Promotion of redox and stability features of doped Ce-W-Ti for NH3-SCR reaction over a wide temperature range

被引:79
作者
Zhao, Kun [1 ,2 ]
Han, Weiliang [1 ]
Lu, Gongxuan [1 ]
Lu, Jiangyin [2 ]
Tang, Zhicheng [1 ]
Zhen, Xinping [2 ]
机构
[1] Chinese Acad Sci, Natl Engn Res Ctr Fine Petrochem Intermediates, State Key Lab Oxo Synth & Select Oxidat, Lanzhou Inst Chem Phys, Lanzhou 730000, Peoples R China
[2] Xinjiang Univ, Coll Chem & Chem Engn, Minist Educ, Key Lab Oil & Gas Fine Chem, Urumqi 830046, Peoples R China
基金
中国国家自然科学基金; 中国科学院西部之光基金;
关键词
NH3-SCR; Hydrothermal stability; Ce-W-Ti; Additional catalyst; Activity sites; SELECTIVE CATALYTIC-REDUCTION; MIXED-OXIDE CATALYST; SUPERIOR CATALYST; NO REDUCTION; NH3; CU; SCR; SURFACE; CO; PERFORMANCE;
D O I
10.1016/j.apsusc.2016.04.090
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, transition metals Co, Mn, and Cu were introduced into a Ce-W-Ti catalyst to promote low-temperature catalytic activity. Among these metal-modified M/Ce-W-Ti catalysts (M represents Co, Mn, or Cu), the Cu/Ce-W-Ti catalyst with an optimized Cu content of 5 wt.% exhibited more than 90% conversion of nitrogen oxide (NO,) in the selective catalytic reduction by NH3 over a wide temperature range (260-400 degrees C). This catalyst likewise exhibited higher resistance to SO2 gas and water vapor under severe test conditions. On the basis of the characterization results by powder X-ray diffraction and X-ray photoelectron spectroscopy, we concluded that the superior catalytic properties of the Cu/Ce-W-Ti catalyst could be attributed to the highly dispersed Cu species, which increased the contents of Ce3+ species and adsorbed oxygen species in the catalysts. In addition, the NH3 temperature-programmed desorption results demonstrated that the Cu species doped into the Ce-W-Ti catalysts optimized surface acid content. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:316 / 322
页数:7
相关论文
共 46 条
[1]   DRIFT study of the interaction of NO and O2 with the surface of Ce0.62Zr0.38O2 as deNOx catalyst [J].
Adamowska, Malgorzata ;
Krzton, Andrzej ;
Najbar, Mieczyslawa ;
Da Costa, Patrick ;
Djega-Mariadassou, Gerald .
CATALYSIS TODAY, 2008, 137 (2-4) :288-291
[2]   REACTIVITY AND PHYSICOCHEMICAL CHARACTERIZATION OF V2O5-WO3/TIO2 DE-NOX CATALYSTS [J].
ALEMANY, LJ ;
LIETTI, L ;
FERLAZZO, N ;
FORZATTI, P ;
BUSCA, G ;
GIAMELLO, E ;
BREGANI, F .
JOURNAL OF CATALYSIS, 1995, 155 (01) :117-130
[3]   Chemical and mechanistic aspects of the selective catalytic reduction of NOx by ammonia over oxide catalysts:: A review [J].
Busca, G ;
Lietti, L ;
Ramis, G ;
Berti, F .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (1-2) :1-36
[4]   Comparative study of 3D ordered macroporous Ce0.75Zr0.2M0.05O2-δ (M = Fe, Cu, Mn, Co) for selective catalytic reduction of NO with NH3 [J].
Cai, Sixiang ;
Zhang, Dengsong ;
Zhang, Lei ;
Huang, Lei ;
Li, Hongrui ;
Gao, Ruihua ;
Shi, Liyi ;
Zhang, Jianping .
CATALYSIS SCIENCE & TECHNOLOGY, 2014, 4 (01) :93-101
[5]   SCR of NO by NH3 over TiO2-supported V2O5-MoO3 catalysts:: reactivity and redox behavior [J].
Casagrande, L ;
Lietti, L ;
Nova, I ;
Forzatti, P ;
Baiker, A .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1999, 22 (01) :63-77
[6]   Screening of doped MnOx-CeO2 catalysts for low-templerature NO-SCR [J].
Casapu, Maria ;
Kroecher, Oliver ;
Elsener, Martin .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2009, 88 (3-4) :413-419
[7]  
Cavataio G., 2007, SAE TECH PAP, V01, P1575
[8]   SELECTIVE CATALYTIC REDUCTION OF NO WITH NH3 ON SO4(-2)/TIO2 SUPERACID CATALYST [J].
CHEN, JP ;
YANG, RT .
JOURNAL OF CATALYSIS, 1993, 139 (01) :277-288
[9]   Promotional Effect of Ce-doped V2O5-WO3/TiO2 with Low Vanadium Loadings for Selective Catalytic Reduction of NOx by NH3 [J].
Chen, Liang ;
Li, Junhua ;
Ge, Maofa .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (50) :21177-21184
[10]   Role of cerium in promoting the stability of CuHM catalyst against HCl to reduce NO with NH3 [J].
Choung, Jin Woo ;
Nam, In-Sik .
APPLIED CATALYSIS A-GENERAL, 2006, 312 :165-174