An efficient electrochemical degradation of toxic pollutants in wastewater using BiOBr/BiVO4 hierarchical structured electrode material.

The electrochemical degradation of alizarin red dye was studied using bismuth oxyhalide attached to bismuth vanadate nanocomposite synthesized via a simple solvothermal method. The electrochemical degradation of alizarin red dye was treated at current densities of 3 and 5 mA cm-1 for 30 min under different supporting electrolyte mediums (NaCl and KCl). Also, the electrochemical degradation of BiOBr/BiVO4 electrode shows higher degradation percentages of 97 and 99 for NaCl and KCl electrolyte solutions, which are higher degradation percentages than pure BiVO4 electrode (88 and 91 for NaCl and KCl). Also, the BiOBr/BiVO4 electrode shows 100% COD reduction during the 30th min of alizarin red dye using both NaCl and KCl electrolyte solutions. This may indicate that the prepared BiOBr/BiVO4 electrode shows an efficient electrode material for the degradation of textile dyes.

A synergistic consequence of catalyst dosage, pH solution and reactive species of Fe-doped CdAl2O4 nanoparticles on the degradation of toxic environmental pollutants.

Industrial wastewater treatment techniques are one of the biggest challenges of the scientific community that necessitate an increased consciousness to address water scarcity worldwide. Herein, an eco-friendly and cost-effective process was demonstrated to cope with tannery, textile and pharmaceutical dye wastes through the co-precipitation of highly reusable Fe-doped CdAl2O4 samples. The XRD studies exposed the space group R 3‾ with no secondary phase step being found for all samples. The outcomes of optical absorbance spectra demonstrate that Fe doping diminished the energy gap from 3.66 to 1.67 eV. HR-TEM images of existing spherical particles and some of the particles' rod-like structures with little agglomeration were found for Fe (0.075 M) doped CdAl2O4 nanoparticles. The PL emission outcomes show that Fe doping effectively prevented the charge carrier's recombination in CdAl2O4 during photocatalysis. All Fe-doped CdAl2O4 samples demonstrated higher photodegradation behaviors towards the effectual degradation of both dye solutions as compared to pure CdAl2O4 samples. Particularly, Fe (0.075 M)-doped CdAl2O4 samples exhibited improved photodegradation performance of 93 and 95% for both dye solutions. The amount of photodegradation was noticed to rely on dye pH, irradiation time, catalyst dosage, initial dye amount, and reactive species. The recyclability of the Fe (0.075 M) doped CdAl2O4 nanoparticles denotes that 78 and 82% of BB and BG were removed up to the 6th run of usage. The outcomes of trapping tests,.OH- and h+ radicals were the major Scavenging in the photodegradation reaction. COD studies affirmed the whole mineralization of BB and BG dye molecules. It is expected that our present examination could offer to improve various spinal oxide materials for the photodegradation activity of pharmaceutical contaminants and environmental issues and can also resolve energy storage applications.

A critical review on recent research progress on microplastic pollutants in drinking water.

Plastic pollution is an emerging issue in recent days. Persistent plastic particles reach the atmosphere, land and water by multiple pathways. Research has confirmed that the existence of plastic particles is found surprisingly everywhere, from the Artic to the Antarctic region. The probability of ingestion of plastic by all living forms is quite natural, as the whole planet's environment is polluted with microplastic particles. The bioaccumulation of microplastics is a threat and the consequences for living beings are yet to be explored. Microplastics present in different drinking water sources like rivers, lakes, treatment units etc. are studied by several researchers, covering various aspects. Research carried out by various scientists on the microplastics in different drinking water sources is highlighted in this review. In view of the previous research carried out on various aspects of microplastic particles, the necessity of a uniform protocol for qualitative and quantitative analysis of microplastic is ascertained. Microplastic pollution is an ongoing environmental concern, it must be addressed and research should be expanded.

Experimental investigation of the electrochemical detection of sulfamethoxazole using copper oxide-MoS2 modified glassy carbon electrodes.

An electrochemical sensor detection of sulfamethoxazole was performed using a copper oxide Molybdenum sulfide modified glassy carbon electrode using Molybdenum sulfide (CuO/MoS2) functionalization. As part of the characterization process, materials were characterized via cyclic voltammetry (CV), Square wave voltammetry (SWV), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD) and scanning electron microscopy (SEM). To optimize the performance of the experiment, parameters like the scan rate and pH, the electrolytes study, the stability, the comparative study and repeatability were optimized. In comparison to CuO, MoS2 and bare Glassy carbon electrode (GCE), an electrochemical sensor that incorporated CuO/MoS2 exhibited exceptional electrochemical performance. CuO/MoS2 modified electrodes showed a higher peak current for oxidation compared with bare, CuO and MoS2 modified electrodes, which demonstrated enhanced electrochemical conductivity for detection of SMX by minimizing oxidation potential from +0.18 V to +0.10 V. In the range of 100-800 µl SMX concentrations, the peak current linearly correlated with the concentration of SMX. In the calibration plot, the modified electrode showed linearity under ideal circumstances for SMX concentrations starting at 0.3 µM. This study investigated the presence of SMX with a detection limit of 0.34 Pg/L. CuO/MoS2 based electrochemical sensor, according to our analysis, are potentially useful in applications requiring the detection of trace amounts of SMX.