个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:中国科学院兰州化学物理研究所
学位:博士
所在单位:环境学院
办公地点:环境楼 B415
联系方式:Tel: 0411-84706658
电子邮箱:xyli@dlut.edu.cn
Combined Spectroscopic and Theoretical Approach to Sulfur-Poisoning on Cu-Supported Ti-Zr Mixed Oxide Catalyst in the Selective Catalytic Reduction of NOx
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论文类型:期刊论文
发表时间:2014-08-01
发表刊物:ACS CATALYSIS
收录刊物:SCIE、EI、Scopus
卷号:4
期号:8
页面范围:2426-2436
ISSN号:2155-5435
关键字:selective catalytic reduction; SO2-poisoning; -CN species; in situ Fourier transform infrared spectroscopy; density functional theory calculations
摘要:The SO2-poisoning on a Cu-supported Ti-Zr mixed oxide catalyst (Cu/Ti0.7Zr0.3O2-delta) in selective catalytic reduction (SCR) of NOx with C3H6 was investigated, and the different effects of SO2 at varying reaction temperatures were clarified by in situ Fourier transform infrared (FTIR) spectroscopy combined with density functional theory (DFT) calculations. In situ FTIR results of the catalyst at low temperatures (150-250 degrees C) implied that the formation of sulfates on the surface inhibited the activation of NO and C3H6 as well as the reactivity of nitrates and NO2. The weakened capacity of the catalyst toward acetate formation is an important reason for the decline of catalytic activity at low temperatures. At high temperatures (above 275 degrees C), the negative effect of SO2 on the C3H6 activation to acetate is quite weak. More importantly, the generation of -NCO species is enhanced significantly via the reaction -CN + SO2/SO42- -> -NCO, which is confirmed by both in situ FTIR experimental observations and DFT calculations. The promotion in the generation of -NCO species is the primary reason for the elevation of SCR activity at high temperatures.