催化作用
臭氧
分解
空间速度
化学
相对湿度
氧化物
共沉淀
无机化学
化学工程
环境化学
有机化学
选择性
热力学
物理
工程类
作者
Yunhe Li,Hao Li,Baogang Zhao,Yanming Ma,Peiyuan Liang,Tianjun Sun
标识
DOI:10.1007/s11356-023-29642-y
摘要
The escalating levels of surface ozone concentration pose detrimental effects on public health and the environment. Catalytic decomposition presents an optimal solution for surface ozone removal. Nevertheless, catalyst still encounters challenges such as poisoning and deactivation in the high humidity environment. The influence of support on catalytic ozone decomposition was examined at a gas hourly space velocity of 300 L·g-1·h-1 and 85% relative humidity under ambient temperature using Cu-Mn-doped oxide catalysts synthesized via a straightforward coprecipitation method. Notably, the Cu-Mn/SiO2 catalyst exhibited remarkable performance on ozone decomposition, achieving 98% ozone conversion and stability for 10 h. Further characterization analysis indicated that the catalyst's enhanced water resistance and activity could be attributed to factors such as an increased number of active sites, a large surface area, abundant active oxygen species, and a lower Mn oxidation state. The catalytic environment created by mixed oxides can offer a clearer understanding of their synergistic effects on catalytic ozone decomposition, providing significant insights into the development of water-resistant catalysts with superior performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI