GB818826A - Method of processing hydrocarbon polymers - Google Patents

Method of processing hydrocarbon polymers

Info

Publication number
GB818826A
GB818826A GB9667/57A GB966757A GB818826A GB 818826 A GB818826 A GB 818826A GB 9667/57 A GB9667/57 A GB 9667/57A GB 966757 A GB966757 A GB 966757A GB 818826 A GB818826 A GB 818826A
Authority
GB
United Kingdom
Prior art keywords
polymer
isobutylene
per cent
condensation product
styrene
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
GB9667/57A
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.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering 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 Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of GB818826A publication Critical patent/GB818826A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/18Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • C08L23/20Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
    • C08L23/22Copolymers of isobutene; Butyl rubber ; Homo- or copolymers of other iso-olefins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

In a process for preparing a rubbery isoolefinic polymer at low temperature in the presence of a Friedel-Crafts catalyst in a nonaqueous diluent agglomeration of the polymer is avoided by mixing the slurry with an aqueous solution of 0.01 to 1 per cent by weight of an oxygenated hydrocarbon of the general formula A(O(CH2)x)yB, where A is hydrogen or an alkyl, aryl, aralkyl, alkaryl or an alkyl, aryl, aralkyl or alkaryl carboxyl radical containing 2 to 50 carbon atoms and B is a hydroxy radical or an acyloxy radical containing 2 to 50 carbon atoms and X and Y are integers between 2 and 50, and 4 and 30 respectively, and the rubbery polymer is then separated and dried. Polyisobutylene or copolymers of C4-C14 olefines with multi-olefines such as isoprene, butadiene, dimethallyl, myrcene and allo-ocymene and aromatic mono-olefinic compounds such as styrene, a - methylstyrene, p - methylstyrene, indene, p-chlorostyrene or dichloro styrene and divinyl benzene and mixtures thereof may be prepared and examples describe the polymerization of isobutylene, isobutylene-isoprene, and styrene-isobutylene. Oxygenated hydrocarbons mentioned are mono-carboxylic fatty or rosin acid esters of polyethylene glycol, e.g. the condensation product of ethylene oxide and abietic acid; alkyl phenoxy polyoxyethylene glycols, e.g. the condensation product of nonyl phenol and ethylene oxides; and aliphatic polyoxyethylene ethers e.g. the condensation product of tridecyl alcohol and ethylene oxide and they may be retained in the polymer in amounts in the range 0.005 to 0.5 per cent of polymer. An oxidation stabilizer such as n-lauroyl-paminophenol, ditertiary butyl p-cresol, phenyl b -naphthylamine or mixtures thereof may be added to the slurry, in an amount from 0.05 to 1.0 per cent based on the polymer.
GB9667/57A 1956-04-16 1957-03-25 Method of processing hydrocarbon polymers Expired GB818826A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US818826XA 1956-04-16 1956-04-16

Publications (1)

Publication Number Publication Date
GB818826A true GB818826A (en) 1959-08-26

Family

ID=22167006

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9667/57A Expired GB818826A (en) 1956-04-16 1957-03-25 Method of processing hydrocarbon polymers

Country Status (2)

Country Link
DE (1) DE1065615B (en)
GB (1) GB818826A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1255319B (en) * 1960-03-31 1967-11-30 Phillips Petroleum Co Process for the production of a rubbery homopolymer or copolymer

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1255319B (en) * 1960-03-31 1967-11-30 Phillips Petroleum Co Process for the production of a rubbery homopolymer or copolymer

Also Published As

Publication number Publication date
DE1065615B (en) 1959-09-17

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