Synthesis of High-Crystallinity Mg-Al Hydrotalcite with a Nanoflake Morphology and Its Adsorption Properties for Cu2+ from an Aqueous Solution

• Published in: Inorganics 2023-09, Vol.11 (9), p.369
• Main Authors: Xu, Nai-Cai, Shi, Dan-Dan, Zhang, Ying, Zhong, Kai-Peng, Liu, Jing, Zhao, Qi, Gao, Qiang, Bian, Shao-Ju
• Format: Article
• Language: English
• Subjects: Adsorbents; Adsorption; Aluminum; Aqueous solutions; Copper; Copper chloride; Cu2; Environmental impact; Experiments; Heavy metals; Hydroxides; kinetics; lamellar morphology; Liquid-solid interfaces; Magnesium; Membrane separation; Mg-Al LDH; Morphology; Nitrates; Polyethylene; Scanning electron microscopy; Spectrum analysis; Thermal stability
• ISSN: 2304-6740; 2304-6740
• DOI: 10.3390/inorganics11090369

A magnesium–aluminum-layered double hydroxide (Mg-Al LDH) with a nano-lamellar morphology was prepared by using a homogeneous precipitation and hydrothermal method, and a calcination product (Mg-Al LDO) of the Mg-Al LDH was also obtained in this work. The XRD, TEM, SEM, FTIR, N2 ad/desorption, and TG-DTG techniques were employed to characterize the microstructures, morphologies, and thermostability levels of these two materials in detail. The results showed that both the Mg-Al LDH and Mg-Al LDO had mesoporous structures and nanoplate morphologies, with diameters of 50~200 nm. The Mg-Al LDH was transformed into Mg-Al LDO at 773 K in an air atmosphere. The adsorption properties of the Mg-Al LDH were investigated systematically with a copper chloride solution as a simulated waste. The experimental results demonstrated that the pH value of the solution had an obvious influence on its Cu2+ adsorption capacity, and the optimal pH value was approximately 5.0. The adsorption kinetics results showed that the Mg-Al LDH had a rapid adsorption rate, and the equilibrium adsorption capacity was 62.11 mg/g. Additionally, the Cu2+ adsorption could be commendably described using a pseudo-second-order model, demonstrating that the adsorption behavior is regulated by chemical sorption. The adsorption thermodynamic results indicated that the adsorption process was spontaneous at temperatures above 318 K. Moreover, the ΔG0 values decreased as the temperature was raised, which indicated that a higher temperature can cause a greater impetus for Cu2+adsorption. In addition, the positive values of the ΔH0 indicated that the Cu2+ adsorption was endothermic, and the positive ΔS0 values revealed an increase in the confusion at the solid–liquid interface of the adsorbent.