Impact of environmental variables on the reduction of nitric acid by proxies for volatile organic compounds emitted by motor vehicles
| Autor: | Robert J. Griffin, H. Y. Wong, C. Gutierrez, M. Junaid, Longwen Gong, Y. J. Leong, Frank K. Tittel, Jack E. Dibb, Eric Scheuer, Andrew P. Rutter, R. Lewicki |
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| Rok vydání: | 2016 |
| Předmět: |
Atmospheric Science
Nitrous acid Reaction mechanism Ozone 010504 meteorology & atmospheric sciences 010501 environmental sciences Photochemistry 01 natural sciences Pollution Redox Aerosol chemistry.chemical_compound Ammonia chemistry Nitric acid Relative humidity Waste Management and Disposal 0105 earth and related environmental sciences |
| Zdroj: | Atmospheric Pollution Research. 7:221-227 |
| ISSN: | 1309-1042 |
| Popis: | Recent work has identified nitric acid (HNO3) as a potential precursor of nitrous acid (HONO), which is an important source of oxidants that regulate ozone and particulate pollution. Recent work in our laboratory has indicated that the reduction of HNO3 to HONO can occur homogeneously in the presence of surrogates for volatile organic compounds (VOCs) emitted by motor vehicles. This study focuses on the impact of environmental variables on the rate of formation of HONO in this process. The observed base case (25.0 °C and ∼20.0% relative humidity (RH)) HONO formation rate was 0.54 ± 0.09 ppb h−1, values comparable to enhancements observed in HONO during morning rush hour in Houston, TX. The rate was enhanced at lower temperatures of ∼20.0 °C, but the rate remained statistically similar (1σ) for experiments conducted at temperatures of 25 °C, 30 °C, and 35 °C. The assumption that multiple reactive components of the VOC mixture react with HNO3 is supported by this observation, and the relative importance of each reactive species in the reaction may vary with temperature. The enhanced rate at lower temperatures could make the proposed reaction mechanism more important at night. The formation rate of HONO does not change substantially when initial HNO3 concentration is varied between 400 and 4600 ppt, suggesting that the concentration of reactive VOCs was the limiting factor. The reduction of HNO3 to HONO appears not to occur heterogeneously on the aerosol surfaces tested. The presence of ∼120 ppb of ammonia has no observable impact on the reaction. However, it is likely that UV irradiation (λ = 350 nm) decreases the formation rate of HONO either by consuming the reactive VOCs involved or by directly interfering with the reaction. The “renoxification” of less reactive HNO3 to more reactive HONO has significant implications for daytime ozone and particulate pollution. |
| Databáze: | OpenAIRE |
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