Conversion of dilute nitrous oxide (N2O) in N2 and N2-O2 mixtures by plasma and plasma-catalytic processes

被引:27
作者
Fan, Xing [1 ]
Kang, Sijing [1 ]
Li, Jian [1 ]
Zhu, Tianle [2 ]
机构
[1] Beijing Univ Technol, Coll Environm & Energy Engn, Key Lab Beijing Reg Air Pollut Control, Beijing 100124, Peoples R China
[2] Beihang Univ, Sch Space & Environm, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
CORONA DISCHARGE REACTOR; LOW-CONCENTRATION FORMALDEHYDE; LOW-CONCENTRATION BTX; NONTHERMAL PLASMA; FLUE-GAS; REMOVAL; DECOMPOSITION; AIR; OXYGEN; PERFORMANCE;
D O I
10.1039/c8ra05607b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A coaxial dielectric barrier discharge (DBD) reactor has been developed for plasma and plasma-catalytic conversion of dilute N2O in N-2 and N-2-O-2 mixtures at both room and high temperature (300 degrees C). The effects of catalyst introduction, O-2 content and inlet N2O concentration on N2O conversion and the mechanism involved in the conversion of N2O have been investigated. The results show that N2O in N-2 could be effectively decomposed to N-2 and O-2 by plasma and plasma-catalytic processes at both room and high temperature, with much higher decomposition efficiency at 300 degrees C than at room temperature for the same discharge power. Under an N-2-O-2 atmosphere, however, N2O could be removed only at high temperature, producing not only N-2 and O-2 but also NO and NO2. Production and conversion of N2O occur simultaneously during the plasma and plasma-catalytic processing of N2O in a N-2-O-2 mixture, with production and conversion being the dominant processes at room and high temperature, respectively. N2O conversion increases with the increase of discharge power and decreases with the increase of O-2 content. Increasing the inlet N2O concentration from 100 to 400 ppm decreases the conversion of N2O under an N-2 atmosphere but increases that under an N-2-O-2 atmosphere. Concentrating N2O in the N-2-O-2 mixture could alleviate the negative influence of O-2 by increasing the involvement of plasma reactive species (e.g., N-2(A(3)Sigma(+)(u)) and O(D-1)) in N2O conversion. Packing the discharge zone with a RuO2/Al2O3 catalyst significantly enhances the conversion of N2O and improves the selectivity of N2O decomposition under an N-2-O-2 atmosphere, revealing the synergy of plasma and catalyst in promoting N2O conversion, especially its decomposition to N-2 and O-2.
引用
收藏
页码:26998 / 27007
页数:10
相关论文
共 37 条
[31]   Combining non-thermal plasma with heterogeneous catalysis in waste gas treatment: A review [J].
Van Durme, Jim ;
Dewulf, Jo ;
Leys, Christophe ;
Van Langenhove, Heirman .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2008, 78 (3-4) :324-333
[32]   Removal of low-concentration formaldehyde in air by DC corona discharge plasma [J].
Wan, Yajuan ;
Fan, Xing ;
Zhu, Tianle .
CHEMICAL ENGINEERING JOURNAL, 2011, 171 (01) :314-319
[33]   Removal of NO from flue gas over HZSM-5 by a cycling adsorption-plasma process [J].
Yu, Qingjun ;
Gao, Yueming ;
Tang, Xiaolong ;
Yi, Honghong ;
Zhang, Runcao ;
Zhao, Shunzheng ;
Gao, Fengyu ;
Zhou, Yuansong .
CATALYSIS COMMUNICATIONS, 2018, 110 :18-22
[34]   The catalytic activity of NiO for N2O decomposition doubly promoted by barium and cerium [J].
Zhang, Fengfeng ;
Wang, Xinping ;
Zhang, Xiaoxiao ;
Turxun, Mamutjan ;
Yu, Haibiao ;
Zhao, Jingjing .
CHEMICAL ENGINEERING JOURNAL, 2014, 256 :365-371
[35]   The byproduct generation analysis of the NOx conversion process in dielectric barrier discharge plasma [J].
Zhang, Yajie ;
Tang, Xiaolong ;
Yi, Honghong ;
Yu, Qingjun ;
Wang, Jiangen ;
Gao, Fengyu ;
Gao, Yueming ;
Li, Dianze ;
Cao, Yumeng .
RSC ADVANCES, 2016, 6 (68) :63946-63953
[36]   Effect of oxygen on nonthermal plasma reactions of nitrogen oxides in nitrogen [J].
Zhao, GB ;
Garikipati, SVB ;
Hu, XD ;
Argyle, MD ;
Radosz, M .
AICHE JOURNAL, 2005, 51 (06) :1800-1812
[37]   N atom radicals and N2(A3Σu+) found to be responsible for nitrogen oxides conversion in nonthermal nitrogen plasma [J].
Zhao, GB ;
Hu, XD ;
Argyle, MD ;
Radosz, M .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2004, 43 (17) :5077-5088