4.3 Article

Mass effects for thermodiffusion in dilute aqueous solutions

期刊

EUROPEAN PHYSICAL JOURNAL E
卷 45, 期 4, 页码 -

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SPRINGER
DOI: 10.1140/epje/s10189-022-00193-3

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资金

  1. European Research Council under the European Union [757111]
  2. Initiative d'Excellence program from the French State (Grant DYNAMO) [ANR11-LABX-0011-01]
  3. European Research Council (ERC) [757111] Funding Source: European Research Council (ERC)

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Thermodiffusion is a phenomenon where molecules in a mixture exhibit concentration gradients under a temperature gradient. Research suggests that the difference in masses between mixture components affects the Soret coefficient significantly, and adjusting the mass of solute and solvent can change the solution from thermophobic to thermophilic.
Thermodiffusion is the phenomenon by which molecules in a mixture present concentration gradients in response to an imposed temperature gradient. Despite decades of investigations, this effect remains poorly understood at a molecular level. A common, phenomenological approach is to individuate the molecular factors that influence the Soret coefficient, the parameter that quantifies the resulting concentration-gradient. Experimental studies, often performed on organic mixtures, as well as simulations of model particle systems have evidenced that the difference in masses between the mixture components has an important effect on the amplitude of the Soret coefficient. Here, we use molecular dynamics simulations of a thermophoretic setting to investigate the mass dependence of the Soret coefficient in dilute aqueous solutions. An advantage of simulation approaches is that they are not limited in the range of explored molecular masses, which is often limited to isotopic substitutions in the experiments. Our simulations reveal that the mass dependence of the Soret coefficient in these solutions is in agreement with previous experimental and simulation work on molecular-size systems. In particular, it is sensitive to the relative mass difference between the solute and the solvent, but not to their absolute mass. Adjusting the mass of the solvent and of the solute can turn a thermophobic solution into a thermophilic one, where solute accumulation is reversed. This demonstrates that the mass effect can indeed compensate for the other contributions to the Soret coefficient. Finally, we find that changing the molecular moments of inertia has a much more limited impact as compared to a change in the total molecular mass.

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