钒
氧化还原
催化作用
轨道能级差
吸附
氮氧化物
电子转移
兴奋剂
催化氧化
氧气
化学
无机化学
化学工程
材料科学
光化学
工程类
物理化学
分子
有机化学
燃烧
光电子学
作者
Jianqiang Shi,Zhen Wang,Jinxing Mi,Hao Liu,Bing Wang,Haiyan Liu,Jiancheng Wang,Jianjun Chen,Junhua Li
标识
DOI:10.1016/j.jhazmat.2023.131489
摘要
Ce-modified commercial vanadium-based catalysts are still in a rapid development stage in terms of optimizing Hg0 oxidation performance. Due to the universal property of ceria, it can act as either support or promoter to supported vanadium-based catalysts. However, the introduction mode of Ce on the Hg0 oxidation is still unclarified. Herein, introducing Ce to vanadium-based catalysts as a promoter (VCe/Ti) plays a more effective role in the Hg0 oxidation than only doping Ce into TiO2 support (V/CeTi). It is revealed that the strong interaction between V and Ce increases the orbital hybridization, and reduces the lowest unoccupied molecular orbital (LUMO) of V, which is conducive to adsorbing and activating HCl. The excellent performance of the VCe/Ti catalyst can be ascribed to its superior redox ability, stronger HCl adsorption capacity, abundant surface oxygen vacancies, and the redox equilibrium (Ce3+ + V5+ ↔ Ce4+ + V4+), which improves electron transfer, and thus the catalytic activity. This work provides the potential application of Ce-modified V-based catalysts for the simultaneous control of NOx and Hg0 in stationary sources.
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