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颗粒物成分和粒径的时间变化概述

Synopsis of the temporal variation of particulate matter composition and size.

作者信息

Demerjian Kenneth L, Mohnen Volker A

机构信息

Department of Earth and Atmospheric Sciences, Atmospheric Sciences Research Center, University at Albany, State University of New York, Albany, NY 12203, USA.

出版信息

J Air Waste Manag Assoc. 2008 Feb;58(2):216-33. doi: 10.3155/1047-3289.58.2.216.

Abstract

A synopsis of the detailed temporal variation of the size and number distribution of particulate matter (PM) and its chemical composition on the basis of measurements performed by several regional research consortia funded by the U.S. Environmental Protection Agency (EPA) PM Supersite Program is presented. This program deployed and evaluated a variety of research and emerging commercial measurement technologies to investigate the physical and chemical properties of atmospheric aerosols at a level of detail never before achieved. Most notably these studies demonstrated that systematic size-segregated measurements of mass, number, and associated chemical composition of the fine (PM2.5) and ultrafine (PM0.1) fraction of ambient aerosol with a time resolution down to minutes and less is achievable. A wealth of new information on the temporal variation of aerosol has been added to the existing knowledge pool that can be mined to resolve outstanding research and policy-related questions. This paper explores the nature of temporal variations (on time scales from several minutes to hours) in the chemical and physical properties of PM and its implications in the identification of PM formation processes, and source attribution (primary versus secondary), the contribution of local versus transported PM and the development of effective PM control strategies. The PM Supersite results summarized indicate that location, time of day, and season significantly influence not only the mass and chemical composition but also the size-resolved chemical/elemental composition of PM. Ambient measurements also show that ultrafine particles have different compositions and make up only a small portion of the PM mass concentration compared with inhalable coarse and fine particles, but their number concentration is significantly larger than their coarse or fine counterparts. PM size classes show differences in the relative amounts of nitrates, sulfates, crustal materials, and most especially carbon as well as variations in seasonal and diurnal patterns.

摘要

本文介绍了由美国环境保护局(EPA)的颗粒物超级站点计划资助的几个区域研究联盟所进行的测量结果,概述了颗粒物(PM)的大小和数量分布及其化学成分的详细时间变化情况。该计划部署并评估了各种研究和新兴商业测量技术,以前所未有的详细程度研究大气气溶胶的物理和化学性质。最值得注意的是,这些研究表明,能够实现对环境气溶胶中细颗粒物(PM2.5)和超细颗粒物(PM0.1)的质量、数量及相关化学成分进行系统的按粒径分类测量,时间分辨率可达数分钟甚至更低。关于气溶胶时间变化的大量新信息已被添加到现有的知识宝库中,可用于解决悬而未决的研究和政策相关问题。本文探讨了PM化学和物理性质的时间变化特性(时间尺度从几分钟到几小时)及其在确定PM形成过程、源归因(一次源与二次源)、本地与传输PM的贡献以及有效PM控制策略制定方面的意义。总结的PM超级站点结果表明,地理位置、一天中的时间和季节不仅对PM的质量和化学成分有显著影响,而且对PM按粒径解析的化学/元素组成也有显著影响。环境测量还表明,超细颗粒物具有不同的组成,与可吸入的粗颗粒物和细颗粒物相比,它们仅占PM质量浓度的一小部分,但其数量浓度明显高于粗颗粒物或细颗粒物。PM粒径类别在硝酸盐、硫酸盐、地壳物质,尤其是碳的相对含量方面存在差异,并且在季节和昼夜模式上也存在变化。

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