Textile Azo Dyes Research Articles

One-step Ag-doped ZnO nanoparticle synthesis for textile azo dye sorption and antibacterial activity

One-step Ag-doped ZnO nanoparticle synthesis for textile azo dye sorption and antibacterial activity

A Sustainable Solution for the Adsorption of C.I. Direct Black 80, an Azoic Textile Dye with Plant Stems: Zygophyllum gaetulum in an Aqueous Solution.

The presence of pollutants in water sources, particularly dyes coming by way of the textile industry, represents a major challenge with far-reaching environmental consequences, including increased scarcity. This phenomenon endangers the health of living organisms and the natural system. Numerous biosorbents have been utilized for the removal of dyes from the textile industry. The aim of this study was to optimize discarded Zygophyllum gaetulum stems as constituting an untreated natural biosorbent for the efficient removal of C.I. Direct Black 80, an azo textile dye, from an aqueous solution, thus offering an ecological and low-cost alternative while recovering the waste for reuse. The biosorbent was subjected to a series of characterization analyses: scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET) method, X-ray diffraction (XRD), and infrared spectroscopy (IR) were employed to characterize the biosorbent. Additionally, the moisture and ash content of the plant stem were also examined. The absorption phenomenon was studied for several different parameters including the effect of the absorption time (0 to 360 min), the sorbent mass (3 to 40 g/L), the pH of the solution (3 to 11), the dye concentration (5 to 300 mg/L), and the pH of the zero-charge point (2-12). Thermodynamic studies and desorption studies were also carried out. The results showed that an increase in plant mass from 3 to 40 g/L resulted in a notable enhancement in dye adsorption rates, with an observed rise from 63.96% to 97.08%. The pH at the zero-charge point (pHpzc) was determined to be 7.12. The percentage of dye removal was found to be highest for pH values ≤ 7, with a subsequent decline in removal efficiency as the pH increased. Following an initial increase in the amount of adsorbed dye, equilibrium was reached within 2 h of contact. The kinetic parameters of adsorption were investigated using the pseudo-first-order, pseudo-second-order and Elovich models. The results indicated that the pseudo-first-order kinetic model was the most appropriate for the plant adsorbent. The isotherm parameters were determined using the Langmuir, Frendlich, Temkin, and Dubinin-Radushkevich models. The experimental data were more satisfactory and better fitted using the Langmuir model for the adsorption of dye on the plant. This study demonstrated that Zygophyllum gaetulum stems could be employed as an effective adsorbent for the removal of our organic dye from an aqueous solution.

Hydrothermal synthesis of cadmium sulfide decorated reduced graphene oxide photocatalyst for the degradation of photostable naphthol blue black dye

Photocatalysis is being used for the mineralization of recalcitrant organic pollutants in water that cannot be treated with conventional methods. Cadmium sulfide decorated reduced graphene oxide (rGO-CdS) nanocomposite photocatalyst was synthesized by hydrothermal method and evaluated for the removal of a photostable textile azo dye, naphthol blue black (NBB) under ultraviolet light (UV-A, 365 nm). The rGO-CdS combination was opted for due to utilizing the narrow band gap (Eg = ~2.4 eV) of CdS and robust rGO support, capable of attracting organic pollutants to surface, bear, and protect CdS from photocorrosion. The formation of rGO-CdS was proved from the findings of physiochemical characterization UV–visible-, X-ray diffraction photoelectron, Raman, energy dispersive X-ray-spectroscopic, and scanning, transmission electron, and atomic force microscopic studies. The spherical CdS was decorated on the random shaped rGO sheets. Eg of CdS and rGO-CdS were 2.42 and 2.39 eV, respectively. After 2 h of light exposure, 2 g/L of rGO-CdS mineralized 95 % of NBB (2 × 10−4 mol/L). After 5 cycles, 80 % of photocatalytic efficiency was retained. In gas chromatography-mass spectrometry studies, 8 fragments of NBB were found after 1 h and confirmed that the degradation was mediated by photocatalytic dilapidation. The optimum pH for NBB degradation was 9. The rGO-CdS was found to be a potentially stable and reusable photocatalyst for environmental applications.

