Upper limit for the generation of N2O from reaction of O-2(A(3)Sigma(+)(u)) and N-2

被引:7
作者
Hwang, ES [1 ]
Buijsse, B [1 ]
Copeland, RA [1 ]
Riris, H [1 ]
Carlisle, CB [1 ]
Slanger, TG [1 ]
机构
[1] SRI INT,MENLO PK,CA 94025
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1997年 / 93卷 / 16期
关键词
D O I
10.1039/a701719g
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 ; 081704 ;
摘要
Evidence from several sources suggest possible in situ production of N2O in the stratosphere. Considering that solar photoabsorption provides a large stratospheric source of O-2(A (3) Sigma(u)(+)), and since vibrational levels of upsilon greater than or equal to 6 are primarily removed by N-2, the O-2(A (3) Sigma(u)(+)) + N-2 system is studied to determine whether it is an atmospherically significant N2O source. Using 243-250 nm photoexcitation to produce vibrationally excited O-2(A (3) Sigma(u)(+), upsilon = 7-10), and frequency modulation diode laser spectroscopy as the detector of N2O, we examine the products generated in a closed cell. We thereby set an upper limit of 0.002% on the N2O yield for the process, and conclude that stratospheric N2O production by this route is not significant compared to existing groundbased sources. The stability of N2O in an N2O-O-3-N-2 mixture subjected to prolonged 245 nm radiation is also studied. For low levels of O-3 (10 ppm) and N2O (40-90 ppb), no loss of N2O is observed.
引用
收藏
页码:2657 / 2663
页数:7
相关论文
共 43 条
[11]   PRODUCT BRANCHING RATIOS FROM THE N-2(A3-SIGMA-U+)+O-2 INTERACTION [J].
FRASER, ME ;
PIPER, LG .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (03) :1107-1111
[12]   TUNABLE DIODE-LASER RATIO MEASUREMENTS OF ATMOSPHERIC CONSTITUENTS BY EMPLOYING DUAL FITTING ANALYSIS AND JUMP SCANNING [J].
FRIED, A ;
HENRY, B ;
DRUMMOND, JR .
APPLIED OPTICS, 1993, 32 (06) :821-827
[13]   An explanation for symmetry-induced isotopic fractionation in ozone [J].
Gellene, GI .
SCIENCE, 1996, 274 (5291) :1344-1346
[14]   BRANCH INTENSITIES AND OSCILLATOR-STRENGTHS FOR THE HERZBERG ABSORPTION SYSTEMS IN OXYGEN [J].
HUESTIS, DL ;
COPELAND, RA ;
KNUTSEN, K ;
SLANGER, TG ;
JONGMA, RT ;
BOOGAARTS, MGH ;
MEIJER, G .
CANADIAN JOURNAL OF PHYSICS, 1994, 72 (11-12) :1109-1121
[15]   Temperature dependence of the collisional removal of O-2(A(3)Sigma(+)(u), v=9) with O-2 and N-2 [J].
Hwang, ES ;
Copeland, RA .
GEOPHYSICAL RESEARCH LETTERS, 1997, 24 (06) :643-646
[16]   PRODUCT CHANNELS OF THE N-2(A3 SIGMA-U+)+O2 INTERACTION [J].
IANNUZZI, MP ;
JEFFRIES, JB ;
KAUFMAN, F .
CHEMICAL PHYSICS LETTERS, 1982, 87 (06) :570-574
[17]   2-TONE FREQUENCY-MODULATION SPECTROSCOPY [J].
JANIK, GR ;
CARLISLE, CB ;
GALLAGHER, TF .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 1986, 3 (08) :1070-1074
[18]   RATE-CONSTANT FOR THE DEACTIVATION OF O2(A 3-SIGMA-U+) BY N2 [J].
KENNER, RD ;
OGRYZLO, EA .
CHEMICAL PHYSICS LETTERS, 1983, 103 (03) :209-212
[19]   DEACTIVATION OF O2(A3-SIGMA-U+) BY O2, O, AND AR [J].
KENNER, RD ;
OGRYZLO, EA .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1980, 12 (07) :501-508
[20]  
KENNER RD, 1983, CAN J CHEM, V61, P922