GB861814A - A process for improving the adhesion of fibrous materials to rubber - Google Patents

A process for improving the adhesion of fibrous materials to rubber

Info

Publication number
GB861814A
GB861814A GB7786/58A GB778658A GB861814A GB 861814 A GB861814 A GB 861814A GB 7786/58 A GB7786/58 A GB 7786/58A GB 778658 A GB778658 A GB 778658A GB 861814 A GB861814 A GB 861814A
Authority
GB
United Kingdom
Prior art keywords
rubber
butyl rubber
latex
fibrous material
butadiene
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
GB7786/58A
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 GB861814A publication Critical patent/GB861814A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/04Reinforcing macromolecular compounds with loose or coherent fibrous material
    • C08J5/06Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2321/00Characterised by the use of unspecified rubbers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Reinforced Plastic Materials (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Fibrous material, e.g. cotton, silk, viscose rayon and nylon, is coated with a phenolicaldehyde resin-containing rubber latex other than a butadiene-styrene-vinyl pyridine latex and then with a brominated butyl rubber cement containing sufficient bromine to improve the adhesion of the fibrous material to natural and synthetic rubber. The phenolic-aldehyde resin-containing rubber latex, which may be a natural rubber, butyl rubber or polyhaloalkadiene rubber latex, is preferably adjusted to a pH of 7-13 and aged at 40-150 DEG F. for 20 minutes to 30 hours before application, and the latex-coated fibrous material may be dried, preferably with stretching, for 0.05 to 30 minutes at 200 DEG to 550 DEG F., whereby the resin is partially set and the volatile materials driven off. The dried, coated fibrous materials are then treated with the brominated butyl rubber cement which preferably contains at least 0.5% by weight of combined bromine but not more than 3 combined atoms of bromine per double bond in the polymer and preferably contains fillers such as silica, clays, alumina, diatomaceous earth, calcium carbonate, silicaalumina and carbon black, with or without curatives such as sulphur, zinc oxide, derivatives of thiuram or carbamic acid, quinoid compounds, primary or polyfunctional amines, phenol-dialcohol resins of the polymethylolphenol type, benzothiazyl disulphide, mercaptobenzothiazole, mercapto imidazoline and sulphonamides. The brominated butyl rubber may be dissolved in a C5 to C10 hydrocarbon or halogenated hydrocarbon such as ethylene dichloride, chloroform or carbon tetrachloride, and after application of the solution the fibrous material may be dried at 150-300 DEG F. for 0.5-30 minutes. The material may then be imbedded as by calendering in an unvulcanized rubber matrix such as natural rubber, butyl rubber, chlorinated or brominated butyl rubber, neoprene rubber, GR-S rubber, "Buna-N" rubber ("Buna" is a Registered Trade Mark), vinyl pyridine-butadiene copolymers and tripolymers of butadiene-acrylonitrile-vinyl pyridine and vulcanized in situ for 0.5 to 90 minutes at 200 DEG to 450 DEG F. Butyl rubber comprises a copolymer containing 85 to 99.5% of a C4 to C8 iso-olefin, e.g. isobutylene, the remainder being a C4 to C10 multiolefin, preferably a C4 to C10 conjugated diolefin such as butadiene, dimethyl butadiene, piperylene or isoprene, and the butyl rubber latex may be prepared by dissolving butyl rubber in a hydrocarbon solution which is then emulsified with water using non-ionic, anionic or cationic emulsifiers and the hydrocarbon solvent removed by stripping; alternatively, the latex may be prepared in intensive mixing equipment, e.g. colloidal mills or sanic mixers, a protective colloid, e.g. polyvinyl alcohol, being added. Methods of brominating butyl rubber are described, and a number of reagents for this purpose are specified. The treated fibrous material may be used in constructing tyre carcasses, conveyer belts, transmission belting, rubber hosing, e.g. steam hose, air springs and other products built up of a plurality of laminations of cord and rubber. Specifications 243,016 and 565,974 are referred to.ALSO:Fibrous material, e.g. cotton, silk, viscose rayon and nylon, is coated with a phenolicaldehyde resin-containing rubber latex other than a butadiene styrene-vinyl pyridine latex and then with a brominated butyl