4.7 Article

Effect of low concentration of impurity gases on the hydrogen absorption performance of uranium

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 48, 期 58, 页码 22161-22173

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2023.03.082

关键词

Uranium; Hydrogen absorption; Blanketing; Poisoning; Retardation

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The hydrogen absorption properties of depleted uranium in impure hydrogen containing various gases were studied. The behavior of these impurities can be classified into three categories: inert gases that hinder hydrogen diffusion, gases that form nitrides and oxides reducing capacity, and gases that chemically adsorb on the uranium surface inhibiting hydrogen adsorption and dissociation. These conclusions are important for studying mixed gas reactivity with uranium and can be used as a reference for other hydrogen storage systems.
The performance of uranium as a hydrogen storage material has attracted much attention. Herein, the hydrogen absorption properties of depleted uranium in impure hydrogen containing He, Ar, CH4, N-2, CO, CO2 and O-2 were studied by PVT method and XPS analysis. When these impurity gases were mixed in H-2 at low concentrations (0.1%similar to 1.5%), their behavior can be classified into three categories. The He, CH4 and Ar were chemically inert to the activated uranium powder under room condition. These three gases inhibited the absorption kinetics during the whole stage by hindering the diffusion of H-2 molecules, showing a blanketing effect. The N-2 and O-2 did not affect the absorption kinetics but reduced the capacity by forming nitrides and oxides. The poisoning effect of N-2 was weaker than that of O-2. The CO and CO2 not only affected the hydrogen absorption capacity, but also strongly inhibited the absorption kinetics. These two gases are chemically adsorbed on the uranium surface to form passivation layers, thus inhibiting the adsorption and dissociation of H-2 molecules and the diffusion of H atoms. The poisoning and retardation effect of CO2 were much stronger than that of CO. The above conclusions are important to further study the reactivity of mixed gas with uranium, and can also be used as a reference for other hydrogen storage systems. (c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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