催化作用
空间速度
分解
铈
臭氧
X射线光电子能谱
锰
无机化学
热分解
化学
材料科学
化学工程
有机化学
工程类
选择性
作者
Jinzhu Ma,Xiaotong Li,Changbin Zhang,Qingxin Ma,Hong He
标识
DOI:10.1016/j.apcatb.2019.118498
摘要
Novel CeMnaOx (a is the molar ratio of Mn to Ce) catalysts for catalytic decomposition of ozone (O3) under high GHSV conditions were successfully synthesized by a facile homogeneous precipitation method. CeMn10Ox showed ozone conversion of 96 % for 40 ppm O3 under relative humidity (RH) of 65 % and space velocity of 840 L·g−1 ·h-1 after 6 h at room temperature, which is far superior to the performance of the α-Mn2O3 (38 %). The ozone decomposition activity of α-Mn2O3 increased by a factor of 2.5 with the addition of Ce. XRD, XPS, H2-TPR, O2-TPD, EXAFS and DFT calculations data confirmed that cerium-manganese complex oxides with enhanced surface area were formed, which played a key role in the decomposition of ozone. This study provides important insights for developing improved catalysts for gaseous ozone decomposition that can be prepared by a simple method, and promoting the performance of manganese oxides for practical ozone elimination.
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