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Visible active reduced graphene oxide loaded Titania for photodecomposition of ciprofloxacin and its antibacterial activity
摘要： The reduced Graphene Oxide based titanium dioxide (rGO-TiO2) nanocomposite was synthesized by a simple hydrothermal preparation and characterized by X-ray Diffraction Analysis (XRD), UV–Vis absorption spectroscopy (UV), Fourier Transform Infrared spectroscopy (FT-IR), Thermogravimetric Analysis (TGA), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). The XRD pattern of rGO-TiO2 indicates the presence of anatase TiO2 and average crystalline size of particles is 32 nm. The optical band gaps of TiO2, GO and rGO-TiO2 nanocomposite are 3.24 eV, 4.3 eV and 2.7 eV respectively. Comparison of efficiencies of three catalysts shows that ciprofloxacin degrades at a faster rate under visible light irradiation in the presence of rGO-TiO2 at 60 min than in presence of pure TiO2 commercial TiO2-P25. Higher photocatalytic decomposition efficiency of rGO-TiO2 is explained by its reduced electron-hole recombination and visible light activity. The kinetics of photodecomposition reaction was analyzed. Antibacterial activity analysis of rGO-TiO2 nanoparticles reveals that it is more active against S. aureus than E.coli.
关键词： Titania,Antibacterial activity,Photocatalytic decomposition,Ciprofloxacin,Reduced graphene oxide
更新于2025-09-04 15:30:14
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Antibacterial and photocatalytic activity of hydrothermally synthesized SnO2 doped GO and CNT under visible light irradiation
摘要： Bacterial and dye pollution are major problems with wastewater treatment. An increasing number of photocatalysts are being used in industry to kill bacterial and reduce pollution. In the present study, highly stable SnO2-doped nanocomposites have been prepared successively by a hydrothermal method. The synthesized nanocomposite was characterized using a range of techniques, such as X-ray diffraction, field emission scanning electron microscopy with energy dispersive X-ray spectroscopy and electron probe micro analysis, ultraviolet–visible spectroscopy, Fourier transform infrared spectroscopy, and high resolution transmission electron microscopy (HR-TEM). The nanocomposites showed significant dose-dependent bactericidal activity in the disc diffusion assay and cell viability test. The S-GO-SnO2 200 μg/mL produced a cell viability of 184.3 ± 11.71 and 172.3 ± 3.05 × 106 CFU/mL for E. coli and P. graminis, respectively. The S-GO-SnO2 showed significant photocatalytic degradation against MB in 120 min. The photocatalyst S-GO-SnO2 showed 159 and 161 × 106 CFU/mL at 150 min in E. coli and P. graminis, respectively. The cells treated with photocatalytic SnO2-doped nanocomposites showed 50% cell death. HR-TEM revealed 50% cell growth inhibition by bacterial damage. This photocatalytic SnO2-doped nanocomposite is a good candidate for treating industrial wastewater treatment contaminated with dyes and bacteria.
关键词： Antibacterial activity,Photocatalytic activity,Hydrothermal syntheses,Visible light irradiation,SGO-SnO2,SCNT-SnO2
更新于2025-09-04 15:30:14
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Synthesis and Characterization of Tio2/C Composite for Photocatalytic Degradation of Dyes.
摘要： Titanium dioxide TiO2 nanoparticles have moderate catalytic activity due to its wide band-gap and high rate of electron-hole recombination [1]. The TiO2 electrical conductivity poor is improved by mixing with other materials. Therefore, TiO2 based nanocomposites have been synthesized to increase the photocatalytic activity, as well as their structural characteristics and electrochemical performance, using dopants like carbon, nitrogen, sulfur and others. TiO2/C composite has been proven to be a promising photocatalyst for pollutants, due to C-doping, morphology, structure and mixed phases [1]. Carbon precursors are reported to synthesize TiO2/C, such as: glucose, oleic acid, carbon nanofiber, graphene oxide, activated carbon, carbon nanotubes, graphite, resorcinol and formaldehyde. Dyes used for industries, are significant sources of environmental pollution, because they are non-biodegradable [2]. Methyl orange (MO) and methyl blue (MB) have been used to help determine the activity of the photocatalyst [3]. The reagents used were: anatase powder 99.8% (metals basis), sucrose (99.5%), H2SO4 (65% wt), distilled water, MO (MW=327.33g/mol) and MB (MW=319.85g/mol). TiO2/C composites were synthesized via infiltrating sucrose into anatase. In a typical synthesis, anatase (A) and sucrose (S) with molar ratio of A/S=6, sulfuric acid and distilled water were mixed completely. The mixture was then put in a drying oven, treated at 100°C for 6h and subsequently at 160°C for 6h. The resulting brown precursor powder was carbonized in a tubular furnace at 800°C for 1h in argon atmosphere. Rigaku D-Max 2200 difractometer was used to obtain XRD patterns using Cu Kα radiation. The surface morphology and the crystalline phases were examined with Field Emission Transmission Electron Microscope, JEM 2010F JEOL. The photocatalytic activity was tested for degradation of MB and MO with an initial concentration of 20 ppm, using 0 and 0.34 g/L of TiO2/C, under radiant flux provided by 175 W UV. The MB and MO concentrations were measured by UV–vis spectroscopy (Aiglet-Vis spectrophotometer). The XRD patterns of TiO2/C composite is shown in Fig. 2, in which all the characteristic diffraction peaks of the TiO2/C composite can be respectively