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Methods for Monitoring a Chloride Volatility Process for Treating Nuclear Materials

机译:监测用于处理核材料的氯化物挥发性过程的方法

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More efficient fuel cycle options are sought for processing nuclear materials, such as spent nuclear fuel, with decreased losses and increased separation efficiencies. Reliable and accurate methods of monitoring and safeguarding materials used in these processes must also be developed. A three-step hydriding-chlorination-volatilization process is reported that was designed to separate impurities from metals while keeping the target bulk material in the solid phase. The bulk material chosen for this preliminary testing was cerium because it is commonly used as a surrogate for actinides and other rare earths. The impurities studied were aluminum, iron, gallium, tantalum, and uranium. The first step uses hydrogen gas between 0 and 300 °C to reduce the particle size of the metal and promote the chemical reaction with anhydrous chlorine gas. It was found that the particle size of the metal was quickly reduced by hydrogen gas from several cm to between 0 and 2,000 um by forming CeH_3 at 100 °C after 12 minutes. The second step results in the formation of porous chloride particles. This step proceeds quickly under flowing Cl_2 by heating first to 250 °C and then to 500 °C with 100% Cl_2. The final step utilizes the different vapor pressures of the chlorides to separate the impurities using chemical vapor transport. In early testing of this process, complete chlorination was prevented by contamination of the metal with dissolved oxygen. When steps were taken to reduce oxygen contamination, chlorination conversion increased up to 97%. The methods used to analyze the materials used in these experiments can also be used to monitor and safeguard materials in an actual process. For example, mass changes in the solid have been shown to indicate the fractional conversion of the metal to chloride based on correlation with conventional chemical analysis methods. Process monitoring signatures were identified that could be identified in real time based on changes in gas pressure, gas temperature, gas flow rate, and sample temperature.
机译:寻求用于处理诸如乏核燃料的核材料的更有效的燃料循环选择,以减少损失并提高分离效率。还必须开发出可靠和准确的方法来监视和保护这些过程中使用的材料。据报道,设计了一个三步氢化-氯化-挥发工艺,用于将杂质从金属中分离出来,同时将目标体材料保持在固相中。选择用于该初步测试的散装材料是铈,因为它通常用作act系元素和其他稀土的替代物。研究的杂质是铝,铁,镓,钽和铀。第一步使用0到300°C之间的氢气来减小金属的粒度并促进与无水氯气的化学反应。发现通过在12分钟后在100°C下形成CeH_3,氢气可以将金属的粒径从几厘米迅速减小到0至2,000 um。第二步骤导致形成多孔氯化物颗粒。通过先加热到250°C,然后再用100%Cl_2加热到500°C,该步骤在流动的Cl_2下快速进行。最后一步利用氯化物的不同蒸气压通过化学蒸气传输来分离杂质。在此过程的早期测试中,由于金属溶解有氧而无法完全氯化。当采取减少氧气污染的措施时,氯化转化率提高了97%。用于分析这些实验中使用的材料的方法也可以用于监视和保护实际过程中的材料。例如,基于与常规化学分析方法的相关性,已显示出固体中的质量变化表明金属向氯化物的分数转化。可以根据气体压力,气体温度,气体流速和样品温度的变化实时识别过程监控签名。

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