Noncombustion Emissions of Organic Acids at a Site near Boise, Idaho.

ACS ES&T Air Pub Date : 2024-11-27 eCollection Date: 2024-12-13 DOI:10.1021/acsestair.4c00138
Andrew J Lindsay, Brigitte M Weesner, Kyle Banecker, Lee V Feinman, Russell W Long, Matthew S Landis, Ezra C Wood
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Abstract

Gas-phase organic acids are ubiquitous in the atmosphere with mixing ratios of several species, such as formic acid and acetic acid, often as high as several parts per billion by volume (ppbv). Organic acids are produced via photochemical reactions and are also directly emitted from various sources, including combustion, microbial activity, vegetation, soils, and ruminants. We present measurements of gas-phase formic, acetic, propionic, pyruvic, and pentanoic acids from a site near Boise, Idaho, in August 2019 made by iodide-adduct chemical ionization mass spectrometry (CIMS). The site is adjacent to a major interstate highway and beyond the urban/suburban core is surrounded by national forests to the north and northeast and by farmland to the west and south. Maximum mixing ratios of formic, acetic, propionic, and pentanoic acid were typically near 10, 3, 0.4, and 0.2 ppbv, respectively. Observed daytime concentrations of these acids were mostly consistent with other studies, but concentrations were persistently the highest at night between 20:00 to 8:00 (local standard time). Such elevated nighttime concentrations are unlike most other reported organic acid measurements. Although there were times when organic acid concentrations were enhanced by mobile source emissions, the organic acid concentrations appear to be mainly controlled by noncombustion surface primary emissions. Source apportionment by positive matrix factorization (PMF) supports the importance of significant noncombustion, nonphotochemical emissions. Two agricultural surface sources were identified and estimated to contribute to greater than half of total observed concentrations of formic and acetic acid. In contrast to the other measured organic acids, but in agreement with all other reported measurements in the literature, pyruvic acid concentrations peaked during the daytime and were largely controlled by photochemistry.

爱达荷州博伊西附近一个站点的非燃烧排放物有机酸。
气相有机酸在大气中无处不在,其混合比例有几种,如甲酸和乙酸,通常高达十亿分之一体积(ppbv)。有机酸是通过光化学反应产生的,也可以从各种来源直接排放,包括燃烧、微生物活动、植被、土壤和反刍动物。我们介绍了2019年8月通过碘化物加合化学电离质谱(CIMS)在爱达荷州博伊西附近的一个地点进行的气相甲酸、乙酸、丙酸、丙酮酸和戊酸的测量。场地毗邻一条主要的州际高速公路,在城市/郊区核心之外,北部和东北部被国家森林包围,西部和南部被农田包围。甲酸、乙酸、丙酸和戊酸的最大混合比分别接近10、3、0.4和0.2 ppbv。白天观察到的这些酸的浓度与其他研究基本一致,但浓度在晚上20:00至8:00(当地标准时间)之间持续最高。如此高的夜间浓度与大多数其他报道的有机酸测量结果不同。虽然流动源排放有时会提高有机酸浓度,但有机酸浓度似乎主要由非燃烧表面一次排放控制。通过正矩阵分解(PMF)的源分配支持显著的非燃烧,非光化学排放的重要性。确定并估计了两个农业地表来源对观察到的甲酸和乙酸总浓度的贡献超过一半。与其他测量的有机酸相反,但与文献中所有其他报告的测量结果一致,丙酮酸浓度在白天达到峰值,并在很大程度上受光化学控制。
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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