氯苯
催化作用
燃烧
化学
氯
催化燃烧
氧气
莫来石
惰性
化学工程
无机化学
有机化学
工程类
陶瓷
作者
Liu Yi,Yinglin Wang,Fei Xie,Jiamin Zheng,Jintong Lan,Furong Guo,Yifei Sun,Lizhi Zhang,Xiao Liu
出处
期刊:ACS Catalysis
日期:2023-07-24
卷期号:13 (15): 10340-10350
被引量:15
标识
DOI:10.1021/acscatal.3c01871
摘要
The degradation of chlorine-containing volatile organic compounds (Cl–VOCs) utilizing catalytic combustion technology is subject to the paradox of toxic byproduct formation and catalyst chlorine poisoning. Herein, a CaO-assisted strategy is proposed to resolve the awkward stuff for improving the catalytic combustion performance of chlorobenzene on SmMn2O5. The CaO-collaborated SmMn2O5 exhibits a significant decrease in T90 by 142 and 125 °C compared with unmodified and inert SiO2-composited SmMn2O5, respectively. The integrated characterization results confirm that CaO collaboration causes electron transfer from CaO to SmMn2O5, resulting in a reduction of the orbital overlap between Mn and O atoms to activate lattice oxygen (Olatt). The activated Olatt enables chlorobenzene to combust completely at a lower temperature of 275 °C at which toxic byproducts are not generated. Furthermore, the switching of the dechlorination site from SmMn2O5 to CaO avoids chlorine poisoning of active sites on SmMn2O5 and thus endows CaO-collaborated SmMn2O5 with prominent stability.
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