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首页> 外文期刊>Journal of the air & waste management association >PM2.5 speciation trends network: Evaluation of whole-system uncertainties using data from sites with collocated samplers
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PM2.5 speciation trends network: Evaluation of whole-system uncertainties using data from sites with collocated samplers

机译:PM2.5物种趋势网络:使用来自并置采样器的站点中的数据评估整个系统的不确定性

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摘要

The objectives of this paper are to contrast the relative variability of replicate laboratory measurements of selected chemical components of fine particulate matter (PM) with total variability from collocated measurements and to compare the magnitudes of the uncertainties determined from collocated sampler data with those currently being provided to U.S. Environmental Protection Agency (EPA)'s Air Quality System (AQS) database by RTI International (RTI). Pointwise uncertainty values are needed for modeling and data analysis and should include all the random errors affecting each data point. Total uncertainty can be decomposed into two primary components: analytical measurement uncertainty and sampling uncertainty. Analytical measurement uncertainties are relatively easy to calculate from routine quality control (QC) data. Sampling uncertainties, on the other hand, are comparatively difficult to measure. In this paper, the authors describe data from collocated samplers to provide a snapshot of whole-system uncertainty for several important chemical species. The components of uncertainty were evaluated for key species from each of the analytical methods employed by the PM2.5 Speciation Trends Network (STN) program: gravimetry, ion chrornatography (IC), X-ray fluorescence (XRF), and thermal-optical analysis for organic carbon and elemental carbon. The results show that the laboratory measurement uncertainties are typically very small compared with uncertainties calculated from the differences between samples collected from collocated samplers. These differences are attributable to the "field" components uncertainty, which may include contamination and/or losses during shipping, handling, and sampling, as well as other distortions of the concentration level due to flow and sample volume variations. Uncertainties calculated from the collocation results were found to be generally similar to the uncertainties currently being loaded into EPA's AQS system, with some exceptions described below.
机译:本文的目的是对比细颗粒物(PM)的选定化学成分的重复实验室测量结果与并置测量的总变异性的相对变异性,并将并列采样器数据确定的不确定性幅度与当前提供的那些进行比较RTI国际(RTI)将其发送给美国环境保护署(EPA)的空气质量系统(AQS)数据库。建模和数据分析需要逐点不确定性值,并且应该包括影响每个数据点的所有随机误差。总不确定度可以分解为两个主要部分:分析测量不确定度和采样不确定度。分析测量不确定度相对容易从常规质量控制(QC)数据计算得出。另一方面,抽样不确定性相对难以衡量。在本文中,作者描述了来自并置采样器的数据,以提供几种重要化学物种的整个系统不确定性的快照。通过PM2.5物种趋势网络(STN)程序采用的每种分析方法,对关键物种的不确定性成分进行了评估:重量分析法,离子色谱法(IC),X射线荧光(XRF)和热光分析用于有机碳和元素碳。结果表明,与根据从并置采样器收集的样本之间的差异计算出的不确定度相比,实验室测量不确定度通常很小。这些差异可归因于“现场”成分的不确定性,其中可能包括运输,处理和采样过程中的污染和/或损失,以及由于流量和样品量的变化而导致的浓度水平的其他失真。发现根据搭配结果计算出的不确定度通常与EPA的AQS系统中当前加载的不确定度相似,但以下所述除外。

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