Ce掺杂和磷酸化对优化废V2O5-WO3/TiO2催化剂低温NH3-SCR活性的协同效应

Qiulin Wang, Xiongfei Qi, Haonan Wang, Minghui Tang, Shengyong Lu, Dunyu Liu, Jing Jin
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引用次数: 0

摘要

废选择性催化还原(SCR)催化剂的再活化和后续再利用具有显著的经济和环境优势。水和酸洗以及热再生通常用于消除催化剂表面的有毒物质,而这些过程通常会导致活性成分的损失。本研究采用浸渍法对废V2O5-WO3/TiO2 (VW/Ti)催化剂中耗尽的活性成分进行补充。实验研究了Ce/P掺杂对该再生催化剂的SCR活性和抗SO2/H2O暴露有害影响的影响。Ce/P共掺杂的VW/Ti催化剂达到了最佳性能,在150至450°C的广泛温度范围内,其去除NOx的效率接近100%。适当含量的Ce的加入使VOx表面密度从亚单层状态增加到单层状态,并促进表面氧空位的形成。这种转化有利于提高催化活性和抗SO2/H2O中毒能力。用H3PO4进一步处理,虽然使催化剂更容易受到水的影响,但在其表面酸度和氧化还原能力之间达到了微妙的平衡。这种优化状态不仅提高了催化剂的鲁棒性,而且进一步拓宽了活性温度窗。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic effect of Ce doping and phosphorylation on optimizing the low temperature NH3-SCR activity of the spent V2O5-WO3/TiO2 catalyst

The reactivation and subsequent reuse of exhausted selective catalytic reduction (SCR) catalysts has significant economic and environmental advantages. Water and acid washing along with thermal regeneration are commonly used to eliminate toxic substances from the catalyst surface, while these processes often result in the undesired loss of active components. In this research, an impregnation approach was adopted to replenish the depleted active constituents of the spent V2O5-WO3/TiO2 (VW/Ti) catalyst. Experimental investigations were conducted to evaluate the influence of Ce/P doping on both the SCR activity of this rejuvenated catalyst and its resistance to the detrimental effects of SO2/H2O exposure. The optimal performance is achieved with the Ce/P co-doped VW/Ti catalyst, demonstrating remarkable efficiency in removing nearly 100% of NOx across a broad range of temperatures from 150 to 450 °C. The incorporation of a proper content of Ce serves to increase the VOx surface density from a sub-monolayer state to a monolayer state and fosters the formation of more surface oxygen vacancies. This transformation positively contributes to enhancing both the catalytic activity and the resistance to SO2/H2O poisoning. Further treatment with H3PO4, although rendering the catalyst more susceptible to H2O, achieves a delicate balance between its surface acidity and redox capabilities. This optimized state not only enhances the catalyst's robustness but also further widens the active temperature window.

Graphical abstract

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