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Denuder/filter sampling of organic acids and organosulfates at urban and boreal forest sites: Gas/particle distribution and possible sampling artifacts

机译:城市和北方森林站点的有机酸和有机硫酸盐的剥蚀/过滤采样:气体/颗粒分布和可能的采样伪像

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Carboxylic acids and organosulfates comprise an important fraction of atmospheric secondary organic aerosols formed from both anthropogenic and biogenic precursors. The partitioning of these compounds between the gas and particle phase is still unclear and further research is warranted to better understand the abundance and effect of organic acids and organosulfates on the formation and properties of atmospheric aerosols. This work compares atmospheric aerosols collected at an urban and a boreal forest site using two side-by-side sampling systems; a high volume sampler (HVS) and a low volume (LVS) denuder/filter sampling system allowing for separate collection of gas- and particle-phase organics. All particle filters and denuder samples were collected at H.C. Andersen Boulevard (HCAB), Copenhagen, Denmark in the summer of 2010, and at the remote boreal forest site at Hyytiala forestry field station in Finland in the summer of 2012. The chemical composition of gas- and particle-phase secondary organic aerosol was investigated by ultra-high performance liquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry (UPLC/ESI-Q-TOFMS), with a focus on carboxylic acids and organosulfates. Results show gas-phase concentrations higher than those observed in the particle phase by a factor of 5-6 in HCAB 2010 and 50-80 in Hyytiala 2012. Although abundant in the particle phase, no organosulfates were detected in the gas phase at either site. Through a comparison of samples collected by the HVS and the LVS denuder/filter sampling system we evaluate the potential artifacts associated with sampling of atmospheric aerosols. Such comparison shows that particle phase concentrations of semi-volatile organic acids obtained from the filters collected by HVS are more than two times higher than concentrations obtained from filters collected using LVS denuder/filter system. In most cases, higher concentrations of organosulfates are observed in particles collected by HVS compared to samples collected by LVS denuder/filter sampling system. The present study shows that volatile organics may absorb onto filter materials in the HVS (and similar sampling systems without denuder) and furthermore undergo subsequent on-filter oxidation and sulfation resulting in formation of both organic acids and organosulfates. (C) 2015 Elsevier Ltd. All rights reserved.
机译:羧酸和有机硫酸盐是由人为和生物前体形成的大气次级有机气溶胶的重要组成部分。这些化合物在气相和颗粒相之间的分配仍然不清楚,有必要进行进一步的研究以更好地理解有机酸和有机硫酸盐对大气气溶胶形成和性质的影响。这项工作使用两个并排的采样系统比较了城市和北方森林站点收集的大气气溶胶。高容量采样器(HVS)和低容量(LVS)剥蚀器/过滤器采样系统,可分别收集气相和颗粒相有机物。在H.C收集所有颗粒过滤器和剥蚀剂样品。于2010年夏季在丹麦哥本哈根的安徒生大道(HCAB)以及在2012年夏季在芬兰Hyytiala林业野外站的偏远的北方森林地带进行了研究。研究了气相和颗粒相二次有机气溶胶的化学成分通过超高效液相色谱/电喷雾电离四极杆飞行时间质谱(UPLC / ESI-Q-TOFMS),重点研究了羧酸和有机硫酸盐。结果表明,气相浓度比颗粒相中的浓度高HCAB 2010中的5-6倍,Hyytiala 2012中的气相中的50-80倍。尽管颗粒相中含量很高,但在任一位置的气相中均未检测到有机硫酸盐。通过比较由HVS和LVS剥蚀器/过滤器采样系统收集的样品,我们评估了与大气气溶胶采样相关的潜在伪影。这样的比较表明,从HVS收集的过滤器中获得的半挥发性有机酸的颗粒相浓度比从LVS剥蚀/过滤器系统收集的过滤器中获得的浓度高两倍以上。在大多数情况下,与通过LVS剥蚀/过滤器采样系统收集的样品相比,在HVS收集的颗粒中观察到更高浓度的有机硫酸盐。本研究表明,挥发性有机物可能会吸收到HVS(以及没有剥蚀剂的类似采样系统)中的过滤材料上,并且随后会在过滤器上进行氧化和硫酸化,从而形成有机酸和有机硫酸盐。 (C)2015 Elsevier Ltd.保留所有权利。

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