Defluoridation performance of electrospun La2O3-CeO2 nanofibers
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Abstract
Nano bimetallic oxides have broad application prospects as fluoride removal agents. La2O3-CeO2 nanofibers were fabricated via electrospinning-calcination method using Ce(NO3)3·6H2O and La(NO3)3·6H2O as raw materials and polyacrylonitrile (PAN) as template. TEM, SEM-EDS, BET, FTIR and XRD were employed to verify the morphology and structure of La2O3-CeO2 nanofibers. The defluoridation properties of La2O3-CeO2 nanofibers were discussed under batch mode, and the effects of adsorbate (F−) initial concentration, pH, contact time, La2O3-CeO2 nanofibers dose and coexisting anions on the defluoridation were explored. The results illustrate that the specific surface area of La2O3-CeO2 adsorbent is 31.04 m2·g−1. The La2O3-CeO2 nanofibers exhibit the best defluoridation performance at pH of 3, and the adsorption capacity of La2O3-CeO2 nanofibers climbs up with rise of the initial concentration of F−. The pseudo-second-order kinetic and Langmuir isotherm model (R2>0.99) simulate the defluoridation process of La2O3-CeO2 nanofibers better, and the maximum uptake of F− by La2O3-CeO2 nanofibers is 111.98 mg·g−1 at 45℃. Thermodynamic studies suggest that the defluoridation process of La2O3-CeO2 nanofibers is a spontaneous (ΔG0<0), entropy increase (ΔS0=56.63 J·mol−1·K−1) and endothermic (ΔH0=9.90 kJ·mol−1) process.
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