indexed with planes of anatase phase of TiO2 (JCPDS No. 21-1272). Moreover, a small peak at 11.5° is observed, characteristic of weakly ordered graphitic microstructure, indicating the trace amount of graphite in the composite [4]. No significant peaks of carbon or rutile are observed after the precursor powders are heat treated under argon atmosphere, which suggesting its amorphous nature and confirmed the high purity of the TiO2/C composite [5], because impurities have been reported due to the transformation from anatase to rutile phase [1]. The broad diffraction peaks indicate the sample’s nanocrystalline nature. Fig. 3a shows the micrographs of TEM bright field of powders; it is clearly seen that the TiO2/C composite powders have mostly spherical morphology. Further, it can be estimated that the particle size of samples is of the microscale order with grain size of the range of 20-30nm. Fig. 3b shows the atomic structure and the crystallinity of TiO2/C composite through HRTEM. The insert image shown in Figure 3b give the corresponding Fast Fourier Transform (FFT) pattern of the anatase; this pattern displays (101) and (200) planes from the interplanar spacing of 0.352 and 0.189 nm respectively (JCPDS No. 21-1272). The results of XRD concurred with the electron diffraction pattern created by FFT from HRTEM. The degradation percentage for MO and MB were 99.95 and 99.99 % at 15 min on TiO2/C whereas 86 and 81 % at 90 min for MB and MO in the absence of catalyst is illustrated in Fig. 5. TiO2/C composite was synthetized using anatase and sucrose by obtaining a precursor powder at low temperature (160°C), which is carbonized at 800°C in argon atmosphere. The XRD analysis reveals that the TiO2/C composite is a phase anatase unique structure with high crystallization, which had no impurities, but it showed a trace amount of graphite in the composite. The TiO2/C composite were found to be efficient catalyst for the photodegradation of MB and MO dyes under UV irradiation. The reaction was found to follow pseudo-first order kinetics described it well. This method could be extended to synthesize a variety of other composites for photocatalytic degradation of dyes.
关键词： anatase,TiO2/C composite,dyes,photocatalytic degradation,sucrose
更新于2025-09-04 15:30:14
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Enhanced photocatalytic simultaneous removals of Cr(VI) and bisphenol A over Co(II)-modified TiO2
摘要： To enhance the electron-hole separation and boost the practical performance of commercial titania (Degussa P25) under natural solar light, in this work, P25 was modified with Co(II) species (CoP25) through post-treatment with decomposition of Co-EDTA precursors in a wet chemical anchoring process. With appropriate Co(II) loading amount as molecular cocatalyst, the resulted CoP25-4 showed significantly improved photocatalytic performance for Cr(VI) reduction and bisphenol A (BPA) oxidation under UV-light irradiation. The co-existence of Cr(VI) and BPA promoted mutually the degradation of both pollutants. Under simulated solar light (AM 1.5G) illumination, the Cr(VI) reduction rate over CoP25-4 was 8.5 times enhanced compared with that over P25, while the simultaneous degradation rate of BPA over CoP25-4 was 8 times higher than that over P25. Further investigations indicated that the covalent atomic Co(II) anchoring on P25 significantly promoted the photogenerated electron-hole separation and facilitated Cr(VI) reduction via the formation of Co(I) intermediate and simultaneously boosted BPA oxidation. Our results demonstrated a facile strategy to modify P25 with remarkably improved performance for the practical application in environmental pollution management under natural light excitation.
关键词： bisphenol A,electron-hole separation,Cr(VI) reduction,photocatalytic,Co(II)-modified TiO2
更新于2025-09-04 15:30:14
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Rational design of yolk–shell nanostructures for photocatalysis
摘要： Photocatalysis is a promising route to convert solar energy into chemical energy directly, providing an alternative solution to environment and natural resource problems. Theoretically, all photocatalytic reactions are driven by charge carriers whose behavior can be divided into charge generation, separation, migration and surface reactions. Efficiencies of charge utilization in every step determine the overall performance of photocatalysis. Yolk–shell (YS) structures can provide an ideal platform for the efficient utilization of charge carriers. Typically, a YS structure is constructed from a hollow shell and an inner core, which can enhance light scattering in the hollow space and provide a large surface to create sufficient active sites, both of which can significantly improve the efficacy of charge utilization. Additionally, many strategies can be adopted to modify the YS structure for further enhancement of charge behaviors in every step. Existing reviews about YS structures mainly concentrate on the universality of the application of YSs, while the strategies to improve photocatalytic performance based on YSs have not been elaborately illustrated. This review describes the classification, synthesis, formation mechanism of YS structures and the rational regulation of the behaviors of photogenerated charge carriers, aiming at their effective utilization based on YS structures in heterogeneous photocatalytic reactions.
关键词： Charge carriers,Heterogeneous photocatalytic reactions,Solar energy conversion,Yolk–shell structures,Photocatalysis
更新于2025-09-04 15:30:14