Sources of Atmospheric Volatile Organic Compounds During the Salt Lake Regional Smoke, Ozone and Aerosol Study (SAMOZA) 2022

IF 3.8 2区 地球科学 Q2 METEOROLOGY & ATMOSPHERIC SCIENCES Journal of Geophysical Research: Atmospheres Pub Date : 2024-09-06 DOI:10.1029/2024JD041640
Emily M. Cope, Damien T. Ketcherside, Lixu Jin, Lu Tan, Marc Mansfield, Colleen Jones, Seth Lyman, Dan Jaffe, Lu Hu
{"title":"Sources of Atmospheric Volatile Organic Compounds During the Salt Lake Regional Smoke, Ozone and Aerosol Study (SAMOZA) 2022","authors":"Emily M. Cope,&nbsp;Damien T. Ketcherside,&nbsp;Lixu Jin,&nbsp;Lu Tan,&nbsp;Marc Mansfield,&nbsp;Colleen Jones,&nbsp;Seth Lyman,&nbsp;Dan Jaffe,&nbsp;Lu Hu","doi":"10.1029/2024JD041640","DOIUrl":null,"url":null,"abstract":"<p>We present measurements of volatile organic compounds (VOCs) and other trace gases taken in Salt Lake City, Utah in August and September 2022. As part of the Salt Lake regional Smoke, Ozone and Aerosol Study (SAMOZA), 35 VOCs were measured with two methods: a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS) and 2,4-dinitrophenylhydrazine (DNPH) cartridges analyzed by high-performance liquid chromatography (HPLC). Over two months, the total measured VOCs averaged 32 ± 24 ppb (mean ± standard deviation) with the hourly maximum at 141 ppb, and the total calculated OH reactivity averaged 3.7 ± 3.0 s<sup>−1</sup> (maximum at 20.7 s<sup>−1</sup>). Among them, methanol and ethanol were the most abundant VOCs, making up 42% of the ambient mixing ratio. Isoprene and monoterpenes contributed 25% of the OH reactivity from VOCs, while formaldehyde and acetaldehyde made up another 30%. The positive matrix factorization analysis showed 5 major sources of VOCs, with 32% of abundance being attributed to secondary production/biogenic sources, 44% from the combination of traffic and personal care products, 15% from industrial solvent use, and the rest from biomass burning (10%). Moderate smoke-impacted days elevated various hazardous air pollutants (HAPs) on average by 45%–217% compared to smoke-free days. The ratio of OH reactivity from NO<sub>x</sub> to that from VOCs showed that ozone production was mostly VOC-limited throughout the campaign, consistent with our modeling study. VOCs and NO<sub>x</sub> both showed increased OH reactivity due to smoke influence. NO<sub>x</sub> featured increased reactivity on weekdays compared to weekends, an effect not shown for VOC reactivity during SAMOZA.</p>","PeriodicalId":15986,"journal":{"name":"Journal of Geophysical Research: Atmospheres","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Geophysical Research: Atmospheres","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1029/2024JD041640","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"METEOROLOGY & ATMOSPHERIC SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

We present measurements of volatile organic compounds (VOCs) and other trace gases taken in Salt Lake City, Utah in August and September 2022. As part of the Salt Lake regional Smoke, Ozone and Aerosol Study (SAMOZA), 35 VOCs were measured with two methods: a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS) and 2,4-dinitrophenylhydrazine (DNPH) cartridges analyzed by high-performance liquid chromatography (HPLC). Over two months, the total measured VOCs averaged 32 ± 24 ppb (mean ± standard deviation) with the hourly maximum at 141 ppb, and the total calculated OH reactivity averaged 3.7 ± 3.0 s−1 (maximum at 20.7 s−1). Among them, methanol and ethanol were the most abundant VOCs, making up 42% of the ambient mixing ratio. Isoprene and monoterpenes contributed 25% of the OH reactivity from VOCs, while formaldehyde and acetaldehyde made up another 30%. The positive matrix factorization analysis showed 5 major sources of VOCs, with 32% of abundance being attributed to secondary production/biogenic sources, 44% from the combination of traffic and personal care products, 15% from industrial solvent use, and the rest from biomass burning (10%). Moderate smoke-impacted days elevated various hazardous air pollutants (HAPs) on average by 45%–217% compared to smoke-free days. The ratio of OH reactivity from NOx to that from VOCs showed that ozone production was mostly VOC-limited throughout the campaign, consistent with our modeling study. VOCs and NOx both showed increased OH reactivity due to smoke influence. NOx featured increased reactivity on weekdays compared to weekends, an effect not shown for VOC reactivity during SAMOZA.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
2022 年盐湖地区烟雾、臭氧和气溶胶研究(SAMOZA)期间的大气挥发性有机化合物来源
我们介绍了 2022 年 8 月和 9 月在犹他州盐湖城对挥发性有机化合物 (VOC) 和其他痕量气体的测量结果。作为盐湖地区烟雾、臭氧和气溶胶研究(SAMOZA)的一部分,我们采用两种方法测量了 35 种挥发性有机化合物:质子转移反应飞行时间质谱仪(PTR-ToF-MS)和通过高效液相色谱法(HPLC)分析的 2,4-二硝基苯肼(DNPH)滤芯。在两个月的时间里,测得的挥发性有机化合物总量平均为 32 ± 24 ppb(平均值 ± 标准偏差),每小时最大值为 141 ppb,计算得出的 OH 反应活性总量平均为 3.7 ± 3.0 s-1(最大值为 20.7 s-1)。其中,甲醇和乙醇是含量最高的挥发性有机化合物,占环境混合比的 42%。异戊二烯和单萜烯占挥发性有机化合物 OH 反应性的 25%,甲醛和乙醛占另外的 30%。正矩阵因式分解分析表明,挥发性有机化合物有 5 个主要来源,32% 的丰度来自二次生产/生物源,44% 来自交通和个人护理产品,15% 来自工业溶剂的使用,其余来自生物质燃烧(10%)。与无烟日相比,中度烟雾影响日的各种有害空气污染物(HAPs)平均升高了 45%-217%。氮氧化物与挥发性有机化合物的羟基反应性之比表明,在整个活动期间,臭氧的产生主要受挥发性有机化合物的限制,这与我们的模型研究结果一致。受烟雾影响,挥发性有机化合物和氮氧化物的羟基反应性都有所提高。与周末相比,氮氧化物在工作日的反应性更高,而在 SAMOZA 期间,挥发性有机化合物的反应性并没有显示出这种效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Geophysical Research: Atmospheres
Journal of Geophysical Research: Atmospheres Earth and Planetary Sciences-Geophysics
CiteScore
7.30
自引率
11.40%
发文量
684
期刊介绍: JGR: Atmospheres publishes articles that advance and improve understanding of atmospheric properties and processes, including the interaction of the atmosphere with other components of the Earth system.
期刊最新文献
Local and Remote Effects of the Sub-Grid Turbulent Orographic Form Drag on the Summer Monsoon Precipitation Over Eastern China Atmospheric Microplastics Emission Source Potentials and Deposition Patterns in Semi-Arid Croplands of Northern China Evaluation of the Representation of Raindrop Self-Collection and Breakup in Two-Moment Bulk Models Using a Multifrequency Radar Retrieval Distinct Radiative and Chemical Impacts Between the Equatorial and Northern Extratropical Volcanic Injections Diagnosing Atmospheric Heating Rate Changes Using Radiative Kernels
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1