DocumentCode
2443194
Title
Experimental investigation on the mechanism for removal of NOX by solution of urea /additive
Author
Yin, Jianpu ; Xiong, Yuanquan ; Xie, Hongyin ; Shi, Zhanfei ; Zheng, Shouzhong
Author_Institution
Sch. of Energy & Environ., Southeast Univ., Nanjing, China
fYear
2011
fDate
24-26 June 2011
Firstpage
1215
Lastpage
1219
Abstract
This paper introduced mass transfer theory and correlation analysis of the NOx liquid absorption. Experiments using urea as the absorbent and triethanolamine as additive were performed in the bubbling absorption reactor. The influencing factors of the NOx removal such as the oxygen existence, sulfur dioxide existence, triethanolamine existence, absorbent concentration and ammonium sulfite were studied, and the ion concentration of NH4+, NO2-, SO32- and SO42- in the solution was analyzed. This study has concluded that oxygen existence could increase oxidation of nitric oxide, which increased the denitrification efficiency. SO2 existence could introduce sulfite ion and also promoted NOx removal efficiency. Triethanolamine could play a buffer and catalytic role in promoting NOx removal efficiency. Ammonium sulfite on denitrification efficiency had an obvious influence.
Keywords
absorption; additives; air pollution; ammonium compounds; chemical engineering; chemical reactors; mass transfer; oxidation; oxygen compounds; sulphur compounds; absorbent concentration; ammonium sulfite; bubbling absorption reactor; catalysis; correlation analysis; denitrification; ion concentration; liquid absorption; mass transfer theory; nitric oxide; oxidation; oxygen existence; sulfur dioxide existence; triethanolamine; triethanolamine existence; urea-additive solution; Absorption; Additives; Hydrogen; Inductors; Ions; Kinetic theory; Publishing; additive; denitrification; mechanism; urea; wetting;
fLanguage
English
Publisher
ieee
Conference_Titel
Remote Sensing, Environment and Transportation Engineering (RSETE), 2011 International Conference on
Conference_Location
Nanjing
Print_ISBN
978-1-4244-9172-8
Type
conf
DOI
10.1109/RSETE.2011.5964498
Filename
5964498
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