Adsorption and anion exchange insight of indigo carmine onto CuAl-LDH/SWCNTs nanocomposite: kinetic, thermodynamic and isotherm analysis

靛蓝胭脂红在CuAl-LDH/SWCNTs纳米复合材料上的吸附和阴离子交换研究:动力学、热力学和等温线分析

阅读:1

Abstract

Two-dimensional layered materials are gaining much attention in the field of wastewater purification. Herein, we report the synthesis and characterization of an anion selective copper-aluminum-layered double hydroxide/single-walled carbon nanotubes (CuAl-LDH/SWCNTs) composite for the scavenging of organic dye indigo carmine (IC) from aqueous solution. A facile urea hydrolysis method was used for the controlled growth of the metal hydroxides over the SWCNTs. Structural characterization of the prepared materials was investigated using X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and X-ray diffraction (XRD) techniques. The obtained results revealed that the CuAl-LDH/SWCNTs composite has a higher potential for the removal of IC in comparison to CuAl-LDH and SWCNTs. The enhanced adsorption capacity of the composite revealed that deposition of CuAl-LDH over SWCNTs increases the active adsorption sites and promotes the interactions between the composite and IC dye via anion exchange, electrostatic, π-π, hydrogen bonding etc. Moreover, adsorption kinetics, isotherms, and thermodynamic studies have been also proposed to illustrate the mechanism of the IC adsorption onto the CuAl-LDH/SWCNTs composite. Thermodynamic parameters showed that the adsorption of IC dye onto the CuAl-LDH/SWCNTs composite was exothermic and spontaneous in nature. Intra-particle diffusion was determined to be the rate-limiting step and adsorption of IC followed the Langmuir isotherm model with the maximum monolayer adsorption capacity 294.117 mg g(-1) at 20 °C. The results suggest that the CuAl-LDH/SWCNTs composite is a potential material for IC adsorption in aqueous solution.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。