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大气中的过氧乙酰硝酸酯(PAN):全球收支与来源归因。

Atmospheric peroxyacetyl nitrate (PAN): a global budget and source attribution.

作者信息

Fischer E V, Jacob D J, Yantosca R M, Sulprizio M P, Millet D B, Mao J, Paulot F, Singh H B, Roiger A, Ries L, Talbot R W, Dzepina K, Pandey Deolal S

机构信息

Department of Atmospheric Science, Colorado State University, Fort Collins, CO, USA.

School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.

出版信息

Atmos Chem Phys. 2014 Mar;14(5):2679-2698. doi: 10.5194/acp-14-2679-2014. Epub 2014 Mar 14.

DOI:10.5194/acp-14-2679-2014
PMID:33758588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7983850/
Abstract

Peroxyacetyl nitrate (PAN) formed in the atmospheric oxidation of non-methane volatile organic compounds (NMVOCs) is the principal tropospheric reservoir for nitrogen oxide radicals (NO = NO + NO). PAN enables the transport and release of NO to the remote troposphere with major implications for the global distributions of ozone and OH, the main tropospheric oxidants. Simulation of PAN is a challenge for global models because of the dependence of PAN on vertical transport as well as complex and uncertain NMVOC sources and chemistry. Here we use an improved representation of NMVOCs in a global 3-D chemical transport model (GEOS-Chem) and show that it can simulate PAN observations from aircraft campaigns worldwide. The immediate carbonyl precursors for PAN formation include acetaldehyde (44% of the global source), methylglyoxal (30 %), acetone (7 %), and a suite of other isoprene and terpene oxidation products (19 %). A diversity of NMVOC emissions is responsible for PAN formation globally including isoprene (37 %) and alkanes (14 %). Anthropogenic sources are dominant in the extratropical Northern Hemisphere outside the growing season. Open fires appear to play little role except at high northern latitudes in spring, although results are very sensitive to plume chemistry and plume rise. Lightning NO is the dominant contributor to the observed PAN maximum in the free troposphere over the South Atlantic.

摘要

在非甲烷挥发性有机化合物(NMVOCs)的大气氧化过程中形成的过氧乙酰硝酸酯(PAN)是对流层中氮氧化物自由基(NO = NO + NO)的主要储存库。PAN使得NO能够向对流层偏远区域传输和释放,这对对流层主要氧化剂臭氧和OH的全球分布具有重大影响。由于PAN对垂直输送以及复杂且不确定的NMVOC源和化学反应的依赖性,对其进行模拟是全球模型面临的一项挑战。在此,我们在一个全球三维化学输送模型(GEOS-Chem)中对NMVOCs采用了改进的表示方法,并表明该模型能够模拟全球范围内飞机观测活动中得到的PAN数据。形成PAN的直接羰基前体包括乙醛(占全球源的44%)、甲基乙二醛(30%)、丙酮(7%)以及其他一系列异戊二烯和萜烯氧化产物(19%)。全球范围内多种NMVOC排放都对PAN的形成有贡献,包括异戊二烯(37%)和烷烃(14%)。在生长季节之外的北半球温带地区,人为源占主导地位。明火似乎作用不大,除了在春季高纬度地区,不过结果对羽流化学和羽流上升非常敏感。闪电产生的NO是南大西洋对流层自由大气中观测到的PAN最大值的主要贡献者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0823/7983850/fdd75bb7ed73/nihms-1669552-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0823/7983850/7d0a30aaa065/nihms-1669552-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0823/7983850/7961aedeb7ce/nihms-1669552-f0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0823/7983850/fdd75bb7ed73/nihms-1669552-f0007.jpg

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