GB737447A - Improvements in or relating to partially hydrohalogenated interpolymers - Google Patents

Improvements in or relating to partially hydrohalogenated interpolymers

Info

Publication number
GB737447A
GB737447A GB35916/53A GB3591653A GB737447A GB 737447 A GB737447 A GB 737447A GB 35916/53 A GB35916/53 A GB 35916/53A GB 3591653 A GB3591653 A GB 3591653A GB 737447 A GB737447 A GB 737447A
Authority
GB
United Kingdom
Prior art keywords
hydrohalogenated
interpolymers
fluorine
interpolymer
per cent
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
GB35916/53A
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.)
Goodrich Corp
Original Assignee
BF Goodrich Corp
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 BF Goodrich Corp filed Critical BF Goodrich Corp
Publication of GB737447A publication Critical patent/GB737447A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/18Introducing halogen atoms or halogen-containing groups
    • C08F8/20Halogenation

Abstract

Partially hydrohalogenated interpolymers are derived from rubbery interpolymers of a major proportion of an isoolefin containing from 4 to 8 carbon atoms and a terminal methylene group with a minor proportion of a polyolefinic hydrocarbon, said hydrohalogenated interpolymer retaining some olefinic unsaturation and having a halogen content of from 0.1 per cent of fluorine, chlorine or bromine up to 1.0 per cent equivalent of fluorine, in the structure <FORM:0737447/IV (a)/1> Isoolefins specified are isobutylene, 3-methyl or 2-ethyl butene-1, 4-methyl or 4-ethyl pentene-1 or mixtures and polyolefins tabulated include acyclic and alicyclic conjugated and non-conjugated diolefins, acyclic and alicyclic triolefins, tetra- and penta-olefins and polyolefinic hydrocarbons containing aromatic nuclei. Other monomers such as styrene, chlorostyrene and acrylyl and methallyl chlorides may be copolymerized with the isoolefin and the polyolefin. The hydrohalogenation may be carried out in solution, dispersion or cement or by passing gaseous hydrogen chloride or bromide over the solid interpolymer. Solvents specified are toluene, chlorobenzene, methyl and ethyl chlorides, trichloroethane, carbon tetrachloride, butane, hexane and heptane. Solvents may be subsequently removed by running the solution, e.g. stabilized with an epoxidized diester of cotton seed fatty acid, into water containing a colloidal protective agent such as zinc stearate. The products may be admixed, by blending dispersions, latices or solutions, with natural or synthetic rubbers and these mixtures or the products alone may be compounded and vulcanized with the usual ingredients, particularly by means of zinc oxide and carbon black. The hydrohalogenated interpolymers may be used as adhesives, for the manufacture of inner tubes and tyre curing bags and in bonding non-hydrohalogenated interpolymers, natural rubber and synthetic rubbers such as butyl rubber.ALSO:A composition comprises natural rubber and a partially hydrohalogenated interpolymer of a major proportion of an isoolefin containing from 4 to 8 carbon atoms and a terminal methylene group, with a minor proportion of a polyolefin, said hydrohalogenated interpolymer retaining some olefinic unsaturation and having a halogen content of from 0.1 per cent of fluorine, chlorine or bromine up to 1.0 per cent equivalent of fluorine, in the structure <FORM:0737447/V/1> The compositions may be obtained by blending dispersions, latices or suspensions and may be compounded and vulcanized with the usual ingredients and also with bivalent metal oxides, in particular zinc oxide in the presence of carbon black, to give products of improved physical properties. Examples 11 to 15 describe the use of the hydrohalogenated interpolymers as adhesives (in heptane solution) for bonding butyl rubber to natural rubber.
GB35916/53A 1953-01-13 1953-12-24 Improvements in or relating to partially hydrohalogenated interpolymers Expired GB737447A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US737447XA 1953-01-13 1953-01-13

Publications (1)

Publication Number Publication Date
GB737447A true GB737447A (en) 1955-09-28

Family

ID=22115552

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35916/53A Expired GB737447A (en) 1953-01-13 1953-12-24 Improvements in or relating to partially hydrohalogenated interpolymers

Country Status (2)

Country Link
FR (1) FR1098977A (en)
GB (1) GB737447A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2968588A (en) * 1955-12-19 1961-01-17 Exxon Research Engineering Co Adhesion of rubbery polymers to tire cords
FR2746802B1 (en) * 1996-03-28 1998-06-12 Derives Resiniques Terpenique PROCESS FOR THE CONTROLLED HYDROHALOGENATION OF POLYOLEFIN-DIENE COPOLYMERS AND POLYMERS THEREOF
GB9615025D0 (en) * 1996-07-17 1996-09-04 Bp Chem Int Ltd Production of substituted polyisobutenes

Also Published As

Publication number Publication date
FR1098977A (en) 1955-08-29

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