The synthesis of a manganese dioxide-iron oxide-graphene magnetic nanocomposite for enhanced uranium(VI) removal

被引:88
作者
Tan, Lichao [1 ]
Wang, Jun [1 ,2 ]
Liu, Qi [1 ]
Sun, Yanbo [3 ]
Jing, Xiaoyan [1 ]
Liu, Lianhe [2 ]
Liu, Jingyuan [1 ]
Song, Dalei [1 ]
机构
[1] Harbin Engn Univ, Minist Educ, Key Lab Superlight Mat & Surface Technol, Harbin 150001, Peoples R China
[2] Harbin Engn Univ, Inst Adv Marine Mat, Harbin 150001, Peoples R China
[3] Jilin Univ, Inst Theoret Chem, State Key Lab Theoret & Computat Chem, Changchun 130023, Peoples R China
基金
中国国家自然科学基金;
关键词
AQUEOUS-SOLUTION; PHOSPHORIC-ACID; METAL IONS; ADSORPTION; COMPOSITE; WATER; RECOVERY; SORPTION; DYE; CYCLODEXTRIN;
D O I
10.1039/c4nj01256a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we have developed a facile route for the fabrication of a manganese dioxide-iron oxide-reduced graphite oxide magnetic nanocomposite (MnO2-Fe3O4-rGO). The as-obtained nanomaterial (MnO2-Fe3O4-rGO) was characterized using transmission electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, vibrating sample magnetometry, and Brunauer-Emmett-Teller surface area measurements. The MnO2-Fe3O4-rGO composite shows extraordinary adsorption capacity and fast adsorption rates for the removal of uranium(VI) in aqueous solution. The influence of factors including the dosage of the MnO2-Fe3O4-rGO composite used, pH of aqueous solution, and temperature were investigated. The thermodynamic parameters, including Gibbs free energy (Delta G degrees), standard enthalpy change (Delta H degrees) and standard entropy change (Delta S degrees) for the process, were calculated using the Langmuir constants. The results show that a pseudo-second-order kinetics model can be used to describe the uptake process using a kinetics test. Our present study suggests that the MnO2-Fe3O4-rGO composite can be used as a potential adsorbent for sorption of uranium(VI) as well as for providing a simple, fast separation method for the removal of uranium(VI) ions from aqueous solution.
引用
收藏
页码:868 / 876
页数:9
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