Facile Synthesis of Sodium Dodecyl Sulfate Intercalated Mg‐Al LDH and its Excellent Adsorption Performances for Cu2+ from Aqueous Solution

吸附 热重分析 水溶液 化学 解吸 无机化学 傅里叶变换红外光谱 十二烷基硫酸钠 化学吸附 吸热过程 弗伦德利希方程 核化学 化学工程 色谱法 有机化学 工程类
作者
Naicai Xu,Xun Wen,Dandan Shi,Xiaojun Liu,Jing Liu,Kai‐Peng Zhong,Qiang Gao,Qi Zhao,Xing Han,Shaoju Bian
出处
期刊:ChemistrySelect [Wiley]
卷期号:9 (14)
标识
DOI:10.1002/slct.202305210
摘要

Abstract In this study, the magnesium aluminum layered double hydroxide intercalated with sodium dodecyl sulfate (Mg‐Al S‐LDH) was synthesized by using a roasting–restoration method based on the Mg‐Al LDH precursor, and their effectiveness in removing Cu 2+ from aqueous solutions was investigated. Detailed microstructural characterization of these adsorption materials involved employing X‐ray diffraction (XRD), Fourier‐transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption/desorption isotherms (N 2 ad/desorption), and thermogravimetric‐differential thermal gravimetric analysis (TG‐DTG). The experimental results revealed that Mg‐Al S‐LDH displayed a plate‐like layered structure with a larger surface area and enhanced adsorption ability. Specifically, the maximum adsorption capacity, reaching 96.15 mg ⋅ g −1 , was achieved at a temperature of 298 K, accompanied by a rapid adsorption rate. The adsorption kinetics adhered to the pseudo‐second‐order model, suggesting that chemisorption controlled the adsorption behavior. Furthermore, the adsorption of Cu 2+ followed the Freundlich model, signifying a multi‐site adsorption mechanism onto the surface and layers of Mg‐Al S‐LDH. Thermodynamic investigations indicated that higher temperatures facilitated Cu 2+ dissolution and strengthened the affinity with Mg‐Al S‐LDH, with a positive Δ H Θ value suggesting that the Cu 2+ adsorption process was endothermic and temperature‐enhancing. Ion selectivity experiments demonstrated that Cd 2+ and Pb 2+ ions had a significant impact on Cu 2+ adsorption, while the effects of Zn 2+ and Fe 2+ ions were less pronounced. The primary adsorption mechanisms of Cu 2+ onto Mg‐Al S‐LDH encompassed precipitation, complexation on the surface and layers, and isomorphous substitution. This study sheds light on the promising potential of Mg‐Al S‐LDH as an effective adsorbent for heavy metal removal and provides valuable insights into its adsorption mechanisms and performance in different environmental conditions.

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