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A new heterocyclic azo dye ligand (L) was synthesized by the combination of 4-amino antipyrine with 4-aminophenol. The new Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Cu(II), Zn(II), and Cd(II) complexes were synthesized in excellent yields. The metal chelate structures were elucidated using elemental analyses, FT-IR, 1H-NMR, mass, magnetic moment, diffused reflectance spectral and thermal analysis (TG-DTG), and molar conductivity measurement. According to the FT-IR study, the azo dye ligand exhibited neutral tri-dentate behavior, binding to the metal ions with the azo N, carbonyl O, and protonated phenolic OH. The 1H-NMR spectral study of the Zn(II) complex supported the coordination of the zo dye ligand without proton displacement of the phenolic OH. Diffused reflectance and magnetic moment studies revealed the octahedral geometry of the complexes, as well as their good electrolytic nature, excepting the Zn(II) and Cd(II) complexes, which were nonelectrolytes, as deduced from the molar conductivity study. The theoretical calculations of optimized HOMO–LUMO energies, geometrical parameters, electronic spectra, natural atomic charges, 3D-plots of MEP, and vibrational wavenumbers were computed and elucidated using LANL2DZ and 6-311G (d, p) basis sets of density functional theory (DFT) with the approach of B3LYP DFT and TD-DFT methods. The ligand and complexes have been assayed for their antimicrobial activity and compared with the standard drugs. Most of the complexes have manifested excellent antimicrobial activity against various microbial strains. A molecular docking investigation was also performed, to acquire more information about the binding mode and energy of the ligand and its metal complexes to the Escherichia coli receptor using molecular docking. Altogether, the newly created ligand and complexes showed positive antibacterial effects and are worth future study.

By releasing of azo dye through textile effluent, textile industry is the main cause of water pollution resulting into acute effect on environment and human health. Development of any eco-friendly and cost-effective method that may address the drawbacks to physical or chemical methods of dye removal is the recent global priority. Physical or chemical methods for textile wastewater pretreatment are of high cost, extremely energy consuming, and environmentally low efficient and generate toxic sludge. Thus, the use of microbial technique for textile dye degradation will be eco-friendly and is probably a lucrative alternative to physico-chemical processes. Microbial enzymes, viz. laccase and azoreductase, are cost-efficient, easy to harvest, easily downstream processable, and effortlessly mobilizable. Recent research trends on nanoparticle-microbial enzyme conjugates are also highly efficient to remove the azo dye from textile waste within a few minutes. But unfortunately, due to some gap between academia and industry, these methods remain only limited up to laboratory and its industrialization is still a challenge. The present review is an illustrated compilation of the use of microbial enzymes in removal of textile dyes.

A number of azo pyrazole derivatives and novel Schiff bases derived from azo diamino pyrazole were synthesized. These included 4-(2-arylhydrazono)-4H-pyrazole-3,5-diamines and N3,N5-dibenzylidene-4-(2-arylhydrazono)-4H-pyrazole-3,5-diamines. The chemical structures of the novel azo dyes were determined using UV–visible, IR, 1H NMR, and 13C NMR spectroscopy. Dyeing process and tautomerism of the aforementioned azo compounds were predicted using DFT calculations. The electronic absorption spectra in methanol were observed and compared to those computed using B3LYP/6-31G(d,p). The dyeing performance of the produced disperse dyes was examined on polyester. The degree of exhaustion and the fastness properties of the dyed samples in terms of washing, perspiration, scorch, and light fastness were assessed. Moreover, the reflectance and color strength of the synthesized dyes were measured and discussed.

The majority of textile wastes are made up of toxic dyes. Additionally, because these compounds are soluble, wastewater may include significant concentrations. In this work, the green alga Lychaete pellucida is used for the bioremoval of four common azo dyes, Reactive Blue 4 (RB4), Reactive Red 120 (RR120), Reactive Brilliant Yellow 3G (RBY3G), and Reactive Green12 (RG12), with the application of two models of sorption isotherms, Langmuir and Freundlich. The spectrophotometer method was used to identify optimum conditions (temperature, pH, dye concentrations, algal biomass, and contact time) to remove these dyes onto dry freshwater macroalgae. The optimum pH for L. pellucida was 8. The optimum biosorbent amount is 2 g/L. Then, the best-removed dye concentration was 5 mg/L, the optimum contact duration was 120 min, and the optimum temperature was 25 °C. Under optimum conditions, the percent of dye removal was about 95% for all used azo dyes. This is the first report on the use of Lychaete pellucida for the efficient biodegradation of hazardous azo dyes .

The textile industry, with its extensive use of dyes and chemicals, stands out as a significant source of water pollution. Exposure to certain textile dyes, such as azo dyes and their breakdown products like aromatic amines, has been associated with health concerns like skin sensitization, allergic reactions, and even cancer in humans. Annually, the worldwide production of synthetic dyes approximates 7 × 10 7 tons, of which the textile industry accounts for over 10,000 tons. Inefficient dyeing procedures result in the discharge of 15–50% of azo dyes, which do not adequately bind to fibers, into wastewater. This review delves into the genotoxic impact of azo dyes, prevalent in the textile industry, on aquatic ecosystems and human health. Examining different families of textile dye which contain azo group in their structure such as Sudan I and Sudan III Sudan IV, Basic Red 51, Basic Violet 14, Disperse Yellow 7, Congo Red, Acid Red 26, and Acid Blue 113 reveals their carcinogenic potential, which may affect both industrial workers and aquatic life. Genotoxic and carcinogenic characteristics, chromosomal abnormalities, induced physiological and neurobehavioral changes, and disruptions to spermatogenesis are evident, underscoring the harmful effects of these dyes. The review calls for comprehensive investigations into the toxic profile of azo dyes, providing essential insights to safeguard the aquatic ecosystem and human well-being. The importance of effective effluent treatment systems is underscored to mitigate adverse impacts on agricultural lands, water resources, and the environment, particularly in regions heavily reliant on wastewater irrigation for food production.