Textile azo dye, Sudan Black B, inducing hepatotoxicity demonstrated in in vivo zebrafish larval model.

Environmental pollution, particularly from textile industry effluents, raises concerns globally. The aim of this study is to investigate the hepatotoxicity of Sudan Black B (SBB), a commonly used textile azo dye, on embryonic zebrafish. SBB exposure led to concentration-dependent mortality, reaching 100% at 0.8mM, accompanied by growth retardation and diverse malformations in zebrafish. Biochemical marker analysis indicated adaptive responses to SBB, including increased SOD, CAT, NO, and LDH, alongside decreased GSH levels. Liver morphology analysis unveiled significant alterations, impacting metabolism and detoxification. Also, glucose level was declined and lipid level elevated in SBB-exposed in vivo zebrafish. Inflammatory gene expressions (TNF-α, IL-10, and INOS) showcased a complex regulatory interplay, suggesting an organismal attempt to counteract pro-inflammatory states during SBB exposure. The increased apoptosis revealed a robust hepatic cellular response due to SBB, aligning with observed liver tissue damage and inflammatory events. This multidimensional study highlights the intricate web of responses due to SBB exposure, which is emphasizing the need for comprehensive understanding and targeted mitigation strategies. The findings bear the implications for both aquatic ecosystems and potentially parallels to human health, underscoring the imperative for sustained research in this critical domain.

New insights into the mechanism of azo dye biodegradation by Lactococcus lactis

Azo dye reduction by syntrophic microbial communities is still unclear, with conflicting observations reported in the literature. In this study, the biodegradation mechanism of a model azo dye by Lactococcus lactis strain LLSP-01 isolated from an acidogenic reactor system was investigated. Proteomics and RT-PCR analysis results showed that LLSP-01 azoreductase (AzoL) was not expressed by the isolate during exposure to Direct Black 22. In contrast, the mechanism appears to involve biosorption by glycoconjugates, particularly exopolysaccharides (EPS) and rhamnolipids, as proteins from the LPS O-antigen metabolism were statistically higher expressed in cells challenged with the target compound. Based on the proteomic observations, it is hypothesized that Direct Black 22 is adsorbed into the biofilm matrix and indirectly reduced by an SDR family oxidoreductase, in a mechanism mediated by riboflavin carriers. Induction of a ring-cleaving dioxygenase in the presence of azo dye indicates further degradation of the resulting aromatic amines. The collected results show that azo dye reduction by L. lactis is mediated by enzymes with broad range specificity, and not the typical azoreductases. This information can assist in the design of new strategies for the bioremediation of textile azo dyes.

Exploring the decolorization efficiency and biodegradation mechanisms of different functional textile azo dyes by Streptomyces albidoflavus 3MGH

Efficiently mitigating and managing environmental pollution caused by the improper disposal of dyes and effluents from the textile industry is of great importance. This study evaluated the effectiveness of Streptomyces albidoflavus 3MGH in decolorizing and degrading three different azo dyes, namely Reactive Orange 122 (RO 122), Direct Blue 15 (DB 15), and Direct Black 38 (DB 38). Various analytical techniques, such as Fourier Transform Infrared (FTIR) spectroscopy, High-Performance Liquid Chromatography (HPLC), and Gas Chromatography-Mass Spectrometry (GC-MS) were used to analyze the degraded byproducts of the dyes. S. albidoflavus 3MGH demonstrated a strong capability to decolorize RO 122, DB 15, and DB 38, achieving up to 60.74%, 61.38%, and 53.43% decolorization within 5 days at a concentration of 0.3 g/L, respectively. The optimal conditions for the maximum decolorization of these azo dyes were found to be a temperature of 35 °C, a pH of 6, sucrose as a carbon source, and beef extract as a nitrogen source. Additionally, after optimization of the decolorization process, treatment with S. albidoflavus 3MGH resulted in significant reductions of 94.4%, 86.3%, and 68.2% in the total organic carbon of RO 122, DB 15, and DB 38, respectively. After the treatment process, we found the specific activity of the laccase enzyme, one of the mediating enzymes of the degradation mechanism, to be 5.96 U/mg. FT-IR spectroscopy analysis of the degraded metabolites showed specific changes and shifts in peaks compared to the control samples. GC-MS analysis revealed the presence of metabolites such as benzene, biphenyl, and naphthalene derivatives. Overall, this study demonstrated the potential of S. albidoflavus 3MGH for the effective decolorization and degradation of different azo dyes. The findings were validated through various analytical techniques, shedding light on the biodegradation mechanism employed by this strain.

