dc.contributor.author |
Anderson, J. |
|
dc.contributor.author |
Jayanetti, J. K. D. S. |
|
dc.contributor.author |
Mayanovic, Robert A. |
|
dc.contributor.author |
Bassett, William A. |
|
dc.contributor.author |
Chou, I-Ming |
|
dc.date.accessioned |
2011-10-05T09:11:08Z |
|
dc.date.available |
2011-10-05T09:11:08Z |
|
dc.date.issued |
2002 |
|
dc.identifier.citation |
American Mineralogist, Volume 87, pages 262–268, 2002 |
en_US |
dc.identifier.uri |
http://archive.cmb.ac.lk:8080/xmlui/handle/70130/225 |
|
dc.description.abstract |
The first direct measurements are reported for the structure of the hydrated La3+ ion in an aqueous
solution (containing 0.007 m La) over a range of temperatures from 25 to 300 ∞C and pressures up to
1600 bars. The radial distribution of atoms around the La3+ ion was measured using the X-ray absorption
fine structure (XAFS) technique. La L3-edge spectra were collected in the fluorescence
mode from nitrate solutions in a modified hydrothermal diamond anvil cell using the PNC-CAT Xray
microprobe at the Advanced Photon Source, Argonne National Laboratory. Analysis of the XAFS
spectra collected at all temperatures indicates that each La3+ ion has a hydration number of nine and
that the solvating waters surround the ion in a tricapped trigonal prismatic arrangement. As temperature
is increased from 25 to 300 ∞C, the bond distance between the equatorial-plane O atoms and the
La3+ ion increases from 2.59 ± 0.02 to 2.79 ± 0.04 Å, whereas the bond distance between La3+ and the
O atoms at the ends of the prism decrease to 2.48 ± 0.03 Å. This study also demonstrates the unique
capability of the modified hydrothermal diamond anvil cell for in situ low energy X-ray spectroscopic
analysis of elements in dilute aqueous solutions at elevated temperatures and pressures. |
en_US |
dc.language.iso |
en |
en_US |
dc.title |
X-ray spectroscopic investigations of fluids in the hydrothermal diamond anvil cell: The hydration structure of aqueous La3+ up to 300 ∞C and 1600 bars |
en_US |
dc.type |
Research abstract |
en_US |