期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 51, 期 12, 页码 6849-6856出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.7b00387
关键词
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资金
- NSF [ATM-0632548, AGS-1216166]
- Directorate For Geosciences
- Div Atmospheric & Geospace Sciences [1216166] Funding Source: National Science Foundation
Photolysis of nitric acid on the surface has been found recently to be greatly enhanced from that in the gas phase. Yet, photolysis of particulate nitrate (pNO(3)) associated with atmospheric aerosols is still relatively unknown. Here, aerosol filter samples were collected both near the ground surface and throughout the troposphere on board the NSF/NACR C-130 aircraft. The photolysis rate constants of pNO(3) were determined from these samples by directly monitoring the production rates of nitrous acid (HONO) and nitrogen dioxide (NO2) under UV light (>290 nm) irradiation. Scaled to the tropical noontime condition on the ground level (solar zenith angle = 0 degrees), the normalized photolysis rate constants (j(pNO3)(N)) are in the range from 6.2 X 10(-6) s(-1) to 5.0 X 10(-4) s(-1) with a median of 8.3 X 10(-5) s(-1) and a mean (+/-1 SD) of (1.3 +/- 1.2) x 10(-4) s(-1). Chemical compositions, specifically nitrate loading and organic matter, affect the rate of photolysis. Extrapolated to ambient pNO(3) loading conditions, e.g. <= 10 nmol m(-3), the mean jpNNo, value is over 1.8 X 10(-4) s(-1) in the suburban,
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