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Titanium tritide radioisotope heat source development: Palladium-coated titanium hydriding kinetics and tritium loading tests

机译:t化钛放射性同位素热源的开发:镀钯钛的氢化动力学和loading负载测试

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摘要

For applications requiring 5-20 mW electrical power for 10-20 years, tritium-based radioisotope thermoelectric generators may be an alternative to Pu-238 based devices. Tritium can be stored compactly on a titanium bed. However, one of the main challenges then becomes loading the heat source at temperatures compatible with existing bismuth telluride thermoelectric module technology (<300 ℃). We find that a 180 nm palladium coating enables titanium to be loaded with hydrogen isotopes without the typical 400-500 ℃ vacuum activation step. Further, we observe that the hydriding kinetics of Pd coated and vacuum activated Ti are similar; both of which can be described by the Mintz-Bloch adherent film model, where the rate of hydrogen absorption is controlled by diffusion through an adherent metal-hydride layer. Finally, we design a prototype heat source vessel and demonstrate that it can be loaded completely, at temperatures below 300 ℃, in less than 10 h.
机译:对于需要10-20年的5-20 mW电力的应用,tri基放射性同位素热电发生器可以替代基于Pu-238的设备。 t可以紧凑地存储在钛床上。然而,接下来的主要挑战之一是将热源加载到与现有的碲化铋热电模块技术兼容的温度(<300℃)下。我们发现180 nm的钯涂层可以使钛负载氢同位素,而无需典型的400-500℃真空活化步骤。此外,我们观察到,Pd涂层和真空活化Ti的氢化动力学相似。两者都可以用Mintz-Bloch粘附膜模型来描述,其中氢的吸收速率由通过粘附金属氢化物层的扩散来控制。最后,我们设计了一个原型热源容器,并证明了它可以在不到300℃的温度下在不到10小时的时间内完全装载。

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