GB806933A - Improved rubbery composition and article made therefrom - Google Patents

Improved rubbery composition and article made therefrom

Info

Publication number
GB806933A
GB806933A GB19066/56A GB1906656A GB806933A GB 806933 A GB806933 A GB 806933A GB 19066/56 A GB19066/56 A GB 19066/56A GB 1906656 A GB1906656 A GB 1906656A GB 806933 A GB806933 A GB 806933A
Authority
GB
United Kingdom
Prior art keywords
acetate
cobaltous
nickel
lead
rubber
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
GB19066/56A
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 GB806933A publication Critical patent/GB806933A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098Metal salts of carboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Reinforced Plastic Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A rubbery composition suitable for use in the bonding of rubber to metal comprises a vulcanizable rubbery material and a partially calcined metal-organic compound in an amount of up to 10 per cent by weight based on the weight of the rubbery material. The metal organic compound may be a cobalt, copper, iron, lead, mercury or nickel salt of an organic acid containing only carbon, hydrogen and oxygen. Specified compounds are cobaltous acetate, cobaltous butyrate, cobaltous citrate, cobaltous formate, cobaltous oleate, cobaltous tartrate, cupric acetate, cupric benzoate, cupric butyrate, cupric stearate, ferric acetate, ferric benzoate, ferric formate, lead acetate, lead citrate, lead palmitate, mercuric acetate, mercuric benzoate, mercuric propionate, nickel acetate, nickel oxalate, nickel propionate, nickel stearate, silver acetate and silver stearate. The compound may be heated for from 150-170 DEG C. for 24-72 hours. The rubbery material may be natural rubber or polymers of butadiene-1,3; isoprene; 2,3-dimethyl butadiene-1,3; 1,4-dimethyl butadiene-1,3; piperylene; chlorobutadiene-1,3; and copolymers of these monomers with isobutylene, styrene, methyl styrene, chlorostyrene, acrylonitrile, methacrylonitrile, alpha chloroacrylonitrile, methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, ethyl methacrylate, and 2-vinyl pyridine, or interpolymers of 3 or more monomers such as that of butadiene-1,3 with styrene and acrylonitrile; rubbery olefin polysulphide polymers, rubbery polyacrylates, rubber polymers containing a curable -COOH or -COOR group formed from a diene and an unsaturated carboxylic acid and the reaction products of a diisocyanate with an hydroxyl terminated polyester. Compounding ingredients such as phenyl-beta-naphthylamine, aldol-alpha-naphthylamine, 2-mercapto benzothiazole disulphide, polymerized trimethyl dihydroquinoline, N-cyclo-hexyl-2-mercaptobenxothiazole sulphene amide, polyaralkylated phenols, 2-mercaptobenzothiazole, precipitated silicon dioxide, precipitated calcium silicate, zinc salt of mercaptobenzothiazole, red iron oxide, zinc oxide, magnesia, titanium dioxide, yellow iron oxide, arc silica, silicon monoxide, clay, carbon black, stearic acid, cellulose flock, hexamethylene tetramine, sulphur, pine tar oil, paraflux heavy oil, tetramethyl thiuram disulphide, calcium hydroxide, triethyl trimethylene triamine, triethylene tetramine, sodium meta silicate, red lead, paraquinone dioxime, rosins and resins may also be added. In a modification the partially calcined metal organic compound can be deposited as a thin layer on the metal or rubber surfaces, and rubber or metal applied and the whole assembly then vulcanized.
GB19066/56A 1955-06-20 1956-06-20 Improved rubbery composition and article made therefrom Expired GB806933A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US806933XA 1955-06-20 1955-06-20

Publications (1)

Publication Number Publication Date
GB806933A true GB806933A (en) 1959-01-07

Family

ID=22159010

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19066/56A Expired GB806933A (en) 1955-06-20 1956-06-20 Improved rubbery composition and article made therefrom

Country Status (1)

Country Link
GB (1) GB806933A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4297159A (en) * 1978-07-21 1981-10-27 Klaus Heckmann Method to directly bond rubber to metal

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4297159A (en) * 1978-07-21 1981-10-27 Klaus Heckmann Method to directly bond rubber to metal

Similar Documents

Publication Publication Date Title
US3317918A (en) Butadiene polymers prepared with a lithium based catalyst characterized by having at least 29 percent of the butadiene as cis-1, 4
US2989504A (en) Vulcanization of polymer with nu, nu'-bismaleimides and compositions thereof
US4843128A (en) Elastomeric composition having increased ozone resistance
GB875947A (en) Vulcanizates of polypropylene and rubber
GB718768A (en) Improvements in chemical process and product
US2395506A (en) Vulcanization of synthetic rubber
GB1007817A (en) Improvements in and relating to aromatic rubber phosphite stabilizers
US3781250A (en) Process for the vulcanization of homo-or copolymers of conjugated dienes
GB806933A (en) Improved rubbery composition and article made therefrom
US3687881A (en) Zinc-containing polymer compositions
GB733134A (en) Improvements in process for chemically modifying butyl rubber and ensuing product
TW200303334A (en) Improved nitrile polymer vulcanizate and process for the production thereof
US3053851A (en) N-(2-vinyl phenyl) maleimide
CA1108347A (en) Age-resisting polymers and their preparation by reactions involving use of certain aminomercaptans
US3909473A (en) Cis-1,4-polyisoprene rubber composition having improved mechanical properties
US2784167A (en) Masticating synthetic rubber
US3023195A (en) Preventing scorch in butyl rubber compositions
US2381059A (en) Synthetic rubber composition
US2983706A (en) Stabilizing brominated rubbery polymers
US3422078A (en) Polymethyleniminethiothiazoles and rubber vulcanization
US2649430A (en) Vulcanization
GB1042293A (en) Metallo organic polymers, their preparation and utility
GB808302A (en) Improvements in or relating to vulcanization of rubbers
GB881482A (en) Method of compounding cis-polybutadiene for improved mill handling and product thereof
GB609086A (en) Improvements in or relating to the vulcanization of natural or synthetic rubber