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Thermal desorption gas chromatography and positron annihilation spectroscopy contribution to alpha decay studies in actinide-doped matrices

机译:热解吸气相色谱和正电子an没光谱对act系元素掺杂基质中α衰变研究的贡献

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A thermal desorption system coupled with a gas analyzer has been adapted and nuclearized to investigate He behavior in actinide-doped samples used to simulate alpha decay aging. This technique widely used in standard laboratories allows measurements of the helium balance and reduced diffusion coefficients, and a preliminary evaluation of helium locations (related to defects and thermal annealing). In our system implemented in a hot cell, small samples are annealed at up to 1100° in controlled atmosphere. They are inserted in a 10 to 20 cm3 vessel connected to a micro gas chromatography detector. Initial system calibration allowed concentration measurements within about 10%. Comparisons with the CNRS/CRPG rare gas analysis laboratory at Nancy, France, were applied on natural uranium oxides originating from Oklo (Gabon) and Mistamisk (Canada). The latest results obtained on Mistamisk samples are in good agreement, with a maximum relative deviation of 14%. The data were used to determine the activation energy of about 1 eV·at−1. On (U,Pu)O2 and PuO2 samples the experiments highlight the impact of defects (up to 100 dpa) on He mobility. The defect population must now be characterized to improve our knowledge of He/defect interactions and mechanisms. In addition and synergy to the macroscopic release measurements by gas chromatography, positron annihilation spectroscopy, an effective nondestructive technique for vacancy defect investigation, was also developed and nuclearized in our hot cell laboratory as part of a project supported by the NOMADE and MATINEX research groups. Specific protocols for doped sample analysis were also developed and validated with UO2 and (U,Pu)O2 samples.
机译:一个热解吸系统与一个气体分析仪相结合,已经过改装和核化,以研究investigate元素掺杂样品中的He行为,以模拟α衰变老化。在标准实验室中广泛使用的这项技术可以测量氦气平衡并降低扩散系数,并可以初步评估氦气位置(与缺陷和热退火有关)。在我们在热室中实施的系统中,小样品在受控气氛中以1100°C退火。将它们插入连接到微型气相色谱检测器的10至20 cm 3 容器中。初始系统校准允许浓度测量在约10%以内。与法国Nancy的CNRS / CRPG稀有气体分析实验室进行了比较,对源自Oklo(加蓬)和Mistamisk(加拿大)的天然铀氧化物进行了分析。在米斯塔米斯克样品上获得的最新结果非常吻合,最大相对偏差为14%。数据用于确定大约1 eV·at -1 的活化能。在(U,Pu)O 2 和PuO 2 样品上,实验强调了缺陷(最大100 dpa)对He迁移率的影响。现在必须对缺陷种群进行表征,以提高我们对He /缺陷相互作用和机制的认识。作为由NOMADE和MATINEX研究小组支持的项目的一部分,我们的热室实验室还开发并利用了气相色谱仪,正电子an没光谱技术(一种用于空缺缺陷调查的有效无损技术)对宏观释放进行测量并产生协同作用。还开发了用于掺杂样品分析的特定方案,并使用UO 2 和(U,Pu)O 2 样品进行了验证。

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