驱动城市环境中甲醛日变化和季节变化的过程

IF 2.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Chenyang Du, Hongli Wang*, Yaqin Gao, Rusha Yan, Sheng’ao Jing, Min Zhou, Qian Wang, Shengrong Lou, Cheng Huang, Dan Dan Huang, Yu Shang* and Jing An, 
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引用次数: 0

摘要

本研究旨在阐明中国最大的特大城市上海甲醛(HCHO)持续升高的物理化学过程。现场测量与统计分析相结合表明,初级来源全年都很突出,而次级生产表现出明显的季节性变化。采用过程级箱形模型对二次生产途径对HCHO时间变异性的贡献进行反卷积。将一系列物理去除方案整合到模型框架中,以解决在基本配置中所有季节对HCHO的高估。观测受限的稀释和夹带大大降低了模拟的HCHO水平,但未能捕捉到观测到的日模式。在较冷的月份,气溶胶液态水的反应性吸收与观测到的二次生产成分有效匹配,但仍不足以完全解决夏季的高估问题。进一步分析发现,异戊二烯光化学是夏季HCHO的主要二次来源,其产率对亚ppb水平的一氧化氮(NO)高度敏感,其中最近发现的异戊二烯过氧相互转化竞争性地调节导致HCHO的碳流。缩放NO测量值显著提高了模型性能,强调了亚ppb NO数据和精细化学机制在代表空气质量稳步改善的城市中心HCHO动态方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Processes Driving Diurnal and Seasonal Variations of Formaldehyde in an Urban Environment

Processes Driving Diurnal and Seasonal Variations of Formaldehyde in an Urban Environment

This study aims to elucidate the physicochemical processes driving the persistently elevated levels of formaldehyde (HCHO) in Shanghai, the largest megacity in China. Field measurements combined with statistical analyses revealed that primary sources remained consistently prominent throughout the year, while secondary production exhibited pronounced seasonal variation. A process-level box model was employed to deconvolute the contributions of secondary production pathways to the temporal variability of HCHO. A sequence of physical removal schemes was integrated into the model framework to resolve the overestimation of HCHO across all seasons in the base configuration. Observation-constrained dilution and entrainment substantially reduced simulated HCHO levels, but failed to capture the observed diurnal patterns. Incorporating reactive uptake onto aerosol liquid water effectively matched the observed secondary production component during colder months, but remained insufficient to fully address the overestimation in summer. Further analysis identified isoprene photochemistry as the major secondary source of summertime HCHO, with its yield highly sensitive to subppb levels of nitric oxides (NO), where the recently discovered isoprene peroxy interconversion competitively regulates the carbon flow that leads to HCHO. Scaling NO measurements notably improved model performance, underscoring the importance of subppb NO data and refined chemical mechanisms in representing HCHO dynamics in urban centers with steadily improved air quality.

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来源期刊
ACS Earth and Space Chemistry
ACS Earth and Space Chemistry Earth and Planetary Sciences-Geochemistry and Petrology
CiteScore
5.30
自引率
11.80%
发文量
249
期刊介绍: The scope of ACS Earth and Space Chemistry includes the application of analytical, experimental and theoretical chemistry to investigate research questions relevant to the Earth and Space. The journal encompasses the highly interdisciplinary nature of research in this area, while emphasizing chemistry and chemical research tools as the unifying theme. The journal publishes broadly in the domains of high- and low-temperature geochemistry, atmospheric chemistry, marine chemistry, planetary chemistry, astrochemistry, and analytical geochemistry. ACS Earth and Space Chemistry publishes Articles, Letters, Reviews, and Features to provide flexible formats to readily communicate all aspects of research in these fields.
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