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Concentration and size distribution of particulate oxalate in marine and coastal atmospheres - Implication for the increased importance of oxalate in nanometer atmospheric particles

机译:海洋和沿海大气中草酸盐颗粒的浓度和尺寸分布-对草酸盐在纳米大气颗粒中重要性的增加表示

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摘要

In literature, particulate oxalate has been widely studied in the total suspended particles (TSP), particles <10 mu m or 2.5 mu m (PM10 and PM2.5) and size-segregated particles >100 nm. In this article, we measured oxalate's concentrations in size-segregated atmospheric particles down to 10 nm or 56 nm during eight campaigns performed at a semi-urban coastal site, over the marginal seas of China and from the marginal seas to the northwest Pacific Ocean (NWPO) in 2012-2015. When the sum of the oxalate's concentration in particles <10 mu m was used for intercomparison, the lowest average values of 0.05-0.06 mu g m(-3) were observed during the two campaigns performed at NWPO. The highest average value of 0.38 mu g m(-3) was observed at the coastal site during a heavy pollution event. Mode analysis results of particulate oxalate and the correlation between oxalate and sulfate suggested that the elevated concentrations of oxalate in PM10 were mainly related to enhanced in-cloud formation of oxalate via anthropogenic precursors. Size distribution data in the total of 136 sets of samples also showed approximately 80% of particulate oxalate's mass existing in atmospheric particles >100 nm. Consistent with previous studies, particulate oxalate in particles >100 nm was a negligible ionic component when comparing to particulate SO42- in the same size range. However, the mole ratios of oxalate/sulfate in particles <100 nm were generally increased by 1-2 orders of magnitude. In approximately 30% of the samples, the mole ratios in atmospheric particles <56 nm were larger than 0.5. Moreover, during Campaign 5, the oxalate's concentrations in <56 nm particles were substantially increased on the days in presence of new particle formation events. These results strongly imply the importance of oxalate in nanometer atmospheric particles, but not in >100 nm atmospheric particles such as PM2.5, PM10, TSP, etc. (C) 2016 Elsevier Ltd. All rights reserved.
机译:在文献中,草酸颗粒已经在总悬浮颗粒(TSP),<10微米或2.5微米的颗粒(PM10和PM2.5)以及尺寸分离的颗粒> 100 nm中得到了广泛的研究。在本文中,我们在半边际沿海站点,中国边缘海以及从边缘海到西北太平洋的八次活动中,测量了尺寸分离到10 nm或56 nm的尺寸分离的大气颗粒中的草酸盐浓度( NWPO)在2012-2015年。当使用草酸盐浓度小于10μm的颗粒进行比对时,在NWPO进行的两次运动中观察到的最低平均值为0.05-0.06μgm(-3)。在严重污染事件期间,沿海地区的最高平均值为0.38μg m(-3)。草酸盐颗粒的模式分析结果以及草酸盐和硫酸盐之间的相关性表明,PM10中草酸盐的浓度升高主要与通过人为前体在云中形成草酸盐的增加有关。总共136套样品的尺寸分布数据还显示,存在于大于100 nm的大气颗粒中的草酸颗粒质量约为80%。与以前的研究一致,当与相同尺寸范围内的SO42-颗粒相比时,> 100 nm颗粒中的草酸颗粒是可忽略的离子成分。然而,<100nm的颗粒中草酸盐/硫酸盐的摩尔比通常增加1-2个数量级。在大约30%的样品中,<56 nm的大气颗粒中的摩尔比大于0.5。此外,在活动5中,存在新的颗粒形成事件的日子里,<56 nm颗粒中草酸盐的浓度大大增加。这些结果强烈暗示草酸盐在纳米大气颗粒中的重要性,而不是在> 100 nm大气颗粒(例如PM2.5,PM10,TSP等)中的重要性。(C)2016 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Atmospheric environment 》 |2016年第10期| 19-31| 共13页
  • 作者单位

    Ocean Univ China, Minist Educ, Key Lab Marine Environm Sci & Ecol, Qingdao 266100, Peoples R China;

    Natl Marine Environm Forecasting Ctr, Beijing 100081, Peoples R China;

    Ocean Univ China, Minist Educ, Key Lab Marine Environm Sci & Ecol, Qingdao 266100, Peoples R China;

    Ocean Univ China, Minist Educ, Key Lab Marine Environm Sci & Ecol, Qingdao 266100, Peoples R China|Qingdao Collaborat Ctr Marine Sci & Technol, Qingdao 266100, Peoples R China;

    Ocean Univ China, Minist Educ, Key Lab Marine Environm Sci & Ecol, Qingdao 266100, Peoples R China|Qingdao Environm Monitoring Ctr, Qingdao 266003, Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Nanometer particles; Oxalate; Sulfate; Submicron particles; New particle formation;

    机译:纳米颗粒;草酸盐;硫酸盐;亚微米颗粒;新颗粒的形成;

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