-11
NL73429C (en)

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