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Oxygen, Carbon, and Sulfur Segregation in Annealed and Unannealed Zerovalent Iron Substrates
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    Oxygen, Carbon, and Sulfur Segregation in Annealed and Unannealed Zerovalent Iron Substrates
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    Department of Chemistry, University of Nebraska, Lincoln, Nebraska 68588-0304 and School of Natural Resources, University of Nebraska, Lincoln, Nebraska 68583-0915
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    Langmuir

    Cite this: Langmuir 2004, 20, 26, 11509–11516
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    https://doi.org/10.1021/la048288j
    Published November 17, 2004
    Copyright © 2004 American Chemical Society

    Abstract

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    Finely ground and pretreated iron substrates known as “zerovalent iron” or “Fe0” are used as reductants in the environmental remediation of halogenated hydrocarbons, and the composition of their surfaces significantly affects their reactivity. Samples of unannealed and annealed (heat-treated under H2/N2) zerovalent iron were analyzed using X-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy (AES). Surface concentration of the iron and of the impurities observed by XPS and AES, carbon, chlorine, sulfur, and oxygen, were measured before and after soaking in trichloroethylene (TCE) and in water saturated with TCE (H2O/TCE) to simulate chlorocarbon remediation conditions. Samples pretreated by annealing at high temperature under H2 contained less iron carbide. The carbide contaminant was evident in both iron and carbon XPS spectra, with binding energies of 709.0 and 283.3 eV for the Fe 2p3/2 and C 1s, respectively. The annealed Fe0 surface also contained more sulfur. The carbide concentration was essentially unchanged by TCE and H2O/TCE exposure, whereas the sulfur decreased in proportion to chlorine adsorption following the dechlorination reaction. While oxygen concentration is initially lower on the annealed substrate surface, it rapidly increased during the model TCE remediative treatment process and thus does not represent a significant effect of the annealing process on surface reactivity.

    Copyright © 2004 American Chemical Society

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     Department of Chemistry.

     School of Natural Resources.

    *

     To whom correspondence should be addressed. E-mail:  [email protected].

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    Langmuir

    Cite this: Langmuir 2004, 20, 26, 11509–11516
    Click to copy citationCitation copied!
    https://doi.org/10.1021/la048288j
    Published November 17, 2004
    Copyright © 2004 American Chemical Society

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