Radiolytic evaluation of a new technetium redox control reagent for advanced used nuclear fuel separations

Anh N Dang; Maya H Rogalski; Corey D Pilgrim; Joseph R Wilbanks; Dean R Peterman; Jesse D Carrie; Peter R Zalupski; Stephen P Mezyk; Gregory P Horne

doi:10.1039/d3cp04987f

Radiolytic evaluation of a new technetium redox control reagent for advanced used nuclear fuel separations

Phys Chem Chem Phys. 2024 Jan 31;26(5):4039-4046. doi: 10.1039/d3cp04987f.

Authors

Anh N Dang¹, Maya H Rogalski¹, Corey D Pilgrim², Joseph R Wilbanks², Dean R Peterman², Jesse D Carrie², Peter R Zalupski², Stephen P Mezyk¹, Gregory P Horne²

Affiliations

¹ Department of Chemistry and Biochemistry, California State University Long Beach, 1250 Bellflower Boulevard, Long Beach California, 90840-9507, USA. stephen.mezyk@csulb.edu.
² Center for Radiation Chemistry Research, Idaho National Laboratory, 1955 N. Freemont Ave., P.O. Box 1625, Idaho Falls, ID, 83415, USA. gregory.holmbeck@inl.gov.

PMID: 38224090
DOI: 10.1039/d3cp04987f

Abstract

Technetium is a problematic radioisotope for used nuclear fuel (UNF) and subsequent waste management owing to its high environmental mobility and coextraction in reprocessing technologies as the pertechnetate anion (TcO₄^-). Consequently, several strategies are under development to control the transport of this radioisotope. A proposed approach is to use diaminoguanidine (DAG) for TcO₄^- and transuranic ion redox control. Although the initial DAG molecule is ultimately consumed in the redox process, its susceptibility to radiolysis is currently unknown under envisioned UNF reprocessing conditions, which is a critical knowledge gap for evaluating its overall suitability for this role. To this end, we report the impacts of steady-state gamma irradiation on the rate of DAG radiolysis in water, aqueous 2.0 M nitric acid (HNO₃), and in a biphasic solvent system composed of aqueous 2.0 M HNO₃ in contact with 1.5 M N,N-di-(2-ethylhexyl)isobutyramide (DEHiBA) dissolved in n-dodecane. Additionally, we report chemical kinetics for the reaction of DAG with key transients arising from electron pulse radiolysis, specifically the hydrated electron (e_aq^-), hydrogen atom (H˙), and hydroxyl (˙OH) and nitrate (NO₃˙) radicals. The DAG molecule exhibited significant reactivity with the ˙OH and NO₃˙ radicals, indicating that oxidation would be the predominant degradation pathway in radiation environments. This is consistent with its role as a reducing agent. Steady-state gamma irradiations demonstrated that DAG is readily degraded within a few hundred kilogray, the rate of which was found to increase upon going from water to HNO₃ containing solutions and solvents systems. This was attributed to a thermal reaction between DAG and the predominant HNO₃ radiolysis product, nitrous acid (HNO₂), k(DAG + HNO₂) = 5480 ± 85 M^-1 s^-1. Although no evidence was found for the radiolysis of DAG altering the radiation chemistry of the contacted DEHiBA/n-dodecane phase in the investigated biphasic system, the utility of DAG as a redox control reagent will likely be limited by significant competition with its degradation by HNO₂.