GB469865A - Improvements in or relating to vulcanisation accelerators and process for their production - Google Patents

Improvements in or relating to vulcanisation accelerators and process for their production

Info

Publication number
GB469865A
GB469865A GB26816/36A GB2681636A GB469865A GB 469865 A GB469865 A GB 469865A GB 26816/36 A GB26816/36 A GB 26816/36A GB 2681636 A GB2681636 A GB 2681636A GB 469865 A GB469865 A GB 469865A
Authority
GB
United Kingdom
Prior art keywords
molecules
acid
examples
condensation
monobutylamine
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
GB26816/36A
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.)
Usines de Melle SA
Original Assignee
Usines de Melle SA
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 Usines de Melle SA filed Critical Usines de Melle SA
Publication of GB469865A publication Critical patent/GB469865A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/29Compounds containing one or more carbon-to-nitrogen double bonds

Abstract

The vulcanization of rubber is accelerated by the addition to the mix of aliphatic aldehydealiphatic amine condensation products which are made by a process which comprises the condensation of one molecule of amine with two molecules of aldehyde and is characterized by the fact that the reaction is conducted with simultaneous cooling of the reactants, and that the reaction product is separated into its constituent components by fractionation. The condensation which is preferably carried out with vigorous agitation of the reactants, may be conducted at either sub-or super-atmospheric pressure. The most valuable and active fraction is that which has a b.p. of 120 DEG C. and over. This fraction may be used as such or in the form of salts with weak acids such as stearic acid, palmitic acid, oleic acid and ricinoleic acid, made by the addition of the stoichiometric amount of acid. In examples: (1) 2 molecules of monobutylamine are condensed with 4 molecules of butyraldehyde at 0 DEG C. and the product fractionated. The most valuable product distills at 120--180 DEG C.; (2) 2,5 molecules of monobutylamine are condensed with 5 molecules of propanol at - 20 DEG C. The accelerator fraction distills above 120 DEG C. Examples are also given to show the efficiency as accelerators of the two products obtained in examples (1) and (2) above. Specifications 180,978, 265,930, and 265,931, [all in Class 70], are referred to.ALSO:The vulcanization of rubber is accelerated by the addition to the mix of aliphatic aldehydealiphatic amine condensation products which are made by a process which comprises the condensation of one molecule of amine with two molecules of aldehyde and is characterized by the fact that the reaction is conducted with simultaneous cooling of the reactants, and that the reaction product is separated into its constituent components by fractionation. The condensation, which is preferably carried out with vigorous agitation of the reactants may be conducted at either sub- or super-atmospheric pressure. The most valuable and active fraction is that which has a b.p. of 120 DEG C. or over. This fraction may be used as such or in the form of salts with weak acids such as stearic acid, palmitic acid, oleic acid and ricinoleic acid, made by the addition of the stoichiometric amount of acid. In examples; (1) 2 molecules of monobutylamine are condensed with 4 molecules of butyraldehyde at 0 DEG C. and the product fractionated. The most valuable product distills at 120-160 DEG C.; (2) 2.5 molecules of monobutylamine are condensed with 4 molecules of propanal at -20 DEG C. The accelerator fractions distills above 120 DEG C. Examples are also given to show the efficiency as accelerators of the two products obtained in examples (1) and (2) above. Specifications 180,978, 265,930, and 265,931, [all in Class 70], are referred to.
GB26816/36A 1935-10-07 1936-10-02 Improvements in or relating to vulcanisation accelerators and process for their production Expired GB469865A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR469865X 1935-10-07

Publications (1)

Publication Number Publication Date
GB469865A true GB469865A (en) 1937-08-04

Family

ID=8902458

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26816/36A Expired GB469865A (en) 1935-10-07 1936-10-02 Improvements in or relating to vulcanisation accelerators and process for their production

Country Status (1)

Country Link
GB (1) GB469865A (en)

Similar Documents

Publication Publication Date Title
GB1037693A (en) Hydrogenation of salts of phthalic acids
GB469865A (en) Improvements in or relating to vulcanisation accelerators and process for their production
US1726713A (en) Art of vulcanizing rubber
US2289266A (en) Method of making casting resins
DE836353C (en) Process for the preparation of polyvalent alkyleneimine esters
GB450592A (en) Process for the manufacture of polymerisation products of olefines
GB451359A (en) Process for the manufacture of valuable products from boron fluoride and oxy-acids of phosphorus
GB171956A (en) Method for the production of a condensation product from naphthalene and glycollic acid
GB620026A (en) Improvements in or relating to the manufacture of 2.4-dinitro-6-cyclohexyl-phenol
US1532651A (en) Manufacture of rubber goods
GB742041A (en) Improvements in or relating to the production of toluic acids
GB175019A (en) The manufacture of ortho-sulphonic acids of aromatic amines
GB224672A (en) A process for the production of sheets, moulded articles and the like, from casein
GB445940A (en) Production of compositions from rubber and the like
GB387738A (en) Process of manufacturing 2-mercaptoarylthiazoles
GB440205A (en) Process for the treatment of mixtures containing dichlorbenzenes
GB437197A (en) Improvements in or relating to the production of methacrylic acid and the alkyl esters thereof
GB452579A (en) Manufacture of fluorinated organic compounds
GB361971A (en) Improvements in or relating to rubber vulcanization accelerators
GB452460A (en) Improved manufacture of citraconic and itaconic acids and anhydrides
GB491932A (en) Process for the polymerisation of mono-olefines
GB457471A (en) Process for the manufacture of a thiourea derivative
GB388615A (en) Method for production of trimethylenetrinitramine
GB420897A (en) Process for the manufacture of new reaction products
CH190643A (en) Process for the preparation of the di-n-propylamide of 3,5-dimethyl-isoxazole-4-carboxylic acid.