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PM2.5 water-soluble elements in the southeastern United States: automated analytical method development, spatiotemporal distributions, source apportionment, and implications for heath studies

机译:PM2.5美国东南部的水溶性元素:自动分析方法开发,时尚分布,源分配,以及对希思研究的影响

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摘要

Water-soluble redox-active metals are potentially toxic due to its ability to catalytically generate reactive oxygen species (ROS) in vivo, leading to oxidative stress. As part of the Southeastern Center for Air Pollution and Epidemiology (SCAPE), we developed a method to quantify water-soluble elements, including redox-active metals, from a large number of filter samples (N = 530) in support of the center's health studies. PM2.5 samples were collected during 2012-2013 at various sites (three urban, two rural, a near-road site, and a road-side site) in the southeastern United States, using high-volume samplers. Water-soluble elements (S, K, Ca, Ti, Mn, Fe, Cu, Zn, As, Se, Br, Sr, Ba, and Pb) were determined by extracting filters in deionized water and re-aerosolized for analyses by X-ray fluorescence (XRF) using an online aerosol element analyzer (Xact, Cooper Environmental). Concentrations ranged from detection limits (nominally 0.1 to 30 ngm(-3)) to 1.2 mu gm(-3), with S as the most abundant element, followed by Ca, K, Fe, Cu, Zn, and Ba. Positive matrix factorization (PMF) identified four factors that were associated with specific sources based on relative loadings of various tracers. These include brake/tire wear (with tracers Ba and Cu), biomass burning (K), secondary formation (S, Se, and WSOC), and mineral dust (Ca). Of the four potentially toxic and relatively abundant metals (redox-active Cu, Mn, Fe, and redox-inactive Zn), 51% of Cu, 32% of Fe, 17% of Mn, and 45% of Zn were associated with the brake/tire factor. Mn was mostly associated with the mineral dust factor (45 %). Zn was found in a mixture of factors, with 26% associated with mineral dust, 14% biomass burning, and 13% secondary formation. Roughly 50% of Fe and 40% of Cu were apportioned to the secondary formation factor, likely through increases in the soluble fraction of these elements by sulfur-driven aerosol water and acidity. Linkages between sulfate and water-soluble Fe and Cu may account for some of the past observed associations between sulfate/sulfur oxide and health outcomes. For Cu, Mn, Fe, and Zn, only Fe was correlated with PM2.5 mass (r = 0.73-0.80). Overall, mobile source emissions generated through mechanical processes (re-entrained road dust, tire and break wear) and processing by secondary sulfate were major contributors to water-soluble metals known to be capable of generating ROS.
机译:由于其在体内催化生成反应性氧物质(ROS),导致氧化应激的能力,水溶性氧化还原活性金属可能毒性。作为海南空气污染和流行病学(SCAPE)的一部分,我们开发了一种量化水溶性元素的方法,包括氧化还原活性金属,从大量的过滤器样本(n = 530),以支持中心的健康学习。 PM2.5在美国东南部的各个地点(三个城市,两个农村,一条路边站点)的2012-2013期间收集了PM2.5样品,使用大批量采样器。通过提取去离子水中的过滤器并通过X分析来确定水溶性元件(S,K,Ca,Ti,Mn,Fe,Cu,Zn,Se,Br,Sr,Ba和Pb),并重新曝光以分析 - 使用在线气溶胶元素分析仪(XACT,Cooper环境) - 射线荧光(XRF)。浓度范围从检测限(名义上是0.1至30ngm(-3))至1.2μgmg(-3),作为最丰富的元素,其次是Ca,K,Fe,Cu,Zn和Ba。正矩阵分解(PMF)确定了基于各种示踪剂的相对载荷与特定来源相关的四个因素。这些包括制动/轮胎磨损(带示踪剂Ba和Cu),生物质燃烧(k),二次形成(S,Se和Wsoc)和矿物粉尘(CA)。在四个潜在的有毒和相对丰富的金属(氧化还原活性Cu,Mn,Fe和氧化氢 - 无活性Zn)中,51%的Cu,32%的Fe,17%的Mn和45%的Zn相关制动/轮胎因子。 Mn大多数与矿物粉尘因子(45%)相关。在因子的混合物中发现Zn,26%与矿物粉尘相关,14%生物质燃烧和13%的二级形成。大约50%的Fe和40%的Cu分配给二次形成系数,可能通过硫驱动的气溶胶水和酸度增加这些元素的可溶性分数。硫酸盐和水溶性Fe和Cu之间的键可以考虑硫酸盐/硫氧化物和健康结果之间的一些过去观察到的关联。对于Cu,Mn,Fe和Zn,只有Fe与PM2.5质量(R = 0.73-0.80)相关。总体而言,通过机械过程(重新夹带的道路灰尘,轮胎和断裂磨损)产生的移动源排放和仲硫酸盐的加工是已知能够产生ROS的水溶性金属的主要贡献者。

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  • 来源
    《Atmospheric chemistry and physics》 |2015年第20期|共16页
  • 作者单位

    Georgia Inst Technol Sch Earth &

    Atmospher Sci Atlanta GA 30332 USA;

    Georgia Inst Technol Sch Earth &

    Atmospher Sci Atlanta GA 30332 USA;

    Georgia Inst Technol Sch Earth &

    Atmospher Sci Atlanta GA 30332 USA;

    Univ Massachusetts Sch Publ Hlth &

    Hlth Sci Amherst MA 01003 USA;

    Georgia Inst Technol Sch Earth &

    Atmospher Sci Atlanta GA 30332 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 大气科学(气象学);
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