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Hydration and ion association of La3+ and Eu3+ salts in aqueous solution

Friesen, S., Krickl, S., Luger, M., Nazet, A., Hefter, G. and Buchner, R. (2018) Hydration and ion association of La3+ and Eu3+ salts in aqueous solution. Physical Chemistry Chemical Physics, 20 (13). pp. 8812-8821.

Link to Published Version: https://doi.org/10.1039/c8cp00248g
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Abstract

Aqueous solutions of five lanthanide salts: LaCl3, La(NO3)3, La2(SO4)3, Eu(NO3)3 and Eu2(SO4)3 have been studied at 25 °C by dielectric relaxation spectroscopy over the frequency range 0.05 ≤ ν/GHz ≤ 89. Detailed analysis of the solvent-related modes located at higher frequencies showed that both La3+ and Eu3+ are strongly hydrated, even including partial formation of a third hydration shell similar to that of Al3+(aq). Up to two solute-related modes could be detected at lower frequencies, due to the formation of various types of 1 : 1 ion pairs (IPs). All five salts showed modest levels of association in the order Cl− < NO3− ≪ SO42−, mostly in the form of double-solvent-separated IPs with small amounts of solvent-shared IPs. Overall association constants, Image ID:c8cp00248g-t1.gif, calculated from the stepwise IP formation constants were consistent with literature values.

Publication Type: Journal Article
Murdoch Affiliation: School of Engineering and Information Technology
Publisher: Royal Society of Chemistry
Copyright: © 2018 Royal Society of Chemistry
URI: http://researchrepository.murdoch.edu.au/id/eprint/40742
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