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Neutron and hard X-ray diffraction studies of the isothermal transformation kinetics in the research reactor fuel candidate U–8 wtMo

机译:研究堆燃料候选U-8 wt%Mo中的等温转变动力学的中子和硬X射线衍射研究

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摘要

Exposing uranium–molybdenum alloys (UMo) retained in the γ phase to elevated temperatures leads to transformation reactions during which the γ-UMo phase decomposes into the thermal equilibrium phases, i.e. U2Mo and α-U. Since α-U is not suitable for a nuclear fuel exposed to high burn-up, it is necessary to retain the γ-UMo phase during the production process of the fuel elements for modern high-performance research reactors. The present work deals with the isothermal transformation kinetics in U–8 wt%Mo alloys for temperatures between 673 and 798 K and annealing durations of up to 48 h. Annealed samples were examined at room temperature using either X-ray or neutron diffraction to determine the phase composition after thermal treatment, and in situ annealing studies disclosed the onset of phase decomposition. While for temperatures of 698 and 673 K the start of decomposition is delayed, for higher temperatures the first signs of transformation are already observable within 3 h of annealing. The typical C-shaped curves in a time–temperature–transformation (TTT) diagram for both the start and the end of phase decomposition could be determined in the observed temperature regime. Therefore, a revised TTT diagram for U–8 wt%Mo between 673 and 798 K and annealing durations of up to 48 h is proposed.
机译:将保留在γ相中的铀钼合金(UMo)暴露在高温下会导致转化反应,在此期间γ-UMo相分解为热平衡相,即U2Mo和α-U。由于α-U不适合暴露在高燃尽的核燃料中,因此有必要在现代高性能研究反应堆的燃料元件生产过程中保留γ-UMo相。目前的工作涉及U–8 wt%Mo合金在673至798 K之间的温度和长达48 h的退火时间下的等温转变动力学。在室温下,使用X射线或中子衍射检查退火样品,以确定热处理后的相组成,并且原位退火研究揭示了相分解的开始。对于698和673 K的温度,分解的开始被延迟了;而对于较高的温度,在退火的3 h内已经观察到了转变的最初迹象。在观察到的温度范围内,可以确定时间-温度-转变(TTT)图中相分解的开始和结束的典型C形曲线。因此,提出了在673和798 K之间的U-8%wt%Mo的修正TTT图,退火时间长达48 h。

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