In this work, we have studied the reaction between H 2 O 2 and UO 2 with particular focus on the nature of the hydroxyl radical formed as an intermediate. Experiments were performed to study the kinetics of H 2 O 2 consumption and uranium dissolution at different initial H 2 O 2 concentrations. The results show that the consumption rates at a given H 2 O 2 concentration are different depending on the initial H 2 O 2 concentration. This is attributed to an alteration of the reactive interface, likely caused by blocking of surface sites by oxidized U/surface-bound hydroxyl radicals. The dissolution yield given by the amount of dissolved uranium divided by the amount of consumed hydrogen peroxide was used to compare the different cases. For all initial H 2 O 2 concentrations, the dissolution yield increases with reaction time. The final dissolution yield decreases with increasing initial H 2 O 2 concentration. This is expected from the mechanism of catalytic decomposition of H 2 O 2 on oxide surfaces. As the experiments were performed in solutions containing 10 mM HCO − 3 and a strong concentration dependence was observed in the 0.2-2.0 mM H 2 O 2 concentration range, we conclude that the intermediate hydroxyl radical is surface bound rather than free.
Hydrogen production by g-radiolysis of the mixture of mordenite, a zeolite mineral, and seawater was studied in order to provide basic points of view for the influences of zeolite minerals, of the salts in seawater, and of rise in temperature on the hydrogen production by the radiolysis of water. These influences are required to be considered in the evaluation of the hydrogen production from residual water in the waste zeolite adsorbents generated in Fukushima Dai-ichi Nuclear Power Station. As the influence of the mordenite, an additional production of hydrogen besides the hydrogen production by the radiolysis of water was observed. The additional hydrogen can be interpreted as the hydrogen production induced by the absorbed energy of the mordenite at the yield of 2.3610 78 mol/J. The influence of the salts was observed as increase of the hydrogen production. The influence of the salts can be attributed to the reactions of bromide and chloride ions inhibiting the reaction of hydrogen with hydroxyl radical. The influence of the rise in temperature was not significantly observed up to 608C in the mixture with seawater. The results show that the additional production of hydrogen due to the mordenite had little temperature dependence.
Radiation-induced oxidative dissolution of uranium dioxide (UO2) is one of the most important chemical processes of U driven by redox reactions. We have examined the effect of UO2 stoichiometry on the oxidative dissolution of UO2 in aqueous sodium bicarbonate solution induced by hydrogen peroxide (H2O2) and γ-ray irradiation. By comparing the reaction kinetics of H2O2 between stoichiometric UO2.0 and hyper-stoichiometric UO2.3, we observed a significant difference in reaction speed and U dissolution kinetics. The stoichiometric UO2.0 reacted with H2O2 much faster than the hyper-stoichiometric UO2.3. The U dissolution from UO2.0 was initially much lower than that from UO2.3 but gradually increased as the oxidation by H2O2 proceeded. Increase in the initial H2O2 concentration caused decrease in the U dissolution yield with respect to the H2O2 consumption both for UO2.0 and UO2.3. This decrease in the U dissolution yield is attributed to the catalytic decomposition of H2O2 on the surface of UO2. The γ-ray irradiation induced the U dissolution that is analogous to the kinetics by the exposure to a low concentration (2 × 10–4 mol dm–3) of H2O2. The exposure to higher H2O2 concentrations caused lower U dissolution and resulted in deviation from the U dissolution behavior by γ-ray irradiation.
The absorption spectra of Br(2)(•-) and Br(3)(-) in aqueous solutions are investigated by pulse radiolysis techniques from room temperature to 380 and 350 °C, respectively. Br(2)(•-) can be observed even in supercritical conditions, showing that this species could be used as a probe in pulse radiolysis at high temperature and even under supercritical conditions. The weak temperature effect on the absorption spectra of Br(2)(•-) and Br(3)(-) is because, in these two systems, the transition occurs between two valence states; for example, for Br(2)(-) we have (2)Σ(u) → (2)Σ(g) transition. These valence transitions involve no diffuse final state. However, the absorption band of Br(-) undergoes an important red shift to longer wavelengths. We performed classical dynamics of hydrated Br(-) system at 20 and 300 °C under pressure of 25 MPa. The radial distribution functions (rdf's) show that the strong temperature increase (from 20 to 300 °C) does not change the radius of the solvent first shell. On the other hand, it shifts dramatically (by 1 Å) the second maximum of the Br-O rdf and introduces much disorder. This shows that the first water shell is strongly bound to the anion whatever the temperature. The first two water shells form a cavity of a roughly spherical shape around the anion. By TDDFT method, we calculated the absorption spectra of hydrated Br(-) at two temperatures and we compared the results with the experimental data.
The radiation stability of the candidate An(III)/Ln(III) separation ligand hexa-n-octylnitrilo-triacetamide (HONTA) under envisioned process conditions was investigated using a combination of solvent test loop gamma and pulsed electron irradiation.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.