Ashbaugh Lowell L, Eldred Robert A
Crocker Nuclear Laboratory, University of California, Davis, California 95616, USA.
J Air Waste Manag Assoc. 2004 Jan;54(1):93-104. doi: 10.1080/10473289.2004.10470878.
The extent of mass loss on Teflon filters caused by ammonium nitrate volatilization can be a substantial fraction of the measured particulate matter with an aerodynamic diameter less than 2.5 microm (PM2.5) or 10 microm (PM10) mass and depends on where and when it was collected. There is no straightforward method to correct for the mass loss using routine monitoring data. In southern California during the California Acid Deposition Monitoring Program, 30-40% of the gravimetric PM2.5 mass was lost during summer daytime. Lower mass losses occurred at more remote locations. The estimated potential mass loss in the Interagency Monitoring of Protected Visual Environments network was consistent with the measured loss observed in California. The biased mass measurement implies that use of Federal Reference Method data for fine particles may lead to control strategies that are biased toward sources of fugitive dust, other primary particle emission sources, and stable secondary particles (e.g., sulfates). This analysis clearly supports the need for speciated analysis of samples collected in a manner that preserves volatile species. Finally, although there is loss of volatile nitrate (NO3-) from Teflon filters during sampling, the NO3- remaining after collection is quite stable. We found little loss of NO3- from Teflon filters after 2 hr under vacuum and 1 min of heating by a cyclotron proton beam.
由硝酸铵挥发导致的聚四氟乙烯滤膜上的质量损失程度,可能是所测空气动力学直径小于2.5微米(PM2.5)或10微米(PM10)颗粒物质量的很大一部分,这取决于样品的采集地点和时间。使用常规监测数据没有直接的方法来校正质量损失。在加利福尼亚酸沉降监测项目期间的南加利福尼亚,夏季白天重量法测定的PM2.5质量损失了30% - 40%。在更偏远的地点质量损失较低。在受保护视觉环境跨部门监测网络中估计的潜在质量损失与在加利福尼亚观测到的实测损失一致。有偏差的质量测量意味着,使用联邦参考方法测定细颗粒物数据可能导致控制策略偏向于扬尘源、其他一次颗粒物排放源以及稳定的二次颗粒物(如硫酸盐)。该分析明确支持对以保存挥发性物种方式采集的样品进行成分分析的必要性。最后,虽然采样期间聚四氟乙烯滤膜上的挥发性硝酸盐(NO3-)会损失,但采集后剩余的NO3-相当稳定。我们发现,在真空下放置2小时并经回旋加速器质子束加热1分钟后,聚四氟乙烯滤膜上的NO3-几乎没有损失。