English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Evolution of anthropogenic aerosols in the coastal town of Salina Cruz,Mexico: part III. Size-segregated elemental composition analysed by total-reflection X-ray fluorescence spectrometry

MPS-Authors
/persons/resource/persons37225

Lammel,  G.
Climate Processes, MPI for Meteorology, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Lammel, G., Baumgardner, D. G., Fittschen, U. E. A., & Peschel, B. (2007). Evolution of anthropogenic aerosols in the coastal town of Salina Cruz,Mexico: part III. Size-segregated elemental composition analysed by total-reflection X-ray fluorescence spectrometry. International Journal of Environmental Analytical Chemistry, 87, 659-672. doi:10.1080/03067310701321967.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-FBA2-F
Abstract
Heavy metals in various size modes of the atmospheric aerosol are a concern for human health. Their and other elements' concentrations are indicative for anthropogenic and natural aerosol sources. Si, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Br, Rb, Sr, Hg, and Pb were determined as a complementary contribution to a study on aerosol cycling during the wet season, June 2004, in a humid, subtropical climate, i.e. in the city of Salina Cruz, situated on the Pacific coast of the Isthmus of Tehuantepec (16.2°N, 95.2°W), Mexico. For mass (gravimetry) and elemental analyses, particles were collected by a Berner low-pressure round nozzle cascade impactor using four stages corresponding to 0.1-0.25, 0.25-1.0, 1.0-4.0, and 4-16 µm of aerodynamic particle size. The impaction plates were modified such that approx. 1/6 consisted of a plastic support (Persplex®) for total reflection X-ray fluorescence spectrometry (TXRF). The elements' total content was determined by TXRF without any further sample pretreatment. Limits of quantification (LOQ) for elemental content in individual impactor stages corresponded to 25-60 ng m-3 for Si; 0.8-4 ng m-3 for Cl, K, Ca, Ti, and V; 3-20 pg m-3 for Cr, Mn, Fe, Cu, Ni, and Zn; and 7-50 pg m-3 for As, Se, Br, Rb, Sr, Hg, and Pb. In some samples, however, high blank values for the supports gave an LOQ = 6-19 ng m-3 for Cl; 3--7 ng m-3 for Ca; 3-7 ng m-3 for Fe, Ni, Cu, and Zn; and 60-70 ng m-3 for Pb. The influence of local natural, industrial, and vehicle traffic sources for heavy-metal mobilization was obvious. Heavy-metal abundances did not coincide with regionally distributed pollutants. V and Ni were found at particularly elevated levels advected with the sea breeze, which points to ships as sources. Br and Pb were found at particularly low levels. The concentrations of Br, Rb, Sr, and Pb were found below LOQ at least in some, As, Co, Se, and Hg in all of the samples. The elements' characteristic differences in mass size distributions were obvious despite the coarse size resolution. During the cycling of air masses from land to sea and back again, enrichment of super-micrometre particles in the near ground aerosol was observed under dry weather conditions. Rain preferentially removed the large particles with which heavy metals have been associated.