Abstract
An imidazole ester skeleton (zeolitic imidazolate framework (ZIF)) was grown on the surface of a ZnAl-layered double hydroxide (ZnAl-LDH) material to form a porous composite (ZIF-ZnAl-LDH). To understand the adsorption characteristics of the two materials, the effects of pH, adsorption time, and adsorption concentration on the adsorption of Congo red (CR) solution were investigated comprehensively. In addition, ZnAl-LDH and ZIF-ZnAl-LDH were characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS). The results clearly showed that ZnAl-LDH had a lamellar structure with a diameter of approximately 200-500 nm and ZIF-ZnAl-LDH had a regular three-dimensional hexagonal structure. The kinetics and thermodynamics of the CR adsorption by ZnAl-LDH and ZIF-ZnAl-LDH can be described using pseudo-second-order (PSO) and Langmuir models, respectively. The highest value of adsorption capacity obtained from the Langmuir equation was equal to 625.00 and 909.09 mg/g for these two compounds, respectively. The values of the standard Gibbs free energy (ΔG°), entropy (ΔS°), and enthalpy (ΔH°) obtained for these adsorption processes prove that the adsorption of CR by ZnAl-LDH and ZIF-ZnAl-LDH is a spontaneous endothermic process. Furthermore, through the analysis of the characterization results, it is concluded that the adsorption mechanisms of ZnAl-LDH and ZIF-ZnAl-LDH on CR are mainly dominated by electrostatic action, functional group action, surface pore adsorption, and anion exchange.