The dyeing process is a very important unit operation in the leather and textile industries; it produces significant amounts of waste effluent containing dyes and poses a substantial threat to the environment. Therefore, degradation of the industrial dye-waste liquid is necessary before its release into the environment. The current is focusing on the reduction of pollutant loads in industrial wastewater through remediating azo and thiazine dyes (synthetic solutions of textile dye consortium). The current research work is focused on the degradation of dye consortium through photo-electro-Fenton (PEF) processes via using dimensionally stable anode (Ti) and graphite cathode. The ideal conditions, which included a pH of 3, 0.1 (g/L) of textile dye consortium, 0.03 (g/L) of iron, 0.2 (g/L) of H2O2, and a 0.3 mAcm-2 of current density, were achieved to the removal of dye consortium over 40 min. The highest dye removal rate was discovered to be 96%. The transition of azo linkages into N2 or NH3 was confirmed by Fourier transforms infra-red spectroscopic analysis. PEF process reduced the 92% of chemical oxygen demand (COD) of textile dye consortium solution, and it meets the kinetics study of the pseudo-first-order. The degradation of dye through the PEF process was evaluated by using the cyclic voltammetric method. The toxicity tests showed that with the treated dye solution, seedlings grew well.

Bisphenol-A, also known as BPA, is commonly used as a building block for epoxy and polycarbonate plastics. However, it has been recently identified as a major source of water pollution due to its release into the water from plastic products. BPA-based resins can also contaminate the water with high concentrations of BPA, which can enter the water bodies through production units and wastewater discharge. Photocatalysis, particularly the photo-Fenton process, is an effective method for wastewater treatment and degrading pollutants. Titanium dioxide (TiO2) is usually chosen based on its high photocatalytic properties and high performance. However, its wide band gap energy is a major issue for the photocatalytic process. This means that the catalyst can only exhibit high photocatalytic performance under UV-light irradiation and usually requires an acidic pH, which limits its use. In order to address the aforementioned issues, a visible-light photoactive photo-Fenton reaction has been successfully developed to degrade bisphenol A at natural pH using H2O2. The process was highly efficient, achieving complete degradation of phenol in just three hours of visible light irradiation with Cu-MOF. This environmentally friendly Fenton process has the advantage of occurring at natural pH levels with the presence of H2O2, providing a new perspective for efficient degradation. The photocatalyst was characterized using single X-ray diffraction (SC-XRD), powder X-ray diffraction (PXRD), Fourier Transform Infrared Spectroscopy (FTIR), and UV–vis diffuse reflectance spectroscopy (DRS).

A liquid-phase exfoliation of few-layer graphene in tea is considered as one of the alternative approaches for the preparation of environment-friendly graphene. However, the removal of chemically adsorbed tea-polyphenols from graphene is known to be difficult and the application of centrifugation or filtration alone for the purification of graphene against tea-polyphenols is regarded to be almost technically impossible. Notably, a strategy for facile deoxygenation of tea-graphene must be established for a green and economical production of graphene to be realized. In this work, a simple purification method of graphene through the application of merely a household bleach ( Clorox®) after the pre-exfoliation in black tea has been proposed. It has been found that the carbon–oxygen (C/O) value for graphene increases from 2.7 to 8.1 while the values of C–OH, C–O–C and C=O region in the C1s spectrum of graphene decrease significantly after being purified in bleach for 5 h. The stretching and shift of C–OH, C=O and C–O–C at 3468 cm−1, 1637 cm−1 and 1008 cm−1 from IR spectrum of purified graphene seems to be in agreement with the produced data from the XPS and Raman spectroscopy. Despite the enhanced ID/IG of Raman from the hybridization of sp2 by hydroxylation, the deoxygenation of tea-graphene does not negatively affect the electrical performance since the sheet resistance was impressively reduced to 193 Ω from 2.1 kΩ. It is believed that this photo-Fenton-inspired purification strategy would assist in the washing issue of polyphenol-stabilized graphene for various future electronic applications.

A nanocomposite consisting of Fe3O4 and MWCNT was produced via sol-gel technique using FeCl3 along with MWCNT by calcination at 300℃. The degradation effect of rhodamine B dye has been investigated under UV illumination in a darkroom. The degradation reaction was studied by monitoring the discoloration of dye as a function of irradiation time using UV-visible spectrophotometeric technique. The Fe3O4-MWCNT samples have continuous degradation ability under the UV illumination with the first order kinetics and the dye removal was better than in the pristine Fe3O4. The resultant composite catalyst was found to be efficient for the photo-Fenton reaction of the dye.