In this study, we investigated the production conditions of Quercus coccifera hydrochar, which is an inexpensive and easy available adsorbent, for the adsorption of Basic Red 18 (BR18) azo dye. The hydrochar was produced in the eco-friendly subcritical water medium (SWM). The effects of the pH (2–10), adsorbent size (45–106 μm), adsorbent dose (0.5–1.5 g/L), dye concentration (40–455 mg/L), and contact time (5–120 min) were studied via optimization experiments. The optimum conditions were pH 10, particle size of 45 μm, particle amount of 1.5 g/L, dye concentration of 455 mg/L, and 60 min. The removal efficiency increased sharply for the first 5 min; after that the removal efficiency reached a steady state at 60 min, with a maximum removal of 88.7%. The kinetic studies for the adsorption of BR18 dye in aqueous solution using hydrochar showed pseudo-second-order kinetics. The Langmuir and Freundlich isotherm models were used to explain the relationship between adsorbent and adsorbate, and Freundlich isotherm was the most suitable model because of its high regression coefficient (R2) value. The intraparticle diffusion model was used to determine the adsorption mechanism of BR18 onto Q. coccifera acorn hydrochar. Desorption studies were also carried out using different types of acid and different molarities.

As dye demand continues to rapidly increase in the food, pharmaceutical, cosmetic, paper, textile, and leather industries, an industrialization increase is occurring. Meanwhile, the degradation and removal of azo dyes have raised broad concern regarding the hazards posed by these dyes to the ecological environment and human health. Physicochemical treatments have been applied but are hindered by high energy and economic costs, high sludge production, and chemicals handling. Comparatively, the bioremediation technique is an eco-friendly, removal-efficient, and cost-competitive method to resolve the problem. This paper provides scientific and technical information about recent advances in the biodegradation of azo dyes. It expands the biodegradation efficiency, characteristics, and mechanisms of various microorganisms containing bacteria, fungi, microalgae, and microbial consortia, which have been reported to biodegrade azo dyes. In addition, information about physicochemical factors affecting dye biodegradation has been compiled. Furthermore, this paper also sketches the recent development and characteristics of advanced bioreactors.

Pollution of waters by azo dyes is a major global issue because some azo dyes have carcinogenic and mutagenic effects. Therefore, advanced methods are required to remove those pollutants from wastewater. For instance, electrochemical oxidation processes have been developed using various approaches to remove azo dyes from wastewater. Here, we review electrochemical processes for the oxidative degradation of azo dyes. Processes include anodic oxidation, electro-Fenton, photo-electro-Fenton, and solar photo-electro-Fenton. The influence of various parameters including process design, design of reactors, and the characteristic degradation products and their toxicity, are discussed. Low molecular weight carboxylic acids are mainly formed as by-products.

Surface -functionalised silica networks are advanced adsorbents. They have been given much attention for treating wastewater using the adsorption technique due to the silanol reactivity, resulting in strong binding affinities towards many pollutants. This review discusses the removal of anionic azo dyes utilising various functional groups such as amines, surfactants, polymers, macrocyclic, and other chelating groups functionalised on silica’s surface. This review also reveals the steadily increasing interest in surface-functionalised silicas as adsorbents, emphasising the scholarly advancements in this field as a platform for future research. For that, adsorption capacities with different experimental conditions have been compared. The possible adsorption mechanisms, rate-limiting step, and factors affecting the anionic azo dye adsorption process have been comprehensively discussed. This review discloses that adsorbent characteristics such as porosity and functional groups, besides structural properties of an anionic azo dye, significantly affect adsorption. The adsorption process followed the Langmuir isotherm and pseudo-second-order models, with a predominantly spontaneous and endothermic nature. Multiple interactions, including electrostatic interaction, π-π interactions, and hydrogen bonding, are observed between dyes and functionalised silicas, indicating the adsorption process’s complexity. Regeneration and cost-economic analysis are also presented to provide a roadmap for sustainable improvements. Chemical and biological regeneration techniques restore > 80% of the spent functionalised silicas. There is a significant opportunity to improve their efficiencies and regenerability, resulting in surface-functionalised silicas being used commercially instead of only in the laboratory. Finally, future research has been proposed by identifying current research gaps, particularly concerning the application of functionalised silicas in wastewater treatment. Graphical abstract

In this study, ZnO was doped and co-doped with rhodium and tungsten to assess the impact of these transition metals on the sonocatalytic degradation of reactive black 5 azo dye (RB-5). Structural analysis revealed that doping ZnO with 1% Rh and W does not alter its wurtzite hexagonal structure, although minor changes in cell parameters were observed due to differences in electronic density. Interestingly, co-doping resulted in lower degradation efficiency than single doping, with W-ZnO emerging as the most effective catalyst, achieving 100% RB-5 degradation within 60 min, likely due to a higher density of oxygen vacancies and hydroxyl groups. Moreover, a 2 k factorial design identified optimal sonocatalytic conditions for W-ZnO, including a catalyst concentration of 0.75 g/L, a power tip of 225 W, and a hydrogen peroxide volume of 27 μL. The findings highlight the potential for doped ZnO nanoparticles in advanced oxidation processes and green chemistry applications, making this method an environmentally friendly alternative for wastewater treatment.