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Probing ion-specific effects on aqueous acetate solutions: Ion pairing versus water structure modifications

The effect of monovalent cations (Li(+), K(+), NH(4)(+), Na(+)) on the water structure in aqueous chloride and acetate solutions was characterized by oxygen K-edge X-ray absorption spectroscopy (XAS), X-ray emission spectroscopy, and resonant inelastic X-ray scattering (RIXS) of a liquid microjet. W...

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Detalles Bibliográficos
Autores principales: Petit, Tristan, Lange, Kathrin M., Conrad, Gerrit, Yamamoto, Kenji, Schwanke, Christoph, Hodeck, Kai F., Dantz, Marcus, Brandenburg, Tim, Suljoti, Edlira, Aziz, Emad F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Crystallographic Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711606/
https://www.ncbi.nlm.nih.gov/pubmed/26798780
http://dx.doi.org/10.1063/1.4884600
Descripción
Sumario:The effect of monovalent cations (Li(+), K(+), NH(4)(+), Na(+)) on the water structure in aqueous chloride and acetate solutions was characterized by oxygen K-edge X-ray absorption spectroscopy (XAS), X-ray emission spectroscopy, and resonant inelastic X-ray scattering (RIXS) of a liquid microjet. We show ion- and counterion dependent effects on the emission spectra of the oxygen K-edge, which we attribute to modifications of the hydrogen bond network of water. For acetates, ion pairing with carboxylates was also probed selectively by XAS and RIXS. We correlate our experimental results to speciation data and to the salting-out properties of the cations.