 |
Ph.D., 2006 Université d'Orsay - Paris XI & Commissariat à l'Energie Atomique (CEA-Saclay), Orsay, France
SES 2456
Phone (312) 413-8271
smekki@uic.edu
Study of uranium-silicate formation kinetics in low temperature aqueous solution.
In the plutonium-production facilities at the U.S. Department of Energy's
Hanford Site, radioactive liquid byproducts were stored in large buried
tanks, constructed in clusters, or 'tank farms.' One of the tank farms was
constructed in 1946 specifically to store and separate solid waste sludges
and liquids. While transferring sludges tank-to-tank in 1951, an
inter-tank pipeline ruptured, and about 350,000 L of waste were released
to the ground, including more than 7000 kg of uranium in alkaline media
(also containing sodium carbonate, nitrate, phosphate, and sulfate).
Beneath the tank farm, a groundwater contaminant plume, 250 m wide and 900
m long, has been shown by uranium isotopic analysis to originate from the
1951 leak. As a radiochemist, I am currently taking part in a research
project with Pr. Kathryn Nagy and Pr. Neil Sturchio, to synthesize and
characterize the different uranium species that may form in the presence
of minerals (feldspar and quartz) and groundwater simulating the vadose
zone chemical conditions of the Hanford Site. We are collaborating with
Lynda Soderholm of the Chemistry Division at Argonne National Laboratory
to obtain insight at the molecular scale of the local structural
environment of uranium species (3-8 Å) using X-ray scattering and
spectroscopic methods (High Energy X-ray Scattering (HEXS), EXAFS
spectroscopy). We hope to construct a complete description of the
formation, structure, and chemical influences on the existence of
different U species observed in the Hanford subsurface.
My previous work is related to the characterization of luminescent heavy
metals (europium and uranium) complexes in novel solvents, Room
Temperature Ionic Liquids (RTILs, which are inflammable, nonvolatile, and
recyclable), potentially usable to replace traditional organic solvents
(volatile, polluting, and flammable). The main goal was to understand
fundamental solvation processes of the luminescent probes and then design
a new extraction path of the heavy metals as a possible replacement for
traditional nuclear fuel reprocessing (involving hazardous volatile
organic compounds). A biphasic extraction system using 'green solvents' -
Supercritical carbon dioxide and RTILs - in conjunction was investigated
and showed quantitative extraction efficiencies (> 95 %) of CO2-philic
ligands/metal complexes. |