Carbon and iron co-doped titanium dioxide catalyst coated on activated carbon (Fe-C-TiO2/AC) was successfully synthesized using the sol-gel method, followed by hydrothermal treatment. Commercial activated carbon was treated by HNO3 prior to being coated by the as-synthesized catalyst. The composite was characterized by XPS, XRD, UV-Vis spectrophotometry, IR, TEM, HR-TEM, and BET. The performance of the supported catalysts was evaluated in the degradation of rhodamine B (RhB) in the solution under visible-light irradiation. The results showed that, with the appropriate amount of activated carbon, prepared Fe-C-TiO2/AC catalysts exhibited higher catalytic activities and Fe-C-TiO2/AC system showed the best performance. The photocatalytic degradation efficiency of Fe-C-TiO2/AC was enhanced due to the synergistic effect between AC (adsorption effect) and Fe-C-TiO2 (photocatalysis effect). This facilitated the photocatalytic degradation of RhB by Fe-C-TiO2.
In the present paper, the synthesis of cobalt ferrite/reduced graphene oxide (Co2Fe2O4/rGO) composite and its use for the simultaneous determination of uric acid (UA), xanthine (XA), and hypoxanthine (HX) is demonstrated. Cobalt ferrite hollow spheres were synthesized by using the carbonaceous polysaccharide microspheres prepared from a D-glucose solution as templates, followed by calcination. The CoFe2O4/rGO composite was prepared with the ultrasound-assisted method. The obtained material was characterized by using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, EDX elemental mapping, and nitrogen adsorption/desorption isotherms. The electrochemical behavior of UA, XA, and HX on the CoFe2O4/rGO-modified electrode was studied with cyclic voltammetry and differential pulse voltammetry (DPV). The modified electrode exhibits excellent electrocatalytic activity towards the oxidation of the three compounds. The calibration curves for UA, XA, and HX were obtained over the range of 2.0–10.0 μM from DPV. The limits of detection for UA, XA, and HX are 0.767, 0.650, and 0.506 μM, respectively. The modified electrode was applied to the simultaneous detection of UA, XA, and HX in human urine, and the results are consistent with those obtained from the high-performance liquid chromatography technique.
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