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基于化学热力学和动力学模型的源排放物在硫酸盐形成途径中的作用。

The role of source emissions in sulfate formation pathways based on chemical thermodynamics and kinetics model.

作者信息

Gao Jie, Wei Yuting, Zhao Huan, Liang Danni, Feng Yinchang, Shi Guoliang

机构信息

State Environmental Protection Key Laboratory of Urban Ambient Air Particulate Matter Pollution Prevention and Control, Tianjin Key Laboratory of Urban Transport Emission Research, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China; CMA-NKU Cooperative Laboratory for Atmospheric Environment-Health Research, Tianjin 300350, China.

State Environmental Protection Key Laboratory of Urban Ambient Air Particulate Matter Pollution Prevention and Control, Tianjin Key Laboratory of Urban Transport Emission Research, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China; CMA-NKU Cooperative Laboratory for Atmospheric Environment-Health Research, Tianjin 300350, China.

出版信息

Sci Total Environ. 2022 Dec 10;851(Pt 1):158104. doi: 10.1016/j.scitotenv.2022.158104. Epub 2022 Aug 18.

Abstract

Sulfate is a major PM constituent and poses a significant threat to ecosystems and human health, which has attracted lots of attention to the sulfate formation mechanism. In recent years, there has been great scientific interest in the multiphase oxidation of SO in aqueous aerosol particles. Many factors are involved in the reaction process, including precursor SO, oxidants/catalysts, and aerosol acidity, which are three channels closely related to the source emission. The conjoint analysis of source emissions and sulfate aqueous formation can provide a scientific basis for designing effective strategies, though the related research is extremely limited. Here, we applied an improved solute strength-dependent chemical Thermodynamics & Kinetics model (for aqueous pathway contribution) and the Partial Target Transformation-Positive matrix factor model (for source apportionment) to explore the role of source emission in sulfate aqueous formation. The results indicated HO aqueous oxidation was the dominant pathway (65.9 %), and secondary nitrate source may grow together with sulfate formation from HO pathway. HO and TMI pathways were related to higher SOR (sulfur oxidation rate). TMI pathway was significant in summer (54.6 %) and increased with secondary sources and vehicle exhaust. NO pathway was more significant at low secondary source and high coal combustion (higher contribution of NO pathway appeared in winter, 24.7 %). While high formation rate of the O pathway always occurred at low source levels. Coal combustion and vehicle exhaust showed obvious effects on sulfate aqueous formation. Notably, aerosol acidity is a significant factor related to sources and plays a key role in sulfate formation. The result also suggested aerosol pH may be more important than the amounts of substances involved in the oxidation reaction. The findings in this work can provide useful information for better understanding sulfate aqueous formation and offer a scientific basis for designing strategies for air pollution control and sulfate mitigation.

摘要

硫酸盐是细颗粒物的主要成分,对生态系统和人类健康构成重大威胁,这使得硫酸盐的形成机制备受关注。近年来,气溶胶颗粒中二氧化硫的多相氧化引起了科学界的极大兴趣。反应过程涉及许多因素,包括前驱体二氧化硫、氧化剂/催化剂和气溶胶酸度,这三个因素与源排放密切相关。尽管相关研究极为有限,但联合分析源排放和硫酸盐在水中的形成可以为设计有效策略提供科学依据。在此,我们应用改进的溶质强度依赖化学热力学与动力学模型(用于水中途径贡献)和偏最小二乘目标转换-正定矩阵因子模型(用于源解析)来探讨源排放在硫酸盐水中形成中的作用。结果表明,羟基自由基在水中的氧化是主要途径(65.9%),二次硝酸盐源可能与羟基自由基途径中的硫酸盐形成共同增长。羟基自由基和过渡金属离子途径与较高的硫氧化率相关。过渡金属离子途径在夏季较为显著(54.6%),并随着二次源和机动车尾气排放的增加而增加。一氧化氮途径在二次源较低和煤炭燃烧较高的情况下更为显著(冬季一氧化氮途径的贡献更高,为24.7%)。而臭氧途径的高形成率总是出现在源水平较低的情况下。煤炭燃烧和机动车尾气排放对硫酸盐在水中的形成有明显影响。值得注意的是,气溶胶酸度是与源相关的一个重要因素,在硫酸盐形成中起关键作用。结果还表明,气溶胶的pH值可能比氧化反应中涉及的物质数量更为重要。这项工作的研究结果可为更好地理解硫酸盐在水中的形成提供有用信息,并为设计空气污染控制和硫酸盐减排策略提供科学依据。

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