The nighttime production of OH radicals in the continental troposphere

被引:35
作者
Bey, I
Aumont, B
Toupance, G
机构
[1] Lab. Interuniv. Syst. A., Créteil
[2] Lab. Interuniv. Syst. A., Universités P12-P7, URA CNRS 1404, 94010 Créteil
关键词
D O I
10.1029/97GL00889
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Chemical pathways involved in the nocturnal production of hydroxyl radical (OH) and associated peroxy radicals (HO2 and RO2) are quantified for various environmental situations of the continental troposphere by means of numerical simulations. In the nocturnal stable layer, most of the OH radicals are directly produced by VOC+O-3 reactions in rural and semipolluted environments while in urban environments, they result mainly from the radical chain propagation from RO2 and HO2. The radical propagation is mainly driven by NO: the nitrate radical (NO3) plays no role in such processes but is significantly involved in the direct formation of RO2 radicals. Above the nocturnal stable layer, whatever the environmental situation, OH radicals are mainly due to radical chain propagation in which NO3 plays a significant role. The nighttime simulated OH concentrations are 3x10(4) to 5x10(5) and 1x10(4) to 5x10(4) molec cm(-3) for the nocturnal stable and residual layers respectively.
引用
收藏
页码:1067 / 1070
页数:4
相关论文
共 23 条
  • [1] REACTIONS OF ALKOXY RADICALS UNDER ATMOSPHERIC CONDITIONS - THE RELATIVE IMPORTANCE OF DECOMPOSITION VERSUS REACTION WITH O-2
    ATKINSON, R
    CARTER, WPL
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 1991, 13 (02) : 195 - 210
  • [2] OH RADICAL PRODUCTION FROM THE GAS-PHASE REACTIONS OF O-3 WITH A SERIES OF ALKENES UNDER ATMOSPHERIC CONDITIONS
    ATKINSON, R
    ASCHMANN, SM
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (07) : 1357 - 1363
  • [3] Tests of some reduction hypotheses made in photochemical mechanisms
    Aumont, B
    JaeckerVoirol, A
    Martin, B
    Toupance, G
    [J]. ATMOSPHERIC ENVIRONMENT, 1996, 30 (12) : 2061 - 2077
  • [4] KINETICS AND PRODUCTS OF THE REACTIONS OF NO3 WITH MONOALKENES, DIALKENES, AND MONOTERPENES
    BARNES, I
    BASTIAN, V
    BECKER, KH
    TONG, Z
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (06) : 2413 - 2419
  • [5] A DETAILED MECHANISM FOR THE GAS-PHASE ATMOSPHERIC REACTIONS OF ORGANIC-COMPOUNDS
    CARTER, WPL
    [J]. ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1990, 24 (03): : 481 - 518
  • [6] KINETICS OF THE REACTIONS CH3O+NO, CH3O+NO3, AND CH3O2+NO3
    DAELE, V
    LAVERDET, G
    LEBRAS, G
    POULET, G
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (05) : 1470 - 1477
  • [7] PRODUCT FORMATION FROM THE GAS-PHASE REACTIONS OF OH RADICALS AND O3 WITH A SERIES OF MONOTERPENES
    HAKOLA, H
    AREY, J
    ASCHMANN, SM
    ATKINSON, R
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 1994, 18 (01) : 75 - 102
  • [8] PRODUCTS AND MECHANISMS OF THE GAS-PHASE REACTIONS BETWEEN NO3 AND A SERIES OF ALKENES
    HJORTH, J
    LOHSE, C
    NIELSEN, CJ
    SKOV, H
    RESTELLI, G
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (19) : 7494 - 7500
  • [9] OZONOLYSIS OF TRANS-2-BUTENES AND CIS-2-BUTENES IN LOW PARTS-PER-MILLION CONCENTRATION RANGES
    HORIE, O
    NEEB, P
    MOORTGAT, GK
    [J]. INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1994, 26 (11) : 1075 - 1094
  • [10] HOUGH A, 1986, R12069 AERE HARW LAB