Transition metals supported on mesoporous ZrO2 for the catalytic control of indoor CO and PM emissions

被引:16
作者
Doggali, Pradeep [1 ]
Waghmare, S. [1 ]
Rayalu, S. [1 ]
Teraoka, Y. [2 ]
Labhsetwar, Nitin [1 ]
机构
[1] CSIR, Natl Environm Engn Res Inst, Environm Mat Div, Nagpur 440020, Maharashtra, India
[2] Kyushu Univ, Fac Engn Sci, Dept Energy & Mat Sci, Fukuoka 8168580, Japan
关键词
Meso-zirconia; CO oxidation; PM oxidation; O-2-TPD studies; Control of emissions; Solid fuel combustion; PEROVSKITE-TYPE CATALYSTS; ZIRCONIA SUPPORT; CARBON-MONOXIDE; TOTAL OXIDATION; COMBUSTION; METHANE; NO;
D O I
10.1016/j.molcata.2011.07.010
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
Mesoporous ZrO2 support has been prepared by using a low cost natural biopolymer chitosan as template, and different transition metals from the first row (Fe, Co, Ni, Cu and Mn) were impregnated on the synthesized support. The synthesized catalysts have been characterized by XRD, BET-SA, SEM, TEM, O-2-TPD and TG analysis to study the material details as well as to understand the catalytic mechanism. The activity of these catalysts has been investigated for CO and PM oxidation. Incorporation of transition metals improved the activity for both CO and PM oxidation. It has been observed that Co-ZrO2 is the most active catalyst for studied reactions while, Ni based catalysts show the lowest activity for both the reactions. The transition metal supported catalysts follow the activity sequence Co-ZrO2 > Mn-ZrO2 > Cu-ZrO2 > Fe-ZrO2 > Ni-ZrO2. The effect of CO2, SO2 and H2O on CO oxidation activity was also investigated, and despite partial deactivation, the catalysts show good CO oxidation activity. The characterization of the materials by O-2-TPD studies explains the better catalytic performance for the Co-ZrO2, Mn-ZrO2 and Cu-ZrO2 catalysts, as compared to Fe-ZrO2 and Ni-ZrO2. Such mesoporous zirconia with reasonably good surface area and without ordered structure could be useful for both CO and PM oxidation reactions. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 59
页数:8
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