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首页> 外文期刊>Journal of Nuclear Materials: Materials Aspects of Fission and Fusion >Kinetics of dissolution of UO 2 in nitric acid solutions: A?multiparametric study of the non-catalysed reaction
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Kinetics of dissolution of UO 2 in nitric acid solutions: A?multiparametric study of the non-catalysed reaction

机译:UO溶解动力学 2 在硝酸溶液中:a?多丙基对非催化反应的研究

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AbstractUO2pellets were prepared by densification of oxides obtained from the conversion of the oxalate precursor. Then characterized in order to perform a multiparametric study of the dissolution in nitric acid medium. In this frame, for each sample, the densification rate, the grain size and the specific surface area of the prepared pellets were determined prior to the final dissolution experiments. By varying the concentration of the nitric acid solution and temperature, three different and successive steps were identified during the dissolution. Under the less aggressive conditions considered, a first transient step corresponding to the dissolution of the most reactive phases was observed at the solid/solution interface. Then, for all the tested conditions, a steady state step was established during which the normalised dissolution rate was found to be constant. It was followed by a third step characterized by a strong and continuous increase of the normalised dissolution rate. The duration of the steady state, also called “induction period”, was found to vary drastically as a function of the HNO3concentration and temperature. However, independently of the conditions, this steady state step stopped at almost similar dissolved material weight loss and dissolved uranium concentration. During the induction period, no important evolution of the topology of the solid/liquid interface was evidenced authorizing the use of the starting reactive specific surface area to evaluate the normalised dissolution rates thus the chemical durability of the sintered pellets. From the multiparametric study of UO
机译:<![CDATA [ 抽象 UO 2 颗粒通过致密化准备从草酸盐前体的转化率获得的氧化物。然后表征以进行硝酸培养基中溶解的多级测定研究。在该框架中,对于每个样品,在最终溶解实验之前测定制备颗粒的致密化率,粒度和比表面积。通过改变硝酸溶液和温度的浓度,在溶解期间鉴定了三种不同和连续的步骤。在考虑的侵略性条件下,在固体/溶液界面中观察到对应于最活性相溶解的第一瞬态步骤。然后,对于所有测试条件,建立了稳态步骤,在此期间发现标准化的溶解速率是恒定的。之后是第三步,其特征在于标准化溶解速率的强烈和连续增加。发现稳定状态的持续时间也称为“诱导时段”,作为HNO 3 浓度和温度的函数剧烈地变化。然而,独立于条件,这种稳态步骤在几乎相似的溶解材料体重减轻和溶解铀浓缩中停止。在诱导期间,证明了固体/液体界面拓扑的重要演变是授权使用起始反应性比表面积来评估烧结粒料的归一化溶解速率。来自UO

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    Institut de Chimie Séparative de Marcoule ICSM UMR 5257 CNRS CEA Univ. Montpellier ENSCM;

    Institut de Chimie Séparative de Marcoule ICSM UMR 5257 CNRS CEA Univ. Montpellier ENSCM;

    Institut de Chimie Séparative de Marcoule ICSM UMR 5257 CNRS CEA Univ. Montpellier ENSCM;

    Institut de Chimie Séparative de Marcoule ICSM UMR 5257 CNRS CEA Univ. Montpellier ENSCM;

    Institut de Chimie Séparative de Marcoule ICSM UMR 5257 CNRS CEA Univ. Montpellier ENSCM;

    AREVA NC;

    Institut de Chimie Séparative de Marcoule ICSM UMR 5257 CNRS CEA Univ. Montpellier ENSCM;

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  • 正文语种 eng
  • 中图分类 原子能技术;
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