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The molecular mobility in an interpenetrating polymeric network (IPN) based on crosslinked polyurethane (1) and styrene–divinylbenzene copolymer (2) was studied by broad‐line NMR spectroscopy and reversed gas chromatography. NMR and infrared investigations show the absence of chemical interaction between the two constituent networks. For an IPN in the temperature range −196 to 120°C transition regions corresponding to the individual networks and to an intermediate region were found, the latter being characterized by an additional transition at 25–60°C (NMR spectroscopy) and 44–78°C (gas chromatography). The existence of an intermediate region, presumably of loosely packed structure, leads to a shift in the beginning of the temperature transition in IPN to lower temperature and to a decrease in activation energies of relaxation in comparison with the individual networks. The activation energies in IPN are decreased with increasing weight fraction of the second network.
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Lipatov et al. (1977) studied this question.
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