Cropper Paul M, Eatough Delbert J, Overson Devon K, Hansen Jaron C, Caka Fern, Cary Robert A
a Department of Chemistry and Biochemistry , Brigham Young University , Provo , UT , USA.
b Division of Atmospheric Sciences , Deseret Research Institute , Reno , NV , USA.
J Air Waste Manag Assoc. 2018 May;68(5):390-402. doi: 10.1080/10962247.2017.1363095.
A study was conducted on the Brigham Young University campus during January and February 2015 to identify winter-time sources of fine particulate material in Utah Valley, Utah. Fine particulate mass and components and related gas-phase species were all measured on an hourly averaged basis. Light scattering was also measured during the study. Included in the sampling was the first-time source apportionment application of a new monitoring instrument for the measurement of fine particulate organic marker compounds on an hourly averaged basis. Organic marker compounds measured included levoglucosan, dehydroabietic acid, stearic acid, pyrene, and anthracene. A total of 248 hourly averaged data sets were available for a positive matrix factorization (PMF) analysis of sources of both primary and secondary fine particulate material. A total of nine factors were identified. The presence of wood smoke emissions was associated with levoglucosan, dehydroabietic acid, and pyrene markers. Fine particulate secondary nitrate, secondary organic material, and wood smoke accounted for 90% of the fine particulate material. Fine particle light scattering was dominated by sources associated with wood smoke and secondary ammonium nitrate with associated modeled fine particulate water.
The identification of sources and secondary formation pathways leading to observed levels of PM (particulate matter with an aerodynmaic diameter <2.5 μm) is important in making regulatory decisions on pollution control. The use of organic marker compounds in this assessment has proven useful; however, data obtained on a daily, or longer, sampling schedule limit the value of the information because diurnal changes associated with emissions and secondary aerosol formation cannot be identified. A new instrument, the gas chromtography-mass spectrometry (GC-MS) organic aerosol monitor, allows for the determination on these compounds on an hourly averaged basis. The demonstrated potential value of hourly averaged data in a source apportionment analysis indicates that significant improvement in the data used for making regulatory decisions is possible.
2015年1月和2月在杨百翰大学校园开展了一项研究,以确定犹他州犹他谷冬季细颗粒物的来源。细颗粒物质量、成分及相关气相物种均按每小时平均值进行测量。研究期间还测量了光散射。采样内容包括首次将一种用于每小时平均测量细颗粒有机标志物化合物的新型监测仪器应用于源解析。所测量的有机标志物化合物包括左旋葡聚糖、脱氢枞酸、硬脂酸、芘和蒽。共有248个每小时平均数据集可用于对一次和二次细颗粒物的来源进行正矩阵因子分解(PMF)分析。共识别出9个因子。木烟排放的存在与左旋葡聚糖、脱氢枞酸和芘标志物相关。细颗粒二次硝酸盐、二次有机物质和木烟占细颗粒物的90%。细颗粒光散射主要由与木烟和二次硝酸铵相关的来源以及相关模型化的细颗粒水主导。
识别导致观测到的PM(空气动力学直径<2.5μm的颗粒物)水平的来源和二次形成途径对于做出污染控制的监管决策很重要。在本评估中使用有机标志物化合物已证明是有用的;然而,按每日或更长采样计划获得的数据限制了信息的价值,因为无法识别与排放和二次气溶胶形成相关的日变化。一种新仪器,气相色谱 - 质谱联用(GC - MS)有机气溶胶监测仪,能够每小时平均测定这些化合物。源解析分析中每小时平均数据所显示的潜在价值表明,用于做出监管决策的数据有可能得到显著改善。