Chemical indicators of sulfate sensitivity to nitrogen oxides and volatile organic compounds

被引:13
作者
Stein, AF [1 ]
Lamb, D [1 ]
机构
[1] Penn State Univ, Dept Meteorol, University Pk, PA 16802 USA
来源
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES | 2002年 / 107卷 / D20期
关键词
aerosols; sulfate and nitrate; chemical indicators; photochemical oxidants; air quality; photochemical modeling;
D O I
10.1029/2001JD001088
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The formation of aerosol sulfate (SO42-) in eastern North America is chemically linked to the emissions of nitrogen oxides (NOx) and volatile organic compounds (VOC) through oxidation of the gaseous precursor, sulfur dioxide (SO2). The response of sulfate production to controls in NOx and VOC emissions depends, in part, on the resulting changes in oxidant levels and the competition that naturally exists between the gas- and aqueous-phase pathways for SO2 oxidation. We propose the use of a combination of concentrations of nitric acid, particulate nitrate, hydrogen peroxide, and ambient sulfate as a nondimensional indicator of the effectiveness of VOC or NOx controls in decreasing SO42- abundance. The concentrations of these indicator species were calculated from a series of photochemical model simulations with varying rates of NOx and VOC emissions using a three-dimensional Eulerian model (MODELS-3) that covers the northeastern United States. This study shows that ambient sulfate concentrations are likely to decrease more effectively as VOC emissions are reduced, when the nondimensional indicator is less than a certain threshold. However, a higher value of the indicator identifies a regime in which NOx emissions reductions are more effective for reducing sulfate than are VOC emissions. In addition, a description of the sulfate-formation pathways, along with a theoretical analysis of the transition between NOx- and VOC-sensitive regimes, provides a strong rationale for the use of the sulfate sensitivity indicator.
引用
收藏
页码:ACH13 / 1
页数:11
相关论文
共 41 条
[1]   The Regional Particulate Matter Model .1. Model description and preliminary results [J].
Binkowski, FS ;
Shankar, U .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1995, 100 (D12) :26191-26209
[2]  
BRUNEKREEF B, 1995, ENVIRON HEALTH PER S, V103, pS3
[3]   MECHANISM OF HOMOGENEOUS OXIDATION OF SULFUR-DIOXIDE IN TROPOSPHERE [J].
CALVERT, JG ;
SU, F ;
BOTTENHEIM, JW ;
STRAUSZ, OP .
ATMOSPHERIC ENVIRONMENT, 1978, 12 (1-3) :197-226
[4]  
CHANG JS, 1990, 4 NATL AC PREC ASS P
[5]   Air pollution and health:: Correlation or causality?: The case of the relationship between exposure to particles and cardiopulmonary mortality [J].
Dab, W ;
Ségala, C ;
Dor, F ;
Festy, B ;
Lameloise, P ;
Le Moullec, Y ;
Le Tertre, A ;
Médina, S ;
Quénel, P ;
Wallaert, B ;
Zmirou, D .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2001, 51 (02) :220-235
[6]   MEASUREMENTS OF THE CHEMICAL-COMPOSITION OF STRATIFORM CLOUDS [J].
DAUM, PH ;
KELLY, TJ ;
SCHWARTZ, SE ;
NEWMAN, L .
ATMOSPHERIC ENVIRONMENT, 1984, 18 (12) :2671-2684
[7]  
DeMore W. B., 1997, JPL PUBL
[8]   The next generation of integrated air quality modeling: EPA's Models-3 [J].
Dennis, RL ;
Byun, DW ;
Novak, JH ;
Galluppi, KJ ;
Coats, CJ ;
Vouk, MA .
ATMOSPHERIC ENVIRONMENT, 1996, 30 (12) :1925-1938
[9]   HOMOGENEOUS OXIDATION OF SULFUR-COMPOUNDS IN ATMOSPHERE [J].
EGGLETON, AEJ ;
COX, RA .
ATMOSPHERIC ENVIRONMENT, 1978, 12 (1-3) :227-230
[10]  
*ENV PROT AG, 1996, EPA600P95001AF OFF R