GB964549A - Improvements relating to the vulcanisation of polymers - Google Patents

Improvements relating to the vulcanisation of polymers

Info

Publication number
GB964549A
GB964549A GB1907262A GB1907262A GB964549A GB 964549 A GB964549 A GB 964549A GB 1907262 A GB1907262 A GB 1907262A GB 1907262 A GB1907262 A GB 1907262A GB 964549 A GB964549 A GB 964549A
Authority
GB
United Kingdom
Prior art keywords
monosulphide
bis
dimethylmorpholinothiocarbonyl
disulphide
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
GB1907262A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and 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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB964549A publication Critical patent/GB964549A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
    • C07D295/21Radicals derived from sulfur analogues of carbonic acid
    • 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
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0025Crosslinking or vulcanising agents; including accelerators

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Bis (2 - 6 - dimethylmorpholinothiocarbonyl) monosulphide is prepared by reacting 2-6-dimethylmorpholine with carbon disulphide in an alkalene aqueous medium to produce a salt of 2-6-dimethyl-4-morpholinecarbodithioic acid, oxidising this to the corresponding thiuram disulphide with an oxidising agent such as potassium ferricyanide, chlorine, bromine, iodine or a peroxide, and converting the disulphide which precipitates to the monosulphide by treatment with sodium or potassium cyanide in an alcoholic medium. In an example 1 mole. of 2-6-dimethylmorpholine, 1 mol. of sodium hydroxide and 900 mol. water were mixed and carbon disulphide slowly dropped in. The clear yellow solution was treated dropwise with aqueous potassium ferricyanide and the dried precipitate was the disulphide. This was dissolved in 95% ethyl alcohol and refluxed with a solution of sodium cyanide in 50% ethyl alcohol and the bis(2-6-dimethylmorpholinothiocarbonyl) monosulphide precipitated by the addition of water. In a similar manner bis(morpholinothiocarbonyl) monosulphide, bis(2-5-dimethylmorpholinothiocarbonyl) monosulphide and bis(3-5-dimethylmorpholinothiocarbonyl) monosulphide are prepared from the appropriate morpholine starting compound.ALSO:A butadiene-styrene elastomeric copolymer is vulcanised with at least 0.4% of its weight of bis(2-6 - dimethylmorpholinothiocarbonyl) monosulphide. The composition may also contain 0.5 to 15% of sulphur, and the usual compounding ingredients.
GB1907262A 1961-05-17 1962-05-17 Improvements relating to the vulcanisation of polymers Expired GB964549A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11063661A 1961-05-17 1961-05-17

Publications (1)

Publication Number Publication Date
GB964549A true GB964549A (en) 1964-07-22

Family

ID=22334097

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1907262A Expired GB964549A (en) 1961-05-17 1962-05-17 Improvements relating to the vulcanisation of polymers

Country Status (3)

Country Link
DE (1) DE1192819B (en)
GB (1) GB964549A (en)
NL (2) NL278499A (en)

Also Published As

Publication number Publication date
NL125173C (en)
DE1192819B (en) 1965-05-13
NL278499A (en)

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