Sorption mechanisms of metals to graphene oxide

被引:5
作者
Showalter, Allison R. [1 ]
Duster, Thomas A. [2 ]
Szymanowski, Jennifer E. S. [2 ]
Na, Chongzheng [2 ]
Fein, Jeremy B. [2 ]
Bunker, Bruce A. [1 ]
机构
[1] Univ Notre Dame, Dept Phys, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Civil & Environm Engn & Earth Sci, Notre Dame, IN 46556 USA
来源
16TH INTERNATIONAL CONFERENCE ON X-RAY ABSORPTION FINE STRUCTURE (XAFS16) | 2016年 / 712卷
关键词
ADVANCED PHOTON SOURCE; AQUEOUS-SOLUTIONS; NANOSHEETS; BEAMLINE;
D O I
10.1088/1742-6596/712/1/012094
中图分类号
O59 [应用物理学];
学科分类号
摘要
Environmental toxic metal contamination remediation and prevention is an ongoing issue. Graphene oxide is highly sorptive for many heavy metals over a wide pH range under different ionic strength conditions. We present x-ray absorption fine structure (XAFS) spectroscopy results investigating the binding environment of Pb(II), Cd(II) and U(VI) ions onto multi-layered graphene oxide (MLGO). Analysis indicates that the dominant sorption mechanism of Pb to MLGO changes as a function of pH, with increasing inner sphere contribution as pH increases. In contrast, the sorption mechanism of Cd to MLGO remains constant under the studied pH range. This adsorption mechanism is an electrostatic attraction between the hydrated Cd+2 ion and the MLGO surface. The U(VI), present as the uranyl ion, changes only subtly as a function of pH and is bound to the surface via an inner sphere bond. Knowledge of the binding mechanism for each metal is necessary to help in optimizing environmental remediation or prevention in filtration systems.
引用
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页数:4
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