Abstract
By means of NMR pulse methods molecular motions of polymer subchains in crosslinked polystyrene gels are studied. The temperature dependence of the effective transverse relaxation timeT 2 eff is explained by a local reorientation process. The local configuration of the elastic chains of the network is shown to be mainly determined by polymer-solvent interaction. The results are compared with those of concentrated solutions. The influence of static-like contributions to the 2nd moments is discussed.
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Geschke, D., Pöschel, K. Dynamic processes in polymeric networks as studied by NMR relaxation methods. Colloid & Polymer Sci 264, 482–487 (1986). https://doi.org/10.1007/BF01422000
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DOI: https://doi.org/10.1007/BF01422000