Kinetics and thermodynamics of Eu(III) adsorption onto synthetic monoclinic pyrrhotite

被引:25
|
作者
Zhu, Yuke [1 ]
Liu, Haibo [1 ]
Chen, Tianhu [1 ]
Xu, Bin [1 ]
Li, Ping [1 ]
机构
[1] Hefei Univ Technol, Sch Resources & Environm Engn, Hefei 230009, Peoples R China
关键词
Pyrrhotite; Eu(III); Adsorption kinetics; Thermodynamics; XPS; GRAPHENE OXIDE NANOSHEETS; AQUEOUS-SOLUTIONS; ENHANCED ADSORPTION; SORPTION; REMOVAL; U(VI); BATCH; PYRITE; DESORPTION; TRANSFORMATION;
D O I
10.1016/j.molliq.2016.01.100
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
The adsorption of Eu(III) from aqueous solutions onto monoclinic pyrrhotite (M-Pyr) was studied by batch experiments under various experimental conditions. M-Pyr was synthesized and characterized by XRD, FT-IR, SEM and potentiometric titration. The macroscopic results showed that the adsorption of Eu(III) on M-Pyr was independent of ionic strength, indicating that inner-sphere surface complexation predominated their adsorption. The kinetic adsorption process was well described by pseudo-second-order model with high correlation coefficient (R-2 > 0.999). The adsorption isotherms indicated that the adsorption of Eu(III) on M-Pyr fitted by Langmuir model was better than Freundlich model. The maximum adsorption capacity of Eu(III) on M-Pyr calculated from Langmuir model was 10.03 mg/g at pH 5.0 and 293 K. The thermodynamic parameters suggested that the adsorption of Eu(III) on M-Pyr was a spontaneous and endothermic processes. According to XPS analysis, the adsorption of Eu(III) on M-Pyr was mainly dominated by ion exchange and inner-sphere surface complexation at low pH and high pH conditions, respectively. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:565 / 570
页数:6
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