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Arsenite and arsenate adsorption on coprecipitated bimetal oxide magnetic nanomaterials: MnFe2O4 and CoFe2O4

机译:MnFe2O4和CoFe2O4共沉淀双金属氧化物磁性纳米材料上的砷和砷吸附

摘要

Bimetal oxide magnetic nanomaterials (MnFe2O4 and CoFe2O4) were synthesized and characterized with transmission electron microscope (TEM), X-ray powder diffraction (XRD), vibrating sample magnetometer (VSM), and X-ray photoelectron spectroscopy (XPS). The adsorption of arsenic on these nanomaterials was studied as a function of pH, initial arsenic concentration, contact time and coexisting anions. The Langmuir and Freundlich isotherm models were applied to fit the adsorption data, and the maximum adsorption capacities of arsenite (As-III) and arsenate (As-V) on MnFe2O4 were 94 and 90 mg g(-1). and on CoFe2O4 were 100 and 74 mg g(-1), respectively. MnFe2O4 and CoFe2O4 showed higher As-III and As-V adsorption capacities than the referenced Fe3O4 (50 and 44 mg g(-1), respectively) prepared by the same procedure. Quantificational calculation from XPS narrow scan results of O(1s) spectra of adsorbents indicated that the higher adsorption capacities of As-III and As-V on MnFe2O4 and CoFe2O4 than on Fe3O4 might be caused by the increase of the surface hydroxyl (M-OH) species. Phosphate and silicate were powerful competitors with arsenic for adsorptive sites on the adsorbent. Desorption study showed that over 80% of As-III and 90% of As-V could be clesorbed from MnFe2O4 with 0.1 M NaOH solution. (C) 2010 Elsevier B.V. All rights reserved.
机译:合成了双金属氧化物磁性纳米材料(MnFe2O4和CoFe2O4)并通过透射电子显微镜(TEM),X射线粉末衍射(XRD),振动样品磁力计(VSM)和X射线光电子能谱(XPS)进行了表征。研究了砷在这些纳米材料上的吸附随pH,初始砷浓度,接触时间和共存阴离子的变化。应用Langmuir和Freundlich等温线模型拟合吸附数据,砷(As-III)和砷酸盐(As-V)在MnFe2O4上的最大吸附容量分别为94和90 mg g(-1)。和在CoFe2O4上分别为100和74 mg g(-1)。 MnFe2O4和CoFe2O4的As-III和As-V吸附容量高于通过相同程序制备的参考Fe3O4(分别为50和44 mg g(-1))。 XPS吸附剂O(1s)光谱的窄扫描结果的定量计算表明,As-III和As-V在MnFe2O4和CoFe2O4上的吸附容量比在Fe3O4上高,这可能是由于表面羟基(M-OH )的物种。磷酸盐和硅酸盐是砷的强力竞争者,它们在吸附剂上的吸附位点上。解吸研究表明,用0.1 M NaOH溶液可以从MnFe2O4中裂解出80%以上的As-III和90%的As-V。 (C)2010 Elsevier B.V.保留所有权利。

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