GB914022A - Production of a finely divided polymer - Google Patents

Production of a finely divided polymer

Info

Publication number
GB914022A
GB914022A GB2846959A GB2846959A GB914022A GB 914022 A GB914022 A GB 914022A GB 2846959 A GB2846959 A GB 2846959A GB 2846959 A GB2846959 A GB 2846959A GB 914022 A GB914022 A GB 914022A
Authority
GB
United Kingdom
Prior art keywords
caprolactam
sulphonyl
phosphinyl
nitroso
acyl
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
GB2846959A
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.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto 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 Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB914022A publication Critical patent/GB914022A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/08Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
    • C08G69/14Lactams
    • C08G69/16Preparatory processes
    • C08G69/18Anionic polymerisation

Abstract

S -caprolactam is polymerized by heating at 80 DEG to 125 DEG C. under substantially anhydrous conditions in the presence of (a) a catalytic amount of an alkali or alkaline earth metal including magnesium, or of a compound of such a metal or of an organo-metallic compound of aluminium or zinc which acts as an anionic polymerization catalyst and (b) a compound containing at least one tertiary nitrogen atom, one group linked to the nitrogen atom being a carbonyl, thiocarbonyl, sulphonyl, phosphinyl or thiophosphinyl group and a second being a carbonyl, thiocarbonyl, sulphonyl, phosphinyl, thiophosphinyl or nitroso group. In a modification of the process there is also present a primary or secondary amine. Specified catalysts include sodium, potassium, lithium, calcium, strontium and barium and hydrides, borohydrides, oxides, hydroxides, amides and carbonates thereof, lithium butyl, di-iso-butyl aluminium chloride and phenyl magnesium bromide. Specified compounds containing tertiary nitrogen atoms include N-substituted imides, e.g. N-acetyl-2-pyrrolidone; N-substituted cyclic imides of dicarboxylic acids, e.g. N-phenyl-succinimide; N:N-diacyl primary alkyl and aryl amines and N:N-diacyl acyl amides, e.g. N:N-diacetyl methylamine; the N:N1:N11-triphenyl ester of isocyanuric acid; N-acyl sulphonamides and N-acyl sulphonimides, e.g. N-acetyl-N-ethyl-p-toluene sulphonamide; disulphonamides of primary alkyl and aryl amines, e.g. N:N-di (p-toluene sulphonyl) amide; N-nitrosoamides, e.g. N-nitroso-2-pyrrolidone; N-nitrososulphonamides, e.g. N-nitroso-N-methyl benzene sulphonamide and N-(dimethyl phosphinyl)-S -caprolactam. Specified primary and secondary amines include methylamine, n-propylamine, iso-propylamine, n-butylamine, t-butylamine, n-pentylamine, t-amylamine, n-hexylamine, stearylamine, benzylamine, cyclohexylamine, dicyclohexylamine and morpholine. The examples disclose the polymerization of S -caprolactam in the presence of N-acetylcaprolactam and sodium hydride. The products of the process may be admixed with glass fibres, clays, calcium carbonate, titanium dioxide, carbon black, molybdenum disulphide, dyes or metallic powders and used as moulding compositions.
GB2846959A 1958-08-20 1959-08-20 Production of a finely divided polymer Expired GB914022A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US75607558A 1958-08-20 1958-08-20

Publications (1)

Publication Number Publication Date
GB914022A true GB914022A (en) 1962-12-28

Family

ID=25041931

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2846959A Expired GB914022A (en) 1958-08-20 1959-08-20 Production of a finely divided polymer

Country Status (2)

Country Link
DE (1) DE1420604A1 (en)
GB (1) GB914022A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4518765A (en) * 1984-03-19 1985-05-21 The Upjohn Company Anionic polymerization of lactam with azetidine-2,4-dione promoter

Also Published As

Publication number Publication date
DE1420604A1 (en) 1968-10-24

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