Search Results (208)

Water polluted by dye colorants has been on the rise in the last decade. This is due to the over reliance on the textile industry, and it is holding a high economic value in most countries. This industry is the highest consumer of fresh water whilst also discharging several natural and synthetic pollutants to the environment. Several methods have been used for the removal of these pollutants and one of the most efficient technologies to be developed includes the photocatalysis method, via advanced oxidation processes. This review highlights the developments of green iron oxide nanoparticles as photocatalysts in the last decade. It was noted that tuning and controlling the phytochemical concentration and synthesis conditions, can assist with forming uniform and non-agglomerated materials, as this has limited the vast usage of these materials in major applications. Also, upon controlling the synthesis conditions, improved surface area and charge separation efficiency was noted. Their limitations and need for modification through forming composites are highlighted. Moreover, future perspectives are given on the use of green IONPs as photocatalysts. Full article

The textile industry widely uses reactive anthraquinone dyes, which exhibit strong resistance to color removal and generate substantial volumes of wastewater containing significant quantities of residual dye requiring treatment prior to discharge. As part of a study aimed at reusing rather than discharging spent reactive anthraquinone dyebaths, Reactive Blue 4 (RB4) dye was used in dyeing cotton, and the generated spent dyebaths were biologically decolorized using a fluidized bed reactor (FBR) operated under hypersaline conditions at a salt concentration of 100 g NaCl/L, which is typically found in commercial spent reactive dyebaths. Across five consecutive runs, the FBR achieved a mean decolorization efficiency of 91.2 ± 2.8% within a 6 h incubation period. The quality of cotton dyed with the treated and reused spent dyebaths was evaluated through shade reproducibility and color consistency assessments. Five repetitive dyeings using the biologically decolorized dyebaths showed that the ΔE_cmc fabric color difference values were 0.58~0.80, which were lower than the industry-accepted value of 1.0. This study demonstrates that biologically decolorized spent dyebaths can be effectively reused, offering substantial reductions in water and salt consumption and improving the economic and environmental sustainability of the reactive dyeing process. Full article

This study investigates the performance of an electrooxidation (EO) process employing Sb₂O₅-doped RuO₂–ZrO₂|Ti anodes integrated into a concave-cover solar still for the degradation of Allura Red dye in aqueous solution and real river water. The anode was synthesized and characterized via scanning electron microscopy (SEM) and X-ray diffraction (XRD) to confirm its porous morphology and crystalline structure. Operational parameters—including supporting electrolyte concentration, initial solution pH, and current density—were systematically optimized. Under optimal conditions (pH 2–3 and 5 mA cm⁻²), the EO process was evaluated under natural solar irradiation. Sunlight exposure increased the solution temperature from approximately 20 °C to 50 °C, enhancing molecular diffusion and mass transport, thereby accelerating decolorization kinetics. Compared to EO performed under laboratory conditions, the solar-assisted system achieved an additional 20% increase in chemical oxygen demand (COD) removal and a fast reduction in color. When applied to real Lerma River water samples under these optimal conditions, the treatment achieved approximately 50% reduction in both COD and true color, demonstrating its applicability to complex environmental matrices. These results confirm that coupling electrooxidation with solar thermal input significantly improves pollutant degradation efficiency and energy performance, establishing this integrated approach as a promising and sustainable technology for advanced wastewater treatment. Full article

The textile industry releases effluents containing toxic contaminants such as azo dyes, which severely affect water quality and aquatic ecosystems. This study optimized the Fe⁰/H₂O₂/UV photo-Fenton process through Response Surface Methodology (RSM) using a Box–Behnken design applied to real textile wastewater. The process relies on in situ hydroxyl radicals (•OH) generation, which degrades refractory organic compounds. Under optimal conditions (pH 3.5, 0.5 g Fe⁰, and 0.55 mL H₂O₂), the system achieved complete color removal, 91% aromatic structures degradation, and an 80% COD reduction within 3 h. Statistical validation indicated an excellent model fit (R² = 1.0; Q² = 1.0), with strong correlation between experimental and predicted results. Spectroscopic analyses (UV–Vis and FTIR) further confirmed the cleavage of chromophoric and aromatic structures, indicating efficient pollutant degradation. Overall, the findings indicate that the Fe⁰/H₂O₂/UV system is an effective and sustainable technology for treating textile wastewater, offering strong potential for industrial-scale application. Full article

