HNO3 forming channel of the HO2+NOreaction as a function of pressure and temperature in the ranges of 72-600 torr and 223-323 K

被引:65
作者
Butkovskaya, Nadezhda
Kukui, Alexandre
Le Bras, Georges
机构
[1] ICARE, CNRS, F-45071 Orleans 2, France
[2] Russian Acad Sci, Inst Chem Phys, Moscow 117334, Russia
[3] IPSL, Serv Aeron, CNRS, Paris, France
关键词
D O I
10.1021/jp074117m
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
A high-pressure turbulent flow reactor coupled with a chemical ionization mass-spectrometer was used to determine the branching ratio of the HO2 + NO reaction: HO2 + NO -> OH + NO2 (1a), HO2 + NO -> HNO3 (1b). The branching ratio, beta = k(1b)/k(1a), was derived from the measurements of "chemically amplified" concentrations of the NO2 and HNO3 products in the presence of O-2 and CO. The pressure and temperature dependence of beta was determined in the pressure range of 72-600 Torr of N-2 carrier gas between 323 and 223 K. At each pressure, the branching ratio was found to increase with the decrease of temperature, the increase becoming less pronounced with the increase of pressure. In the 298-223 K range, the data could be fitted by the expression: beta(T,P) = (530 +/- 10)/T(K) + (6.4 +/- 1.3) x 10(-4)P(Torr) - (1.73 +/- 0.07), giving beta approximate to 0.5% near the Earth's surface (298 K, 760 Tort) and 0.8% in the tropopause region (220 K, 200 Torr). The atmospheric implication of these results is briefly discussed.
引用
收藏
页码:9047 / 9053
页数:7
相关论文
共 13 条
[1]   Formation of nitric acid in the gas-phase HO2+NOreaction:: Effects of temperature and water vapor [J].
Butkovskaya, NI ;
Kukui, A ;
Pouvesle, N ;
Le Bras, G .
JOURNAL OF PHYSICAL CHEMISTRY A, 2005, 109 (29) :6509-6520
[2]  
CHIPPERFIELD MP, UNPUB
[3]   Kinetic and mechanistic studies of the recombination of OH with NO2:: Vibrational deactivation, isotopic scrambling and product isomer branching ratios [J].
D'Ottone, L ;
Bauer, D ;
Campuzano-Jost, P ;
Fardy, M ;
Hynes, AJ .
FARADAY DISCUSSIONS, 2005, 130 :111-123
[4]   Constraining the mechanism of OH+NO2 using isotopically labeled reactants:: Experimental evidence for HOONO formation [J].
Donahue, NM ;
Mohrschladt, R ;
Dransfield, TJ ;
Anderson, JG ;
Dubey, MK .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (09) :1515-1520
[5]   High-pressure flow reactor product study of the reactions of HOx+NO2:: The role of vibrationally excited intermediates [J].
Dransfield, TJ ;
Donahue, NM ;
Anderson, JG .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (09) :1507-1514
[6]   Direct kinetics study of the temperature dependence of the CH2O branching channel for the CH3O2+HO2 reaction [J].
Elrod, MJ ;
Ranschaert, DL ;
Schneider, NJ .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2001, 33 (06) :363-376
[7]   Cis-cis and trans-perp HOONO:: Action spectroscopy and isomerization kinetics [J].
Fry, JL ;
Nizkorodov, SA ;
Okumura, M ;
Roehl, CM ;
Francisco, JS ;
Wennberg, PO .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (03) :1432-1448
[8]   Reaction of OH+NO2+M:: Kinetic evidence of isomer formation [J].
Hippler, H ;
Nasterlack, S ;
Striebel, F .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2002, 4 (13) :2959-2964
[9]   REACTIONS OF SF6- AND I- WITH ATMOSPHERIC TRACE GASES [J].
HUEY, LG ;
HANSON, DR ;
HOWARD, CJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (14) :5001-5008
[10]  
Ikezoe Y., 1987, Gas Phase Ion-Molecule Reaction Rate Constants through 1986