Effects of post-sampling conditions on ambient carbon aerosol filter measurements |
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| Authors: | Ann M Dillner Chin H Phuah Jay R Turner |
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| Institution: | 1. Crocker Nuclear Laboratory, University of California—Davis, One Shields Avenue, Davis, CA 95616, USA;2. Department of Civil and Environmental Engineering, University of California—Davis, One Shields Avenue, Davis, CA 95616, USA;3. Department of Energy, Environmental and Chemical Engineering, Washington University, St. Louis, MO 63130, USA;1. Science and Technology Program, University of Washington-Bothell, Bothell, WA, USA;2. Air Quality Research, Finnish Meteorological Institute, Helsinki, Finland;3. Department of Atmospheric Sciences, University of Washington, Seattle, WA, USA;4. Sunset Laboratory Inc., Portland, OR, USA;1. School of Public and Environmental Affairs, Indiana University, Bloomington, IN 47405, USA;2. Department of Chemistry, Indiana University, Bloomington, IN 47405, USA |
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| Abstract: | Ambient carbonaceous material collected on quartz filters is prone to measurement artifacts due to material gained or lost during post-sampling field latency, shipping, and storage. In seventeen sampling events over a one year period, ambient PM2.5 aerosols were collected on quartz filters (without denuders) and subjected to various filter treatments to assess the potential for and extent of artifacts. The filter treatments simulated post-sampling environments that filters may be exposed to and included: storage at 40 °C for up to 96 h, storage at ?16 °C for 48 h, and storage at room temperature (～21 °C) for 48 h. Carbon mass on the filters was measured using a thermal-optical method. The total carbon (TC), total organic carbon (TOC) and total elemental carbon (TEC) as well as carbon thermal fraction masses were obtained. Statistical analyses were performed to identify significant differences in carbon fraction concentrations between filters analyzed immediately after sampling and after being subjected to treatment.TOC and TC concentrations decreased by on average 15 ± 5% and 10 ± 4%, respectively, for filters maintained at 40 °C for 96 h but did not change for filters stored at room temperature or frozen for 48 h. TEC did not change for any of the filter treatments. The mass concentration for the organic carbon thermal fraction that evolves at the lowest temperature step (OC1) decreased with increasing storage time at 40 °C with average losses of 70 ± 7% after 96 h. Therefore, OC1 is not a stable measurement due to post-sampling conditions that may be encountered. This work demonstrates that TOC and TC can have substantial measurement artifacts on filters subjected to field latency and other non-temperature controlled post-sampling handling, compared to the carbon loadings on the filter at the end of the sampling period. |
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