化学
臭氧
环境化学
甲酸
质谱法
氯
离子
光化学
微粒
离子色谱法
污染物
化学电离
大气化学
试剂
大气(单位)
气团(太阳能)
电离
臭氧消耗
作者
Shira Joudan,John Liggio,Jeremy J.B Wentzell,Jessica T. Clouthier,Na-Yung Seoh,P. M. Edwards,Trevor C. VandenBoer,C. J. S. Young
标识
DOI:10.1021/acs.estlett.6c00211
摘要
Monochloroacetic acid (MCAA) is a regulated disinfection byproduct in drinking water due to its toxicity, but its presence in environmental samples unrelated to disinfection is poorly understood. Here, we apply two online mass spectrometry-based techniques to quantify atmospheric MCAA: chemical ionization mass spectrometry with acetate reagent ions for measurements of gas-phase MCAA every minute and ambient ion monitoring ion chromatography mass spectrometry for hourly measurements of MCAA in the gas and particle phases. Sampling campaigns in Toronto, Canada determined average gas-phase MCAA mixing ratios of 0.57 ± 0.44 pptv from February to April 2022 and 1.4 ± 1.0 pptv from June to August 2022. No MCAA was detected in particulate matter (PM2.5), suggesting particles were not reservoirs of MCAA. Summer gas-phase MCAA data displayed clear diurnal trends and correlated with UV irradiance and known secondary pollutants ozone and formic acid. Thus, we propose MCAA is photochemically formed from volatile precursors. Modeling MCAA from three known precursors accounted for <0.2% of the measured MCAA in July, suggesting unknown MCAA precursors including the potential for it to be a product of chlorine atom-initiated photochemistry.
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