A method based on application of ZnO nanorods loaded on activated carbon (ZnO-NRs-AC) for adsorption of Bromocresol Green (BCG) and Eosin Y (EY) accelerated by ultrasound was described. The present material was synthesized under ultrasound assisted wet-chemical method and subsequently was characterized by FE-SEM, TEM, BET and XRD analysis. The extent of contribution of conventional variables like pH (2.0-10.0), BCG concentration (4-20mgL(-1)), EY concentration (3-23mgL(-1)), adsorbent dosage (0.01-0.03g), sonication time (1-5min) and centrifuge time (2-6min) as main and interaction part were investigated by central composite design under response surface methodology. Analysis of variance (ANOVA) was adapted to experimental data and guide the best operational conditions mass by set at 6.0, 9mgL(-1), 10mgL(-1), 0.02g, 4 and 4min for pH, BCG concentration, EY concentration, adsorbent dosage, sonication and centrifuge time, respectively. At these specified conditions dye adsorption efficiency was higher than 99.5%. The suitability and well prediction of optimum point was tested by conducting five experiments and respective results revel that RSD% was lower than 3% and high quality of fitting was confirmed by t-test. The experimental data were best fitted in Langmuir isotherm equation and the removal followed pseudo second order kinetics. The experimentally obtained maximum adsorption capacities were estimated as 57.80 and 61.73mgg(-1) of ZnO-NRs-AC for BCG and EY respectively from binary dye solutions. The mechanism of removal was explained by boundary layer diffusion via intraparticle diffusion.
In this study, magnetic activated carbon (MAC) nanoparticles were coated with an organic hybrid of silicotungstic acid that makes MAC suitable for adsorption and photocatalytic degradation of dyes. The prepared composite was characterized by Fourier transform infrared spectroscopy, powder X-ray diffraction, thermal analyses, scanning electron microscopy, vibrating sample magnetometer, and N 2 adsorption-desorption isotherms. Dye adsorption and photocatalytic properties of composite were examined by studying the decolorization of model dyes methylene blue (MB), methyl orange (MO), rhodamine B (RhB), and their mixture solutions. The results show that the composite can selectively adsorb MB molecules from binary mixtures of MB/MO or MB/RhB, and its adsorption capacity is enhanced as compared with the MAC. The composite is also, unlike MAC, a good photocatalyst in the degradation of dyes under sunlight, visible, and UV irradiation and can be separated by magnet, recovered and reused. Removal is via combination of adsorption and then photocatalytic degradation through direct oxidation by composite or indirect oxidation by• OH radicals. While the sunlight is not able to degrade alone MO and RhB solution in the presence of composite, it degrades the MO and RhB mixed with MB solution.
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