Controlled removal of textile azo dye Congo red from aqueous system using PEG-ZnO/rGO composite

Controlled removal of textile azo dye Congo red from aqueous system using PEG-ZnO/rGO composite

Performance and hydrodynamic study of a new multi‐stage solar photoreactor with immobilized ZnO for synthetic wastewater treatment

AbstractThis study aims to design a new multi‐stage photoreactor with immobilized ZnO and assess its performance in reducing textile wastewater toxicity using solar energy. The electric conductivity measurement is retained as a detection method to obtain the residence time distribution (RTD) function. The RTD is then used to characterize the hydrodynamic behavior of the photoreactor and to evaluate its deviation from the distribution curves of ideal reactors. Solar experiments are conducted to demonstrate the performance of this multistage reactor towards the degradation of a textile azo dye namely Solophenyl Red 3BL (SR 3BL). The influence of the flow rate and the SR 3BL initial concentration (CO) are considered. The variation of the flow rate slightly influences the SR 3BL photodegradation efficiency and it is inversely proportional to its concentration. The study of the reuse of the immobilized catalyst shows that the degradation efficiency of 98% is reached even after multiple photocatalytic cycles. The figure of merit collector area per order was in the range of 35 to 110 . This result provides useful information for scaling up and estimating energy efficiency of the reactor.

Hues of risk: investigating genotoxicity and environmental impacts of azo textile 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 × 107 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.

Microalgal and activated sludge processing for biodegradation of textile dyes

The textile industry contributes substantially to water pollution. To investigate bioremediation of dye-containing wastewater, the decolorization and biotransformation of three textile azo dyes, Red HE8B, Reactive Green 27, and Acid Blue 29, were considered using an integrated remediation approach involving the microalga Chlamydomonas mexicana and activated sludge (ACS). At a 5 mg L−1 dye concentration, using C. mexicana and ACS alone, decolorization percentages of 39%–64% and 52%–54%, respectively, were obtained. In comparison, decolorization percentages of 75%–79% were obtained using a consortium of C. mexicana and ACS. The same trend was observed for the decolorization of dyes at higher concentrations, but the potential for decolorization was low. The toxic azo dyes adversely affect the growth of microalgae and at high concentration 50 mg L−1 the growth rate inhibited to 50–60% as compared to the control. The natural textile wastewater was also treated with the same pattern and got promising results of decolorization (90%). Moreover, the removal of BOD (82%), COD (72%), TN (64%), and TP (63%) was observed with the consortium. The HPLC and GC-MS confirm dye biotransformation, revealing the emergence of new peaks and the generation of multiple metabolites with more superficial structures, such as N-hydroxy-aniline, naphthalene-1-ol, and sodium hydroxy naphthalene. This analysis demonstrates the potential of the C. mexicana and ACS consortium for efficient, eco-friendly bioremediation of textile azo dyes.

Decolorization of Textile Azo Dye via Solid-State Fermented Wheat Bran by Lasiodiplodia sp. YZH1.

