This study presents a novel method for the development of TiO2/reduced graphene oxide (rGO) nanocomposites for photocatalytic degradation of dyes in an aqueous solution. The synergistic integration of rGO and TiO2, through the formation of Ti–O–C bonds, offers an interesting opportunity to design photocatalyst nanocomposite materials with the maximum absorption shift to the visible region of the spectra, where photodegradation can be activated not only with UV but also with the visible part of natural solar irradiation. TiO2@rGO nanocomposites with different content of rGO have been self-assembled by the hydrothermal method followed by calcination treatment. The morphological and structural analysis of the synthesized photocatalysts was performed by FTIR, XRD, XPS, UV-Vis DRS, SEM/EDX, and Raman spectroscopy. The effectiveness of the synthesized nanocomposites as photocatalysts was examined through the photodegradation of methylene blue (MB) and rhodamine B (RhB) dye under artificial solar-like radiation. The influence of rGO concentration (5 and 15 wt.%) on TiO2 performance for photodegradation of the different dyes was monitored by UV-Vis spectroscopy. The obtained results showed that the synthesized TiO2@rGO nanocomposites significantly increased the decomposition of RhB and MB compared to the synthesized TiO2 photocatalyst. Furthermore, TiO2@rGO nanocomposite with high contents of rGO (15 wt.%) presented an improved performance in photodegradation of MB (98.1%) and RhB (99.8%) after 120 min of exposition to solar-like radiation. These results could be mainly attributed to the decrease of the bandgap of synthesized TiO2@rGO nanocomposites with the increased contents of rGO. Energy gap (Eg) values of nanocomposites are 2.71 eV and 3.03 eV, when pure TiO2 particles have 3.15 eV. These results show the potential of graphene-based TiO2 nanocomposite to be explored as a highly efficient solar light-driven photocatalyst for water purification.
The aim of this work was to identify and characterize three samples of jarosite process tailing waste in Mitrovica, Kosovo, using Raman and Fourier transform infrared (FTIR) spectroscopy. The identification is made based on the assignment of bands in the Raman and FTIR spectra. Both Raman and FTIR spectra show the fundamental stretching and bending vibration mode of SO 4 2 -, OH -and NH 4 + groups. The results obtained by the means of Raman and infrared spectroscopy are compared with cited reference data in order to sum the analysis of vibrational spectra.
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