GB595721A - Polymerization of methylpentadienes - Google Patents
Polymerization of methylpentadienesInfo
- Publication number
- GB595721A GB595721A GB24840/44A GB2484044A GB595721A GB 595721 A GB595721 A GB 595721A GB 24840/44 A GB24840/44 A GB 24840/44A GB 2484044 A GB2484044 A GB 2484044A GB 595721 A GB595721 A GB 595721A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- benzene
- naphthylamine
- azo
- alpha
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
2-Methyl and/or 4-methyl-1 : 3-pentadiene are polymerized without or with other unsaturated compounds by heating above 75 DEG C. in the presence of a diazo-amino aryl compound. Unsaturated compounds specified are other conjugated pentadienes, 1 : 3-butadiene, isoprene, styrene, alpha-methyl styrene, acrylonitrile, methacrylonitrile, vinyl chloride, vinyl acetate, ethyl acrylate, methacrylates, methyl vinyl ketone and isobutylene, and homologues, analogues and substituted derivatives thereof. Diazo compounds specified are diazoaminobenzene, ortho-, meta- and paradiazoamino toluenes, diazoamino xylenes, toluene azo benzylamine, 4 - methyl diazoamino benzene, para toluene azo 5-pseudo cumidine, benzene azo para cuminylamine, benzene azotetrahydro naphthylamine, benzene diazo amino naphthalene and alpha- and betadiazo amino naphthalenes. Solvent, mass or emulsion methods may be used. Soaps, glue, gelatine, methyl cellulose or polyvinyl alcohol may be used in emulsion. Plasticisers, antioxidants, inhibitors, lubricants, dyes, pigments, fillers, perborates, persulphates, peroxides and ozonides, carbon tetrachloride, tetrachlor- and hexachlorethanes, chlorinated aromatic hydrocarbons, amyl alcohol and other alcohols of 5-8 C atoms, aldehydes, mercaptans, amines, phosphates, carbonates and acetates may be present. Air may be excluded. The products may be mixed with dibutyl phthalate, tricresyl phosphate, triacetin, tetrahydro-naphthalene, coal tar and oils therefrom, cumarone resins, soft factice, wool grease, stearic and lauric acids, waxes, ketone-aldehyde resins, phenyl beta-naphthylamine, p-hydroxy diphenyl, hydroquinone, p-aminophenol, p,p1-diamino diphenylmethane, 2,4-n-toluylene diamine, diphenylamine, o-ditolylamine, p-ditolylamine, phenyl alpha-naphthylamine, phenyl beta-naphthyl nitrosamine, sym-di-beta-naphthyl p-phenylene diamine, diphenyl diamino ethane and 2,4-diaminodiphenylamine, and pigments such as carbon black, iron oxide, titanium dioxide, barytes, zinc oxide, hydrated alumina, lithopone and whiting. Vulcanization can be carried out with sulphur, sulphur dioxide, hydrogen sulphide and sulphur thiocyanate, ozone, organic and inorganic peroxides, selenium, halogens and nitrobenzene, tetramethyl thiuram disulphide, zinc dibutyl dithiocarbamate, tetramethyl thiuram monosulphide, hexamethylene tetramine, benzo thiazyl disulphide, dipentamethylene thiuram tetrasulphide, mercapto benzo thiazole, aldehyde ammonia, diphenylguanidine, diphenylthiourea, piperidinium pentamethylene dithiocarbamate, di-o-tolylguanidine, triphenylguanidine and lead dimethyldithiocarbamate. The compositions may be applied to fibrous material to give balloon coverings, table covers, electrical insulation and friction tape, and hose. Other articles specified are paints, self-sealing tanks, gaskets, belts, vibration dampers, soles, aprons, gloves, gas masks, tyre tubes and casings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US595721XA | 1959-10-05 | 1959-10-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB595721A true GB595721A (en) | 1947-12-15 |
Family
ID=22023840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24840/44A Expired GB595721A (en) | 1943-12-16 | 1944-12-11 | Polymerization of methylpentadienes |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE595721A (en) |
GB (1) | GB595721A (en) |
-
1944
- 1944-12-11 GB GB24840/44A patent/GB595721A/en not_active Expired
-
1960
- 1960-10-04 BE BE595721A patent/BE595721A/en unknown
Also Published As
Publication number | Publication date |
---|---|
BE595721A (en) | 1961-04-04 |
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