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The corrosion of coated and uncoated Mo and of uncoated Mo-ZrO_2 in glass melts under a. c. loading

机译:玻璃熔体涂覆和未涂覆的MO和未涂覆的MO-ZRO_2的腐蚀。 C。装载

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Sintered and deformed molybdenum, molten and deformed molybdenum and Mo-5ZrO_2 (Mo with 5 volume % ZrO_2) were exposed to molten C-, white- and green-glass under an alternating current loading of 1 A/cm~2. Via mass loss measurement and chemical analysis of the glass melts corrosion rates of the various materials were determined. The most significant deviation to lower corrosion could be found for Mo-5ZrO_2 in green-glass. Retardation of intercrystalline corrosion by the dopant itself or - more likely - the formation of a viscous layer promoted by the presence of the dopant are responsible for this behaviour. Sibor (Si-B) coated molybdenum was also tested in C-glass melt under the same conditions. After an initial period of strong dissolution and bubbling the corrosion rate decreased and became lower than that of the 3 uncoated materials. Presumably the preferential dissolution of Si (B) over the period observed is responsible for this effect.
机译:烧结和变形的钼,熔融和变形的钼和Mo-5zRO_2(Mo,具有5体积%ZrO_2),在1A / cm〜2的交流负载下暴露于熔融C-,白色和绿色玻璃。通过质量损失测量和玻璃的化学分析测定了各种材料的腐蚀速率。为绿色玻璃中的Mo-5zro_2可以找到对降低腐蚀的最显着偏差。掺杂剂本身或更可能 - 通过掺杂剂存在促进的粘性层的形成延迟了促进的粘性层对该行为负责。在相同条件下,Sibor(Si-B)涂覆的钼也在C玻璃熔体中进行测试。经过初始溶解和鼓泡腐蚀速率的初始时期,变得低于3个未涂覆材料的腐蚀速率。据推测,观察到的时期Si(B)的优先溶解是对这种效果的原因。

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