rubber cement containing sufficient bromine to improve the adhesion of the fibrous material to natural and synthetic rubber. The phenolic-aldehyde resin-containing rubber latex, which may be a natural rubber, butyl rubber or polyhaloalkadiene rubber latex, is preferably adjusted to a pH of 7-13 and aged at 40 DEG -150 DEG F. for 20 minutes to 30 hours before application, and the latex-coated fibrous material may be dried, preferably with stretching, for 0,05 to 30 minutes at 200 DEG to 550 DEG F., whereby the resin is partially set and the volatile materials driven off. The dried, coated fibrous materials are then treated with the brominated butyl rubber cement which preferably contains at least 0,5% by weight of combined bromine but not more than 3 combined atoms of bromine per double bond in the polymer and preferably contains fillers such as silica, clays, alumina, diatomaceous earth, calcium carbonate, silica-alumina and carbon black, with or without curatives such as sulphur, zinc oxide, derivatives of thiuram or carbamic acid, quinoid compounds, primary or poly-functional amines, phenoldialcohol resins of the polymethylol-phenol type, benzothiazyl disulphide, mercaptobenzothiazole, mercapto imidazoline and sulphonamides. The brominated butyl rubber may be dissolved in a C5 to C10 hydrocarbon or halogenated hydrocarbon such as ethylene dichloride, chloroform or carbon tetrachloride, and after application of the solution the fibrous material may be dried at 150 DEG -300 DEG F. for 0,5 to 30 minutes. The material may then be embedded as by calendering in an unvulcanized rubber matrix such as natural rubber, butyl rubber, chlorinate or brominated butyl rubber, neoprene rubber, GR-S rubber, Buna-N rubber ("Buna" is a Registered Trade Mark), vinyl pyridine-butadiene copolymers and tripolymers of butadieneacrylonitrile-vinyl pyridine and vulcanized in situ for 0,5 to 90 minutes at 200 DEG to 450 DEG F. Butyl rubber comprises a copolymer containing 85 to 99,5% of a C4 to C8 isoolefin, e.g. isobutylene, the remainder being a C4 to C10 multiolefin, preferably a C4 to C10 conjugated diolefin such as butadiene, dimethyl butadiene, piperylene or isoprene, and the butyl rubber latex may be prepared by dissolving butyl rubber in a hydrocarbon solution which is then emulsified with water using non-ionic, anionic or cationic emulsifiers and the hydrocarbon solvent removed by stripping; alternatively, the latex may be prepared in intensive mixing equipment, e.g. colloidal mills or sonic mixers, a protective colloid, e.g. polyvinyl alcohol, being added. Methods of brominating butyl rubber are described, and a number of reagents for this purpose are specified. The treated fibrous material may be used in constructing tire carcasses, conveyer belts, transmission belting, rubber hosing, e.g. steam hose, air springs and other products built up of a plurality laminations of cord and rubber. Specifications 243,016 and 565,974 are referred to.
GB7786/58A 1957-05-03 1958-03-11 A process for improving the adhesion of fibrous materials to rubber Expired GB861814A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US861814XA 1957-05-03 1957-05-03

Publications (1)

Publication Number Publication Date
GB861814A true GB861814A (en) 1961-03-01

Family

ID=22196826

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7786/58A Expired GB861814A (en) 1957-05-03 1958-03-11 A process for improving the adhesion of fibrous materials to rubber

Country Status (2)

Country Link
FR (1) FR1205988A (en)
GB (1) GB861814A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1524293A1 (en) * 2003-10-16 2005-04-20 The Goodyear Tire & Rubber Company Airsleeve
CN111621040A (en) * 2020-06-09 2020-09-04 贵州大学 Method for reducing heat generation of butadiene styrene rubber vulcanized rubber, product and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1524293A1 (en) * 2003-10-16 2005-04-20 The Goodyear Tire & Rubber Company Airsleeve
CN111621040A (en) * 2020-06-09 2020-09-04 贵州大学 Method for reducing heat generation of butadiene styrene rubber vulcanized rubber, product and preparation method thereof
CN111621040B (en) * 2020-06-09 2022-11-18 贵州大学 Method for reducing heat generation of butadiene styrene rubber vulcanized rubber, product and preparation method thereof

Also Published As

Publication number Publication date
FR1205988A (en) 1960-02-05

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