Synthesis of nZnO from waste batteries by hydrometallurgical method for photocatalytic degradation of organic pollutants under visible light irradiation.

Waste zinc carbon (Zn-C) batteries are generated worldwide in a large amount. They are non-rechargeable and costly to recycle. Therefore, they end up in the landfills where they create hazards for humans and for environment as well. Zn-C batteries are rich in concentration of different heavy metals so they can be subjected for the recovery of metals for the development of valuable new materials. In this study authors have proposed an easy hydrometallurgical method for the recovery of zinc from waste Zn-C batteries to synthesize nano zinc oxide (nZnO) photocatalyst. The prepared nZnO particles were irregular in shape, highly crystalline in nature with crystallite size 23.94 nm. The band gap of the photocatalyst was 3.1 eV. The photocatalytic activity of the synthesised nZnO was tested for the degradation of three organic pollutants namely; phenol, p-nitrophenol (PNP) and crystal violet dye (CV) in an aqueous solution under visible light irradiation. nZnO showed a good catalytic efficiency for the degradation of all the three pollutants, however, the crystal violet (CV) removal was best in comparison with the other pollutants, it was minimally effected by the increase in CV concentration. The maximum degradation of phenol, PNP and CV was found to be 95.03 ± 0.2%, 88.63 ± 0.1% and 97.87 ± 0.4%, respectively. The degradation data was fitted best with pseudo-first-order kinetic model. The photocatalyst was recyclable and its regeneration ability was higher for initial three cycles. The intermediate compounds formed in the process of degradation were determined by liquid chromatography and mass spectroscopy (LC-MS) analysis.

Photocatalytic Degradation of Orange G Dye by Using Bismuth Molybdate: Photocatalysis Optimization and Modeling via Definitive Screening Designs.

In the current study, Bismuth molybdate was synthesized using simple co-precipitation procedure, and their characterization was carried out by various methods such as FT-IR, SEM, and P-XRD. Furthermore, the photocatalytic degradation of Orange G (ORG) dye using synthesized catalyst under visible light irradiation was studied. Response surface Method was used for the optimization of process variables and degradation kinetics evaluated by modeling of experimental data. Based on the experimental design outcomes, the first-order model was proven as a practical correlation between selected factors and response. Further ANOVA analysis has revealed that only two out of six factors have a significant effect on ORG degradation, however ORG concentration and irradiation time indicated the significant effects sequentially. Maximum ORG degradation of approximately 96% was achieved by keeping process parameters in range, such as 1 g L-1 loading of catalyst, 50 mg L-1 concentration of ORG, 1.4 mol L-1 concentration of H2O2 at pH 7 and a temperature of 30 °C. Kinetics of ORG degradation followed the pseudo first order, and almost complete degradation was achieved within 8 h. The effectiveness of the Bi2MoO6/H2O2 photo-Fenton system in degradation reactions is due to the higher number of photo-generated e- available on the catalyst surface as a result of their ability to inhibit recombination of e- and h+ pair.

Corn husk derived magnetized activated carbon for the removal of phenol and para-nitrophenol from aqueous solution: Interaction mechanism, insights on adsorbent characteristics, and isothermal, kinetic and thermodynamic properties.

In this study, waste corn husk was used for the synthesis of an effective adsorbent (cornhusk activated carbon, CHAC) and by treating at two different temperatures, 250 °C (CHAC-250) and 500 °C (CHAC-500) to check adsorption efficiency. The synthesized adsorbents were characterized with the help of scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy, Particle size analysis and x-ray diffraction (XRD), which revealed the different properties of the two adsorbents. The synthesized adsorbents were applied for the removal of phenol and p-nitrophenol (PNP) from aqueous solution. CHAC-500 was more efficient than the CHAC-250. The maximum adsorptions of phenol and PNP by CHAC-500 were ∼96% and ∼94%, respectively, while the maximum adsorptions of phenol and PNP by CHAC-250 were ∼81% and ∼84%, respectively. The adsorption processes were best fitted with the Langmuir adsorption isotherm and the pseudo-second-order kinetic model. The adsorption of phenol was an exothermic process, while that of PNP was an endothermic process, on both adsorbents.