TY - JOUR
T1 - Aerosol quantification with the Aerodyne Aerosol Mass Spectrometer: Detection limits and ionizer background effects
AU - Drewnick, F.
AU - Hings, S. S.
AU - Alfarra, M. R.
AU - Prevot, A. S H
AU - Borrmann, S.
N1 - AMT 1867-1381
PY - 2009
Y1 - 2009
N2 - Systematic laboratory experiments were performed to investigate quantification of various species with two versions of the Aerodyne Aerosol Mass Spectrometer, a Quadrupole Aerosol Mass Spectrometer (Q-AMS) and a compact Time-of-Flight Aerosol Mass Spectrometer (c-ToF-AMS). Here we present a new method to continuously determine the detection limits of the AMS analyzers during regular measurements, yielding detection limit (DL) information under various measurement conditions. Minimum detection limits range from 0.03 μgm -3 (nitrate, sulfate, and chloride) up to 0.5 μg m -3 (organics) for the Q-AMS. Those of the c-ToF-AMS are found between 0.003 μg m -3 (nitrate, sulfate) and 0.03 μgm -3 (ammonium, organics). The DLvalues found for the c-ToF-AMS were ∼10 times lower than those of the Q-AMS, mainly due to differences in ion duty cycle. Effects causing an increase of the detection limits include long-term instrument contamination, measurement of high aerosol mass concentrations and short-term instrument history. The self-cleaning processes which reduce the instrument background after measurement of large aerosol concentrations as well as the influences of increased instrument background on mass concentration measurements are discussed. Finally, improvement of detection limits by extension of averaging time intervals, selected or reduced ion monitoring, and variation of particle-to-background measurement ratio are investigated.
AB - Systematic laboratory experiments were performed to investigate quantification of various species with two versions of the Aerodyne Aerosol Mass Spectrometer, a Quadrupole Aerosol Mass Spectrometer (Q-AMS) and a compact Time-of-Flight Aerosol Mass Spectrometer (c-ToF-AMS). Here we present a new method to continuously determine the detection limits of the AMS analyzers during regular measurements, yielding detection limit (DL) information under various measurement conditions. Minimum detection limits range from 0.03 μgm -3 (nitrate, sulfate, and chloride) up to 0.5 μg m -3 (organics) for the Q-AMS. Those of the c-ToF-AMS are found between 0.003 μg m -3 (nitrate, sulfate) and 0.03 μgm -3 (ammonium, organics). The DLvalues found for the c-ToF-AMS were ∼10 times lower than those of the Q-AMS, mainly due to differences in ion duty cycle. Effects causing an increase of the detection limits include long-term instrument contamination, measurement of high aerosol mass concentrations and short-term instrument history. The self-cleaning processes which reduce the instrument background after measurement of large aerosol concentrations as well as the influences of increased instrument background on mass concentration measurements are discussed. Finally, improvement of detection limits by extension of averaging time intervals, selected or reduced ion monitoring, and variation of particle-to-background measurement ratio are investigated.
U2 - 10.5194/amt-2-33-2009
DO - 10.5194/amt-2-33-2009
M3 - Article
SN - 1867-1381
VL - 2
SP - 33
EP - 46
JO - Atmospheric Measurement Techniques
JF - Atmospheric Measurement Techniques
IS - 1
ER -