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Generation and Control of Electrohydrodynamic Flows in Aqueous Electrolyte Solutions
Published on: September 7, 2018
Hydration and ion association of La3+ and Eu3+ salts in aqueous solution
Sergej Friesen1, Sebastian Krickl, Magdalena Luger
1Institute of Physical and Theoretical Chemistry, University of Regensburg, 93040 Regensburg, Germany. richard.buchner@chemie.uni-regensburg.de.
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, , calculated from the stepwise IP formation constants were consistent with literature values.
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