Arsenic removal from aqueous solutions by mixed magnetite-maghemite nanoparticles

被引:143
作者
Chowdhury, Saidur Rahman [1 ]
Yanful, Ernest K. [1 ]
Pratt, Allen R. [2 ]
机构
[1] Univ Western Ontario, Dept Civil & Environm Engn, London, ON N6A 5B9, Canada
[2] Nat Resources Canada, CANMET Min & Mineral Sci Labs, Ottawa, ON K1A 0G7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Arsenic; Groundwater; Magnetite-maghemite nanoparticles; Langmuir isotherm; Adsorption; X-RAY PHOTOELECTRON; MULTIPLET STRUCTURE; ADSORPTION; IRON; PRECIPITATION; SPECTROSCOPY; ADSORBENT; SORPTION;
D O I
10.1007/s12665-010-0865-z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, magnetite-maghemite nanoparticles were used to treat arsenic-contaminated water. X-ray photoelectron spectroscopy (XPS) studies showed the presence of arsenic on the surface of magnetite-maghemite nanoparticles. Theoretical multiplet analysis of the magnetite-maghemite mixture (Fe3O4-gamma Fe2O3) reported 30.8% of maghemite and 69.2% of magnetite. The results show that redox reaction occurred on magnetite-maghemite mixture surface when arsenic was introduced. The study showed that, apart from pH, the removal of arsenic from contaminated water also depends on contact time and initial concentration of arsenic. Equilibrium was achieved in 3 h in the case of 2 mg/L of As(V) and As(III) concentrations at pH 6.5. The results further suggest that arsenic adsorption involved the formation of weak arsenic-iron oxide complexes at the magnetite-maghemite surface. In groundwater, arsenic adsorption capacity of magnetite-maghemite nanoparticles at room temperature, calculated from the Langmuir isotherm, was 80 mu mol/g and Gibbs free energy (a dagger G(0), kJ/mol) for arsenic removal was -35 kJ/mol, indicating the spontaneous nature of adsorption on magnetite-maghemite nanoparticles.
引用
收藏
页码:411 / 423
页数:13
相关论文
共 38 条
  • [1] ARSENATE ADSORPTION ON AMORPHOUS ALUMINUM HYDROXIDE
    ANDERSON, MA
    FERGUSON, JF
    GAVIS, J
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1976, 54 (03) : 391 - 399
  • [2] *BGS, 2001, WC0019 BGS GOV PEOPL, V1
  • [3] Cornell R.M., 1996, The Iron Oxide: Structure, Properties, Reactions, Occurance and Uses
  • [4] Arsenic removal using a polymeric/inorganic hybrid sorbent
    DeMarco, MJ
    Sengupta, AK
    Greenleaf, JE
    [J]. WATER RESEARCH, 2003, 37 (01) : 164 - 176
  • [5] Comparison of arsenic(V) and arsenic(III) sorption onto iron oxide minerals: Implications for arsenic mobility
    Dixit, S
    Hering, JG
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (18) : 4182 - 4189
  • [6] Granular ferric hydroxide - a new adsorbent for the removal of arsenic from natural water
    Driehaus, W
    Jekel, M
    Hildebrandt, U
    [J]. JOURNAL OF WATER SERVICES RESEARCH AND TECHNOLOGY-AQUA, 1998, 47 (01): : 30 - 35
  • [7] Fairley N, 1999, CASAXPS VERSION 2 2
  • [8] Investigation of multiplet splitting of Fe 2p XPS spectra and bonding in iron compounds
    Grosvenor, AP
    Kobe, BA
    Biesinger, MC
    McIntyre, NS
    [J]. SURFACE AND INTERFACE ANALYSIS, 2004, 36 (12) : 1564 - 1574
  • [9] Examination of the oxidation of iron by oxygen using X-ray photoelectron spectroscopy and QUASES™
    Grosvenor, AP
    Kobe, BA
    McIntyre, NS
    [J]. SURFACE SCIENCE, 2004, 565 (2-3) : 151 - 162
  • [10] Guha S., 1990, Asian Environ, V12, P42