A major obstacle to textile recycling is the presence of dyes, which limits the reuse of fibers in high-value applications. Despite previous studies on, cotton decolorization, the systematic development of an optimal formulation that preserves fabric integrity remains lacking. This study addresses this gap by investigating a decolorization method for mixed-dyed cotton textiles that enables successful redyeing while preserving fabric quality. Reactive and vat-dyed cotton fabrics were treated with sequential reductive and oxidative processes, in a full factorial design. The impact of input parameters on tensile strength was evaluated through statistical analysis using analysis of variance at a significance level of α = 0.05. The developed recipe was subsequently validated on post-consumer cotton textiles. Stripping efficiency was assessed using K/S values, and fabric quality was evaluated through tensile strength, pilling, and fuzzing appearance. Temperature showed the strongest influence on dye removal. Fabric strength was significantly affected by temperature and oxidizing agent, and by interactions of temperature with reducing agent and oxidation time. The optimized process achieved 98–99.5% color removal and retained 95% of the fabric’s tenacity. A stripping efficiency of >90% for post-consumer cotton validates the method’s applicability in real-world circular systems. Full article

Road-marking operations generate alkaline wash water with intense color and soluble cationic additives. A new biomass adsorption material (LML) was developed to address dye pollution in road-marking wash water effectively. Enzymatically hydrolyzed lignin was used as the raw material for the first time. L-lysine was modified to the structure of the lignin benzene ring using a simple one-step synthesis method, which endowed lignin with a large number of active carboxyl and amino functional groups to improve its adsorption capacity. The adsorption performance of LML for methylene blue in water was also investigated. The experimental results show that the LML has a high dye removal rate under alkaline conditions. The fitted adsorption model shows that the saturated adsorption capacity of LML for methylene blue (MB) is 129.4 mg g⁻¹ and malachite green (MG) is 244.9 mg g⁻¹, which is in line with the Langmuir isotherm adsorption model. The adsorption process is endothermic, which means that the adsorption capacity increases with increasing temperature. Kinetic studies showed that the adsorption process reached equilibrium within 120 min following a pseudo-second-order kinetic model. The cycle experiment shows that the removal efficiency of the adsorbent for dyes can still reach 90% after five cycles, indicating a good practical application value for the polishing of road-marking wash water. Full article

The discharge of dye-laden effluents remains an environmental challenge since conventional treatments remove color but not the organic load. This study systematically compared anodic oxidation (AO), electro-Fenton (EF), and photoelectro-Fenton (PEF) processes for three representative industrial dyes, such as Coriasol Red CB, Brown RBH, and Blue VT, and their ternary mixture, using boron-doped diamond (BDD) and Ti/IrO₂–SnO₂–Sb₂O₅ (MMO) anodes. Experiments were conducted in a batch reactor with 50 mM Na₂SO₄ at pH = 3.0 and current densities of 20–60 mA cm⁻². Kinetic analysis showed that AO-BDD was most effective at low pollutant loads, EF-BDD became superior at medium loads due to efficient H₂O₂ electrogeneration, and PEF-MMO dominated at higher loads by fast UVA photolysis of surface Fe(OH)²⁺ complexes. In a ternary mixture of 120 mg L⁻¹ of dyes, EF-BDD and PEF-MMO achieved >98% decolorization in 22–23 min with pseudo-first-order rate constants of 0.111–0.136 min⁻¹, whereas AO processes remained slower. COD assays revealed partial mineralization of 60–80%, with EF-BDD providing the most consistent reduction and PEF-MMO minimizing treatment time. These findings confirm that decolorization overestimates efficiency, and electrode selection must be tailored to dye structure and effluent composition. Process selection rules allow us to conclude that EF-BDD is the best robust dark option, and PEF-MMO, when UVA is available, offers practical guidelines for cost-effective electrochemical treatment of textile wastewater. Full article

