State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China; University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China; Center for Excellence in Regional Atmospheric Environment, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, China.
J Environ Sci (China). 2018 Sep;71:76-88. doi: 10.1016/j.jes.2017.11.021. Epub 2017 Dec 11.
Chemical speciation of fine particles or PM collected on filters is still a costly and time-consuming task. In this study, filter-based PM samples were collected during November-December 2013 at four sites in Guangzhou, and the major components were fast screened (~7min per filter sample) by Attenuated Total Reflectance (ATR)-Fourier Transform Infrared Spectroscopic (FTIR) in comparison with that measured by Organic carbon/Element carbon (OC/EC) analyzer and Ion Chromatography (IC). The concentrations of nitrate, ammonium, sulfate, primary organic carbon (POC) and secondary organic carbon (SOC) measured by OC/EC and IC analyzers were better correlated with their infrared absorption peak heights at 1320cm for nitrate, 1435, 3045 and 3215cm for ammonium, 615cm for sulfate, 690, 760 and 890cm for POC and 1640 and 1660cm for SOC respectively, during polluted days (PM>75μg/m) than during clean days (PM≤75μg/m). With the evolution of a haze episode during our field campaign, the concentrations of the major PM components displayed consistent variations with their infrared absorption peak heights, suggesting ATR-FTIR could be a fast and useful technique to characterize filter-based PM compositions particularly during pollution events although cautions should be taken when PM levels are low. Notably, elevated PM mass concentrations occurred with enhanced ratios of [NO]/[SO] and [NH]/[SO], implying that nitrogenous components play vital roles in the PM pollution events in the study region.
采集到滤膜上的细颗粒物(PM)的化学形态仍然是一项既昂贵又耗时的工作。本研究于 2013 年 11 月至 12 月在广州的四个地点采集基于滤膜的 PM 样本,并用衰减全反射(ATR)-傅里叶变换红外光谱(FTIR)快速筛选(每个滤膜样品约 7 分钟),与有机碳/元素碳(OC/EC)分析仪和离子色谱(IC)的测量结果进行比较。在污染日(PM>75μg/m),OC/EC 和 IC 分析仪测量的硝酸盐、铵、硫酸盐、一次有机碳(POC)和二次有机碳(SOC)浓度与它们在 1320cm 处的红外吸收峰高度的相关性更好,而在清洁日(PM≤75μg/m)相关性较差。在污染日,硝酸盐在 1435、3045 和 3215cm 处,铵在 1435、3045 和 3215cm 处,硫酸盐在 615cm 处,POC 在 690、760 和 890cm 处,SOC 在 1640 和 1660cm 处,OC/EC 和 IC 分析仪测量的硝酸盐、铵、硫酸盐、POC 和 SOC 浓度与红外吸收峰高度的相关性更好。随着我们野外考察期间一场霾事件的发展,主要 PM 成分的浓度与它们的红外吸收峰高度显示出一致的变化,这表明 ATR-FTIR 可能是一种快速有用的技术,可以用于描述基于滤膜的 PM 成分,特别是在污染事件期间,尽管在 PM 水平较低时应谨慎使用。值得注意的是,PM 质量浓度的升高伴随着[NO]/[SO]和[NH]/[SO]比值的增加,这意味着含氮成分在研究区域的 PM 污染事件中起着重要作用。