Photochemical Removal of N2O in N2 or Air Using 172 nm Excimer Lamps

被引:6
作者
Tsuji, Masaharu [1 ,2 ]
Kamo, Naohiro [2 ]
Senda, Makoto [2 ]
Kawahara, Masashi [2 ]
Kawahara, Takashi [2 ]
Hishinuma, Nobuyuki [3 ]
机构
[1] Kyushu Univ, Inst Mat Chem & Engn, Fukuoka 8168580, Japan
[2] Kyushu Univ, Dept Appl Sci Elect & Mat, Grad Sch Engn Sci, Fukuoka 8168580, Japan
[3] Ushio Inc, Himeji, Hyogo 6710224, Japan
关键词
NITROUS-OXIDE; O-2; DECOMPOSITION; NO2; DISCHARGE; LASER; CONVERSION; CATALYSTS;
D O I
10.1143/JJAP.48.046002
中图分类号
O59 [应用物理学];
学科分类号
摘要
N2O removal was investigated in N-2 or air using 172 nm Xe-2 excimer lamps (50 or 300 mW/cm(2)) without using any expensive catalysts. The residual amount of N2O and the formation ratios of products were measured as functions of photoirradiation time, N2O concentration, and O-2 concentration. N2O (100 ppm) was completely converted to N-2 and O-2 without NOx emission in N-2 at atmospheric pressure after 30 min photoirradiation using a high-power Xe-2 excimer lamp (300 mW/cm(2)). 76% of N2O (100 ppm) was also converted to N-2, O-2, and HNO(0)3 in air (20% O-2) after 30 min photoirradiation using the high-power lamp. We concluded that N2O is dominantly decomposed by 172 nm photolysis in N-2 and by the O(D-1) + N2O reaction in air, where O(D-1) atoms dominantly arise from the 172 nm photolysis Of O-2. The conversion of N2O in air increased more than twofold by decreasing the total pressure from atmospheric pressure to 20 kPa by suppressing the collisional quenching of O(D-1) by N-2 and O-2 buffer gases. In a flow experiment, the conversion of N2O in N-2 was only 6-18% in the total flow rate range of 0.1-1 L/min owing to the short residence time of N2O in the photolysis chamber. (c) 2009 The Japan Society of Applied Physics
引用
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页数:8
相关论文
共 24 条
[1]   Evaluated kinetic and photochemical data for atmospheric chemistry: Supplement VI - IUPAC subcommittee on gas kinetic data evaluation for atmospheric chemistry [J].
Atkinson, R ;
Baulch, DL ;
Cox, RA ;
Hampson, RF ;
Kerr, JA ;
Rossi, MJ ;
Troe, J .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1997, 26 (06) :1329-1499
[2]  
EPA, INV US GREENH GAS EM
[3]   Transformations and destruction of nitrogen oxides -: NO, NO2 and N2O -: in a pulsed corona discharge reactor [J].
Hu, XD ;
Zhang, JJ ;
Mukhnahallipatna, S ;
Hamann, J ;
Biggs, MJ ;
Agarwal, P .
FUEL, 2003, 82 (13) :1675-1684
[4]   The destruction of N2O in a pulsed corona discharge reactor [J].
Hu, XD ;
Nicholas, J ;
Zhang, JJ ;
Linjewile, TM ;
de Filippis, P ;
Agarwal, PK .
FUEL, 2002, 81 (10) :1259-1268
[5]  
Jacob D, 1999, INTRO ATMOSPHERIC CH, DOI DOI 10.1515/9781400841547
[6]   Nitrous oxide processing by a combination of gliding and microwave discharges [J].
Krawczyk, Krzysztof ;
Drozdowski, Michal ;
Naperty, Katarzyna .
CATALYSIS TODAY, 2007, 119 (1-4) :239-242
[7]  
Krawczyk K, 2006, J ADV OXID TECHNOL, V9, P160
[8]   Detection of O(D-1) produced in the photodissociation of O-2 in the Schumann-Runge continuum [J].
Nee, JB ;
Lee, PC .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (36) :6653-6657
[9]  
Okabe H., 1978, PHOTOCHEMISTRY SMALL
[10]   Direct decomposition of nitrous oxide over Ru/Al2O3 catalysts prepared by deposition-precipitation method [J].
Reddy, P. Siva Sankar ;
Pasha, Nayeem ;
Rao, M. G. V. Chalapathi ;
Lingaiah, N. ;
Suryanarayana, I. ;
Prasad, P. S. Sai .
CATALYSIS COMMUNICATIONS, 2007, 8 (09) :1406-1410