Preparation of ferric oxide modified diatomite and its application in the remediation of As(III) species from solution

被引:27
|
作者
Knoerr, R. [1 ]
Brendle, J. [1 ]
Lebeau, B. [1 ]
Demais, H. [2 ]
机构
[1] Univ Haute Alsace, CNRS, Equipe Mat Porosite Controlee, Inst Sci Mat Mulhouse,LRC 7228, F-68200 Mulhouse, France
[2] SA OLMIX, F-56580 Za Du Haut Du Bois, Brehan, France
关键词
Diatomite; Composite; Lepidocrocite; Goethite; Remediation; SULFATED AQUEOUS-MEDIUM; FERROUS HYDROXIDE; ARSENIC REMOVAL; IRON-OXIDE; ADSORPTION; FERRIHYDRITE; ADSORBENTS; WATER; SPECIATION; OXIDATION;
D O I
10.1016/j.micromeso.2012.09.036
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new iron oxide-diatomite system was synthesized in one pot by mixing natural diatomite with a ferrous sulfate solution at room temperature. The characterization of the materials (Diatom-Fe) by XRD and chemical analysis revealed that iron (29% w/w) was crystallized under goethite phase (alpha-FeOOH). Analysis conducted by SEM further highlighted the preferential presence of goethite on the surface of diatomite, which involves hydrogen bonding between diatomite surface silanol groups and ion species. The mechanism of formation of goethite is suggested to occur through the precipitation of ferrous ions by hydroxyls ions followed by the oxidation of the iron species to yield first to lepidocrocite (gamma-FeOOH) then goethite that is thermodynamically more stable. Within this mechanism, the contribution of calcium carbonate through its dissolution into hydroxyls species is evidenced by XRD and FIR analyses. The remediation properties of Diatom-Fe towards arsenite species cations were investigated in batch jar tests for 24 h at auto-equilibrium pH. The materials showed a noticeable higher As (III) sorption capacity (16 mg/g) than the native diatomite (0.5 mg/g). These results can be explained by the strong affinity of arsenites to goethite which is further emphasized by the dispersion of the iron oxide crystals on diatomite surface. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:185 / 191
页数:7
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