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首页> 外文期刊>Atmospheric chemistry and physics >Pseudo steady states of HONO measured in the nocturnal marine boundary layer: A conceptual model for HONO formation on aqueous surfaces
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Pseudo steady states of HONO measured in the nocturnal marine boundary layer: A conceptual model for HONO formation on aqueous surfaces

机译:夜间海洋边界层中测得的HONO的伪稳态:在水表面形成HONO的概念模型

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A complete understanding of the formation mechanism of nitrous acid (HONO) in the ambient atmosphere is complicated by a lack of understanding of processes occurring when aqueous water is present. We report nocturnal measurements of HONO, SO_2 and NO_2 by differential optical absorption spectroscopy over the ocean surface in a polluted marine environment. In this aqueous environment, we observed reproducible pseudo steady states (PSS) of HONO every night, that are fully formed shortly after sunset, much faster than seen in urban environments. During the PSS period, HONO is constant with time, independent of air mass source and independent of the concentration of NO _2. The independence of HONO on the concentration of NO_2 implies a 0° order formation process, likely on a saturated surface, with reversible partitioning of HONO to the gas phase, through vaporization and deposition to the surface. We observed median HONO/NO_2 ratios starting at 0.13 at the beginning of the PSS period (with an apparent lower bound of 0.03), rising to median levels of ~0.30 at the end of the PSS period (with an upper bound >1.0). The implication of these numbers is that they suggest a common surface mechanism of HONO formation on terrestrial and aqueous surfaces, with an increase in the HONO/NO2 ratio with the amount of water available at the surface. The levels of HONO during the nocturnal PSS period are positively correlated with temperature, consistent with a partitioning of HONO from the surface to the gas phase with an apparent enthalpy of vaporization of ΔHSNL (HONO)=55.5±5.4 κJ mol-1. The formation mechanism on aqueous surfaces is independent of relative humidity (RH), despite observation of a negative HONO-RH correlation. A conceptual model for HONO formation on ambient aqueous surfaces is presented, with the main elements being the presence of a surface nanolayer (SNL), highly acidic and saturated with N(IV) precursors, production of HNO 3, that diffuses to underlying water layers, and HONO, which partitions reversibly between the SNL and the gas phase. Implications of the conceptual model are discussed.
机译:对环境中亚硝酸(HONO)形成机理的完整理解由于缺乏对存在含水时发生的过程的理解而变得复杂。我们报告了在受污染的海洋环境中通过海洋表面的差分光学吸收光谱法对HONO,SO_2和NO_2的夜间测量结果。在这种水环境中,我们每天晚上观察到可再现的HONO伪稳态(PSS),该状态在日落后不久就完全形成,比在城市环境中观察到的速度快得多。在PSS期间,HONO随时间恒定,与空气质量源无关,与NO _2浓度无关。 HONO对NO_2浓度的独立性意味着可能在饱和表面上形成0°阶的形成过程,通过蒸发和沉积到表面,HONO与气相可逆分配。我们观察到,HONO / NO_2的中值比率在PSS阶段开始时从0.13开始(明显的下限为0.03),在PSS阶段结束时上升到中位数水平〜0.30(上限> 1.0)。这些数字的含义是,它们暗示了地面和水表面形成HONO的常见表面机制,随表面可用水量的增加,HONO / NO2的比例增加。夜间PSS期间HONO的水平与温度呈正相关,这与HONO从表面到气相的分配相一致,其表观汽化焓为ΔHSNL(HONO)= 55.5±5.4κJmol-1。尽管观察到负的HONO-RH相关性,但在水表面的形成机理与相对湿度(RH)无关。提出了在周围水表面形成HONO的概念模型,其主要元素是存在高酸性且被N(IV)前驱物饱和的表面纳米层(SNL)的存在,HNO 3的产生扩散到下面的水层和HONO,它们在SNL和气相之间可逆地分配。讨论了概念模型的含义。

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