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An empirical equation relating electrophoretic mobility and ionic strength was proposed. The equation includes a number of parameters that are found using the mobilities of reference ions: two coefficients in the numerator describing the linear relationship of the multiplier in front of the square root of the ionic strength with the product of the ion mobility in the background electrolyte (BGE) without additives by the modulus of the charge number, raised to a certain power, and also the multiplier in the denominator before the square root of the ionic strength. The proposed equation was tested using the mobilities measured in BGEs with the addition of sodium chloride to adjust ionic strength and sulfated β-cyclodextrin (S-β-CD) for 11 anions with charge numbers from -1 to -4.

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In this study, novel anion photo-responsive supramolecular hydrogels based on cysteine-silver sol (CSS) and iodate anions (IO) were prepared. The peculiarities of the self-assembly process of gel formation in the dark and under visible-light exposure were studied using a complex of modern physico-chemical methods of analysis, including viscosimetry, UV spectroscopy, dynamic light scattering, electrophoretic light scattering, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. In the dark phase, the formation of weak snot-like gels takes place in a quite narrow IO ion concentration range.

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The present work reports on the preparation, characterization, and evaluation of a set of novel triphenyl-modified silica-based stationary phases without and with embedded ion-exchange sites for mixed-mode liquid chromatography. The three synthesized triphenyl phases differed in additionally incorporated ion-exchange sites. In one embodiment, allyltriphenylsilane was bonded to thiol-modified silica by thiol-ene click reaction, leading to particles with no ion-exchange sites.

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Quantification of vehicular uncorrelated Li-solvent transport in highly concentrated electrolytes solvent-related Onsager coefficients.

Phys Chem Chem Phys

December 2024

Department of Chemistry and Center for Materials Science (WZMW), University of Marburg, Hans-Meerwein-Straße 4, 35032 Marburg, Germany.

Highly concentrated salt solutions are promising electrolytes for battery applications due to their low flammability, their high thermal stability, and their good compatibility with electrode materials. Understanding transport processes in highly concentrated electrolytes is a challenging task, since strong ion-ion and ion-solvent interactions lead to highly correlated movements on the microscopic scale. Here, we use an experimental overdetermination method to obtain accurate Onsager transport coefficients for concentrated binary electrolytes composed of either sulfolane (SL) or dimethyl carbonate (DMC) as solvent and either LiTFSI or LiFSI as salt.

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