锰铁氧体纳米颗粒吸附/光催化同时去除单组分和二元组分体系中的有机染料和六价铬

N. Das, Priyamabada Mahapatra
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引用次数: 0

摘要

作为主要的污染源,染料工业的废水大多与几种有毒重金属有关。通过吸附/光催化工艺同时去除这些废水中的染料和重金属的努力有限。尖晶石铁氧体具有窄带隙和高稳定性,适合进一步开发。铁酸锰纳米颗粒的合成和表征,并评估其在单一和二元组分系统中去除有机染料和六价铬的效率是本研究的目标。通过x射线衍射、扫描电镜、透射电镜、紫外-可见漫反射和磁性测量等手段对共沉淀法制备的铁酸锰纳米颗粒(MF NPs)进行了表征。采用不同染料和Cr(VI)水溶液,考察了材料在可见光下的吸附和光催化性能。通过各种技术表征发现形成了具有窄带隙(1.78 eV)和中等饱和磁化强度(38.5 emu/g)的立方MF纳米颗粒。阴离子染料和Cr(VI)在MF上的吸附效果较好,而阳离子染料的光活性更明显。在可见光下,MF NPs显示出单独或同时光降解/还原不同染料和Cr(VI)的潜力。催化剂可以从反应混合物中磁性回收,以便再循环和进一步利用。
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Simultaneous Adsorptive/photocatalytic Removal of Organic Dyes and Hexavalent Chromium in Single and Binary Component Systems by Manganese Ferrite Nanoparticles
As a major source of pollutant, the effluents of dye based industries are mostly associated with several toxic heavy metals. Limited efforts have been made on simultaneous removal of both dyes and heavy metals from these effluents through adsorption/photocatalysis processes. Spinel ferrites with narrow band gap and high stability are suitable for further exploitation in this regard. Synthesis and characterisation of manganese ferrite nanoparticle and to assess its efficiency towards removal of organic dyes and hexavalent chromium in single and binary component systems are the objectives of this study. Manganese ferrite nanoparticle (MF NPs), prepared by coprecipitation, was characterised systematically by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV-Visible diffuse reflectance and magnetic measurement. Adsorptive and photocatalytic performances of the material under visible light were evaluated using aqueous solutions of different dyes and Cr(VI). Characterisation by various techniques revealed the formation of cubic MF nanoparticles with narrow band gap (1.78 eV) and moderate saturation magnetization (38.5 emu/g). In comparison, the anionic dyes and Cr(VI) were better adsorbed on MF, while photoactivity was more pronounced in the case of cationic dye. MF NPs displayed potential for photo-degradation/reduction of different dyes and Cr(VI) individually or simultaneously under visible light. The catalyst can be recovered magnetically from the reaction mixture for recycling and further use.
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