Textile dyes are one of the major water pollutants released into water in various ways, posing serious hazards for both aquatic organisms and human beings. Bioremediation is a significantly promising technique for dye decolorization. In the present study, the fungal strain Lasiodiplodia sp. was isolated from the fruiting bodies of Schizophyllum for the first time. The isolated fungal strain was examined for laccase enzyme production under solid-state fermentation conditions with wheat bran (WB) using ABTS and 2,6-Dimethoxyphenol (DMP) as substrates, then the fermented wheat bran (FWB) was evaluated as a biosorbent for Congo red dye adsorption from aqueous solutions in comparison with unfermented wheat bran. A Box-Behnken design was used to optimize the dye removal by FWB and to analyze the interaction effects between three factors: fermentation duration, pH, and dye concentration. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) were applied to study the changes in the physical and chemical characteristics of wheat bran before and after fermentation. An additional experiment was conducted to investigate the ability of the Lasiodiplodia sp. YZH1 to remove Congo red in the dye-containing liquid culture. The results showed that laccase was produced throughout the cultivation, reaching peak activities of ∼6.2 and 22.3 U/mL for ABTS and DMP, respectively, on the fourth day of cultivation. FWB removed 89.8% of the dye (100 mg L-1) from the aqueous solution after 12 h of contact, whereas WB removed only 77.5%. Based on the Box-Behnken design results, FWB achieved 93.08% dye removal percentage under the conditions of 6 days of fermentation, pH 8.5, and 150 mg L-1 of the dye concentration after 24 h. The fungal strain removed 95.3% of 150 mg L-1 of the dye concentration after 8 days of inoculation in the dye-containing liquid culture. These findings indicate that this strain is a worthy candidate for dye removal from environmental effluents.

Development of manganese peroxidase based voltammetric biosensor for detection of textile Azo dyes RR 195 & RB 221

Azo dyes are extensively applied in textile and leather industries. Monitoring the toxicity and rate of exhaustion of such pollutants besides their mineralization are extremely important for environmental safety and sustainability. Detection of dyes based on enzyme inhibition mechanism and exploration of effect of various dyes on enzymes such as manganese peroxidase (MnP) for such purpose are not studied previously. The goal of the study is to develop MnP based biosensor and to determine whether all dyes impart inhibitory effect on enzyme or not. Thereby, two different dyes i.e. Reactive Red 195 (RR195) and Reactive Blue 221 (RB221) were used for the study and purified MnP was co-immobilized on carbon felt electrode for quantitative measurement of these dyes using electrochemical signals. Voltammetric analysis was carried out to determine the effects of different dye concentrations on the enzyme activity in the form electric signal (I) at an applied voltage of −1 to +1. It was revealed that increase in concentrations(10 μg/L −50 mg/L) of RR195 and RB221 transfuse inhibitory and non-inhibitory effect on MnP activity resulting in current (I) output reduction and enhancement respectively. To validate the study, another study was also conducted, which investigated the effect of these dyes on fungal growth and manganese peroxidase enzyme activity in-vitro. The results obtained authenticated the biosensing results obtained by CV as RR195 inhibit MnP activity (highly toxic) and RB221 impart no effect on MnP activity (less toxic). The fabricated biosensors demonstrated reproducibility, durability, and low threshold of detection with little interference from other substances. Even 100 days later, the MnP-based biosensors showed minor fluctuation in its current (I) outputs with 96–36 % and 86-65 % stability in case of RR195 and RB221 respectively. The study demonstrated the application of enzyme-based biosensors for both detection and toxicological monitoring of dyes.

Degradation and decolorization of textile azo dyes by effective fungal-bacterial consortium.

Synthetic dyes are one of the main pollutants in the textile industry and bioremediation is considered as an environmentally friendly method to degrade them. Soil microbial consortia (MCs) are reported having the potential of decolorizing most of textile dyes. This study aimed at evaluating dye-degrading ability of MCs developed from fungi and bacteria. Fungi and bacteria were isolated from the soil samples obtained from textile waste dumping site at Horana industrial zone, Sri Lanka and were screened for crystal violet (CV) and congo red (CR) dyes to develop MCs. Decolorization assay was performed for MCs along with individual isolates under variable pH levels. Metabolized products were characterized to confirm the biodegradation. A. tamari (F5) and P. putida (B3) significantly (P < 0.05) decolorized both dyes. All the MCs showed higher decolorization percentages over the individual microorganisms. Neutral pH (pH 7) was the optimum pH for the decolorization of both dyes by individual isolates and the percentages were significantly changed under the acidic and basic pH levels. However, decolorization ability by all MCs was not significantly changed with pH. Consortium with A. tamari - P. putida significantly (P < 0.05) decolourized both dyes under optimum pH 7. All MCs showed better pH tolerance in degrading CV and CR. Thus, it can be concluded that the selected MC with A. tamari - P. putida can degrade CV and CR textile dyes efficiently into non-toxic compounds against plants under neutral pH. Degradation and decolorization of textile azo dyes by effective fungal-bacterial consortium.

