Comparing Short-Term Volatile Organic Compound Measurements in Fenceline Environments Using Multiple Mobile Air Monitoring Platforms and Methods

Justin G. Coughlin*, Antonios Tasoglou, Katherine Haile, Leslie P. Silva, Scott Hamilton, Marta Fuoco, Samuel Porter, Aikaterini Liangou and Eben Thoma, 
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Abstract

The presence of volatile organic compounds (VOCs) can increase the air pollution burden in fenceline communities. Technological advancements have made mobile air toxic monitoring a useful and attractive approach to spatially quantify VOC concentrations in real-time, but there is a need to evaluate the accuracy of these measurements in real-world applications using intercomparison techniques. Here, we conducted a two-week field campaign near different VOC-emitting facilities using three different mobile monitoring platforms and four different ambient VOC-measurement technologies. Our primary focus was the intercomparison of a proton transfer reaction time-of-flight mass spectrometer (PTR-ToF-MS) and canister samples analyzed by an offline gas chromatograph mass spectrometer (GC-MS), but we also collected measurements using a closed-path ultraviolet differential optical absorption spectrometer (UV-DOAS) and a selected ion flow tube mass spectrometer (SIFT-MS). The PTR-ToF-MS and offline GC-MS analyses show strong agreement in stationary settings (all targeted VOCs R2 = 0.92, slope = 1.1) for aromatic compounds including benzene (R2 = 0.95, p < 0.001), naphthalene (R2 = 0.84, p < 0.01), and xylenes + ethylbenzene (R2 = 0.93, p < 0.01). PTR-ToF-MS and UV-DOAS comparisons have varied results. The UV-DOAS compared well at some monitoring locations but had poor agreement in ambient air matrices containing naphthalene, which caused uncorrectable interferences for measurements of benzene, toluene, and xylenes. Lastly, the PTR-ToF-MS and SIFT-MS showed strong agreement (all targeted VOCs R2 = 0.68, slope = 0.85) in mobile format comparisons but only when aldehyde compounds with high background noise were removed. Our results highlight some potential interferences that should be accounted for when performing monitoring of mobile air toxics and demonstrate multi-instrument comparison techniques that can be used to ensure robust data collection.

Abstract Image

使用多种移动空气监测平台和方法比较围栏环境中挥发性有机化合物的短期测量
挥发性有机化合物(VOCs)的存在会增加围栏社区的空气污染负担。技术进步使移动空气毒性监测成为一种有用且有吸引力的方法,可以实时定量VOC浓度的空间,但需要使用相互比较技术来评估这些测量在实际应用中的准确性。在这里,我们使用三种不同的移动监测平台和四种不同的环境voc测量技术,在不同的voc排放设施附近进行了为期两周的实地调查。我们的主要焦点是质子转移反应飞行时间质谱仪(PTR-ToF-MS)和离线气相色谱质谱仪(GC-MS)分析的罐样的相互比较,但我们也收集了使用闭路紫外微分光学吸收光谱仪(UV-DOAS)和选择离子流管质谱仪(SIFT-MS)的测量结果。PTR-ToF-MS和离线GC-MS分析显示,在固定环境下(所有目标VOCs R2 = 0.92,斜率= 1.1),芳香族化合物包括苯(R2 = 0.95, p <;0.001)、萘(R2 = 0.84, p <;0.01),二甲苯+乙苯(R2 = 0.93, p <;0.01)。PTR-ToF-MS和UV-DOAS比较有不同的结果。UV-DOAS在一些监测地点比较好,但在含有萘的环境空气基质中一致性较差,这对苯、甲苯和二甲苯的测量造成了不可纠正的干扰。最后,PTR-ToF-MS和SIFT-MS在移动格式比较中显示出很强的一致性(所有目标VOCs R2 = 0.68,斜率= 0.85),但仅在去除高背景噪声的醛类化合物时才如此。我们的研究结果强调了在进行移动空气毒物监测时应该考虑的一些潜在干扰,并展示了可用于确保可靠数据收集的多仪器比较技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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