Theory of the thermodynamics, structure, and dynamics of polymer blends

Kenneth S Schweizer, John G. Curro

Research output: Contribution to journalConference articlepeer-review

Abstract

The authors have recently developed a microscopic statistical mechanical theory of the structure and thermodynamics of polymer melts blends and copolymer liquids which goes far beyond the traditional lattice/mean field models. The approach is based on nonperturbative, continuous space RISM integral equation methods of modern liquid state theory. This theory is capable of numerically calculating the scattering structure factors, intermolecular monomer-monomer pair correlation functions, equation-of-state and other equilibrium properties of nonpolar polymer liquids as functions of temperature, density, molecular weight, intramolecular structure, and intermolecular forces. This paper focuses on binary polymer mixtures. The authors studied two general classes of model binary blends. The first type is the 'athermal' blend for which there is no heat or volume change of mixing. The second general class of blends are those which exhibit a heat of mixing.

Original languageEnglish (US)
Pages (from-to)50-51
Number of pages2
JournalAmerican Chemical Society, Polymer Preprints, Division of Polymer Chemistry
Volume30
Issue number1
StatePublished - Apr 1 1989
Externally publishedYes
EventPapers Presented at the Dallas, Texas Meeting - Dallas, TX, USA
Duration: Apr 9 1989Apr 14 1989

ASJC Scopus subject areas

  • Polymers and Plastics

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