Efficient sorption and reduction of U(VI) on zero-valent iron-polyaniline-graphene aerogel ternary composite

被引:109
作者
Chen, Lili [1 ,2 ]
Feng, Shaojie [1 ]
Zhao, Donglin [1 ]
Chen, Shaohua [1 ]
Li, Feifei [1 ]
Chen, Changlun [2 ,3 ]
机构
[1] Anhui Jianzhu Univ, Key Lab Adv Funct Mat, Key Lab Funct Mol Design & Interface Proc, Hefei 230601, Peoples R China
[2] Chinese Acad Sci, Key Lab Novel Thin Film Solar Cells, Inst Plasma Phys, POB 1126, Hefei 230031, Peoples R China
[3] Soochow Univ, Collaborat Innovat Ctr Radiat Med, Jiangsu Higher Educ Inst, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
U(VI); Fe-PANI-GA composite; Sorption; OXIDE NANOSHEETS; HIGHLY-EFFICIENT; SELECTIVE ADSORPTION; PLASMA TECHNIQUE; AQUEOUS-SOLUTION; WASTE-WATER; REMOVAL; CARBON; PARTICLES; ADSORBENT;
D O I
10.1016/j.jcis.2016.11.050
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, zero-valent iron-polyaniline-graphene aerogel composite (Fe-PANI-GA) was prepared and applied in the removal of U(VI) from aqueous solutions by batch sorption experiments. The experimental results showed that the Fe-PANI-GA composite had an excellent removal capacity for the removal of U (VI) in acidic solutions. The results also showed that the maximum removal capacity of the Fe-PANI-GA toward U(VI) was 350.47 mg/g at pH 5.5. The sorption kinetics data were well-described by pseudo-second-order. The sorption isotherms of U(VI) fitted well with Langmuir isotherm and exhibited better removal efficiency with the increase of temperature. The thermodynamic parameters (AG, AS, AH) indicated that the sorption of U(VI) on the Fe-PANI-GA was an endothermic and spontaneous process. Moreover, removal mechanisms were studied based on the results of XRD, FTIR and XPS. Both U(VI) sorption and partially reductive precipitation of U(VI) to U(IV) contributed to the removal of U(VI) on Fe-PANI-GA. Therefore, Fe-PANI-GA was an economic and effective material for the removal of uranium from nuclear waste in practical application. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:197 / 206
页数:10
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