Theoretical predictions of diffusion from Brownian motion in superstrong polymers

This paper presents a summary of unique highly nonlinear static and dynamic theories for chain molecules (actually, for almost any kind of organic molecule), including the first superstrong polymers. These theories have been used to predict and explain (1) the physical self-assembly (self-ordering) of specific kinds of molecules into liquid crystalline (LC) phases (i.e., partially ordered phases) and (2) the diffusion of these molecules in various LC phases and the isotropic (I) liquid phase.By acceptance of this article, the publisher recognizes that the U. S. Government retains a nonexclusive, royality-free license to publish or reproduce the published form of this contribution, or to allow others to do so, for U.S. Government purposes.