We have investigated the influence of the chain length and the size of the Kuhn segment on the thermal diffusion coefficient D T of dilute solutions of polymers in organic solvents. For oligomers and short polymer chains, D T increases with molar mass M and reaches a molar mass independent constant plateau value. A similar increase and plateau is observed for high polymers with increasing chain stiffness. For chains with Kuhn segments above 1 kg/mol, the plateau value is independent of the polymer and inversely proportional to the solvent viscosity. The thermal diffusion coefficient of such a polymer can be estimated to be D T ≈ 0.6 × 10 −14 Pa m 2 K −1 × η −1 . No simple relation holds for short chains and flexible high polymers.
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Stadelmaier et al. (2009) studied this question.
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