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Apportionment of sources of fine and coarse particles in four major Australian cities by positive matrix factorisation

机译:通过正矩阵分解对澳大利亚四个主要城市中细颗粒和粗颗粒的来源进行分配

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摘要

In this study, 437 days of 6-daily, 24-h samples of PM2.5, PM2.5-10 and PM10 were collected over a 12-month period during 2003-2004 in Melbourne, Sydney, Brisbane and Adelaide. The elemental, ionic and polycyclic aromatic hydrocarbon composition of the particles were determined. Source apportionment was carried out by using the positive matrix factorisation software (PMF2). Eight factors were identified for the fine particle samples including 'motor vehicles', 'industry', 'other combustion sources', 'ammonium sulphates', 'nitrates', 'marine aerosols', 'chloride depleted marine aerosols' and 'crustal/soil dust'. On average combustion sources, secondary nitrates/sulphates and natural origin dust contributed about 46%, 25% and 26% of the mass of the fine particle samples, respectively. 'Crustal/soil dust', 'marine aerosols', 'nitrates' and 'road side dust' were the four factors identified for the coarse particle samples. On average natural origin dust contributed about 76% of the mass of the coarse particle samples. The contributions of the sources to the sample mass basically reflect the emission source characteristics of the sites. Secondary sulphates and nitrates were found to spread out evenly within each city. The average contribution of secondary nitrates to fine particles was found to be rather uniform in different seasons, rather than higher in winter as found in other studies. This could be due to the low humidity conditions in winter in most of the Australian cities which made the partitioning of the particle phase less favourable in the NH4NO3 equilibrium system. A linear relationship was found between the average contribution of marine aerosols and the distance of the site from the bay side. Wind erosion was found associated with higher contribution of crustal dust on average and episodes of elevated concentration of coarse particles in spring and summer.
机译:在这项研究中,在2003年至2004年的12个月内,从墨尔本,悉尼,布里斯班和阿德莱德收集了437天的PM2.5,PM2.5-10和PM10,每天6小时,24小时采样。测定了颗粒的元素,离子和多环芳烃组成。使用正矩阵分解软件(PMF2)进行源分配。确定了细颗粒样品的八个因素,包括“汽车”,“工业”,“其他燃烧源”,“硫酸铵”,“硝酸盐”,“海洋气溶胶”,“氯化物贫化的海洋气溶胶”和“地壳/土壤”。灰尘'。在平均燃烧源中,次要硝酸盐/硫酸盐和天然尘埃分别占细颗粒样品质量的46%,25%和26%。 “地壳/土壤粉尘”,“海洋气溶胶”,“硝酸盐”和“路边粉尘”是确定粗颗粒样品的四个因素。平均而言,自然来源的灰尘约占粗颗粒样品质量的76%。源对样品质量的贡献基本上反映了站点的排放源特征。发现次级硫酸盐和硝酸盐在每个城市中平均分布。发现在不同季节,次要硝酸盐对细颗粒的平均贡献相当均匀,而不是在其他研究中发现的冬季较高。这可能是由于澳大利亚大多数城市冬季的湿度低,这使得在NH4NO3平衡系统中颗粒相的分配不那么理想。发现海洋气溶胶的平均贡献与站点距海湾一侧的距离之间存在线性关系。发现风蚀与地壳粉尘的平均贡献较高以及春季和夏季的粗颗粒浓度升高有关。

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