"Pertechnetate-Induced Addition of Sulfide in Small Olefinic Acids: Formation of [TcO(dimercaptosuccinate)2] 5- and [TcO(mercaptosuccinate)2] 3- Analogues"
Silvia Jurisson, Kimberly Reinig, Rachel Seibert, Daniel Velazquez, Jakob Baumeister, Firouzeh Najafi Khosroshahi, Wei Wycoff, Jeff Terry, John Adams, Carol Deakyne,
Inorganic Chemistry
Vol. 56
2017
13214-13227
Link
Technetium-99 (99Tc) is important to the nuclear
fuel cycle as a long-lived radionuclide produced in ∼6% fission
yield from 235U or 239Pu. In its most common chemical form,
namely, pertechnetate (99TcO4
−), it is environmentally mobile.
In situ hydrogen sulfide reduction of pertechnetate has been proposed
as a potential method to immobilize environmental 99TcO4
−
that has entered the environment. Reactions of 99TcO4
− with
sulfide in solution result in the precipitation of Tc2S7 except when
olefinic acids, specifically fumaric or maleic acid, are present; a
water-soluble 99Tc species forms. NMR (1
H, 13C, and 2D methods)
and X-ray absorption spectroscopy [XAS; near-edge (XANES)
and extended fine structure (EXAFS)] studies indicate that sulfide adds across the olefinic bond to generate mercaptosuccinic
acid (H3MSA) and/or dimercaptosuccinic acid (H4DMSA), which then chelate(s) the 99Tc to form [99TcO(MSA)2]
3−,
[
99TcO(DMSA)2]
5−, or potentially [99TcO(MSA)(DMSA)]4−. 2D NMR methods allowed identification of the products by
comparison to 99Tc and nonradioactive rhenium standards. The rhenium standards allowed further identification by electrospray
ionization mass spectrometry. 99TcO4
− is essential to the reaction because no sulfide addition occurs in its absence, as determined
by NMR. Computational studies were performed to investigate the structures and stabilities of the potential products. Because
olefinic acid is a component of the naturally occurring humic and fulvic acids found in soils and groundwater, the viability of in
situ hydrogen sulfide reduction of environmental 99TcO4
− as an immobilization method is evaluated. |
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