Plutonium Redox Transformation in the Presence of Iron, Organic Matter, and Hydroxyl Radicals: Kinetics and Mechanistic Insights.

Chao Pan, Yongqin Jiao, Annie B Kersting, Mavrik Zavarin

Environmental science & technology 2021 Feb 02

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Plutonium (Pu) redox and complexation processes in the presence of natural organic matter and associated iron can impact the fate and transport of Pu in the environment. We studied the fate of Pu(IV) in the presence of humic acid (HA) and Fe(II) upon reaction with H2O2 that may be generated by photochemical and other reactions. A portion of Pu(IV) was oxidized to Pu(V/VI), which is primarily ascribed to the generation of reactive intermediates from the oxidation of Fe(II) and Fe(II)-HA complexes by H2O2. The kinetics of Pu(IV) oxidation is pH-dependent and can be described by a model that incorporates Pu redox kinetics with published HA-modified Fenton reaction kinetics. At pH 3.5, the presence of HA slowed Pu(IV) oxidation, while at pH 6, HA accelerated Pu(IV) oxidation in the first several hours followed by a reverse process where the oxidized Pu(V/VI) was reduced back to Pu(IV). Analysis of Pu-associated particle size suggests that Pu oxidation state is a major driver in its complexation with HA and formation of colloids and heteroaggregates. Our results revealed the H2O2-driven oxidation of Pu(IV)-HA-Fe(II) colloids with implications to the transient mobilization of Pu(V/VI) in organic-rich redox transition zones.

Citation

Chao Pan, Yongqin Jiao, Annie B Kersting, Mavrik Zavarin. Plutonium Redox Transformation in the Presence of Iron, Organic Matter, and Hydroxyl Radicals: Kinetics and Mechanistic Insights. Environmental science & technology. 2021 Feb 02;55(3):1800-1810