4.7 Article

Iron isotopic fractionation in industrial emissions and urban aerosols

Journal

CHEMOSPHERE
Volume 73, Issue 11, Pages 1793-1798

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2008.08.042

Keywords

Fe acrosols; Fe isotopes; Single-particle analysis; SEM-EDX; Industrial emissions; Steel metallurgy

Funding

  1. Communaute Urbaine de Dunkerque
  2. Nord - Pas de Calais County Council
  3. French Ministry for Higher Education and Research
  4. European funds (FEDER)

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A study on tropospheric aerosols involving Fe particles with an industrial origin is tackled here. Aerosols were collected at the largest exhausts of a major European steel Metallurgy plant and around its near urban environment. A combination of bulk and individual particle analysis performed by SEM-EDX provides the chemical composition of Fe-bearing aerosols emitted within the factory process (hematite, magnetite and agglomerates of these oxides with sylvite (KCl), calcite (CaCO3) and graphite carbon). Fe isotopic compositions of those emissions fall within the range (0.08 parts per thousand < delta Fe-56 < +0.80 parts per thousand) of enriched ores processed by the manufacturer (-0.16 parts per thousand < delta Fe-56 < +1.19 parts per thousand). No significant evolution of Fe fractionation during steelworks processes is observed. At the industrial Source. Fe is mainly present as oxide particles, to some extent in 3-4 mu m aggregates. In the close urban area, 5 km away from the steel plant, individual particle analysis of collected aerosols presents, in addition to the industrial particle type, aluminosilicates and related natural particles (gypsum, quartz, calcite and reacted sea salt). The Fe isotopic composition (delta Fe-56 = 0.14 +/- 0.11 parts per thousand) measured in the close urban environment of the steel metallurgy plant appears coherent with an external mixing of industrial and continental Fe-containing tropospheric aerosols, as evidenced by individual particle chemical analysis. Our isotopic data provide a first estimation of an anthropogenic Source term as part of the study of photochemically promoted dissolution processes and related Fe fractionations in tropospheric aerosols. (C) 2008 Elsevier Ltd. All rights reserved.

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