Effect of Vaporizer Temperature on Ambient Non-Refractory Submicron Aerosol Composition and Mass Spectra Measured by the Aerosol Mass Spectrometer

被引:7
作者
Docherty, Kenneth S. [1 ,2 ,3 ]
Lewandowski, Michael [4 ]
Jimenez, Jose L. [1 ,2 ]
机构
[1] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80302 USA
[2] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80302 USA
[3] Alion Sci & Technol Inc, Res Triangle Pk, NC USA
[4] US EPA, Off Res & Dev, Res Triangle Pk, NC 27711 USA
基金
美国国家科学基金会;
关键词
ORGANIC AEROSOLS; COLLECTION EFFICIENCIES; VOLATILITY MEASUREMENTS; PARTICLE COMPOSITION; COMPONENTS; PRESSURES; SECONDARY; SYSTEM; PHASE; FIELD;
D O I
10.1080/02786826.2015.1042100
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Aerodyne Aerosol Mass Spectrometers (AMS) are routinely operated with a constant vaporizer temperature (T-vap) of 600 degrees C in order to facilitate quantitative detection of non-refractory submicron (NR-PM1) species. By analogy with other thermal desorption instruments, systematically varying T-vap may provide additional information regarding NR-PM1 chemical composition and relative volatility, and was explored during two ambient studies. The performance of the AMS generally and the functional integrity of the vaporizer were not negatively impacted during vaporizer temperature cycling (VTC) periods. NR-PM1 species signals change substantially as T-vap decreases with that change being consistent with previous relative volatility measurements: large decreases in lower volatility components (e.g., sulfate, organic aerosol [OA]) with little, if any, decrease in higher volatility components (e.g., nitrate, ammonium) as T-vap decreases. At T-vap < 600 degrees C, slower evaporation was observed as a shift in particle time-of-flight distributions and an increase in "particle beam blocked" (background) concentrations. Some chemically reduced (i.e., CxHy+) OA ions at higher m/z are enhanced at lower T-vap, indicating that this method may improve the analysis of some chemically reduced OA systems. The OA spectra changes dramatically with T-vap; however, the observed trends cannot easily be interpreted to derive volatility information. Reducing T-vap increases the relative O:C and CO2+, contrary to what is expected from measured volatility. This is interpreted as continuing decomposition of low volatility species that decreases more slowly (as T-vap decreases) than does the evaporation of reduced species. The reactive vaporizer surface and the inability to reach T-vap much below 200 degrees C of the standard AMS limit the ability of this method to study the volatility of oxidized OA species. Copyright 2015 American Association for Aerosol Research
引用
收藏
页码:485 / 494
页数:10
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