| Title | Reduction of Pertechnetate by Acetohydroxamic Acid: Formation of [Tc(II)(NO)(AHA)2(H2O)](+) and Implications for the UREX Process. | | Author(s) | Gong CM, Lukens WW, Poineau F, Czerwinski KR | | Institution | Harry Reid Center for Environmental Studies, Nuclear Science and Technology Division, University of Nevada, Las Vegas, Las Vegas, Nevada 89154-4009, and Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720-8175 czerwin2@unlv.nevada.edu. | | Source | Inorg Chem 2008 Jul 2. | | Abstract | Reductive nitrosylation and complexation of ammonium pertechnetate by acetohydroxamic acid has been achieved in aqueous nitric and perchloric acid solutions. The kinetics of the reaction depend on the relative concentrations of the reaction components and are accelerated at higher temperatures. The reaction does not occur unless conditions are acidic. Analysis of the X-ray absorption fine structure spectroscopic data is consistent with a pseudo-octahedral geometry and the linear Tc-N-O bond typical of technetium nitrosyl compounds, and electron spin resonance spectroscopy is consistent with a d (5) Tc(II) nitrosyl complex. The nitrosyl source is generally AHA, but it may be augmented by some products of the reaction with nitric acid. The resulting low-valency trans-aquonitrosyl(diacetohydroxamic)-technetium(II) complex ([Tc (II)(NO)(AHA) 2H 2O] (+), 1) is highly soluble in water, extremely hydrophilic, and is not extracted by tri- n-butylphosphate in a dodecane diluent. Its extraction properties are not pH-dependent: potentiometric-spectrophotometric titration studies indicate a single species from pH 4 down to -0.6 (calculated). This molecule is resistant to oxidation by H 2O 2, even at high pH, and can undergo substitution to form other technetium nitrosyl complexes. The potential formation of 1 during reprocessing may strongly impact the fate of technetium in the nuclear fuel cycle. | | Language | ENG | | Pub Type(s) | JOURNAL ARTICLE
| | PubMed ID | 18597420 |
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