标题:Experimental and Modeling Study on de-NOx Characteristics of Selective Non-catalytic Reduction in O-2/CO2 Atmosphere
作者:Li, Hui; Han, Kuihua; Liu, Hongtao; Lu, Chunmei
通讯作者:Han, Kuihua
作者机构:[Li Hui] School of Energy and Power Engineering, Shandong University, National Engineering Laboratory for Coal-fired Pollutants Emission Reduction, Ji 更多
会议名称:International conference on structured catalysts and reactions
会议日期:SEP 25-27, 2013
来源:中国化学工程学报
出版年:2014
卷:22
期:8
页码:943-949
DOI:10.1016/j.cjche.2014.06.002
关键词:Selective non-catalytic reduction; Denitrification; Ammonia; Kinetic; modeling; O-2/CO2; SO2; Additives
摘要:An experimental study of thermal de-NOx using NH3 as reductant in O-2/CO2 atmosphere with the effect of SO2 and different additives was performed in a drop tube furnace. Results show that the optimum temperature window is 841-1184 degrees C, and the optimum reaction temperature is about 900 degrees C with a de-NOx efficiency of 95.4%. A certain amount of SO2 has an inhibiting effect on NO reduction. The effect of additives, including Na2CO3, C2H5OH and FeCl3, on NO reduction by NH3 is also explored. The addition of Na2CO3 and FeCl3 is useful to widen the temperature window and shift the reaction to lower temperature for the efficiency is increased from 30.5% to 74.0% and 67.4% respectively at 800 degrees C. Qualitatively, the modeling results using a detailed kinetic modeling mechanism represent well most of the process features. The effect of Na2CO3, C2H5OH and FeCl3 addition can be reproduced well by the Na2CO3, C2H5OH and Fe(CO)(5) sub-mechanism respectively. The reaction mechanism analysis shows that the effects of these additives on NO reduction are achieved mainly by promoting the production of OH radicals at lower temperature. (C) 2014 The Chemical Industry and Engineering Society of China, and Chemical Industry Press. All rights reserved.
收录类别:CPCI-S;EI;CSCD;SCOPUS;SCIE
WOS核心被引频次:2
Scopus被引频次:2
资源类型:会议论文;期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84927692570&doi=10.1016%2fj.cjche.2014.06.002&partnerID=40&md5=e9e441247028eab212ea790adc188244
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