Water pollution is a globally recognized serious problem that is hindering human development and societal progress. One of the most feasible methods to eliminate this problem is wastewater treatment and reuse. Emerging micropollutants, such as pesticides, are notorious for not being removed using traditional treatment methods. Therefore, novel techniques such as advanced oxidation processes (AOPs) have been proposed, among which photocatalytic ozonation is arguably the best option. Sulfoxaflor belongs to a relatively newer class of compounds known as sulfoximines and has not been studied for degradation using photocatalytic ozonation. In this work, we explore the degradation of sulfoxaflor, specifically a Dow product containing sulfoxaflor as an active ingredient using various AOPs, particularly photocatalytic ozonation. Photocatalytic ozonation has shown a synergy of 2.23 times compared to photocatalysis and ozonation alone. Fe-zeolite can improve the treatment time as an ozonation catalyst, reducing the removal time from 22 min to 18 min while reducing the electrical energy per order and electrical energy per order (EEO) from 69.5 to 42.92 kWh m⁻³ order⁻¹. Catalysts have been characterized using scanning electron microscopy and point of zero charge. The effects of the initial concentration, UV intensity, catalyst dose, and catalyst reuse have been studied. Moreover, the rate constants have been determined using curve fitting, and the mechanism is proposed.

Glycerol pretreatment is a promising method for the environmentally-friendly transformation of lignocellulosic materials into sustainable cellulose-rich raw materials (i.e., biopolymer) to fabricate biocomposites. Here, a comparison of aqueous acidified glycerol (AAG) pretreatment of wheat straw (WS) with alkaline, hot water, and dilute acid pretreatments on the thermal and mechanical characteristics of their fabricated composite board is presented. A comparison of total energy expenditure during WS pretreatment with AAG and other solutions was estimated and a comparative influence of AAG processing on lignocellulosic constituents and thermal stability of WS fiber was studied. Results imply that AAG pretreatment was superior in generating cellulose-rich fiber (CRF) as compared to other pretreatments and enhanced the cellulose contents by 90% compared to raw WS fiber. Flexural strength of acidic (40.50 MPa) and hot water treated WS composite (38.71 MPa) was higher compared to the value of 33.57 MPa for untreated composite, but AAG-treated composites exhibited lower values of flexural strength (22.22 MPa) compared to untreated composite samples. Conversely, AAG pretreatment consumed about 56% lesser energy for each kg of WS processed as compared to other pretreatments. These findings recognize that glycerol pretreatment could be a clean and new pretreatment strategy to convert agricultural waste into high-quality CRF as a sustainable raw material source for engineered biocomposite panels.

Due to the importance of water for human survival and scarcity of freshwater resources, wastewater treatment has become very important recently. Some persistent pollutants, such as pesticides, are not removed even after multiple conventional wastewater treatment techniques. Advanced oxidation processes (AOPs) are one of the novel techniques that can be used to treat these persistent compounds. Photocatalytic ozonation is a promising AOP that combines photocatalysis and ozonation for synergistic effects and faster degradation of persistent pollutants. However, usually, only a photocatalyst is used while combining photocatalysis and ozonation. In this work, both a photocatalyst and ozonation catalyst have been simultaneously used for the degradation of commercially available CONFIDOR^® pesticide, a Bayer product with Imidacloprid as the active ingredient. TiO₂ is employed as a photocatalyst, and Fe-coated Zeolite is employed as an ozonation catalyst. The results show that the reaction rate increases by 1.4 times if both catalysts are used as compared to the use of one photocatalyst only. Almost complete removal (>99%) of pollutant is achieved after 20 min with the simultaneous use of a catalyst when imidacloprid with an initial concentration of 100 mg/L is subjected to 250 W/m² UV of a wavelength of 253.7 nm and 100 mg/h ozone, where it takes 30 min if only one photocatalyst is used. The paper also explores the effect of initial concentration, UV intensity, catalyst dose and catalyst reuse while also briefly discussing the kinetics and mechanism.

Clean water is a necessity for all life to survive and flourish. However, natural waters are being continuously contaminated due to the release of waste streams in water. Hence, it is important to remove pollutants from wastewater to fulfill human needs. Conventional treatment methods are neither efficient nor economical for wastewaters that especially contain refractory toxic pollutants. This requires novel techniques like Advanced oxidation processes (AOPs), that may successfully degrade persistent micropollutants more efficiently. In this study, an azo dye Acid Red 1 was removed by three AOPs, namely Photocatalytic oxidation, Ozonation and Photocatalytic Ozonation, by employing heterogenous catalysts. TiO₂ was used as photocatalyst, whereas Fe-Zeolite has been further added as Ozonation catalyst. The study revealed that photocatalysis degraded only 28% Acid red dye after 15 min, whereas for ozonation, the degradation percentage was 95% in same time. In combined photocatalytic ozonation process using TiO₂, 95% degradation was achieved in just 9 min and treatment time further reduced to 5 min when Fe-zeolite was added. Optimization studies for initial concentration, UV intensity and catalyst loading were performed. Finally, rate constants and Electrical Energy per Order (EEO) values were determined for all AOPs, and mechanism was proposed.

The purpose of this work was to consider the decolorization efficiency of reactive yellow 160 (Ry-160) dye utilizing cobalt aluminum oxide (AlCo₂O₄)-anchored Multi-Walled Carbon Nanotubes (AlCo₂O₄/MWCNTs) nanocomposites as catalysts for the first time in a photocatalytic process under natural sunlight irradiation. The compositional, morphological, and functional group analyses of AlCo₂O₄ and AlCo₂O₄/MWCNTs were performed by utilizing Energy Dispersive Spectroscopy (EDS), Field Emission Scanning Electron Microscopy (FE-SEM), and Fourier Transform Infrared (FTIR) Spectroscopy, respectively. A UV-Vis (UV-Vis) spectrophotometer was used to investigate degradation efficiency. The results exhibited a reduction in the optical bandgap for AlCo₂O₄/MWCNTs nanocomposites as catalysts from 1.5 to 1.3 eV compared with pure spinel AlCo₂O₄ nanocomposites. AlCo₂O₄/MWCNTs nanocomposites showed excellent photocatalytic behavior, and around 96% degradation of Ry-160 dye was observed in just 20 min under natural sunlight, showing first-order kinetics with rate constant of 0.151 min⁻¹. The results exhibited outstanding stability and reusability for AlCo₂O₄/MWCNTs by maintaining more than 90% photocatalytic efficiency even after seven successive operational cycles. The betterment of the photocatalytic behavior of AlCo₂O₄/MWCNTs nanocomposites as compared to AlCo₂O₄ nanocomposites owes to the first-rate storage capacity of electrons in MWCNTs, due to which the catalyst became an excellent electron acceptor. Furthermore, the permeable structure of MWCNTs results in a greater surface area leading to the onset of more active sites, and, in turn, it also boosts conductivity and reduces the formation of agglomerates on the surface of catalysts, which inhibits e−/h⁺ pair recombination. Concisely, the synthesis of a novel AlCo₂O₄/MWCNTs catalyst with excellent and fast photocatalytic activity was the aim of this study.