GB849027A - Improvements in polymers of ethylene - Google Patents

Improvements in polymers of ethylene

Info

Publication number
GB849027A
GB849027A GB4549/58A GB454958A GB849027A GB 849027 A GB849027 A GB 849027A GB 4549/58 A GB4549/58 A GB 4549/58A GB 454958 A GB454958 A GB 454958A GB 849027 A GB849027 A GB 849027A
Authority
GB
United Kingdom
Prior art keywords
free radical
ethylene
compound
compounds
reaction
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
GB4549/58A
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.)
Godfrey L Cabot Inc
Original Assignee
Godfrey L Cabot Inc
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 Godfrey L Cabot Inc filed Critical Godfrey L Cabot Inc
Publication of GB849027A publication Critical patent/GB849027A/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
    • C08K5/14Peroxides
    • 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

Landscapes

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

Abstract

A homo-polymer of ethylene characterised by an average molecular weight above 50,000, a melting point above 125 DEG C., a density above 0,94, a modulus of elasticity at 23 DEG C. of at least 60,000 p.s.i., an ultimate tensile strength above 2500 p.s.i. when measured at 23 DEG C., at an extension rate of 20 inches/minute, a melt index as measured by A.S.T.M. test D1238-52T of at least 0,2 gram/10 minutes, and the ability to resist cracking for a period of at least 7 days continuous exposure to air at 80 DEG C. when moulded strips-of same are cut and stressed in the manner described on pages 25-26 of A.S.T.M. Bulletin No. 218, published December 1956 by reacting a homopolymer of ethylene having the above properties except that it is susceptible to embrittlement, stress cracking and other forms of degradation at a temperature above 80 DEG C., with a free radical generating compound which does not boil below 100 DEG C. at atmospheric pressure and which decomposes to form free radicals in the range of 140 DEG to 200 DEG C. and which is present in an amount of from 0,1 to 0,4 parts by weight per 100 parts of polyethylene, by decomposing by heat the free radical generating compound. The reaction with the free radical compound may be effected in the presence of carbon blacks, antixoidants, and plasticisers. If desired these ingredients may also be compounded with the aftertreated polymer. The free radical compounds may be peroxides or hydroperoxides, compounds containing an <N-Cl grouping, metal alkyls, amine oxides, hydrasine salts, organic disulphides, and azo compounds. The preferred compound is dicumyl peroxide. In Example 2, the reaction with cicumyl peroxide is carried out in the presence of carbon black and phenyl-beta-naphthalmine and the product extruded into pipes.
GB4549/58A 1957-02-13 1958-02-12 Improvements in polymers of ethylene Expired GB849027A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US63984957A 1957-02-13 1957-02-13

Publications (1)

Publication Number Publication Date
GB849027A true GB849027A (en) 1960-09-21

Family

ID=24565812

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4549/58A Expired GB849027A (en) 1957-02-13 1958-02-12 Improvements in polymers of ethylene

Country Status (7)

Country Link
BE (1) BE564735A (en)
CH (1) CH381858A (en)
DE (1) DE1131005B (en)
FR (1) FR1198844A (en)
GB (1) GB849027A (en)
IT (1) IT588438A (en)
NL (2) NL103085C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3352817A (en) * 1964-01-31 1967-11-14 Glanzstoff Ag Stability of polyolefines
US3407172A (en) * 1964-01-31 1968-10-22 Glanzstoff Ag Stability of polyolefines

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB872439A (en) * 1959-10-23 1961-07-12 Grace W R & Co Improvements in polyethylene compositions and methods for their production

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2455910A (en) * 1945-02-20 1948-12-14 Du Pont Method for curing ethylene polymers
US2628214A (en) * 1945-10-27 1953-02-10 Du Pont Curing of polyethylenes
US2528523A (en) * 1948-06-12 1950-11-07 Du Pont Process for extruding and insolubilizing polymers of ethylene

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3352817A (en) * 1964-01-31 1967-11-14 Glanzstoff Ag Stability of polyolefines
US3407172A (en) * 1964-01-31 1968-10-22 Glanzstoff Ag Stability of polyolefines

Also Published As

Publication number Publication date
BE564735A (en)
DE1131005B (en) 1962-06-07
IT588438A (en)
CH381858A (en) 1964-09-15
FR1198844A (en) 1959-12-09
NL103085C (en)
NL224546A (en)

Similar Documents

Publication Publication Date Title
US4578431A (en) Process for improving melt strength of ethylene polymers by treatment with organic peroxide
IE42665B1 (en) Bromine-containing fluoropolymer composition
GB1535039A (en) Compositions with dicumyl peroxide and process for avoiding scorching of ethylene polymer composition
US2619481A (en) Curing rubbery olefinic copolymers
GB849023A (en) Polypropylene-butyl rubber blends
US4172939A (en) Vulcanizable ethylene/vinyl acetate/carbon monoxide terpolymers
US3153014A (en) Maleimides and citraconimides as curing agents for vulcanizable rubbers
GB849027A (en) Improvements in polymers of ethylene
US3531455A (en) Peroxide-cured chlorinated polyethylene
US2567135A (en) Vulcanization of butadiene copolymer rubbers
JPS5638341A (en) Polypropylene resin composition
US3050503A (en) Chlorosulfonated elastomers and methods for making the same
US2975159A (en) Rubber-like interpolymers of ethylene and two other monoolefins
US2453689A (en) Vulcanizing synthetic rubber with dixanthic sulfides
US2958680A (en) Chloroprene polymers containing trialkyl thiourea accelerators
US2944995A (en) Acceleration of the peroxide cure of hexafluoropropylene-vinylidene fluoride elastomer with methylene bisacrylamide
US2448154A (en) Use of symmetrical xenyltriazenes in making gas expanded organic plastics
KR940018418A (en) Improved Ethylene-Vinyl Acetate Vulcanizer
US2504295A (en) Curing copolymers of butadiene-1, 3 and acrylonitrile with organic halogen compounds
US2985632A (en) Gr-s cured with dicamyl peroxide and sulfur
CN110128706B (en) Degradable random copolymerization BOPP composition and application thereof
US2819255A (en) Vulcanizable rubber compositions and process
GB969657A (en) Production and use of nitrosoanilinonitroalkanes
US2340699A (en) Synthetic rubber composition
US3468855A (en) Vulcanization with p,p&#39;-oxybis(thiophenol) and at least one activator selected from sulfur and an organic peroxide curative