Two-Dimensional Ti3C2Tx MXene Nanosheets for Efficient Copper Removal from Water

吸附 X射线光电子能谱 吸热过程 弗伦德利希方程 扫描电子显微镜 透射电子显微镜 能量色散X射线光谱学 材料科学 核化学 水溶液 化学工程 化学 冶金 纳米技术 物理化学 复合材料 工程类
作者
Asif Shahzad,Kashif Rasool,Waheed Miran,Mohsin Nawaz,Jiseon Jang,Khaled A. Mahmoud,Dae Sung Lee
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:5 (12): 11481-11488 被引量:456
标识
DOI:10.1021/acssuschemeng.7b02695
摘要

The performance of two-dimensional (2D) Ti3C2Tx MXene nanosheets in the adsorption and copper removal from aqueous media was investigated. Delaminated (DL)-Ti3C2Tx exhibited excellent Cu removal ability, because of their large specific surface area, hydrophilicity, and unique surface functional properties. Scanning electron microscopy coupled with energy-dispersive spectroscopy (SEM–EDS), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD) analyses were performed to analyze the structural changes in Ti3C2Tx MXene and its interaction with Cu ions. Oxygenated moieties in the layered structure of MXene facilitated reductive adsorption of Cu2+ forming Cu2O and CuO species. DL-Ti3C2Tx exhibited a higher and faster Cu uptake, compared to multilayer (ML)-Ti3C2Tx. The maximum experimental adsorption capacity (Qexp,max) was 78.45 mg g–1, and 80% of the total content of metal ions was adsorbed within 1 min. A pseudo-second-order kinetic model and the Freundlich adsorption isotherm accurately describe the equilibrium time and maximum Cu uptake onto the adsorbent material, respectively. Thermodynamic analysis revealed that the adsorption process was endothermic. The adsorption capacity (Qe) of DL-Ti3C2Tx was 2.7 times higher than that of a commercially available activated carbon. The present results illustrate the promising potential of 2D MXene nanosheets for the removal of toxic metals from water.
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