• DocumentCode
    3122630
  • Title

    Adsorption of Phosphate and Arsenate on Polynuclear Aluminum-Oxalate Precipitate: Spectroscopic and Adsorption Investigations

  • Author

    Liu Jing ; Li Wenjie

  • Author_Institution
    Key Lab. of Solid Waste Treatment & Resource Recycle, Southwest Univ. of Sci. & Technol., Mianyang, China
  • fYear
    2010
  • fDate
    18-20 June 2010
  • Firstpage
    1
  • Lastpage
    5
  • Abstract
    Aluminum organic coprecipitates play important roles in the transport of oxyanions in soil environment. Al13-Oxalate precipitate representing common aluminum organomineral components in soil environment was prepared to investigate the adsorption behavior of phosphate and arsenate on noncrystalline aluminum precipitate. Important thermodynamic parameters (ΔG, ΔH and ΔS) of adsorption reactions were evaluated using macroscopic adsorption data and equations. The low values of active energy of arsenate and phosphate adsorption reactions (Ea = 21.9KJ·moL-1 and 10.6 KJ·moL-1, respectively) indicate that the adsorption reaction basically is a diffusion process. The XPS studies indicate that phosphate has stronger chemical interaction with substrate than arsenate. FTIR spectroscopic studies have provide evidence for the formation of two different types of complexes in substrate.
  • Keywords
    Fourier transform spectra; adsorption; aluminium compounds; diffusion; geochemistry; infrared spectra; minerals; precipitation; precipitation (physical chemistry); soil; FTIR spectroscopy; XPS; aluminum organic coprecipitates; arsenate adsorption; chemical interaction; diffusion; noncrystalline aluminum precipitate; oxyanions transport; phosphate adsorption; polynuclear aluminum-oxalate precipitate; soil environment; thermodynamic parameters; Aluminum; Crystals; Educational technology; Laboratories; Minerals; Recycling; Soil; Solids; Spectroscopy; Thermodynamics;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
  • Conference_Location
    Chengdu
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-4712-1
  • Electronic_ISBN
    2151-7614
  • Type

    conf

  • DOI
    10.1109/ICBBE.2010.5516515
  • Filename
    5516515