Azo dyes are widely used in the textile industry due to their vibrant colors and chemical stability; however, wastewater containing these dyes poses significant environmental and health risks due to their toxic, persistent, and potentially carcinogenic properties. In this study, the treatment of wastewater containing trypan blue dye was investigated using the electrooxidation process with boron-doped diamond electrodes, and the efficiency of the process was modeled through the Extreme Gradient Boosting (XGBoost) algorithm. In the experimental phase, the effects of key operational parameters, including current density, pH, electrolysis time, and supporting electrolyte concentration, on TB dye removal efficiency were systematically evaluated. Based on the experimental data obtained, a machine learning-based XGBoost prediction model was developed, and hyperparameter optimization was performed to enhance its predictive performance. The model achieved high accuracy (R² = 0.996 for training and 0.954 for testing) and yielded low error metrics (RMSE and MAE), confirming its reliability in predicting removal efficiency. This study presents an integrated and data-driven approach for improving the efficiency and sustainability of electrooxidation processes and offers an environmentally friendly and effective method for the treatment of azo dye-contaminated wastewater. Full article

Ceramic membrane technology plays an important role in water and wastewater treatment. Strategic sourcing of various natural mineral resources has contributed to developing low-cost ceramic membranes. The combination with calcination of inorganic and organic wastes from domestic and agricultural activities results in fully sustainable ceramic membrane materials. In this work, ceramic membranes were developed using 96% clay, 2% almond shells and 2% lime. Sintering at 900, 950, and 1000 °C enabled the production of membranes (MK-900, MK-950, and MK-1000) in a clean, simple, and cost-effective manner. The average pore diameter and porosity decreased slightly from 44 to 42 nm and from about 30% to 26% with increasing sintering temperature, while the flexural strength increased from 25 to 40 MPa. The pure water permeability was 68 and 59 L·m⁻²·h⁻¹·bar⁻¹ for MK-900 and MK-950, respectively. Effective color (as Indigo blue) removal of 78% and 92% was observed for MK-900 and MK-950, respectively. More than 90% of the initial permeability was recovered after three cycles of dye filtration using water backwashing at each stage, indicating good fouling resistance of the prepared membranes. Full article

The discharge of printing and dyeing wastewater has become a key concern in global water pollution control due to its high pollutant concentration, dark color, refractory biodegradability and toxic characteristics. Photoelectrocatalytic (PEC) technology has gained widespread attention as it can effectively treat refractory organic pollutants. In this study, titanium dioxide (TiO₂)–bismuth vanadate (BiVO₄) composite materials were synthesized through the sol–gel/solvothermal hybrid method, and layered heterojunction structures were fabricated via sol–gel precursor preparation followed by spin-coating deposition. The PEC degradation efficiency of rhodamine B (RhB) was systematically evaluated under varying operational conditions in the presence of TiO₂-BiVO₄. The four-layer BiVO₄/four-layer TiO₂ material showed the optimal catalytic activity among the tested structures, achieving an 80.3% removal of RhB under an applied bias of 4 V and illumination intensity of 14,000 lx. Through the equilibrium adjustment of the Fermi levels, the type Ⅱ heterostructure was formed. Moreover, superoxide radical (O₂⁻) was identified as the predominant reactive oxygen species driving the degradation mechanism. Mechanistic analysis revealed that RhB degradation was accomplished through deethylation, benzene ring cleavage, and subsequent ring-opening mineralization. This study prepared an efficient PEC material, which provides a theoretical basis for the PEC treatment of printing and dyeing wastewater. Full article

This study explores the visible-light-driven photolysis of Ferrioxalate complexes for the degradation of Toluidine Blue (TB), a persistent phenothiazine dye, using a 1 L recirculating batch-loop photoreactor. The reactor system incorporated two tubular photochemical units (35 cm × 3 cm each) in series: the first equipped with an immersed blue fluorescent lamp (12 W, 30 cm-tube), and the second with dual external blue LED lamps (18 W total, 30 cm) encasing a double-walled glass cell. Continuous flow between the units was maintained via a peristaltic pump. Experimental investigations were used to evaluate the effects of key parameters such as Fe(III) and oxalate concentrations, initial TB load, pH, light source, flow rate, ligand type, dissolved gas type, external H₂O₂ addition, and the presence of various inorganic ions. The results demonstrate efficient dye degradation, with ~75% TB removal within 1 h under combined fluorescent and LED irradiation, where each reactor contributing comparably. The optimal performance was achieved at pH 4, with a 10 oxalate-to-Fe(III) molar ratio (1 mM:0.1 mM) and a flow rate of 25 mL s⁻¹. Among various ligands tested (oxalate, acetate, citrate, EDTA), oxalate proved to be the most effective. The presence and type of anions significantly influenced degradation efficiency due to their potential scavenging effects. Although the process achieved high dye removal, TOC analysis indicated only moderate mineralization, suggesting the accumulation of non-colored intermediates. External H₂O₂ addition moderately improved TOC removal, likely due to enhanced hydroxyl radical generation via the Fenton mechanism. These findings highlight the promise of Ferrioxalate-based photochemical systems under visible light for dye removal, while also emphasizing the need for further research into by-product identification, mineralization enhancement, and toxicity reduction to ensure safe effluent discharge. Full article

