Abstract

The influence of the morphology on the local motion in the noncrystalline regions and chain diffusion between crystalline and noncrystalline regions is studied in ultrahigh molecular weight linear polyethylene: The behaviors of samples of the same material crystallized from the melt and from solution are compared. The geometrical restrictions of the conformational transitions are probed via anisotropic NMR interactions, i.e., 13C−1H dipole–dipole couplings and 13C chemical shift anisotropy. As they are averaged out under MAS, recoupling techniques are applied to yield sideband patterns or quasi-static NMR spectra, from which residual anisotropies are determined. Chain diffusion is probed by 13C exchange NMR. As expected, the local conformational transitions are more restricted in the solution crystallized sample compared with the melt crystallized one. Moreover, the motional narrowing observed by both techniques indicates that the local mobility in the noncrystalline regions of the solution crystallized s...

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