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This article in SSSAJ

  1. Vol. 70 No. 1, p. 215-221
     
    Received: Apr 26, 2005


    * Corresponding author(s): cornejo@irnase.csic.es
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doi:10.2136/sssaj2005.0131

Heavy Metal Adsorption by Montmorillonites Modified with Natural Organic Cations

  1. M. Cruz-Guzmána,
  2. R. Celisa,
  3. M. C. Hermosína,
  4. W. C. Koskinenb,
  5. E. A. Naterb and
  6. J. Cornejo *a
  1. a Instituto de Recursos Naturales y Agrobiología de Sevilla, CSIC, P.O. Box 1052, 41080 Sevilla, Spain
    b USDA-ARS, 1991 Upper Buford Circle, Rm. 439, St. Paul, MN 55108

Abstract

Agricultural and industrial pollution release large amounts of heavy metals into the atmosphere, surface water, soil, and plants. The protection and restoration of soils and water contaminated with heavy metals generate a great need to develop efficient adsorbents for these pollutants. This study reports the adsorption of Pb(II) and Hg(II) by two reference montmorillonites, Wyoming (SWy-2) and Arizona (SAz-1), that were pretreated with various natural organic cations containing different functional groups (L-carnitine, L-cysteine ethyl ester, L-cystine dimethyl ester, and thiamine cations) and with synthetic, nonfunctionalized organic cations (hexadecyltrimethylammonium [HDTMA] and phenyltrimethylammonium [PTMA] cations). Most of the organoclays adsorbed less Pb(II) than the untreated montmorillonites, with the exception of the L-carnitine–treated montmorillonites. The carboxyl functional group on L-carnitine was apparently effective for complexing Pb. In contrast, Hg(II) adsorption was greatly increased by several of the organic cation pretreatments. Sulfur-containing organic functional groups enhanced Hg(II) adsorption. The synthetic organic cations PTMA and HDTMA suppressed adsorption of Pb(II) and Hg(II) because these organic cations competed with the metals for adsorption sites on the clay surfaces and lack organic functional groups capable of interacting with the heavy metals. These findings are consistent with prior understanding of organic functional group-metal complexation reactions but go further by demonstrating that organoclays can be selectively functionalized with natural organic cations to enhance their affinity for heavy metals.

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