A lightweight NO2-to-NOx conversion model for quantifying NOx emissions of point sources from NO2 satellite observations

IF 5.2 1区 地球科学 Q1 ENVIRONMENTAL SCIENCES
Sandro Meier, Erik F. M. Koene, Maarten Krol, Dominik Brunner, Alexander Damm, Gerrit Kuhlmann
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引用次数: 0

Abstract

Abstract. Nitrogen oxides (NOx = NO + NO2) are air pollutants which are co-emitted with CO2 during high-temperature combustion processes. Monitoring NOx emissions is crucial for assessing air quality and for providing proxy estimates of CO2 emissions. Satellite observations, such as those from the TROPOspheric Monitoring Instrument (TROPOMI) on board the Sentinel-5P satellite, provide global coverage at high temporal resolution. However, satellites measure only NO2, necessitating a conversion to NOx. Previous studies have applied a constant NO2-to-NOx conversion factor. In this paper, we develop a more realistic model for NO2-to-NOx conversion and apply it to TROPOMI data of 2020 and 2021. To achieve this, we analysed plume-resolving simulations from the MicroHH large-eddy simulation model with chemistry for the Bełchatów (PL), Jänschwalde (DE), Matimba (ZA) and Medupi (ZA) power plants, as well as a metallurgical plant in Lipetsk (RU). We used the cross-sectional flux method to calculate NO, NO2 and NOx line densities from simulated NO and NO2 columns and derived NO2-to-NOx conversion factors as a function of the time since emission. Since the method of converting NO2 to NOx presented in this paper assumes steady-state conditions and that the conversion factors can be modelled by a negative exponential function, we validated the conversion factors using the same MicroHH data. Finally, we applied the derived conversion factors to TROPOMI NO2 observations of the same sources. The validation of the NO2-to-NOx conversion factors shows that they can account for the NOx chemistry in plumes, in particular for the conversion between NO and NO2 near the source and for the chemical loss of NOx further downstream. When applying these time-since-emission-dependent conversion factors, biases in NOx emissions estimated from TROPOMI NO2 images are greatly reduced from between −50 % and −42 % to between only −9.5 % and −0.5 % in comparison with reported emissions. Single-overpass estimates can be quantified with an uncertainty of 20 %–27 %, while annual NOx emission estimates have uncertainties in the range of 4 %–21 % but are highly dependent on the number of successful retrievals. Although more simulations covering a wider range of meteorological and trace gas background conditions will be needed to generalise the approach, this study marks an important step towards a consistent, uniform, high-resolution and near-real-time estimation of NOx emissions – especially with regard to upcoming NO2-monitoring satellites such as Sentinel-4, Sentinel-5 and CO2M.
从二氧化氮卫星观测量化点源氮氧化物排放的轻量级二氧化氮-氮氧化物转换模型
摘要氮氧化物(NOx = NO + NO2)是高温燃烧过程中与二氧化碳共同排放的空气污染物。监测氮氧化物的排放对评估空气质量和提供二氧化碳排放的替代估算值至关重要。卫星观测,如 Sentinel-5P 卫星上的 TROPOspheric Monitoring Instrument(TROPOMI)所进行的观测,以高时间分辨率覆盖全球。不过,卫星只能测量二氧化氮,因此需要转换成氮氧化物。以往的研究采用的是恒定的二氧化氮到氮氧化物转换系数。在本文中,我们为二氧化氮到氮氧化物的转换建立了一个更现实的模型,并将其应用于 2020 年和 2021 年的 TROPOMI 数据。为此,我们分析了 MicroHH 大涡流模拟模型的羽流解析模拟,该模型包含 Bełchatów(波兰)、Jänschwalde(德国)、Matimba(南非)和 Medupi(南非)电厂以及利佩茨克(俄罗斯)冶金厂的化学模拟。我们使用横截面通量法,从模拟的一氧化氮和二氧化氮柱计算一氧化氮、二氧化氮和氮氧化物的线密度,并得出二氧化氮与氮氧化物的换算系数与排放后时间的函数关系。由于本文提出的将二氧化氮转换为氮氧化物的方法假定了稳态条件,并且转换系数可以用负指数函数来模拟,因此我们使用相同的 MicroHH 数据验证了转换系数。最后,我们将得出的转换因子应用于相同来源的 TROPOMI NO2 观测数据。二氧化氮到氮氧化物转换因子的验证结果表明,它们可以解释羽流中的氮氧化物化学反应,特别是源附近的氮氧化物和二氧化氮之间的转换以及下游氮氧化物的化学损失。应用这些与排放时间相关的转换因子后,从 TROPOMI NO2 图像估算出的氮氧化物排放量与报告排放量相比,偏差大大减小,从-50%到-42%之间减小到只有-9.5%到-0.5%之间。单次穿越估计值的不确定性为 20%-27% ,而氮氧化物年排放量估计值的不确定性在 4%-21% 之间,但高度依赖于成功检索的次数。虽然需要进行更多的模拟,涵盖更广泛的气象和痕量气体背景条件,才能推广这种方法,但这项研究标志着向一致、统一、高分辨率和近实时估算氮氧化物排放量迈出了重要一步--尤其是在即将发射的二氧化氮监测卫星(如哨兵-4、哨兵-5 和 CO2M)方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Atmospheric Chemistry and Physics
Atmospheric Chemistry and Physics 地学-气象与大气科学
CiteScore
10.70
自引率
20.60%
发文量
702
审稿时长
6 months
期刊介绍: Atmospheric Chemistry and Physics (ACP) is a not-for-profit international scientific journal dedicated to the publication and public discussion of high-quality studies investigating the Earth''s atmosphere and the underlying chemical and physical processes. It covers the altitude range from the land and ocean surface up to the turbopause, including the troposphere, stratosphere, and mesosphere. The main subject areas comprise atmospheric modelling, field measurements, remote sensing, and laboratory studies of gases, aerosols, clouds and precipitation, isotopes, radiation, dynamics, biosphere interactions, and hydrosphere interactions. The journal scope is focused on studies with general implications for atmospheric science rather than investigations that are primarily of local or technical interest.
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