Abstract
In this research, cerium oxide (CeO 2 ) nanoparticles were synthesized by the homogeneous precipitation. Cerium nitrate hexahydrate and ammonia solution were used as precursors. A mixture of water and ethylene glycol was used as solvent. The ratio of ethylene glycol /water mixed solvent was 80% by volume of ethylene glycol. Pure CeO 2 nanoparticles were yellow powder. Particle size was found to be in the range of 5–6 nm with BET specific surface area of 140.62 m2/g. TGA/DSC was used to find the appropriate temperature for calcination. X-ray diffraction analysis showed that the particles exhibited cubic fluorite structure. Then, cerium oxide nanoparticles were impregnated with ferric nitrate at 0.25, 0.50, 0.75, 1.00, 1.50 and 2.00 mol.% of CeO 2 by calcining the mixture at 400 C˚. Color of Fe-doped CeO 2 became deeper yellow when mol.% Fe increased. Cerium oxide nanoparticles and the doped samples were characterized by using X-ray diffraction (XRD), the Brunauer, Emmett and Teller (BET), Transmission electron microscopy (TEM), Scanning electron microscopy (SEM) and Energy dispersive X-ray spectroscopy analysis (EDS). The photocatalytic activity of pure CeO 2 and Fe-doped CeO 2 were investigated for the degradation of oxalic acid and formic acid under visible irradiation using photocatalytic reactor. The effect of Fe on photocatalytic activity of CeO 2 nanoparticles was verified. It was found that Fe-doped CeO 2 was more effective than pure CeO 2 . The photocatalytic activity of Fe-doped CeO 2 for mineralization of formic acid was better than that of oxalic acid (the mineralization time to degrade formic acid was less than that of oxalic acid). The best result of photocatalytic activity for the degradation of oxalic was obtained from 2.00 mol.% Fe-doped CeO 2 nanoparticles. 1.00 mol.% Fe-doped CeO 2 demonstated the highest photocatalytic activity for the degradation of formic acid under visible irradiation. The enhanced performance observed for the Fe-doped CeO 2 system was likely due to the formation of ferrioxalate and ferriformate complexes which could generate hydroxyl radical.
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