Formation, structure, and elasticity of loosely crosslinked epoxy‐amine networks. II. Mechanical and optical properties
- 1 February 1984
- journal article
- research article
- Published by Wiley in Journal of Polymer Science: Polymer Physics Edition
- Vol. 22 (2) , 265-278
- https://doi.org/10.1002/pol.1984.180220211
Abstract
The mechanical and optical behavior in the dry and swollen states of loosely crosslinked epoxy networks prepared from the diglycidyl ether of bisphenol A, phenylglycidyl ether, and 4,4′‐diaminodiphenylmethane was investigated, and the weight fraction of sol in the networks was determined. The crosslinking density was controlled by an excess of diamine and by the fraction of monoepoxide. The reaction proceeded to almost full conversion of epoxy groups. With increasing content of monoepoxide or with increasing excess of diamine, the main transition region is shifted to lower temperatures. The dependence of the viscoelastic modulus on temperature and the optical behavior indicate that the networks are homogeneous. In all cases, the sol fraction is adequately described by the theory of branching processes (cf. Part I). The equilibrium modulus related to the dry state is the same irrespective of whether it is obtained by measurements in the dry or swollen state. The mechanical behavior in the rubbery state can be described by the theory of phantom networks with fully suppressed fluctuations of crosslinking (front factor A = 1) or by the theory of phantom networks with fully released fluctuations of crosslinks (front factor) A = fe−2/fe] and contribution of trapped entanglements of the Langley‐Graessley type (cf. Part I). In the analysis of the equilibrium behavior, it is advantegeous to use the plot of superimposed dependences of Ge on the gel fraction, which considerably reduces the effect of experimental inaccuracy in determination of composition and degree of conversion.Keywords
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