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Here, we used a modified single-particle soot photometer (SP2) coupled with a concentric pneumatic nebulizer to measure the size-resolved number and mass concentrations of light-absorbing iron oxide aerosols (FeOx) in liquid water (CNFeOx and CMFeOx, respectively). The SP2 could selectively detect individual FeOx particles in mixed wüstite–fullerene soot laboratory samples and melted Arctic snow samples. The nebulizer efficiency for FeOx particles was about 50% within the 70–650 nm diameter range, as derived from the ratio of the volume of ammonium sulfate before and after extraction by the nebulizer and the size-resolved transmission efficiency in the nebulizer–SP2 sampling line. Uncertainty from the boundary lines empirically drawn to discriminate the scatterplots of FeOx and black carbon in the mixed wüstite–fullerene soot suspensions and snow samples was approximately 3.0% and 10%, respectively. Overall uncertainty in total CNFeOx and CMFeOx (220–1400 nm) was approximately 19% and 18%, respectively. After storage at 4 °C for 16 months, the FeOx particle size distributions in melted Arctic snow had remained stable, and CNFeOx and CMFeOx had changed by less than 19% and 1.0%, on average, respectively. Most of the FeOx on dust particles measured by this system was estimated to be in the diameter range smaller than 1000 nm, considering the nebulizer efficiency for dust particles. The high accuracy of the CNFeOx and CMFeOx measurements will help to improve our quantitative understanding of the wet deposition of FeOx and provide more accurate estimates of the effects of FeOx on snow surface albedo. [ABSTRACT FROM AUTHOR]

We developed an improved technique for measuring the size distribution of black carbon (BC) particles suspended in liquid water to facilitate quantitative studies of the wet deposition of BC. The measurement system, which consists of a nebulizer and a single-particle soot photometer, incorporates two improvements into the system that we developed earlier. First, we extended the upper limit of the detectable BC size from 0.9 μm to about 4.0 μm by modifying the photo-detector for measuring the laser-induced incandescence signal. Second, we introduced a pneumatic nebulizer (Marin-5) with a high extraction efficiency (∼50.0%) that was independent of particle diameter up to 2.0 μm. For BC mass concentrations less than 70 μg L−1, we experimentally showed that the diameters of BC particles did not appreciably change during the Marin-5 extraction process, consistent with theoretical calculations. Finally, we demonstrated by laboratory experiments that the size distributions of ambient BC particles changed little during their growth into cloud droplets under supersaturation of water vapor. Using our improved system, we measured the size distributions of BC particles simultaneously in air and rainwater in Tokyo during summer 2014. We observed that the size distributions of BC particles in rainwater shifted to larger sizes compared with those observed in ambient air, indicating that larger BC particles in air were removed more efficiently by precipitation. Copyright © 2016 American Association for Aerosol Research [ABSTRACT FROM AUTHOR]