The Effects of the Quantity and Placement of Copolymer Units Within the Polymeric Chain on the Crystallization Phenomena in Polymers.

Abstract

The crystallization kinetics of random copolymers containing linear polyethylene as the major constituent and methyl and m-propyl side groups as counits have been studied by dilatometric techniques. Major attention has been given to the analysis of the temperature coefficient of the process which is demonstrated to be nucleation controlled. It is found that, irrespective of the mode of nucleation selected, there is a systematic increase in the crystallite interfacial free energy with increasing copolymeric content. The major increase occurs at copolymer compositions where spherulitic structures are no longer resolved. The values deduced for the interfacial free energy strongly favor the three-dimensional mode of nucleation. (Author)

Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1970
Accession Number
AD0716824

Entities

People

  • L. Mandelkern

Organizations

  • Florida State University

Tags

Communities of Interest

  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Coefficients
  • Copolymers
  • Crystallites
  • Crystallization
  • Dielectric Polymers
  • Energy
  • Free Energy
  • Kinetics
  • Macromolecules
  • Molecules
  • Nucleation
  • Polymers
  • Temperature Coefficients
  • Three Dimensional
  • Transition Temperature

Fields of Study

  • Chemistry

Readers

  • Materials Science and Engineering.
  • Polymer Science and Technology

Technology Areas

  • Microelectronics