{"title":"随州工业区和居民区 PM2.5 和 PM1 中水溶性无机离子和碳质成分的季节变化","authors":"Mi Zhang , Yu Gong , Hao Huang , Hui Hu","doi":"10.1016/j.apr.2024.102276","DOIUrl":null,"url":null,"abstract":"<div><p>Seasonal variations of fine particulate matter (PM) and its chemical components in Suizhou are investigated by collecting PM<sub>2.5</sub> and PM<sub>1</sub> samples from industrial and residential areas between March 2017 and February 2018. The findings reveal more severe PM pollution in industrial areas compared to residential areas. Concentrations and percentages of water-soluble inorganic ions (WSII) in PM are higher in spring and winter. Notably, the high levels of SO<sub>4</sub><sup>2−</sup> and NO<sub>3</sub><sup>−</sup> in PM<sub>1-2.5</sub> indicate that secondary transformation of SO<sub>2</sub> and NO<sub>x</sub> significantly contribute to the rapid increase in PM<sub>1-2.5</sub>. The conversion of NO<sub>2</sub> to NO<sub>3</sub><sup>−</sup> is a key factor in the winter increase of mass concentrations of PM<sub>2.5</sub> [<em>ρ</em>(PM<sub>2.5</sub>)], while photochemical reactions involving NO<sub>2</sub> drive the summer increase of <em>ρ</em>(PM<sub>2.5</sub>). Organic carbon (OC) and elemental carbon (EC) are mainly distributed in PM<sub>1</sub>, with OC peaking in winter. Chemical fractionation of PM reveals that carbonaceous components have a greater impact on PM<sub>1</sub> concentration than WSII, whereas WSII more significantly affects <em>ρ</em>(PM<sub>2.5</sub>) than carbonaceous components. The OC to EC ratio in industrial areas (2.5 ± 1.4) and residential areas (1.9 ± 0.8) suggests more prominent secondary aerosol pollution in industrial areas. Significant correlations between secondary organic carbon (SOC), SOC conversion rate (<em>η</em><sub>SOC</sub>), and concentrations of O<sub>3</sub>-8h and NO<sub>2</sub> in Suizhou further indicate that O<sub>3</sub> and NO<sub>2</sub> levels in the atmosphere influence the generation of SOC and <em>η</em><sub>SOC</sub>.</p></div>","PeriodicalId":8604,"journal":{"name":"Atmospheric Pollution Research","volume":"15 11","pages":"Article 102276"},"PeriodicalIF":3.9000,"publicationDate":"2024-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Seasonal variation of water-soluble inorganic ions and carbonaceous components of PM2.5 and PM1 in industrial and residential areas of Suizhou, China\",\"authors\":\"Mi Zhang , Yu Gong , Hao Huang , Hui Hu\",\"doi\":\"10.1016/j.apr.2024.102276\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Seasonal variations of fine particulate matter (PM) and its chemical components in Suizhou are investigated by collecting PM<sub>2.5</sub> and PM<sub>1</sub> samples from industrial and residential areas between March 2017 and February 2018. The findings reveal more severe PM pollution in industrial areas compared to residential areas. Concentrations and percentages of water-soluble inorganic ions (WSII) in PM are higher in spring and winter. Notably, the high levels of SO<sub>4</sub><sup>2−</sup> and NO<sub>3</sub><sup>−</sup> in PM<sub>1-2.5</sub> indicate that secondary transformation of SO<sub>2</sub> and NO<sub>x</sub> significantly contribute to the rapid increase in PM<sub>1-2.5</sub>. The conversion of NO<sub>2</sub> to NO<sub>3</sub><sup>−</sup> is a key factor in the winter increase of mass concentrations of PM<sub>2.5</sub> [<em>ρ</em>(PM<sub>2.5</sub>)], while photochemical reactions involving NO<sub>2</sub> drive the summer increase of <em>ρ</em>(PM<sub>2.5</sub>). Organic carbon (OC) and elemental carbon (EC) are mainly distributed in PM<sub>1</sub>, with OC peaking in winter. Chemical fractionation of PM reveals that carbonaceous components have a greater impact on PM<sub>1</sub> concentration than WSII, whereas WSII more significantly affects <em>ρ</em>(PM<sub>2.5</sub>) than carbonaceous components. The OC to EC ratio in industrial areas (2.5 ± 1.4) and residential areas (1.9 ± 0.8) suggests more prominent secondary aerosol pollution in industrial areas. Significant correlations between secondary organic carbon (SOC), SOC conversion rate (<em>η</em><sub>SOC</sub>), and concentrations of O<sub>3</sub>-8h and NO<sub>2</sub> in Suizhou further indicate that O<sub>3</sub> and NO<sub>2</sub> levels in the atmosphere influence the generation of SOC and <em>η</em><sub>SOC</sub>.