Modifications to the surface chemistry of low-rank coal-based carbon catalysts to improve flue gas nitric oxide removal

被引:61
作者
Izquierdo, MT
Rubio, B
Mayoral, C
Andrés, JM
机构
[1] CSIC, Inst Carboquim, Dept Energia & Medio Ambiente, Zaragoza 50015, Spain
[2] CSIC, Inst Carboquim, Dept Proc Quim, Zaragoza 50015, Spain
关键词
selective catalytic reduction; nitric oxide removal; coal-based carbon catalyst; surface modification;
D O I
10.1016/S0926-3373(01)00192-8
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 [物理化学]; 081704 [应用化学];
摘要
The effectiveness of carbons as low-temperature selective catalytic reduction (SCR) catalysts will depend upon their physical and chemical properties. Surface functional groups containing oxygen are closely related to the catalytic activity of carbons. These groups are expected to change the interaction between the carbon surface and the reactants through a variation in adsorption and reaction characteristics. This paper presents a more detailed study of the effects of either gas-phase sulfuric acid or oxygen oxidation treatments on the catalytic NO reduction by low-rank coal-based carbon catalysts. Raw and treated carbons were characterized by N-2 and CO2 surface areas, TPD and ash content. NO removal capacity of carbons was determined by passing a flow containing NO, H2O, O-2, NH3 and N-2 through a fixed bed of carbon at 150 degreesC and 4 s of residence time, the effluent concentration being monitored continuously during the reaction. The effects of varying the type and conditions of the treatment on the physicochemical features of carbons were studied. The gas-phase sulfuric acid treatment (corresponding to a first step SO2 removal) markedly enhanced carbon activities for NO removal. On the contrary, oxygen oxidation enhanced NO removal capacity of chars to a lower extent. Therefore, the carbons studied could be used in a combined SO2/NO removal process, because the use and regeneration of the carbon in the first step is beneficial for the performance in the second one. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:315 / 324
页数:10
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