Abstract
A statistical molecular model of polymer networks, which takes into account inter‐molecular orientational interaction and constancy of the chain contour length, is proposed. A simple formula for the network free energy valid for any deformations is obtained. A system of equations which describes orientational‐elastic interactions in polymer networks is derived. The influence of deformation and degree of cross linking on the conditions of network phase transition into the orientationally ordered state of the nematic type is studied. The deformation curves considerably deviate from those predicted by the classical elasticity theory. A comparison of the proposed theory with experimental data for natural rubbers is carried out.
Original language | English |
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Pages (from-to) | 391-400 |
Number of pages | 10 |
Journal | Macromolecular Theory and Simulations |
Volume | 1 |
Issue number | 6 |
DOIs | |
State | Published - 1 Jan 1992 |
Externally published | Yes |
ASJC Scopus subject areas
- Condensed Matter Physics
- Organic Chemistry
- Polymers and Plastics
- Inorganic Chemistry
- Materials Chemistry