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Modeling organic aerosol concentrations and properties during winter 2014 in the northwestern Mediterranean region

机译:2014年冬季地中海地区冬季建模有机气溶胶浓度和特性

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Organic aerosols are measured at a remote site (Ersa) on the cape of Corsica in the northwestern Mediterranean basin during the winter campaign of 2014 of the CHemistry and AeRosols Mediterranean EXperiment (CharMEx), when high organic concentrations from anthropogenic origins are observed. This work aims to represent the observed organic aerosol concentrations and properties (oxidation state) using the air-quality model Polyphemus with a surrogate approach for secondary organic aerosol (SOA) formation. Because intermediate and semi-volatile organic compounds (I/S-VOCs) are the main precursors of SOAs at Ersa during winter 2014, different parameterizations to represent the emission and aging of I/S-VOCs were implemented in the chemistry-transport model of Polyphemus (different volatility distribution emissions and single-step oxidation vs multi-step oxidation within a volatility basis set – VBS – framework, inclusion of non-traditional volatile organic compounds – NTVOCs). Simulations using the different parameterizations are compared to each other and to the measurements (concentration and oxidation state). The highly observed organic concentrations are well reproduced in all the parameterizations. They are slightly underestimated in most parameterizations. The volatility distribution at emissions influences the concentrations more strongly than the choice of the parameterization that may be used for aging (single-step oxidation vs multi-step oxidation), stressing the importance of an accurate characterization of emissions. Assuming the volatility distribution of sectors other than residential heating to be the same as residential heating may lead to a strong underestimation of organic concentrations. The observed organic oxidation and oxygenation states are strongly underestimated in all simulations, even when multigenerational aging of I/S-VOCs from all sectors is modeled. This suggests that uncertainties in the emissions and aging of I/S-VOC emissions remain to be elucidated, with a potential role of formation of organic nitrate and low-volatility highly oxygenated organic molecules.
机译:在2014年的冬季运动中,在西北地中海盆地的偏远地点(ERSA)偏远地点(ERSA)测量了有机气溶胶在2014年的化学和气溶胶地中海实验(Charmex)中,当观察到来自人为起源的高有机浓度。该工作旨在代表观察到的有机气溶胶浓度和性质(氧化态),使用具有替代有机气溶胶(SOA)形成的替代方法的空气质量模型复分。因为中间体和半挥发性有机化合物(I / S-VOC)是2014年冬季ERSA的SOA的主要前体,所以在化学运输模型中实施了不同的参数化以代表I / S-VOC的发射和老化多孔(不同的挥发性分布排放和单步氧化与挥发性基于挥发性的多步氧化 - VBS框架,包含非传统挥发性有机化合物 - NTVOC)。使用不同参数化的模拟彼此相互比较和测量(浓度和氧化状态)。在所有参数化中,高度观察到的有机浓度很好地再现。它们在大多数参数化中略微低估。排放的波动分布影响比可用于老化的参数化的浓度更强烈(单步氧化对多步氧化),强调了精确表征排放的重要性。假设除了住宅加热之外的扇区的波动率分布与住宅加热相同,可能导致有机浓度的强烈低估。在所有模拟中,所观察到的有机氧化和氧合态在所有模拟中都非常低估,即使所有扇区的I / S-VOC的多酿造老化都是为模拟的。这表明I / S-VOC排放的排放和老化的不确定性仍然阐明,具有有机硝酸盐和低挥发性高度含氧有机分子的潜在作用。

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