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首页> 外文期刊>Journal of Nuclear Materials: Materials Aspects of Fission and Fusion >Long-term alteration mechanisms in water for SON68 radioactive borosilicate glass
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Long-term alteration mechanisms in water for SON68 radioactive borosilicate glass

机译:SON68放射性硼硅酸盐玻璃在水中的长期变化机理

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Experimental results obtained with high-level radioactive glass specimens typically containing 10(9) to 10(10) Bq g(-1) of beta gamma -emitters confirm the behavior observed on simulated non-radioactive glass, Most of the current knowledge of the alteration mechanisms of nuclear glass in water and the kinetic laws of glass alteration developed to model their longterm behavior is based on studies of inactive material. No difference was found between the initial alteration rates measured on active and inactive glass specimens, nor in the long-term alteration rates at advanced stages of reaction progress (typically three or four orders of magnitude lower than the initial rates). At high reaction progress under conditions with very low solution renewal. however. the time necessary for the highly radioactive specimens to reach the low final rate is longer than for the non-radioactive glass. This behavior would suggest that the alteration films are slightly less protective under high beta gamma dose rates (> 100 rad h(-1)). The alteration layer has strong retention capacities for the actinides. The key processes, and the corresponding retention models, are highlighted. (C) 2001 Elsevier Science B.V. All rights reserved. [References: 29]
机译:使用通常包含10(9)至10(10)Bq g(-1)Bγ发射体的高水平放射性玻璃样品获得的实验结果证实了在模拟非放射性玻璃上观察到的行为。水中核玻璃的化学变化机理以及为模拟玻璃的长期行为而建立的玻璃化学动力学规律是基于对非活性物质的研究。在活性和非活性玻璃样品上测得的初始变化率之间没有发现差异,在反应进展的晚期阶段也没有发现长期变化率(通常比初始变化率低三个或四个数量级)。在溶液更新非常低的条件下,以较高的反应进度进行。然而。高放射性样品达到低最终率所需的时间比非放射性玻璃更长。此行为表明,在高βγ剂量率(> 100 rad h(-1))下,涂膜的保护性稍差。蚀变层对the系元素具有强的保留能力。重点过程和相应的保留模型将突出显示。 (C)2001 Elsevier Science B.V.保留所有权利。 [参考:29]

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