Co-Mn-Al Nonstoichiometric Spinel-Type Catalysts Derived from Hydrotalcites for the Simultaneous Removal of Soot and Nitrogen Oxides

被引:8
|
作者
Wang, Zhongpeng [1 ,2 ]
Zhang, Xiaomin [1 ]
Wang, Liguo [1 ]
Zhang, Zhaoliang [1 ]
Jiang, Zheng [2 ]
Xiao, Tiancun [2 ]
Umar, Ahmad [3 ,4 ]
Wang, Qiang [5 ]
机构
[1] Univ Jinan, Sch Resources & Environm, Jinan 250022, Peoples R China
[2] Univ Oxford, Inorgan Chem Lab, Oxford OX1 3QR, England
[3] Najran Univ, Coll Arts & Sci, Dept Chem, Najran 11001, Saudi Arabia
[4] Najran Univ, PCSED, Najran 11001, Saudi Arabia
[5] Beijing Forestry Univ, Coll Environm Sci & Engn, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
CoMnAl; Nonstoichionnetric Spinel; Hydrotalcites; Mixed Oxides; Soot Oxidation; NOx Removal; DIESEL SOOT; MIXED OXIDES; MG-AL; COBALT CATALYSTS; CARBON-DIOXIDE; NOX; COMBUSTION; POTASSIUM; OXIDATION; CU;
D O I
10.1166/sam.2013.1606
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A series of Co-Mn-Al nonstoichiometric spinet-type oxides were synthesized from hydrotalcites precursors prepared through co-precipitation method, and their catalytic activities for the simultaneous removal of soot and NOx were investigated. The solids were characterized by XRD, BET, H-2-TPR, in situ FTIR and TPO techniques. Manganese carbonate was formed during the hydrotalcite synthesis for Mn containing precursors. Thermal decomposition at 800 degrees C led to nonstoichiometric spinel-type oxides for Co containing mixed oxides with specific surface areas ranged from 16 to 25 m(2)/g. CoMnAl ternary oxides exhibited much higher NOx storage capacities than CoAl and MnAl binary oxides, which may be due to the improved reducibility. The presence of NO in the feed gas significantly enhanced the soot oxidation activity. A cooperative effect between Co and Mn in the spinel oxides was found for the simultaneous catalytic removal of soot and NOx. The in situ FTIR spectroscopy over catalyst-soot mixtures in O-2 indicated the presence of surface oxygen complexes (SOC), existing mainly as carboxyl species and phenol groups, in soot oxidation process. In the case of O-2/NO atmosphere, NO was easily oxidized to NO2 over the mixed oxides. NO2, a more powerful oxidant, acts as an intermediate which oxidizes soot to CO2 at a lower temperature with itself reduced to NO or N-2, resulting in the high catalytic performances in simultaneous soot-NOx removal.
引用
收藏
页码:1449 / 1457
页数:9
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