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Concurrent measurements of size-segregated particulate sulfate, nitrate and ammonium using quartz fiber filters, glass fiber filters and cellulose membranes

机译:使用石英纤维过滤器,玻璃纤维过滤器和纤维素膜同时测量粒度分离的硫酸盐,硝酸盐和铵盐

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摘要

Current science and policy requirements have focused attention on the need to expand and improve particulate matter (PM) sampling methods. To explore how sampling filter type. affects artifacts in PM composition measurements, size-resolved particulate SO42-, NO3- and NH4+ (SNA) were measured on quartz fiber filters (QFF), glass fiber filters (GFF) and cellulose membranes (CM) concurrently in an urban area of Beijing on both clean and hazy days. The results showed that SNA concentrations in most of the size fractions exhibited the following patterns on different filters: CM > QFF > GFF for NH4+; GFF > QFF > CM for SO42-; and GFF > CM > QFF for NO3-. The different patterns in coarse particles were mainly affected by filter acidity, and that in fine particles were mainly affected by hygroscopicity of the filters (especially in size fraction of 0.65-2.1 mu m). Filter acidity and hygroscopicity also shifted the peaks of the annual mean size distributions of SNA on QFF from 0.43-0.65 mu m on clean days to 0.65-1.1 mu m on hazy days. However, this size shift was not as distinct for samples measured with CM and GFF. In addition, relative humidity (RH) and pollution levels are important factors that can enhance particulate size mode shifts of SNA on clean and hazy days. Consequently, the annual mean size distributions of SNA had maxima at 0.65-1.1 mu m for QFF samples and 0.43-0.65 mu m for GFF and CM samples. Compared with NH4+ and SO42-, NO3- is more sensitive to RH and pollution levels, accordingly, the annual mean size distribution of NO3- exhibited peak at 0.65-1.1 mu m for CM samples instead of 0.43-0.65 mu m. These methodological uncertainties should be considered when quantifying the concentrations and size distributions of SNA under different RH and haze conditions. (C) 2016 Elsevier Ltd. All rights reserved.
机译:当前的科学和政策要求将注意力集中在扩展和改进颗粒物(PM)采样方法的需求上。探索如何采样过滤器类型。影响PM成分测量中的伪影,在北京市区同时测量了石英纤维过滤器(QFF),玻璃纤维过滤器(GFF)和纤维素膜(CM)上的尺寸分解颗粒SO42-,NO3-和NH4 +(SNA)在干净和朦胧的日子里。结果表明,在不同滤膜上,大多数大小部分中的SNA浓度均显示以下模式:NH 4+的CM> QFF> GFF;对于SO42-,GFF> QFF> CM;对于NO3-,GFF> CM> QFF。粗颗粒的不同模式主要受过滤器酸度的影响,细颗粒的模式主要受过滤器吸湿性的影响(尤其是0.65-2.1μm的粒径分数)。过滤器的酸度和吸湿性还将QFF上SNA的年平均尺寸分​​布的峰值从清洁日的0.43-0.65微米转移到朦胧日的0.65-1.1微米。但是,对于使用CM和GFF测量的样品,这种尺寸变化并不明显。另外,相对湿度(RH)和污染水平是重要的因素,可以在清洁和朦胧的日子里增强SNA的颗粒尺寸模式变化。因此,SNA的年平均粒径分布最大,QFF样品为0.65-1.1μm,GFF和CM样品为0.43-0.65μm。与NH4 +和SO42-相比,NO3-对RH和污染水平更敏感,因此,CM样品中NO3-的年平均分布峰值出现在0.65-1.1μm处,而不是0.43-0.65μm。在定量不同相对湿度和雾度条件下SNA的浓度和大小分布时,应考虑这些方法学上的不确定性。 (C)2016 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Atmospheric environment》 |2016年第11期|293-298|共6页
  • 作者单位

    Chinese Acad Sci, State Key Lab Atmospher Boundary Layer Phys & Atm, Inst Atmospher Phys, Beijing 100029, Peoples R China;

    Chinese Acad Sci, State Key Lab Atmospher Boundary Layer Phys & Atm, Inst Atmospher Phys, Beijing 100029, Peoples R China;

    Chinese Acad Sci, State Key Lab Atmospher Boundary Layer Phys & Atm, Inst Atmospher Phys, Beijing 100029, Peoples R China|Cangzhou Normal Univ, Sch Chem & Chem Engn, Cangzhou 061001, Peoples R China;

    Chinese Acad Sci, State Key Lab Atmospher Boundary Layer Phys & Atm, Inst Atmospher Phys, Beijing 100029, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    SNA; Size distribution; Haze; Glass fiber filters; Quartz fiber filters; Cellulose membranes;

    机译:SNA;尺寸分布;雾度;玻璃纤维过滤器;石英纤维过滤器;纤维素膜;

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