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中国嘉兴的 PM 特征和来源解析。

Characteristics and source apportionment of PM in Jiaxing, China.

机构信息

Instrumental Analysis Center, Shanghai Jiao Tong University, Shanghai, 200240, China.

Jiaxing Environmental Monitoring Station, Jiaxing, 314000, China.

出版信息

Environ Sci Pollut Res Int. 2019 Mar;26(8):7497-7511. doi: 10.1007/s11356-019-04205-2. Epub 2019 Jan 18.

Abstract

Herein we investigated the morphology, chemical characteristics, and source apportionment of fine particulate matter (PM) samples collected from five sites in Jiaxing. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that soot aggregates and coal-fired fly ash were generally the most abundant components in the samples. All the samples were analyzed gravimetrically for mass concentrations and their various compositions were determined. Our results revealed that the PM concentrations in the samples were in the following order: winter > spring > autumn > summer. The PM concentrations in winter and spring were higher than those in autumn and summer, except for inorganic elements. Carbonaceous species and water-soluble inorganic ions were the most abundant components in the samples, accounting for 26.17-50.44% and 34.27-49.6%, respectively. The high secondary organic carbon/organic carbon ratio indicated that secondary organic pollution in Jiaxing was severe. The average ratios of NO/SO, ranging from 1.01 to 1.25 at the five sites, indicated that mobile pollution sources contributed more to the formation of PM than stationary sources. The BeP/(BeP + BaP) ratio (0.52-0.71) in samples reflected the influence of transportation from outside of Jiaxing. The positive matrix factorization (PMF) model identified eight main pollution sources: secondary nitrates (26.95%), secondary sulfates (15.49%), secondary organic aerosol (SOA) (19.64%), vehicle exhaust (15.67%), coal combustion (8.6%), fugitive dust (7.7%), ships and heavy oil (5.23%), biomass burning, and other sources (0.91%). Therefore, PM pollution in Jiaxing during the winter and spring seasons was more severe than that in the summer and autumn. Secondary aerosols were the most important source of PM pollution; therefore, focus should be placed on controlling gaseous precursors.

摘要

在此,我们研究了采集自嘉兴五个地点的细颗粒物(PM)样品的形态、化学特征和来源分配。扫描电子显微镜(SEM)和透射电子显微镜(TEM)显示,烟尘团聚物和燃煤飞灰通常是样品中最丰富的成分。对所有样品进行了质量浓度的重量分析,并确定了它们的各种成分。我们的结果表明,样品中的 PM 浓度顺序为:冬季>春季>秋季>夏季。冬季和春季的 PM 浓度高于秋季和夏季,除了无机元素。碳质物种和水溶性无机离子是样品中最丰富的成分,分别占 26.17-50.44%和 34.27-49.6%。较高的二次有机碳/有机碳比值表明,嘉兴的二次有机污染严重。五个采样点的 NO/SO 平均值比值(1.01-1.25)表明,移动污染源比固定污染源对 PM 的形成贡献更大。样品中 BeP/(BeP+BaP)的比值(0.52-0.71)反映了来自嘉兴以外的运输影响。正定矩阵因子(PMF)模型识别出了 8 个主要的污染来源:二次硝酸盐(26.95%)、二次硫酸盐(15.49%)、二次有机气溶胶(SOA)(19.64%)、机动车尾气(15.67%)、煤燃烧(8.6%)、扬尘(7.7%)、船舶和重油(5.23%)、生物质燃烧及其他来源(0.91%)。因此,嘉兴冬季和春季的 PM 污染比夏季和秋季更为严重。二次气溶胶是 PM 污染的最重要来源,因此应重点控制气态前体物。

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