scholarly journals Estimation of Emission Sources of Trace Elements in an Atmospheric Aerosol by Particle Size Distributions

1977 ◽  
pp. 902-906 ◽  
Author(s):  
Mitsuru FUJIMURA ◽  
Yoshikazu HASHIMOTO
1992 ◽  
Vol 02 (04) ◽  
pp. 637-644 ◽  
Author(s):  
GUANGHUA ZHU ◽  
XINFU WANG ◽  
XINYIN SHEN

The atmospheric aerosol samples are collected in Beijing using a ten-stage cascade impactor sampler, and the elemental concentrations are analyzed by the PIXE analytical method. The parameters of particle size distributions are determined by the use of log-normal plots and the least-squares minimization. From these parameters the total amount of deposit in a day at the naso-pharyngeal, tracheo-bronchial and pulmonary are evaluated based on the deposition and retention models.


2021 ◽  
Vol 21 (3) ◽  
pp. 2105-2124
Author(s):  
Songyun Fan ◽  
Yuan Gao ◽  
Robert M. Sherrell ◽  
Shun Yu ◽  
Kaixuan Bu

Abstract. Size-segregated particulate air samples were collected during the austral summer of 2016–2017 at Palmer Station on Anvers Island, western Antarctic Peninsula, to characterize trace elements in aerosols. Trace elements in aerosol samples – including Al, P, Ca, Ti, V, Mn, Ni, Cu, Zn, Ce, and Pb – were determined by total digestion and a sector field inductively coupled plasma mass spectrometer (SF-ICP-MS). The crustal enrichment factors (EFcrust) and k-means clustering results of particle-size distributions show that these elements are derived primarily from three sources: (1) regional crustal emissions, including possible resuspension of soils containing biogenic P, (2) long-range transport, and (3) sea salt. Elements derived from crustal sources (Al, P, Ti, V, Mn, Ce) with EFcrust<10 were dominated by the coarse-mode particles (>1.8 µm) and peaked around 4.4 µm in diameter, reflecting the regional contributions. Non-crustal elements (Ca, Ni, Cu, Zn, Pb) showed EFcrust>10. Aerosol Pb was primarily dominated by fine-mode particles, peaking at 0.14–0.25 µm, and likely was impacted by air masses from southern South America based on air mass back trajectories. However, Ni, Cu, and Zn were not detectable in most size fractions and did not present clear size patterns. Sea-salt elements (Ca, Na+, K+) showed a single-mode distribution and peaked at 2.5–4.4 µm. The estimated dry deposition fluxes of mineral dust for the austral summer, based on the particle-size distributions of Al measured at Palmer Station, ranged from 0.65 to 28 mg m−2 yr−1 with a mean of 5.5±5.0 mg m−2 yr−1. The estimated dry deposition fluxes of the target trace elements in this study were lower than most fluxes reported previously for coastal Antarctica and suggest that atmospheric input of trace elements through dry deposition processes may play a minor role in determining trace element concentrations in surface seawater over the continental shelf of the western Antarctic Peninsula.


1987 ◽  
Vol 30 (6) ◽  
pp. 44-49
Author(s):  
David Ensor ◽  
Robert Donovan ◽  
Bruce Locke

Measurements of particle size distributions smaller than 0.1 μm in Class 100 clean rooms are summarized. The size distributions were measured in operational rooms during periods of time with little activity—the so-called "at rest" conditions. A simple particle number balance model is proposed, illustrating the importance of filter penetration and atmospheric aerosol on the concentration of submicrometer particles. Preliminary calculations are used to explain the absence of &lt; 0.1 μm diameter particles in the clean rooms tested. A ratio of condensation nucleus counter concentration to optical particle counter concentration is suggested as a parameter to provide an indication of changes in clean room particle size distribution.


AIHAJ ◽  
1972 ◽  
Vol 33 (9) ◽  
pp. 569-575 ◽  
Author(s):  
GORDON D. NIFONG ◽  
EDWARD A. BOETTNER ◽  
JOHN W. WINCHESTER

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