GB407948A - Improved methods of making plastic elastic materials - Google Patents

Improved methods of making plastic elastic materials

Info

Publication number
GB407948A
GB407948A GB26728/32A GB2672832A GB407948A GB 407948 A GB407948 A GB 407948A GB 26728/32 A GB26728/32 A GB 26728/32A GB 2672832 A GB2672832 A GB 2672832A GB 407948 A GB407948 A GB 407948A
Authority
GB
United Kingdom
Prior art keywords
rubber
aluminium chloride
plastic materials
reacting
absence
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
GB26728/32A
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.)
Uniroyal Chemical Co Inc
Original Assignee
Naugatuck 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 Naugatuck Chemical Co filed Critical Naugatuck Chemical Co
Publication of GB407948A publication Critical patent/GB407948A/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
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes

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

Plastic materials prepared by reacting an aromatic compound of the general formula R-C6H4-R<1> (where R and R<1> represent hydrogen or a saturated aliphatic hydrocarbon radical containing more than one carbon atom) with an ethylene dihalide in the presence of aluminium chloride and in the presence or absence of rubber may be dispersed in water in the presence of nitrobenzene, soap, casein or sodium hydroxide.ALSO:Plastic materials, which are resistant to abrasion and to the action of water, acid, alkali and many organic liquids are prepared by reacting an aromatic compound of the general formula R--C6H4--R<1> (where R and R<1> each represent hydrogen or a saturated aliphatic hydrocarbon radical containing more than one carbon atom) with an ethylene dihalide, such as the chloride or bromide, in the presence of aluminium chloride and in the presence or absence of rubber. The reaction yields a jelly like mass which is washed with water which may contain butyl acetate, acid or alkali preferably in the presence of steam and then dried. The products, which may be chlorinated, may be milled and mixed with fillers, pigments or fibrous materials such as carbon black, zinc oxide, whiting, clay, asbestos fibres and rubber or rubber compounds and used in the manufacture of heat-resisting covers for conveyer belts and flexible linings for tanks, barrels, ball mills and pipe lines. Suitable aromatic compounds include benzene, ethyl- and diethylbenzene, iso-propylbenzene and butyl benzene. In examples: (1) benzene; (2) ethylbenzene; (3) benzene and crepe; (4) n-butylbenzene; (5) p-diethylbenzene and (6) sym-diphenylethane are condensed with ethylene dichloride in the presence of aluminium chloride. The Specification as open to inspection under Sect. 91 referred to the use of other Friedel-Kraft's type catalysts and was not limited to the use of any catalyst. This subject-matter does not appear in the Specification as accepted.ALSO:Flexible linings for ball mills are prepared from plastic materials obtained by reacting an aromatic compound of the general formula R - C6H4 - R1(where R and R1 each represent hydrogen or a saturated aliphatic hydrocarbon radical containing more than one carbon atom) with an ethylene dihalide in the presence of aluminium chloride in the presence or absence of rubber. Pigments, fillers and fibrous materials may be added to the plastic materials.ALSO:Plastic materials prepared by reacting an aromatic compound of the general formula R-C6H4-R1 (where R and R1 represent hydrogen or a saturated aliphatic hydrocarbon radical containing more than one carbon atom) with an ethylene dihalide in the presence or absence of rubber and in the presence of aluminium chloride may be milled and mixed with pigments, fillers or fibrous materials such as carbon black, zinc oxide, whiting, clay, asbestos fibres, rubber or rubber compounds and used in the manufacture of covers for conveyer belts and linings for tanks, barrels, ball mills and pipe lines.
GB26728/32A 1931-10-27 1932-09-26 Improved methods of making plastic elastic materials Expired GB407948A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US407948XA 1931-10-27 1931-10-27

Publications (1)

Publication Number Publication Date
GB407948A true GB407948A (en) 1934-03-26

Family

ID=21912992

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26728/32A Expired GB407948A (en) 1931-10-27 1932-09-26 Improved methods of making plastic elastic materials

Country Status (1)

Country Link
GB (1) GB407948A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3213041A (en) * 1957-07-05 1965-10-19 Kellogg M W Co Process of pyrolyzing a paraxylyl halide
US3294531A (en) * 1959-07-22 1966-12-27 Azoplate Corp Photoconductive layers for electrophotographic purposes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3213041A (en) * 1957-07-05 1965-10-19 Kellogg M W Co Process of pyrolyzing a paraxylyl halide
US3294531A (en) * 1959-07-22 1966-12-27 Azoplate Corp Photoconductive layers for electrophotographic purposes

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