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Influence of Seed Aerosol Surface Area and Oxidation Rate on Vapor-Wall Deposition and SOA Mass Yields: A case study with α-pinene Ozonolysis

机译:种子气溶胶表面积和氧化率对蒸汽壁沉积和SOA质量产量的影响:一种α-叉烯臭氧溶解的案例研究

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摘要

Laboratory chambers, invaluable in atmospheric chemistry and aerosol formation studies, are subject to particle and vapor wall deposition, processes that need to be accounted for in order to accurately determine secondary organic aerosol (SOA) mass yields. Although particle wall deposition is reasonably well understood and usually accounted for, vapor wall deposition is less so. The effects of vapor wall deposition on SOA mass yields in chamber experiments can be constrained experimentally by increasing the seed aerosol surface area to promote the preferential condensation of SOA-forming vapors onto seed aerosol. Here, we study the influence of seed aerosol surface area and oxidation rate on SOA formation in α-pinene ozonolysis. The observations are analyzed using a coupled vapor–particle dynamics model to interpret the roles of gas–particle partitioning (quasi-equilibrium vs. kinetically limited SOA growth) and α-pinene oxidation rate in influencing vapor wall deposition. We find that the SOA growth rate and mass yields are independent of seed surface area within the range of seed surface area concentrations used in this study. This behavior arises when the condensation of SOA-forming vapors is dominated by quasi-equilibrium growth. Faster α-pinene oxidation rates and higher SOA mass yields are observed at increasing O3 concentrations for the same initial α-pinene concentration. When the α-pinene oxidation rate increases relative to vapor wall deposition, rapidly produced SOA-forming oxidation products condense more readily onto seed aerosol particles, resulting in higher SOA mass yields. Our results indicate that the extent to which vapor wall deposition affects SOA mass yields depends on the particular volatility organic compound system and can be mitigated through the use of excess oxidant concentrations.
机译:实验室室在大气化学和气溶胶形成研究中具有不可估量的价值,它经受颗粒和蒸气壁沉积的影响,这些过程必须加以考虑才能准确确定次要有机气溶胶(SOA)的产量。尽管合理地理解并通常考虑了颗粒壁沉积,但是气相壁沉积却很少。通过增加种子气溶胶表面积以促进形成SOA的蒸汽优先凝结到种子气溶胶上,可以通过实验限制蒸汽室壁沉积对室实验中SOA产量的影响。在这里,我们研究了α-pine烯臭氧分解中种子气溶胶表面积和氧化速率对SOA形成的影响。使用耦合的蒸汽-颗粒动力学模型分析观测结果,以解释气体-颗粒分配(准平衡与动力学受限的SOA生长)和α-pine烯氧化速率在影响气相壁沉积中的作用。我们发现,在本研究中使用的种子表面积浓度范围内,SOA的生长速率和产量与种子表面积无关。当形成SOA的蒸汽的冷凝主要由准平衡生长引起时,就会出现这种现象。在相同的初始α-pine烯浓度下,随着O3浓度的增加,观察到更快的α-pine烯氧化速率和较高的SOA质量产率。当α-pine烯的氧化速率相对于气相壁沉积增加时,快速生成的形成SOA的氧化产物更容易凝结在种子气溶胶颗粒上,从而导致更高的SOA质量产率。我们的结果表明,蒸汽壁沉积影响SOA量产的程度取决于特定的挥发性有机化合物系统,可以通过使用过量的氧化剂来缓解。

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