Bioremediation of Azo Dye Brown 703 by Pseudomonas aeruginosa: An Effective Treatment Technique for Dye-Polluted Wastewater

Dye-polluted wastewater poses a serious threat to humans’, animals’ and plants’ health, and to avoid these health risks in the future, the treatment of wastewater containing dyes is necessary before its release to environment. Herein, a biological approach is used; the textile azo dye brown 703 is degraded utilizing Pseudomonas aeruginosa. The bacterial strain was isolated from textile wastewater dumping sites in Mingora, Swat. The optimization for bacterial degradation was carried out on the nutrient broth medium, which was then subjected to a variety of environmental physicochemical conditions and nutritional source supplementation before being tested. Under micro-aerophilic circumstances, the maximum decolorization and degradation of dye occurred at a 20 ppm dye concentration within 3 days of incubation at a neutral pH and 38 °C. The decrease in the intensity of the absorbance peak in the UV–Vis spectrum was used to measure the extent of decolorization. Initially, 15 bacterial strains were isolated from the textile effluent. Out of these strains, Pseudomonas aeruginosa was found to be the most potent degrading bacteria, with a degradation extent of around 71.36% at optimum conditions. The appearance and disappearance of some new peaks in the FT-IR analysis after the degradation of brown 703 showed that the dye was degraded by Pseudomonas aeruginosa. The GC–MS analysis performed helped in identifying the degraded compounds of azo dye that were utilized in illustrating the under-study process of brown 703 degradation. The biodegradation brought about by Pseudomonas aeruginosa can be employed successfully in the future as an eco-friendly approach with far reaching results.

Rice Husk-Cellulose-Based Agricultural Waste Enhances the Degradation of Synthetic Dyes Using Multiple Enzyme-Producing Extremophiles.

The brightly colored synthetic dyes used in the textile industry are discharged at high concentrations-for example, various azo dyes including Methylene Blue (MB) and Methyl Orange (MO)-which is a matter of global concern, as such dyes are harmful to humans and the environment. Microbial degradation is considered an efficient alternative for overcoming the disadvantages of conventional physical and chemical dye removal methods. In this study, we investigated the potential of multiple types of the enzyme-producing extremophilic bacteria Bacillus FW2, isolated from food waste leachate, for the decolorization and bioremediation of artificial synthetic dyes. The screening of enzyme production and assaying of bacterial strain enzymes are essential for enhancing the breakdown of azo bonds in textile azo dyes. The degradation efficiencies of the water-soluble dyes MB and MO were determined at different concentrations using rice husk, which is an efficient substrate. Using the rice husks, the MO was removed completely within 20 h, and an estimated 99.8% of MB was degraded after 24 h by employing shaking at 120 rpm at 40 °C-whereas a removal efficiency of 98.9% was achieved for the combination of MB + MO. These results indicate the possibility of applying an extremophilic bacterial strain, Bacillus sp., for large-scale dye degradation in the future.

Molecular characterization of azoreductase and its potential for the decolorization of Remazol Red R and Acid Blue 29

Azoreductase is a reductive enzyme that efficiently biotransformed textile azo dyes. This study demonstrated the heterologous overexpression of the azoreductase gene in Escherichia coli for the effective degradation of Remazol Red-R and Acid-Blue 29 dyes. The AzK gene of Klebsiella pneumoniae encoding a ≈22 kDa azoreductase enzyme was cloned into the pET21+C expression vector. The inoculum size of 1.5%, IPTG concentration of 0.5 mM, and incubation time of 6 h were optimized by response surface methodology a statistical tool. The crude extract showed 76% and 74%, while the purified enzyme achieved 94% and 93% decolorization of RRR and AB-29, respectively in 0.3 h. The reaction kinetics showed that RRR had a Km and Vmax value of 0.058 mM and 1416 U mg−1, respectively at an NADH concentration of 10 mM. HPLC and GC-MS analyses showed that RRR was effectively bio-transformed by azoreductase to 2-[3-(hydroxy-amino) benzene-1-sulfonyl and AB-29 to aniline and 3-nitrosoaniline. This study explored the potential of recombinant azoreductase isolated from K. pneumoniae in the degradation of toxic textile azo dyes into less toxic metabolites.

