首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Alkyl nitrate photochemistry during the tropospheric organic chemistry experiment
Authors:David R Worton  Claire E Reeves  Stuart A Penkett  William T Sturges  Jana Slemr  David E Oram  Brian J Bandy  William J Bloss  Nicola Carslaw  James Davey  Kathryn M Emmerson  Thomas J Gravestock  Jacqueline F Hamilton  Dwayne E Heard  James R Hopkins  Anne Hulse  Trevor Ingram  Mark J Jacob  James D Lee  Roland J Leigh  Shona C Smith
Institution:1. State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing, China;2. Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Juelich GmbH, Juelich, Germany;3. International Joint laboratory for Regional pollution Control (IJRC), Peking University, Beijing, China;4. Beijing Innovation Center for Engineering Sciences and Advanced Technology, Peking University, Beijing, China;5. CAS Center for Excellence in Regional Atmospheric Environment, Chinese Academy of Science, Xiamen, China;1. Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of Environmental Science & Engineering, Institute of Atmospheric Sciences, Fudan University, Shanghai 200433, China;2. Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China;3. Collaborative Innovation Center of Atmospheric Environment and Equipment Technology (CICAEET), Nanjing University of Information Science and Technology, Nanjing 210044, China;1. Department of Environmental and Natural Resource Science, Faculty of Agriculture, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo 183-8538, Japan;2. Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, 1-1, Gakuen-cho, Naka-ku, Sakai, Osaka 599-8531, Japan;3. Tokyo Metropolitan Research Institute for Environmental Protection, 1-7-5 Shinsuna, Koto-ku, Tokyo 136-0075, Japan
Abstract:Alkyl nitrates (C1–C5) were measured at two sites (near urban and rural) in southeast England during the Tropospheric Organic Chemistry Experiment (TORCH). Methyl nitrate was the dominant species during both campaigns accounting for on average about one third of the total measured alkyl nitrates. High mixing ratios (>50 pptv) and variability of methyl nitrate were observed at the near urban site (TORCH1) that were not seen at the rural site (TORCH2) and which could not be explained by local photochemical production or direct emissions. The diurnal variation of methyl nitrate during TORCH1 showed a morning maximum that would be consistent with nighttime chemistry followed by transport to the surface by boundary layer dynamics. Similarly, elevated morning mixing ratios were also observed during TORCH2 although the magnitudes were much smaller. As a result, methyl nitrate could represent a tracer for nighttime chemistry seen at the ground the following day. At both campaigns, the dominant source of short chain alkyl nitrates and carbonyl precursor radicals (≤C4) were from decomposition of larger compounds. The magnitude of the source increased with decreasing carbon number consistent with increasing total precursor abundance. Non-photochemical emissions of acetaldehyde and acetone could not be accounted for by automobile exhaust emissions alone and indicated that other direct sources are likely important in this environment.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号