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Annals of the New York Academy of Sciences | 1953

BRANCHING IN POLYETHYLENE

Frank M. Rugg; Joseph J. Smith; Lloyd H. Wartman

The principal purpose of this paper is to present the current status, as viewed by the authors, of our knowledge of branching in polyethylene and the effects of branching on its properties. Another purpose is to present some speculative material, and some challenging observations, in an attempt to stimulate, in some measure, future work on the structure and chemistry of polyethylene. In endeavoring to achieve these aims, the authors have drawn heavily upon their own work and liberally from the literature, particularly the published results of R. B. Richards and his collaborators. Polyethylene resins are made by polymerizing ethylene at elevated temperatures and high pressures.’, The polymer molecules formed under these conditions are branched hydrocarbon chains3* 4 . 6 * and their average molecular size varies from approximately 50 carbon atoms per molecule, for the greasy products, to more than 1000 carbon atoms per molecule for rigid resins. The degree of branching in polyethylene has been shown to play an important role in determining the properties of the resin.’ In fact, it is now generally recognized that degree of branching and molecular weight are the most important molecular variables in polyethylene resins. In this paper, degree of branching is defined as the number of branches per 100 carbon atoms, and the number of branches per molecule is defined as the number of -CH3 groups per molecule more than two. Although some chains and branches are terminated by vinyl groups (-CH=CHJ, the concentration of these is very small compared to the concentration of methyl groups. Side chain methylene groups (RR’C=CHZ) may be regarded as short branches but, as such, represent not more than 15 per cent, and generally a much smaller proportion, of the total number of branches. As a result, this configuration is not considered significant for the purposes of this paper.


Journal of Polymer Science | 1958

Structure and mechanism of dehydrochlorination of polyvinyl chloride

B. Baum; Lloyd H. Wartman


Journal of the American Chemical Society | 1960

Transition Metal Catalysts. I. Ethylene Polymerization with a Soluble Catalyst Formed from an Aluminum Halide, Tetraphenyltin and a Vanadium Halide1

Wayne L. Carrick; Rudolph W. Kluiber; Eugene F. Bonner; Lloyd H. Wartman; Frank M. Rugg; Joseph J. Smith


Journal of Polymer Science | 1953

Infrared spectrophotometric studies on polyethylene. I. Structure

Frank M. Rugg; Joseph J. Smith; Lloyd H. Wartman


Archive | 1965

Ethylene-acrylic acid copolymers plasticized with polyols

Jr Clarence E Roth; Lloyd H. Wartman


Archive | 1967

Ethylene copolymers with vinyl esters plasticized with phosphate and carboxylic esters

Lloyd H. Wartman


Archive | 1967

Ethylene-acrylic acid copolymers plasticized with adducts of alkylene oxides and amines

Clarence Edward Roth; Lloyd H. Wartman


Archive | 1962

Molten phase extraction of polymeric olefins

Richard W Quarles; Lloyd H. Wartman


Archive | 1967

Plasticized ethylene-acrylic acid copolymers

Lloyd H. Wartman; Clarence Edward Roth


Archive | 1966

Die verwendung von alkylphosphaten zum weichmachen von aethylen-metharylsaeure-mischpolymerisaten The use of alkyl phosphates to soften from ethylene copolymers metharylsaeure

Lloyd H. Wartman; Jun Roth

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