THE NATURE AND ORIGINS OF ACID SUMMER HAZE AIR-POLLUTION IN METROPOLITAN TORONTO, ONTARIO

被引:20
作者
THURSTON, GD
GORCZYNSKI, JE
CURRIE, JH
HE, D
ITO, K
HIPFNER, J
WALDMAN, J
LIOY, PJ
LIPPMANN, M
机构
[1] ONTARIO MINIST ENVIRONM & ENERGY,ETIBICOKE,ON,CANADA
[2] UNIV MED & DENT NEW JERSEY,ROBERT WOOD JOHNSON MED SCH,DEPT ENVIRONM & COMMUNITY MED,PISCATAWAY,NJ 08854
关键词
D O I
10.1006/enrs.1994.1036
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
During July and August of 1986, 1987, and 1988, a field study was conducted of ambient acidic aerosol levels in Toronto, Ontario. Fine particle mass (d(a) < 2.5 mu m) samples were collected twice daily at a central-city site for the determination of particulate-phase strong acidity (H+) and sulfate (SO4=). Two additional H+-monitoring sites were concurrently operated during the summers of 1986 and 1987 to examine the spatial variability of H+ within the metropolitan area. During the summer of 1986, a quasicontinuous total sulfate/sulfuric acid analyzer was also deployed to allow a determination of the chemical form of H+. Results indicate that acid aerosol episodes (H+ greater than or similar to 100 nmole/m(3)) did occur in this city during the summer months, and that H+ peaks were well correlated with sulfate peaks. Virtually all of the H+ was found to be present as ammonium bisulfate (NH4HSO4). While H+ concentrations were highly correlated among the three monitoring sites (r = 0.9), the highest H+/SO4= ratios prevailed during SO4= episode periods and at the least urbanized site. This latter trend was apparently due to greater neutralization of H+ by local ammonia at the more urbanized sites. Comparisons of day vs night H+/SO4= ratios, an examination of air mass back-trajectories, and contemporaneous H+ measurements at surrounding sites collectively indicated that transported regional haze air pollution from the United States is a major contributor to the H+ events recorded within Toronto. (C) 1994 Academic Press, Inc.
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页码:254 / 270
页数:17
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