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The Ion Pairing and Hydration Structure of Ni2+ in Supercritical Water at 425°C Determined by X-Ray Absorption Fine Structure and Molecular Dynamics Studies
SL Wallen, BJ Palmer, and JL Fulton. J. Chemical Physics, 108(10):4039-4046 (1998).
Abstract: The ion pairing structure of Ni(Br)2
solutions (0.2 and 0.4 molal) under supercritical conditions was
determined using x-ray absorption fine structure (XAFS) spectroscopy.
These first measurements of the average bulk structure show that
approximately one Br- counterion is associated with each
Ni2+. The Ni2+ -to-Br- distance
of 2.40 Å is very accurately determined and the strength of this
interaction, as indicated by the Debye-Waller factor (s2=0.009 Å2),
shows that the bromine anion is very tightly bound to the niobium
cation under these supercritical conditions. In addition to the
onset of ion pairing interactions, there is also a dramatic transition
in the hydration structure. Results show a loss of about 50% of
the waters in the first shell upon going from ambient to a hydrothermal
condition of 425°C and 690 bar. Finally, we use molecular dynamics
simulations with refined intermolecular potentials to directly calculate
XAFS spectra that are shown to quantitatively reproduce the experimental
results for the ion pair and hydration structure.
For information about supercritical fluid capabilities at PNNL, please contact Clement Yonker, at (509) 372-4748, clem.yonker@pnl.gov.
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