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Assessing The Potential For Diol And Hydroxy Sulfate Ester Formation From The Reaction Of Epoxides In Tropospheric Aerosols

机译:通过对流层气溶胶中环氧化合物的反应评估生成二羟醇和羟硫酸酯的可能性

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摘要

Polyols and sulfate esters have recently been identified in the secondary organic aerosol (SOA) formed in the photooxidation of biogenic hydrocarbons both in the laboratory and under ambient atmospheric conditions, Inthe present study, the potential role of the reactions of epoxides in SOA to form diols and hydroxy sulfate esters is explored. Nuclear magnetic resonance methods were used to monitor the bulk reaction kinetics of the epoxide hydrolysis reactions for a number of simple epoxides. The experiments were carried out at various acid concentrations in order to confirm the acid-catalysis rate order and to determine the second-order rate constants for such reactions in aerosols under the previously studied laboratory conditions and under ambient atmospheric conditions. The measured rate constants depended systematically on the carbon substitution nature of the epoxide ring, with the tertiary epoxides characterized by the largest rate constants. The hydroxy sulfate yield was observed to depend linearly on the total sulfate concentration, with yields as high as 30% observed at high sulfate concentrations. Due to the large values of the observed rate constants, these reactions are expected to be efficient even for mostly neutralized tropospheric SOA, let alone the much more acidic SOA particles previously studied in laboratory experiments. Therefore, the epoxide hydrolysis mechanism appears to be a kinetically feasible route to the formation of the diols and hydroxy sulfate esters observed inthe SOA resulting from the photooxidation of biogenic hydrocarbons.
机译:最近在实验室和环境大气条件下,在生物碳氢化合物的光氧化中形成的次级有机气溶胶(SOA)中,均已鉴定出多元醇和硫酸酯。在本研究中,环氧化物在SOA中反应生成二醇的潜在作用并研究了羟基硫酸酯。核磁共振方法用于监测许多简单环氧化物的环氧化物水解反应的整体反应动力学。在各种酸浓度下进行实验,以确认酸催化速率的阶次,并确定在先前研究的实验室条件下和环境大气条件下在气溶胶中进行此类反应的二级速率常数。测得的速率常数系统地取决于环氧化物的碳取代性质,其中叔环氧化物的特征在于最大的速率常数。观察到羟基硫酸盐的产率线性依赖于总硫酸盐的浓度,在高硫酸盐浓度下观察到的产率高达30%。由于观察到的速率常数值很大,因此即使对于大多数中和的对流层SOA,这些反应也有望有效,更不用说以前在实验室实验中研究过的酸性更高的SOA颗粒。因此,环氧化物水解机理似乎是从生物碳氢化合物的光氧化反应中形成的,在SOA中观察到的二醇和羟基硫酸酯形成的动力学可行途径。

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  • 来源
    《Environmental Science & Technology》 |2009年第5期|1386-1392|共7页
  • 作者单位

    Department of Chemistry and Biochemistry, 119 WoodlandrnStreet, Oberlin College, Oberlin, Ohio 44074;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-17 14:04:21

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