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Direct aerosol chemical composition measurements to evaluate the physicochemical differences between controlled sea spray aerosol generation schemes

机译:直接气溶胶化学成分测量,以评估受控海喷雾气溶胶生成方案之间的理化差异

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Controlled laboratory studies of the physical and chemical properties of sea spray aerosol (SSA) must be under-pinned by a physically and chemically accurate representation of the bubble-mediated production of nascent SSA particles. Bubble bursting is sensitive to the physico-chemical properties of seawater. For a sample of seawater, any important differences in the SSA production mechanism are projected into the composition of the aerosol particles produced. Using direct chemical measurements of SSA at the single-particle level, this study presents an intercomparison of three laboratory-based, bubble-mediated SSA production schemes: gas forced through submerged sintered glass filters ("frits"), a pulsed plunging-waterfall apparatus, and breaking waves in a wave channel filled with natural seawater. The size-resolved chemical composition of SSA particles produced by breaking waves is more similar to particles produced by the plunging waterfall than those produced by sintered glass filters. Aerosol generated by disintegrating foam produced by sintered glass filters contained a larger fraction of organic-enriched particles and a different size-resolved elemental composition, especially in the 0.8–2 μm dry diameter range. Interestingly, chemical differences between the methods only emerged when the particles were chemically analyzed at the single-particle level as a function of size; averaging the elemental composition of all particles across all sizes masked the differences between the SSA samples. When dried, SSA generated by the sintered glass filters had the highest fraction of particles with spherical morphology compared to the more cubic structure expected for pure NaCl particles produced when the particle contains relatively little organic carbon. In addition to an intercomparison of three SSA production methods, the role of the episodic or "pulsed" nature of the waterfall method on SSA composition was under-taken. In organic-enriched seawater, the continuous operation of the plunging waterfall resulted in the accumulation of surface foam and an over-expression of organic matter in SSA particles compared to those produced by a pulsed plunging waterfall. Throughout this set of experiments, comparative differences in the SSA number size distribution were coincident with differences in aerosol particle composition, indicating that the production mechanism of SSA exerts important controls on both the physical and chemical properties of the resulting aerosol with respect to both the internal and external mixing state of particles. This study provides insight into the inextricable physicochemical differences between each of the bubble-mediated SSA generation mechanisms tested and the aerosol particles that they produce, and also serves as a guideline for future laboratory studies of SSA particles.
机译:海洋喷雾气溶胶(SSA)的物理和化学性质的受控实验室研究必须通过气泡介导的新生SSA颗粒的物理和化学精确表示来加强。气泡破裂对海水的物理化学性质敏感。对于海水样品,SSA产生机理中的任何重要差异都将推算为产生的气溶胶颗粒的组成。使用单颗粒水平上SSA的直接化学测量结果,本研究提出了三种基于实验室的,气泡介导的SSA生产方案的比较:气体通过浸入式烧结玻璃过滤器(“玻璃料”),脉冲骤降式瀑布仪,并在充满天然海水的海浪通道中冲破海浪。通过破碎波产生的SSA颗粒的尺寸分辨化学组成与由瀑布形成的颗粒比由烧结玻璃过滤器产生的颗粒更相似。分解由烧结玻璃过滤器产生的泡沫而产生的气溶胶含有较大比例的有机物富集颗粒和不同的尺寸分辨元素组成,尤其是在干直径0.8–2μm范围内。有趣的是,两种方法之间的化学差异仅在对颗粒进行单分子水平的化学分析时才出现,这是粒径的函数。对所有尺寸的所有颗粒的元素组成取平均值,可以掩盖SSA样品之间的差异。干燥后,与烧结的玻璃滤光片产生的SSA相比,具有球形形态的颗粒比例最高,而当颗粒中有机碳含量相对较低时,所产生的纯NaCl颗粒具有更立方的结构。除了对三种SSA生产方法的比较之外,还采用了瀑布方法的情景式或“脉冲式”性质对SSA组成的作用。在富含有机物的海水中,瀑布的连续运行导致SSA颗粒中表面泡沫的积累和有机物过表达,而脉冲状瀑布则产生了有机泡沫。在这组实验中,SSA数量大小分布的相对差异与气溶胶颗粒组成的差异相吻合,这表明SSA的生成机制对所得气溶胶的内部和内部物理化学特性均起重要控制作用和颗粒的外部混合状态。这项研究提供了对所测试的每个气泡介导的SSA生成机制与它们产生的气溶胶颗粒之间不可分割的物理化学差异的了解,并且还为将来的SSA颗粒实验室研究提供了指南。

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