• DocumentCode
    2507218
  • Title

    Environmental Geochemistry of Sediments in Endemic Arseniasis at Western Hetao Plain

  • Author

    Tan, Ting ; Ma, Teng ; He, Jun

  • Author_Institution
    Key Lab. of Biogeology & Environ. Geol. of Minist. of Educ., China Univ. of Geosci., Wuhan, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    Arsenic and As-bearing solid phases in sediments was studied to provide a further evidence for researches of enrichment mechanism of arsenic at western Hetao Plain. The content of arsenic in 23 core sediment samples varies from 7.7 to 34.6 mg/Kg, with great value in clay and mild clay layer. The obvious positive relationship in content between Fe2O3, Mn, Sb, B, V and As indicates that the distribution of arsenic in the sediments may be related to Fe and Mn oxides, and mobilization of Sb, B and V may be affected by similar geochemical processes as that of As. Sequential extraction show that in addition to recalcitrant mineral phase dissolved by acid, the major forms of arsenic in the sediment are strongly adsorbed As, followed by As coprecipitated with amorphous Fe oxyhydroxides, As coprecipitated with acid volatile sulfide (AVS), carbonates, Mn oxides, and very amorphous Fe oxyhydroxides. The release of arsenic from the sediment is mainly affected by the competition of phosphate absorption and reductive dissolution of iron hydroxide.
  • Keywords
    clay; dissolving; geochemistry; sediments; soil pollution; acid volatile sulfide; coprecipitation; endemic arseniasis; enrichment mechanism; environmental geochemistry; extraction; mild clay; oxyhydroxides; phosphate absorption; recalcitrant mineral phase; reductive dissolution; sediments; western Hetao Plain; Absorption; Amorphous materials; Chemicals; Geology; Helium; Iron; Laboratories; Minerals; Sediments; Solids;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5162780
  • Filename
    5162780