Diffusion of liquid n-alkanes: Free-volume and density effects

• Published in: The Journal of chemical physics 1998-03, Vol.108 (10), p.4299-4304
• Main Authors: von Meerwall, E., Beckman, S., Jang, J., Mattice, W. L.
• Format: Article
• Language: English
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.475829

In support of our numerical simulations of self-diffusion D of chain molecules in the melt, we have used the pulsed-gradient spin-echo NMR method to make detailed D measurements in 15 liquid n-paraffins (8–60 carbons; molecular weight M=114–844) at eight temperatures T from 30 to 170 °C. We find that D∼Mβ, with β changing approximately linearly from −2.72 to −1.85 as T increases. Thus the apparent activation energies also rises linearly with log M. In the absence of molecular entanglements, Rouse kinetics predicts β=−1, but Cohen–Turnbull–Bueche free-volume effects due to molecular chain ends add a further nonpower-law term, enhancing D increasingly at low M. The combined D vs M theory does, however, closely mimic a power law with the exponents observed at all our measurement temperatures. To obtain this result it is necessary to include in the free-volume term the dependence of the liquid’s density on M and T, analytically modeled based on the incomplete literature data. The fitted density model itself is useful as a guide for the molecular modeling effort. The success of this approach makes it possible to deduce a small intrinsic thermal activation energy contained within the larger, free-volume dominated, apparent values.