Recyclable superparamagnetic adsorbent based on mesoporous carbon for sequestration of radioactive Cesium

被引:42
作者
Husnain, Syed M. [1 ]
Um, Wooyong [1 ,2 ]
Chang, Yoon-Young [3 ]
Chang, Yoon-Seok [1 ]
机构
[1] Sch Environm Sci & Engn, Kwangju, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Div Adv Nucl Engn, Pohang 790784, South Korea
[3] Kwangwoon Univ, Dept Environm Engn, Seoul 139701, South Korea
基金
新加坡国家研究基金会;
关键词
Fe3O4-O-CMK-3; Carbonaceous adsorbent; Superparamagnetic nanoparticles; Nuclear waste; Cesium; BLUE/GRAPHENE OXIDE NANOCOMPOSITES; AQUEOUS-SOLUTION; EFFICIENT REMOVAL; MAGNETIC COMPOSITES; SURFACE COMPLEXES; HIGHLY EFFICIENT; ADSORPTION; WATER; COPPER; ACID;
D O I
10.1016/j.cej.2016.09.116
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Novel and recyclable superparamagnetic adsorbent Fe3O4-O-CMK-3 was synthesized by in situ growth of nanometer sized magnetite particles (m-NPs) on the surface of mesoporous carbon at low temperature (70 degrees C) using ecologically-benign materials. Structural characterization by transmission electron microscopy (TEM) confirmed the formation of 20 nm thick oxidized mesoporous carbon layers around the magnetic NPs. Thermogravimetric analysis (TGA) results revealed dense carboxylic and phenolic groups on the surface of Fe3O4-O-CMK-3. Because of these abundant polar groups the Fe3O4-O-CMK-3 had stronger adsorption affinity towards Cs than did magnetic mesoporous carbons O-Fe-CMK-3 synthesized by impregnation, and Fe-O-CMK-3 synthesized by co-casting, even in the presence of high concentrations of competing cations (K+,Na+, Ca2+ and Sr2+). The Fe3O4-O-CMK-3 adsorbent reached a steady state quickly (<5 min) with maximum adsorption capacity of 205 mg g(-1) which is sufficiently higher than other magnetic adsorbents (usually lower than 110 mg g(-1)) reported in the literature. The synthesized nanostructure adsorbent could be retrieved in a few seconds using an external magnet and reused at least six times for contaminant removal. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:798 / 808
页数:11
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