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利用稳定硫同位素追踪 2017-2019 年冬季华北地区天津的硫氧化途径。

Using Stable Sulfur Isotope to Trace Sulfur Oxidation Pathways during the Winter of 2017-2019 in Tianjin, North China.

机构信息

Institute of Surface-Earth System Science, School of Earth System Science, Tianjin University, Tianjin 300072, China.

出版信息

Int J Environ Res Public Health. 2022 Sep 2;19(17):10966. doi: 10.3390/ijerph191710966.

Abstract

After the implementation of the Coal Replacing Project (CRP) in the northern parts of China in 2017, its effect on PM composition is still unclear. In the study, water-soluble ionic components (WSICs) and stable sulfur isotope ratios (δS) of SO in PM collected during the domestic heating period before and after the implementation of CRP in Tianjin were analyzed. Results showed that the average concentrations of both PM and WSICs have dropped dramatically after the CRP, especially for the SO (by approximately 57-60%). After the CRP, the range of δS was significantly narrowed to 4.1-7.5‱ in January 2018 and 1.4-6.1‱ in January 2019, which suggested that the sulfur source was becoming simple. It was interesting that the δS value in the pollution period before the CRP was higher than that in the clean period, whereas it showed the opposite tendency after the CRP, which implied that the contribution of sea salt was high during the pollution period before the CRP. The MIXSIAR model calculated that the contributions of the transition-metal ion (TMI) oxidation and NO oxidation pathways in the three sampling stages were higher than those of the OH radical oxidation and HO/O oxidation pathways, indicating that the formation pathway of sulfate was mainly dominated by heterogeneous oxidation. Before the CRP, the NO oxidation pathway was the dominant sulfate oxidation pathway during a haze episode, and the TMI oxidation pathway dominated the formation of sulfates after the CRP.

摘要

2017 年中国北方地区实施煤炭替代计划(CRP)后,其对 PM 成分的影响尚不清楚。本研究分析了 CRP 实施前后天津采暖期采集的 PM 中水溶性离子成分(WSICs)和 SO 的稳定硫同位素比值(δS)。结果表明,CRP 后 PM 和 WSICs 的平均浓度均大幅下降,尤其是 SO(下降约 57-60%)。CRP 后,2018 年 1 月和 2019 年 1 月δS 的范围分别显著缩小至 4.1-7.5‱和 1.4-6.1‱,表明硫源变得单一。有趣的是,CRP 前污染期的δS 值高于清洁期,而 CRP 后则相反,这表明 CRP 前污染期海盐的贡献较高。MIXSIAR 模型计算得出,在三个采样阶段,过渡金属离子(TMI)氧化和 NO 氧化途径的贡献高于 OH 自由基氧化和 HO/O 氧化途径,表明硫酸盐的形成途径主要由非均相氧化主导。CRP 前,NO 氧化途径是霾事件中硫酸盐氧化的主要途径,而 CRP 后 TMI 氧化途径主导硫酸盐的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cff/9518053/f68581de3b9c/ijerph-19-10966-g001.jpg

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