Cerium and tin oxides anchored onto reduced graphene oxide for selective catalytic reduction of NO with NH3 at low temperatures

被引:20
|
作者
Wang, Yanli [1 ]
Kang, Ying [1 ]
Ge, Meng [1 ]
Zhang, Xiu [1 ]
Zhan, Liang [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Multiphase Mat Chem Engn, Key Lab Specially Funct Polymers & Related Techno, State Key Lab Chem Engn,Minist Educ, Shanghai 200237, Peoples R China
[2] Chinese Acad Sci, Inst Coal Chem, CAS Key Lab Carbon Mat, Taiyuan 030001, Shanxi, Peoples R China
来源
RSC ADVANCES | 2018年 / 8卷 / 63期
基金
美国国家科学基金会;
关键词
MNOX-CEO2 MIXED OXIDES; STRUCTURAL-CHARACTERIZATION; CE; OXIDATION; AMMONIA; SN; PERFORMANCE; NH3-SCR; SO2; CEO2-TIO2;
D O I
10.1039/c8ra05151h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of cerium and tin oxides anchored on reduced graphene oxide (CeO2-SnOx/rGO) catalysts are synthesized using a hydrothermal method and their catalytic activities are investigated by selective catalytic reduction (SCR) of NO with NH3 in the temperature range of 120-280 degrees C. The results indicate that the CeO2-SnOx/rGO catalyst shows high SCR activity and high selectivity to N-2 in the temperature range of 120-280 degrees C. The catalyst with a mass ratio of (Ce + Sn)/GO = 3.9 exhibits NO conversion of about 86% at 160 degrees C, above 97% NO conversion at temperatures of 200-280 degrees C and higher than 95% N-2 selectivity at 120-280 degrees C. In addition, the catalyst presents a certain SO2 resistance. It is found that the highly dispersed CeO2 nanoparticles are deposited on the surface of rGO nanosheets, because of the incorporation of Sn4+ into the lattice of CeO2. The mesoporous structures of the CeO2-SnOx/rGO catalyst provides a large specific surface area and more active sites for facilitating the adsorption of reactant species, leading to high SCR activity. More importantly, the synergistic interaction between cerium and tin oxides is responsible for the excellent SCR activity, which results in a higher ratio of Ce3+/(Ce3+ + Ce4+), higher concentrations of surface chemisorbed oxygen and oxygen vacancies, more strong acid sites and stronger acid strength on the surface of the CeSn(3.9)/rGO catalyst.
引用
收藏
页码:36383 / 36391
页数:9
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