Tu Yao-Jen, Chan Ting-Shan, Tu Hao-Wei, Wang Shan-Li, You Chen-Feng, Chang Chien-Kuei
Institute of Urban Study, Shanghai Normal University, No. 100, Guilin Rd., Shanghai 200234, China.
National Synchrotron Radiation Research Center (NSRRC), No 101, Hsin-Ann Road, Hsincho 30076, Taiwan.
Chemosphere. 2016 Apr;148:452-8. doi: 10.1016/j.chemosphere.2016.01.054. Epub 2016 Feb 4.
An efficient method for removing and recovering molybdenum (Mo) from water was developed by using ZnFe2O4 nanoparticles. The Mo adsorption displayed a nonlinear isotherm that fitted well with the Langmuir isotherm, showing limited adsorption sites on the surface of ZnFe2O4. The adsorption of Mo(VI) was dependent on solution pH. With increasing pH, the build-up of negative charges of both adsorbent and adsorbate led to enhanced electric repulsion between them. The K-edge XANES spectra for the adsorbents collected after Mo adsorption revealed that Mo(VI) was the predominant oxidation state sorbed on ZnFe2O4, indicating that the reduction of Mo(VI) did not occur on ZnFe2O4. The different peak positions of k-space and R-space shown in K-edge EXAFS spectra demonstrated that the adsorbed Mo could be bound on the surface or be slipped in the vacancy position of the ZnFe2O4 crystal. Importantly, Mo could be efficiently adsorbed from photoelectric industrial wastewater and these adsorbed Mo anions were rapidly replaced by OH(-) ions, implying the potential for Mo removing and recovering in industrial wastewater.
通过使用ZnFe2O4纳米颗粒开发了一种从水中去除和回收钼(Mo)的有效方法。钼的吸附呈现出非线性等温线,与朗缪尔等温线拟合良好,表明ZnFe2O4表面的吸附位点有限。Mo(VI)的吸附取决于溶液的pH值。随着pH值的升高,吸附剂和吸附质的负电荷积累导致它们之间的电排斥增强。钼吸附后收集的吸附剂的K边XANES光谱表明,Mo(VI)是吸附在ZnFe2O4上的主要氧化态,这表明在ZnFe2O4上没有发生Mo(VI)的还原。K边EXAFS光谱中显示的k空间和R空间的不同峰位表明,吸附的钼可以结合在表面上,也可以滑入ZnFe2O4晶体的空位位置。重要的是,钼可以从光电工业废水中被有效吸附,并且这些吸附的钼阴离子会迅速被OH(-)离子取代,这意味着在工业废水中去除和回收钼的潜力。