The unavailability of clean drinking water is one of the significant health issues in modern times. Industrial dyes are one of the dominant chemicals that make water unfit for drinking. Among these dyes, methylene blue (MB) is toxic, carcinogenic, and non-biodegradable and can cause a severe threat to human health and environmental safety. It is usually released in natural water sources, which becomes a health threat to human beings and living organisms. Hence, there is a need to develop an environmentally friendly, efficient technology for removing MB from wastewater. Photodegradation is an advanced oxidation process widely used for MB removal. It has the advantages of complete mineralization of dye into simple and nontoxic species with the potential to decrease the processing cost. This review provides a tutorial basis for the readers working in the dye degradation research area. We not only covered the basic principles of the process but also provided a wide range of previously published work on advanced photocatalytic systems (single-component and multi-component photocatalysts). Our study has focused on critical parameters that can affect the photodegradation rate of MB, such as photocatalyst type and loading, irradiation reaction time, pH of reaction media, initial concentration of dye, radical scavengers and oxidising agents. The photodegradation mechanism, reaction pathways, intermediate products, and final products of MB are also summarized. An overview of the future perspectives to utilize MB at an industrial scale is also provided. This paper identifies strategies for the development of effective MB photodegradation systems.

Recent developments in nanoscience have appreciably modified how diseases are prevented, diagnosed, and treated. Metal nanoparticles, specifically silver nanoparticles (AgNPs), are widely used in bioscience. From time to time, various synthetic methods for the synthesis of AgNPs are reported, i.e., physical, chemical, and photochemical ones. However, among these, most are expensive and not eco-friendly. The physicochemical parameters such as temperature, use of a dispersing agent, surfactant, and others greatly influence the quality and quantity of the synthesized NPs and ultimately affect the material’s properties. Scientists worldwide are trying to synthesize NPs and are devising methods that are easy to apply, eco-friendly, and economical. Among such strategies is the biogenic method, where plants are used as the source of reducing and capping agents. In this review, we intend to debate different strategies of AgNP synthesis. Although, different preparation strategies are in use to synthesize AgNPs such as electron irradiation, optical device ablation, chemical reduction, organic procedures, and photochemical methods. However, biogenic processes are preferably used, as they are environment-friendly and economical. The review covers a comprehensive discussion on the biological activities of AgNPs, such as antimicrobial, anticancer anti-inflammatory, and anti-angiogenic potentials of AgNPs. The use of AgNPs in water treatment and disinfection has also been discussed in detail.

Microplastics (MPs) have become a critical pollutant, accumulating in aquatic ecosystems and posing significant environmental and human health risks. Approximately 5.25 trillion plastic particles float in global oceans, releasing up to 23,600 metric tonnes of dissolved organic carbon annually, which disrupts microbial dynamics. MPs arise from the breakdown of larger plastics, degraded by photodegradation, thermal degradation, and biological processes, which are influenced by polymer type and environmental factors. As carriers, MPs absorb and transport contaminants such as heavy metals, per- and polyfluoroalkyl substances (PFAS), and persistent organic pollutants (POPs) across trophic levels, thereby increasing toxicity within food webs. Key aquatic organisms, including microalgae, molluscs, and fish, experience cellular toxicity, oxidative stress, and disruptions in essential functions due to MP ingestion or adhesion, raising concerns about their bioaccumulation in humans through ingestion, inhalation, and dermal contact. The complex surface chemistry of MPs enhances their pollutant adsorption, a process modulated by environmental pH, salinity, and contamination levels, while aging and structural attributes further impact their bioavailability and toxicity. This review consolidates knowledge on MPs’ occurrence, transformation, pollutant interactions, and methodologies for sampling and analysis, emphasizing advancements in spectroscopy and imaging techniques to improve MP detection in aquatic environments. These insights underscore the pressing need for standardized analytical protocols and comprehensive toxicological research to fully understand MPs’ effects on ecosystems and human health, informing future mitigation strategies and policy development. Graphical

In this study, initially 11 different bacterial strains were tested for the degradation capabilities against Basic Orange 2 dye. In initial screening with 78.90% degradation activity, Escherichia coli emerged as the most promising strain to degrade the selected dye, and was then employed in subsequent experiments. For further enhancing the degradation capability of selected bacteria, the effects of various physicochemical parameters were also evaluated. Among the tested parameters, 20 ppm dye concentration, 1666 mg/L glucose concentration, a temperature of 40 °C, 666 mg/L sodium chloride concentration, pH 7, 1000 mg/L urea concentration, a 3-day incubation period and the use of sodium benzoate as a redox mediator (666 mg/L) were found to be ideal conditions to get the highest decolorization/degradation activities. Finally, all the mentioned parameters were combined in a single set of experiments, and the decolorization capacity of the bacteria was enhanced to 89.88%. The effect of pH, dye concentration, incubation time and temperature were found to be responsible for the optimum degradation of dye (p < 0.05), as predicted from the ANOVA (analysis of variance) of the response surface methodology. The metabolites were collected after completion of the process and characterized through Fourier transform irradiation (FTIR) and gas chromatography mass spectrometry (GC-MS). From the data obtained, a proposed mechanism was deduced where it was assumed that the azo bond of the dye was broken by the azoreductase enzyme of the bacteria, resulting in the formation of aniline and 3, 4-diaminobezeminium chloride. The aniline was then further converted to benzene by deamination by the action of the bacterial deaminase enzyme. The benzene ring, after subsequent methylation, was transformed into o-xylene, while 3, 4-diaminobezeminium chloride was converted to p-xylene by enzymatic action. These findings suggest that Escherichia coli is a capable strain to be used in the bioremediation of textile effluents containing azo dyes. However, the selected bacterial strain may need to be further investigated for other dyes as well.

The main issues with mainstream anammox application is loss of bacterial activity by low temperatures and by a high organic content of wastewater. We demonstrate a novel switching method between sidestream and mainstream wastewater. The wastewater flow was switched between sidestream (reject water at >22 °C) and mainstream (municipal wastewater at 16.5 °C), so that the anammox biomass activity and biomass growth could benefit from sidestream conditions. Real sidestream wastewater (biogas plant effluent) (≈1000 mg NH₄⁺-N L^-1) and synthetic mainstream (municipal wastewater-like source) (≈100 mg NH₄⁺ -N) wastewater were used for 20 L biofilm reactor feeding. The highest total nitrogen removal rate (TNRR) of 527 g N m^-3 d^-1 (average TNRR 180 (±140) g N m^-3 d^-1) was achieved with sidestream wastewater at a low chemical oxygen demand (COD)/TN ratio of 1.1/1. For reactor feeding with mainstream, the highest TNRR achieved was 61 g N m^-3d^-1. Average TNRR for mainstream of 20 (±15) g N m^-3 d^-1 was low due to a higher COD/N ratio of 3.2/1. The highest TNRR in a batch test was achieved at the COD concentration of 480 mg L^-1, reflecting a TNRR of ≈ 5 mg N g^-1 TSS h^-1. With a high COD concentration of 2600 mg L^-1 (TOC/TN = 8/1), TNRR decreased similarly in both feeds to 1.6 mg N g^-1 TSS h^-1. The anammox microorganism’s genus Candidatus Brocadia enrichment in deammonification biofilm reactor was higher in the mainstream operation (7.6% of all bacteria) than in sidestream operation period (<0.7% of all bacteria).