使用从过期多糖零食/铁盐中提取的混合多孔碳材料去除六价铬

M. Baikousi, Konstantinos Moustaklis, Angeliki Karakassides, Georgios Asimakopoulos, D. Moschovas, Apostolos Avgeropoulos, A. Bourlinos, A. Douvalis, C. Salmas, M. Karakassides
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引用次数: 1

摘要

目前,由于环境污染的加剧,科学兴趣越来越集中在开发废物回收利用的新策略以及开发清洁技术上。本文研究了一种过期的奶酪番茄风味玉米零食多糖食品,通过生产先进的环境修复复合磁性材料,对其进行了增值处理。利用氢氧化钾对这种零食进行碳化化学活化,得到了具有高表面积(SgBET ~800 m2/g)的微孔活性炭。以醋酸铁配合物为前驱体制备铁基磁性纳米颗粒,采用原位技术合成了磁性杂化材料。所得材料保留了微孔结构的一部分,表面积为SgBET ~500 m2/g。这种材料由均匀分散的磁隔离零价铁纳米颗粒和碳基体中的碳化铁(Fe3C)组成。磁性碳在Cr(VI)去除应用中表现出高吸附能力,符合准二级动力学模型。pH = 3时的最大吸附量为88.382 mgCr(VI)/gAC。最后,氧化实验结合FT-IR、Mössbauer和VSM测量表明,可能的Cr6+去除机制包括铁相氧化和Cr6+还原为Cr3+。
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Use of a Hybrid Porous Carbon Material Derived from Expired Polysaccharides Snack/Iron Salt Exhibiting Magnetic Properties, for Hexavalent Chromium Removal
Nowadays, the scientific interest is focused more and more on the development of new strategies in recycling of waste products as well as on the development of clean technologies due to the increased environmental pollution. In this work we studied the valorization of an expired cheese-tomato flavor corn snack, which is polysaccharide food product, by producing advanced hybrid magnetic materials for environmental remediation purposes. The carbonization-chemical activation of this snack using potassium hydroxide leads to a microporous activated carbon with high surface area (SgBET ~800 m2/g). The magnetic hybrid material was synthesized via an in-situ technique using iron acetate complex as the precursor to produce iron based magnetic nanoparticles. The resulting material retains a fraction of the microporous structure with surface area SgBET ~500 m2/g. Such material consists, of homogenously dispersed magnetic isolated zero valent iron nanoparticles and of iron carbides (Fe3C), into the carbon matrix. The magnetic carbon exhibited high adsorption capacity in Cr(VI) removal applications following a pseudosecond order kinetic model. The maximum adsorption capacity was 88.382 mgCr(VI)/gAC at pH = 3. Finally, oxidation experiments, in combination with FT-IR, Mössbauer, and VSM measurements indicated that the possible Cr6+ removal mechanism involves oxidation of iron phases and reduction of Cr6+ to Cr3+.
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