Emissions lifetimes and ozone formation in power plant plumes

被引:174
作者
Ryerson, TB
Buhr, MP
Frost, GJ
Goldan, PD
Holloway, JS
Hubler, G
Jobson, BT
Kuster, WC
McKeen, SA
Parrish, DD
Roberts, JM
Sueper, DT
Trainer, M
Williams, J
Fehsenfeld, FC
机构
[1] NOAA, Aeron Lab, Boulder, CO 80303 USA
[2] Univ Colorado, NOAA, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
关键词
D O I
10.1029/98JD01620
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The concept of ozone production efficiency (OPE) per unit NOx is based on photochemical models and provides a tool with which to assess potential regional tropospheric ozone control strategies involving NOx emissions reductions. An aircraft study provided data from which power plant emissions removal rates and measurement-based estimates of OPE are estimated. This study was performed as part of the Southern Oxidants Study-1995 Nashville intensive and focuses on the evolution of NOx, SO2, and ozone concentrations in power plant plumes during transport. Two approaches are examined. A mass balance approach accounts for mixing effects within the boundary layer and is used to calculate effective boundary layer removal rates for NOx and SO2 and to estimate net OPE. Net OPE is more directly comparable to photochemical model results than previous measurement-based estimates. Derived net production efficiencies from mass balance range from 1 to 3 molecules of ozone produced per molecule of NOx emitted. A concentration ratio approach provides an estimate of removal rates of primary emissions relative to a tracer species. This approach can be combined with emissions ratio information to provide upper limit estimates of OPE that range from 2 to 7. Both approaches illustrate the dependence of ozone production on NOx source strength in these large point source plumes. The dependence of total ozone production, ozone production efficiency, and the rate of ozone production on NOx source strength is examined. These results are interpreted in light of potential ozone control strategies for the region.
引用
收藏
页码:22569 / 22583
页数:15
相关论文
共 43 条
[1]   BOUNDARY-LAYER DEPTH AND ENTRAINMENT ZONE CHARACTERIZATION WITH A BOUNDARY-LAYER PROFILER [J].
ANGEVINE, WM ;
WHITE, AB ;
AVERY, SK .
BOUNDARY-LAYER METEOROLOGY, 1994, 68 (04) :375-385
[2]  
ANTHES RA, 1987, 282 NCAR
[3]   THE BIOGEOCHEMICAL SULFUR CYCLE IN THE MARINE BOUNDARY-LAYER OVER THE NORTHEAST PACIFIC-OCEAN [J].
BATES, TS ;
JOHNSON, JE ;
QUINN, PK ;
GOLDAN, PD ;
KUSTER, WC ;
COVERT, DC ;
HAHN, CJ .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1990, 10 (01) :59-81
[4]   OZONE PRECURSOR RELATIONSHIPS IN THE AMBIENT ATMOSPHERE [J].
CHAMEIDES, WL ;
FEHSENFELD, F ;
RODGERS, MO ;
CARDELINO, C ;
MARTINEZ, J ;
PARRISH, D ;
LONNEMAN, W ;
LAWSON, DR ;
RASMUSSEN, RA ;
ZIMMERMAN, P ;
GREENBERG, J ;
MIDDLETON, P ;
WANG, T .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D5) :6037-6055
[5]   RELATIONSHIP OF OZONE AND CARBON-MONOXIDE OVER NORTH-AMERICA [J].
CHIN, M ;
JACOB, DJ ;
MUNGER, JW ;
PARRISH, DD ;
DODDRIDGE, BG .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D7) :14565-14573
[7]   Chemical and physical properties of plumes of anthropogenic pollutants transported over the North Atlantic during the North Atlantic Regional Experiment [J].
Daum, PH ;
Kleinman, LI ;
Newman, L ;
Luke, WT ;
WeinsteinLloyd, J ;
Berkowitz, CM ;
Busness, KM .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D22) :29029-29042
[8]  
DLUGI R, 1982, J HUNG METEOROL SERV, V86, P82
[9]  
Finlayson-Pitts B.J., 1986, Atmospheric Chemistry: Fundamentals and Experimental Techniques
[10]   GAS-TO-PARTICLE CONVERSION OF SULFUR IN POWER-PLANT PLUMES .1. PARAMETRIZATION OF THE CONVERSION RATE FOR DRY, MODERATELY POLLUTED AMBIENT CONDITIONS [J].
GILLANI, NV ;
KOHLI, S ;
WILSON, WE .
ATMOSPHERIC ENVIRONMENT, 1981, 15 (10-1) :2293-2313