This study explores the sustainable extraction and application of natural dyes from figs (Ficus carica) and Eucalyptus leaves using an aqueous alkaline medium. The dyeing process was optimized for cotton fabric using the exhaust-dyeing method. Fabrics dyed with Ficus carica extract and its blend with Eucalyptus exhibited enhanced color strength, excellent crocking fastness (rated 4–5), and good washing fastness (rated 3–4 on the gray scale). The use of Aloe barbadensis Miller as a bio-mordant significantly improved dye fixation, resulting in deeper, earthy shades, such as green, yellow–green, and yellowish brown. The highest K/S value (5.85) was recorded in samples treated with a mordant, sodium chloride (NaCl), and the combined dye extracts, indicating a synergistic effect among the components. Mosquito repellency tests revealed that treated fabrics exhibited up to 70% repellency, compared to just 20% in undyed samples. Antibacterial testing against E. coli showed that dyed fabrics achieved over 80% bacterial reduction after 24 h, indicating promising antimicrobial functionality. Air permeability slightly decreased post-dyeing due to the potential shrinkage in cotton fabrics. Furthermore, adsorption studies showed a removal efficiency of 57% for Ficus carica dye on graphene oxide (GO) under ultrasonication. These findings confirm the potential of GO as an effective adsorbent material for treating wastewater from natural textile dyes. Overall, the study highlights the environmental safety, functional performance, and multifunctional advantages of plant-based dyeing systems in sustainable textile applications. Full article

Persistent reactive azo dyes released from textile finishing are a serious threat to water systems, but effective methods using sunlight to break them down are still limited. Everzol Yellow 3RS (EY-3RS) is particularly recalcitrant: past studies have relied almost exclusively on physical adsorption onto natural or modified clays and zeolites, and no photocatalytic pathway employing engineered nanomaterials has been documented to date. This study reports the synthesis, characterization, and performance of a visible-active ternary nanocomposite, Cu₄O₃/ZrO₂/TiO₂, prepared hydrothermally alongside its binary (Cu₄O₃/ZrO₂) and rutile TiO₂ counterparts. XRD, FT-IR, SEM-EDX, UV-Vis, and PL analyses confirm a heterostructured architecture with a narrowed optical bandgap of 2.91 eV, efficient charge separation, and a mesoporous nanosphere-in-matrix morphology. Photocatalytic tests conducted under midsummer sunlight reveal that the ternary catalyst removes 91.41% of 40 ppm EY-3RS within 100 min, markedly surpassing the binary catalyst (86.65%) and TiO₂ (81.48%). Activity trends persist across a wide range of operational variables, including dye concentrations (20–100 ppm), catalyst dosages (10–40 mg), pH levels (3–11), and irradiation times (up to 100 min). The material retains ≈ 93% of its initial efficiency after four consecutive cycles, evidencing good reusability. This work introduces the first nanophotocatalytic strategy for EY-3RS degradation and underscores the promise of multi-oxide heterojunctions for solar-driven remediation of colored effluents. Full article

Annually, more than 10,000 synthetic dyes are produced worldwide, generating around 280,000 tons of waste, posing risks to human and aquatic life, and potentially creating even more toxic products than the dyes themselves. This study aims to immobilize organic dyes, forming hybrid pigments using ZnO as support obtained through starch combustion. ZnO was obtained by starch (sago) combustion and characterized by XRD, SEM and the BET method. It was then used for the adsorption of orange and green textile dyes, evaluating the adsorbent dosage, initial dye concentration, contact time, and selectivity with copper ions. The removal studies indicated up to 100% removal of both dyes at low concentrations. The co-adsorption system showed excellent performance, with removal percentages exceeding 90% for both textile dyes and Cu (II) ions. Hybrid pigments were assessed for solvent resistance and durability under extended white light exposure. ZnO immobilized the dyes, showing resistance to organic solvents and good stability under prolonged white light exposure. Full article