BaCeO3 在 Na2SO4+V2O5 混合盐中的高温腐蚀行为

P.V. Sachin Raj, S.P. Kumaresh Babu
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引用次数: 0

摘要

本研究探讨了 BaCeO3 的高温腐蚀响应和热障特性。采用 TG-DSC 分析法研究了 BaCeO3 的相稳定性和分解行为。热扩散率和热膨胀系数是通过激光闪烁分析和稀释测量技术测定的。烧结 BaCeO3 的显微硬度采用维氏微压痕技术测量,弹性模量则采用超声波技术测定。在温度为 900ºC 的 32 wt% Na2SO4 + 68 wt% V2O5 盐溶液中对 BaCeO3 涂层和颗粒样品进行了腐蚀试验,并使用 XRD 和 SEM-EDS 分析了腐蚀过程。在暴露于 32 wt% Na2SO4 + 68 wt% V2O5 混合物中的样品中发现的主要腐蚀产物是 Ba3V2O8,还有少量 CeO2 和 BaSO4。对腐蚀样品进行的扫描电子显微镜-电子显微镜 (SEM-EDS) 检查突出显示了对 BaCeO3 的严重腐蚀作用,表明 Ba2+ 离子被酸性浸出,然后与盐混合物发生反应。NaVO3 的形成增强了原子的流动性,加剧了腐蚀过程。将 BaCeO3 在纯 Na2SO4 和 V2O5 熔体中的热腐蚀与在 32 wt% Na2SO4 + 68 wt% V2O5 混合物中的热腐蚀进行比较,证实了这种效应。在任何一种腐蚀模式中都没有观察到与任何 Ce-V-O 化合物相对应的明显峰值,这表明由于 BaO 的碱性更强,在腐蚀过程中 BaO 比 CeO2 更受青睐。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-temperature corrosion behavior of BaCeO3 in Na2SO4+V2O5 salt mixture

This study examines the high temperature corrosion response and thermal barrier characteristics of BaCeO3. The phase stability and decomposition behaviour of BaCeO3 were studied using TG-DSC analysis. The thermal diffusivity and thermal expansion coefficient were determined using Laser Flash Analysis and Dilatometry techniques. Microhardness of the sintered BaCeO3 was measured using Vickers micro indentation technique whereas the elastic modulus was found using Ultrasonic technique. Corrosion tests were performed on both BaCeO3 coatings and pellet samples in 32 wt% Na2SO4 + 68 wt% V2O5 salt melt at 900ºC, and the corrosion process was analyzed using XRD and SEM-EDS. The main corrosion product found in the samples exposed to 32 wt% Na2SO4 + 68 wt% V2O5 mixture was Ba3V2O8, with small amounts of CeO2 and BaSO4. SEM-EDS examination of the corroded samples highlighted the significant corrosive action on BaCeO3, indicating the acidic leaching of Ba2+ ions, which then reacted with the salt mixture. The formation of NaVO3 intensified atomic mobility, aggravating the corrosion process. Comparing the hot corrosion of BaCeO3 in pure Na2SO4 and V2O5 melts with that in the 32 wt% Na2SO4 + 68 wt% V2O5 mixture confirmed this effect. No discernible peaks corresponding to any Ce-V-O compound were observed in any of the corrosion patterns, suggesting a preference for BaO over CeO2 in the corrosion process due to its stronger basic nature.

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