Article | REF: AM3038 V1

Morphological structure of polymers

Authors: Michel FONTANILLE, Yves GNANOU

Publication date: January 10, 2009

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ABSTRACT

The behavior of polymers in the solid state results from two forms of organization adopted by the macromolecular chains of glass and crystal. In a glass, the macromolecular chains are by essence at the amorphous state and produce entanglements which participate in the visco-elasticity of the mass material. Reversely, the chains characterized by a regular and symmetrical conformational structure or bearing groups capable of strong molecular interactions of polymers are likely to produce crystalline zones. After presenting the various types of oriented polymers, this article also deals with the incompatibility of polymers between themselves and the difficulty mixing them.

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AUTHORS

  • Michel FONTANILLE: Professor Emeritus, Bordeaux 1 University

  • Yves GNANOU: Research Director, CNRS - Université Bordeaux 1 – ENSCPB – CNRS. Pessac

 INTRODUCTION

In the [AM 3 037] dossier, we described the different types of structure that govern the geometry of the isolated macromolecule: assembly of atoms and monomer units, tacticity and conformational architectures. A close relationship exists between this structural level and the mechanical and thermo-mechanical properties of the final material. However, many of these properties can only be interpreted through intermediate structural scales involving the assembly of a greater or lesser number of macromolecular chains.

The behavior of polymers in the solid state – as opposed to the rubbery or viscous state – results from the two forms of organization that macromolecular chains can adopt, namely those of crystal and glass. In crystals, polymer chains are organized in a three-dimensional order, whereas in glass, macromolecular chains are essentially amorphous.

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