The relation between ozone, NOx and hydrocarbons in urban and polluted rural environments

被引:1170
作者
Sillman, S [1 ]
机构
[1] Univ Michigan, Dept Atmospher Ocean & Space Sci, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
ozone; hydrocarbons; nitrogen oxides; photochemical production;
D O I
10.1016/S1352-2310(98)00345-8
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Research over the past ten years has created a more detailed and coherent view of the relation between O-3 and its major anthropogenic precursors, volatile organic compounds (VOC) and oxides of nitrogen (NOx). This article presents a review of insights derived from photochemical models and field measurements. The ozone-precursor relationship can be understood in terms of a fundamental split into a NOx-senstive and VOC-sensitive (or NOx-saturated) chemical regimes. These regimes are associated with the chemistry of odd hydrogen radicals and appear in different forms in studies of urbanized regions, power plant plumes and the remote troposphere. Factors that affect the split into NO, sensitive and VOC-sensitive chemistry include: VOC/NOx ratios, VOC reactivity, biogenic hydrocarbons, photochemical aging, and rates of meteorological dispersion. Analyses of ozone-NOx-VOC sensitivity from 3D photochemical models show a consistent pattern, but predictions for the impact of reduced NOx and VOC in indivdual locations are often very uncertain. This uncertainty can be identified by comparing predictions from different model scenarios that reflect uncertainties in meteorology, anthropogenic and biogenic emissions. Several observation-based approaches have been proposed that seek to evaluate ozone-NOx-VOC sensitivity directly from ambient measurements (including ambient VOC, reactive nitrogen, and peroxides). Observation-based approaches have also been used to evaluate emission rates, ozone production efficiency, and removal rates of chemically active species. Use of these methods in combination with models can significantly reduce the uncertainty associated with model predictions. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1821 / 1845
页数:25
相关论文
共 124 条
[21]  
DOMMEN J, 1998, UNPUB J GEOPHYSICAL
[22]  
DRUMMOND J, 1989, 82 ANN M AIR WAST MA
[23]   Photochemical production and loss rates of ozone at Sable Island, Nova Scotia during the North Atlantic Regional Experiment (NARE) 1993 summer intensive [J].
Duderstadt, KA ;
Carroll, MA ;
Sillman, S ;
Wang, T ;
Albercook, GM ;
Feng, L ;
Parrish, DD ;
Holloway, JS ;
Fehsenfeld, FC ;
Blake, DR ;
Blake, NJ ;
Forbes, G .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D11) :13531-13555
[24]  
FEHSENFELD FC, 1993, J GEOPHYS RES, V101, P28877
[25]   Long-term trends in ground level ozone over the contiguous United States, 1980-1995 [J].
Fiore, AM ;
Jacob, DJ ;
Logan, JA ;
Yin, JH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D1) :1471-1480
[26]   COMPARISON OF EMISSION INVENTORY AND AMBIENT CONCENTRATION RATIOS OF CO, NMOG, AND NOX IN CALIFORNIA SOUTH COAST AIR BASIN [J].
FUJITA, EM ;
CROES, BE ;
BENNETT, CL ;
LAWSON, DR ;
LURMANN, FW ;
MAIN, HH .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 1992, 42 (03) :264-276
[27]  
GAO D, 1996, J GEOPHYS RES, V101, P9071
[28]   REASSESSMENT OF BIOGENIC VOLATILE ORGANIC-COMPOUND EMISSIONS IN THE ATLANTA AREA [J].
GERON, CD ;
PIERCE, TE ;
GUENTHER, AB .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (13) :1569-&
[29]   AN IMPROVED MODEL FOR ESTIMATING EMISSIONS OF VOLATILE ORGANIC-COMPOUNDS FROM FORESTS IN THE EASTERN UNITED-STATES [J].
GERON, CD ;
GUENTHER, AB ;
PIERCE, TE .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D6) :12773-12791
[30]  
GEUNTHER A, 1996, J GEOPHYS RES, V101, P1345