A new statistical theory based on the rotational isomeric state model de-scribing the chain conformational free energy has been proposed. This theory can be usedto predict different tensions of rubber elongation for chemically different polymers
and theenergy term during the elongation of natural rubber coincides with the experimental one.
Abstract
A new statistical theory based on the rotational isomeric state model de-scribing the chain conformational free energy has been proposed. This theory can be usedto predict different tensions of rubber elongation for chemically different polymers
and theenergy term during the elongation of natural rubber coincides with the experimental one.
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