催化作用
氧化物
材料科学
化学工程
复合材料
氧化铈
氧气
基质(水族馆)
X射线光电子能谱
化学
冶金
有机化学
海洋学
地质学
工程类
作者
Zhihua Wang,Fawei Lin,Shanqun Jiang,Kunzan Qiu,Min Kuang,Ron Whiddon,Kefa Cen
出处
期刊:Fuel
[Elsevier]
日期:2016-02-01
卷期号:166: 352-360
被引量:56
标识
DOI:10.1016/j.fuel.2015.11.012
摘要
Oxidation catalysts can be used to achieve highly efficient NO oxidation by residual O2 in flue gas and decrease the power consumption of pollutant oxidation process through ozone injection. Ceria was selected as the catalyst carrier because of its excellent oxygen storage capacity. Ceria substrate composite catalysts were prepared through sol–gel method. The effects of dopant metals (Co, Mn, Fe, Cr, and Ni), calcination temperatures, and Co doping content on NO conversion efficiency were assessed. The physico-chemical characteristics of catalysts prepared were analyzed through BET, XRD, TPR, TEM, and XPS. Cobalt was used as the dopant metal because of its excellent catalytic activity. The optimal condition was 400 °C calcination, and the effective mole ratio of Co to Ce was 0.51. Under the optimal condition, the Ce–Co composite catalyst yielded an NO conversion efficiency of 93% at 230 °C. The catalytic activity of the Ce–Co composite catalyst on NO oxidization was related to structural features, crystalline pattern, redox ability, and interactions between cobalt and ceria. The effect of residual oxygen concentration in flue gas on NO oxidation was evaluated. When the oxygen concentration exceeded 6%, NO conversion efficiency stabilized. The sulfur- and water-resistant ability of the Ce–Co composite catalyst was very weak. Only 53% NO conversion was obtained at 190 °C when 200 ppm SO2 and 3% steam were added.
科研通智能强力驱动
Strongly Powered by AbleSci AI