</p></div>\",\"PeriodicalId\":8604,\"journal\":{\"name\":\"Atmospheric Pollution Research\",\"volume\":\"15 11\",\"pages\":\"Article 102276\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-08-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Atmospheric Pollution Research\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1309104224002411\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric Pollution Research","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1309104224002411","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
通过采集2017年3月至2018年2月期间随州工业区和居民区的可吸入颗粒物和颗粒物样本,研究了随州细颗粒物及其化学成分的季节性变化。研究结果表明,与居民区相比,工业区的可吸入颗粒物污染更为严重。可吸入颗粒物中水溶性无机离子(WSII)的浓度和百分比在春季和冬季较高。值得注意的是,可吸入颗粒物中二氧化硫和氮氧化物的含量较高,这表明二氧化硫和氮氧化物的二次转化在很大程度上导致了可吸入颗粒物的快速增加。将 NO 转化为 NO 是冬季可吸入颗粒物(PM)质量浓度增加的关键因素,而涉及 NO 的光化学反应则推动了夏季可吸入颗粒物(PM)的增加。有机碳(OC)和元素碳(EC)主要分布在可吸入颗粒物中,有机碳在冬季达到峰值。可吸入颗粒物的化学分馏结果表明,碳质成分对可吸入颗粒物浓度的影响比 WSII 更大,而 WSII 对(可吸入颗粒物)的影响比碳质成分更显著。工业区(2.5 ± 1.4)和居民区(1.9 ± 0.8)的 OC 与 EC 比率表明,工业区的二次气溶胶污染更为突出。随州二次有机碳(SOC)、SOC转化率()与O-8h和NO浓度之间的显著相关性进一步表明,大气中的O和NO水平影响着SOC和.NOC的生成。
Seasonal variation of water-soluble inorganic ions and carbonaceous components of PM2.5 and PM1 in industrial and residential areas of Suizhou, China
Seasonal variations of fine particulate matter (PM) and its chemical components in Suizhou are investigated by collecting PM2.5 and PM1 samples from industrial and residential areas between March 2017 and February 2018. The findings reveal more severe PM pollution in industrial areas compared to residential areas. Concentrations and percentages of water-soluble inorganic ions (WSII) in PM are higher in spring and winter. Notably, the high levels of SO42− and NO3− in PM1-2.5 indicate that secondary transformation of SO2 and NOx significantly contribute to the rapid increase in PM1-2.5. The conversion of NO2 to NO3− is a key factor in the winter increase of mass concentrations of PM2.5 [ρ(PM2.5)], while photochemical reactions involving NO2 drive the summer increase of ρ(PM2.5). Organic carbon (OC) and elemental carbon (EC) are mainly distributed in PM1, with OC peaking in winter. Chemical fractionation of PM reveals that carbonaceous components have a greater impact on PM1 concentration than WSII, whereas WSII more significantly affects ρ(PM2.5) than carbonaceous components. The OC to EC ratio in industrial areas (2.5 ± 1.4) and residential areas (1.9 ± 0.8) suggests more prominent secondary aerosol pollution in industrial areas. Significant correlations between secondary organic carbon (SOC), SOC conversion rate (ηSOC), and concentrations of O3-8h and NO2 in Suizhou further indicate that O3 and NO2 levels in the atmosphere influence the generation of SOC and ηSOC.
期刊介绍:
Atmospheric Pollution Research (APR) is an international journal designed for the publication of articles on air pollution. Papers should present novel experimental results, theory and modeling of air pollution on local, regional, or global scales. Areas covered are research on inorganic, organic, and persistent organic air pollutants, air quality monitoring, air quality management, atmospheric dispersion and transport, air-surface (soil, water, and vegetation) exchange of pollutants, dry and wet deposition, indoor air quality, exposure assessment, health effects, satellite measurements, natural emissions, atmospheric chemistry, greenhouse gases, and effects on climate change.