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Eliot Fried

Publications and source records attributed to Eliot Fried.

3 recordsLinked to original sources

Theory for solvent, momentum, and energy transfer between a surfactant solution and a vapor atmosphere.

We develop a complete set of equations governing the evolution of a sharp interface separating a volatile-solvent/nonvolatile-surfactant solution from a vapor atmosphere. In addition to a sorption isotherm equation and the conventional balances for mass, linear momentum, and energy, these equations include an alternative to the Hertz-Knudsen-Langmuir equation familiar from conventional theories of evaporation and condensation. This additional equation arises from a consideration of configurational forces within a thermodynamical framework. While the notion of configurational forces is well developed and understood for the description of materials that, like crystalline solids, possess natural reference configurations, very little has been done regarding their role in materials, such as viscous fluids, that do not possess preferred reference states. We therefore provide comprehensive developments of configurational forces, the balance of configurational momentum, and configurational thermodynamics. Our treatment does not require a choice of reference configuration. The general evolution equations arising from our theory account for the thermodynamic structure of the solution and the interface and for sources of dissipation related to the transport of surfactant, momentum, and heat in the solution and within the interface along with the transport of solute, momentum, kinetic energy, and heat across the interface. Moreover, the equations account for the Soret and Dufour effects in the solution and on the interface and for observed discontinuities of the temperature and chemical potential across the interface. Due to the complexity of these equations, we provide approximate equations which we compare to equations preexistent in the literature.

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Incompatible strains associated with defects in nematic elastomers.

In a nematic elastomer the deformation of the polymer network chains is coupled to the orientational order of the mesogenic groups. Statistical arguments have derived the so-called neoclassical free energy that models this coupling. Here we show that the neoclassical model supplemented by the usual Frank energy predicts incompatible network strains associated with the formation of standard nematic textures. The incompatibility is measured by the Riemann curvature tensor, which we find to be nonzero for both radial hedgehog defects and escaped disclinations of strength +1 in circular cylinders. Analogous problems for conventional nonlinearly elastic solids do not possess solutions with such incompatibilities. Compatibility in nematic elastomers would require either more complicated nematic textures in elastomers than in conventional (polymeric and low molecular weight) liquid crystals or a free-energy density more complicated than the neoclassical expression.

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Orientational order and finite strain in nematic elastomers.

Nematic elastomers exhibit large, spontaneous shape changes at the transition from the high-temperature isotropic phase to the low-temperature nematic phase. These finite deformations are studied here in the context of a nonlinear, properly invariant, variational theory that couples the orientational order and elastic deformation. The theory is based on the minimization of a free-energy functional that consists of two contributions: a nematic one due to the interaction of the mesogenic units and an elastic one arising from the stretching of the cross-linked polymer chains. Suitable choices for these two contributions allow for large, reversible, spontaneous shape changes in which the elastic deformation can affect the isotropic-nematic transition temperature. The change in transition temperature as well as the magnitude of the resulting spontaneous deformation is illustrated for various parameter values. The theory includes soft elasticity as a special case but is not restricted to it.

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