Efficient and environmentally friendly removal of azo textile dye using a low-cost adsorbent: Kinetic and reuse studies with application to textile effluent

Recently, there has been an increasing interest in environmentally friendly methods for the removal of toxic dyes to enable sustainable textile dyeing processes. In this study, a highly efficient, non-toxic, low-cost MgO particles were prepared by sol-gel technique and utilized for the removal of Reactive Red 21 azo dye by adsorption process. The prepared MgO particles were characterized by Scanning Electron Microscopy, Fourier Transform Infrared Spectroscopy, X-Ray Diffraction, and Particle Size Analysis. The batch adsorption studies were performed for optimizing the parameters affecting adsorption. The adsorption behavior of Reactive Red 21 was accurately characterized by the Langmuir model. The adsorption process was found to be thermodynamically spontaneous at room temperatures as indicated by the negative Gibbs free energy change (∆G) value of −30.65 kj/mol. The kinetic studies indicate that the pseudo-second-order model provides a good fit to the adsorption of Reactive Red 21. The adsorption capacity of the prepared MgO particles for Reactive Red 21 was determined to be 355 mg/g at room temperature over a wide pH range of 5–9, with a contact time of 20 min. The regeneration of dye-adsorbed MgO particles was conducted at 500 °C for 2 h. The regenerated MgO particles were then utilized for adsorbing Reactive Red 21 five times with a sufficiently high dye removal efficiency. The prepared MgO particles provided a 98 % dye removal in real textile wastewater containing Reactive Red 21 dye.

Assessment of physically treated banana leaves as a low-cost and eco-friendly adsorbent for removal of a textile azo dye

Assessment of physically treated banana leaves as a low-cost and eco-friendly adsorbent for removal of a textile azo dye

Differently Prepared PbO2/Graphitic Carbon Nitride Composites for Efficient Electrochemical Removal of Reactive Black 5 Dye

In this paper, electrochemical degradation of Reactive Black 5 (RB5) textile azo dye was examined in regard to different synthesis procedures for making PbO2–graphitic carbon nitride (g-C3N4) electrode. The reaction of PbOH3- with ClO− in the presence of different surfactants, i.e., cetyltrimethylammonium bromide (CTAB) and tetrabutylammonium phosphate (TBAP), under conventional conditions, resulted in the formation of PbO2 with varying morphology. The obtained materials were combined with g-C3N4 for the preparation of the final composite materials, which were then characterized morphologically and electrochemically. After optimizing the degradation method, it was shown that an anode comprising a steel electrode coated with the composite of PbO2 synthesized using CTAB as template and g-C3N4, and using 0.15 M Na2SO4 as the supporting electrolyte, gave the best performance for RB5 dye removal from a 35 mg/L solution. The treatment duration was 60 min, applying a current of 0.17 A (electrode surface 4 cm2, current density of 42.5 mA/cm2), while the initial pH of the testing solution was 2. The reusability and longevity of the electrode surface (which showed no significant change in activity throughout the study) may suggest that this approach is a promising candidate for wastewater treatment and pollutant removal.

USE OF BI2S3 AS A PHOTOCATALYST FOR PHOTOCATALYTIC DEGRADATION OF TEXTILE AZO DYE REACTIVE BLUE 160 (RB160)

In apparel industries removal of the color of dye is one of the main problem. In the current work semiconductor photo-catalyst Bi2S3 utilized in photo catalytic decolorizing of textile azo dye Reactive Blue 160 under UV light. Spectrophotometric measurements of the reaction rate were made. It has been investigated how many variables, including dye concentration, photocatalyst quantity, and pH, affect reaction efficiency.