Deciphering the guanidinium cation: Insights into thermal diffusion.

Thermophoresis, or thermodiffusion, is becoming a more popular method for investigating the interactions between proteins and ligands due to its high sensitivity to the interactions between solutes and water. Despite its growing use, the intricate mechanisms behind thermodiffusion remain unclear. This gap in knowledge stems from the complexities of thermodiffusion in solvents that have specific interactions as well as the intricate nature of systems that include many components with both non-ionic and ionic groups.

Overlapping hydration shells in salt solutions causing non-monotonic Soret coefficients with varying concentration.

We investigate the thermodiffusive properties of aqueous solutions of sodium iodide, potassium iodide and lithium iodide, using thermal diffusion forced Rayleigh scattering in a concentration range of 0.5-4 mol kg of solvent, large enough to deal with associated salts, and a temperature range of 15 to 45 °C. All systems exhibit non-monotonic variations of the Soret coefficient with concentration, with a minimum at one mol kg of solvent in all three cases.

Peptide model systems: Correlation between thermophilicity and hydrophilicity.

In recent years, the response of biomolecules to a temperature gradient has been utilized to monitor reactions of biomolecules, but the underlying mechanism is not well understood due to the complexity of the multicomponent system. To identify some underlying principles, we investigate the thermal diffusion of small amide molecules in water systematically. We re-analyze previous measurements of urea and formamide and compare the results with acetamide, N-methylformamide, and N,N-dimethylformamide, amides with a lower hydrophilicity.

Shear-banding in entangled xanthan solutions: tunable transition from sharp to broad shear-band interfaces.

We report on the smooth transition between gradient-banded velocity profiles with a sharp interface and curved velocity profiles, both resulting from strong shear-thinning dispersions of concentrated xanthan (a highly charged poly-saccharide). Pronounced shear-banded flow, where two extended shear-bands are separated by a relatively sharp interface, is observed in a limited range of shear rates, at very low ionic strength and at a high concentration, using heterodyne light scattering to measure spatially resolved velocity profiles. The width of the interface between the coexisting shear-bands broadens to span a sizable fraction of the gap of the shear cell, either by changing the shear rate, by lowering the concentration, or by increasing the ionic strength.

Publisher's Note: Effect of the salt-induced micellar microstructure on the nonlinear shear flow behavior of ionic cetylpyridinium chloride surfactant solutions [Phys. Rev. E 95, 032603 (2017)].

This corrects the article DOI: 10.1103/PhysRevE.95.