Maximum Decolorization Research Articles

Ex situ and in situ decolorization of the textile dye methylene blue by a cheese whey-microbial fuel cell

ABSTRACT Methylene blue (MB) is a textile dye that can be fatal to aquatic life, plants, and human health when discharged into the environment without treatment. A cheese whey-microbial fuel cell (CW-MFC) is a device that generates electricity from the degradation of cheese whey by microbial activity. The microbial activity of the CW-MFC during electricity production was able to decolorize MB. In this study, 50 ppm of MB was used to evaluate the decolorization capability of bacteria of the CW-MFC. A bacterial consortium present in the bioanode of the CW-MFC showed good MB decolorization in both the ex situ and in situ operations. Ex situ operation performed outside the CW-MFC reactor showed 92.2% MB decolorization within 18 h, while the in situ operation conducted inside the CW-MFC reactor showed 97.1% MB decolorization within the same timeframe. The maximum decolorization performance was achieved at pH 4 and 37 °C. The treated MB exhibited very little or no toxicity in the germination, rooting, and shooting of Oryza sativa compared to the untreated MB. Thus, the CW-MFC can be used as a promising technique to decolorize and remove the toxic effects of MB-contaminated wastewater, and the treated wastewater can be applicable for irrigation purposes.

Degradation of Azo-dye (Disperse Red) Using Rhizosphere Bacterial Consortium

This study investigates the degradation of the azo dye (Disperse Red) using a rhizosphere bacterial consortium. Standard microbiological and molecular techniques were employed to isolate and identify organisms from rhizosphere soil. Degradation of azodye was carried out in a fabricated anoxic and oxic chambers with hydraulic retention time of 40hrs. Initial identification of the bacterial isolates through Gram’s reaction and biochemical tests revealed the presence of organisms belonging to the genera Pseudomonas, Lysinibacillus, and Citrobacter. Molecular and phylogenetic analyses confirmed the isolates as Pseudomonas aeruginosa, Lysinibacillus sphaericus, Pseudomonas chengduensis, and Citrobacter freundii. During the preliminary testing, the degradation efficiency was assessed under varying glucose concentrations. Higher decolorization rate of 56.17% was observed in the medium with 10% glucose after 72 hours, while the medium with 5% glucose achieved a 44.17% colour reduction. Notably, lower degradation rates recorded were 11.96% and 12.85% for the 5% and 10% dye enhance glucose mineral salt media, respectively. However, During the actual degradation testing in a double-chamber system enhanced with biochar, the first anaerobic cycle achieved a maximum decolorization of 71.95% after 94 hours, with the first aerobic cycle further enhancing degradation to 90.51%. The second anaerobic cycle increased degradation to 94.78%, and the final aerobic cycle achieved a decolorization of 98.47%. These results show that the rate of Disperse Red degradation is highly dependent on glucose levels and alternating anaerobic-aerobic conditions. This study demonstrates the potential of using rhizosphere bacterial consortia to bioremediate wastewater contaminated with azo dyes, offering an efficient and sustainable method of environmental management. The results underline the need of optimizing ambient conditions to increase microbial degradation processes.

Decolorization of anthraquinone dye (Reactive Blue 4) in the microbial fuel cell by Baker’s yeast: process optimization

The release of anthraquinone dyes in aquatic sources has a huge impact on the environment because of their turbidity, toxicity, mutagenicity, and carcinogenicity effects. Microbial Fuel Cell (MFC) is a hopeful technology for the decolorization of dyes. The goal of the present study is the decolorization of Reactive Blue 4 (RB4) as an anthraquinone dye from an aqueous solution by Baker’s yeast in MFC. The selection of three parameters (dye concentration, glucose concentration, and airflow rate) and optimization of dye decolorization and chemical oxygen demand (COD) removal are performed using response surface methodology (RSM). The results demonstrated that the interaction between parameters does not affect the dye decolorization efficiency, whereas the interaction between dye concentration and glucose concentration was found to be significant for COD removal. Accordingly, the optimum conditions for maximum dye decolorization and COD removal were obtained at a dye concentration of 50 mgL−1, a glucose concentration of 1 gL−1, and an airflow rate of 10 mLmin−1.

Enhancing bioelectricity generation through co-cultivation of bacteria consortium and microalgae in photosynthetic microbial fuel cell

This study investigates the effect of microbial configuration on the electrochemical performance of photosynthetic microbial fuel cells (PMFCs). The PMFC configuration incorporating both bacteria and microalgae exhibited the highest open-circuit voltage (OCV) of 397.95 ± 31.53 mV, significantly higher than that of the OCVs obtained in the sterile control (C1) and the microalgae-only configuration (C2), which were 32.47 ± 22.43 mV and 284.59 ± 12.63 mV, respectively. Furthermore, the PMFC containing only microalgae achieved a current density (CD) of 20.96 ± 0.18 mA/m³ and a power density (PD) of 0.40 ± 0.01 mW/m³ under room temperature conditions. Notably, the combined bacteria and microalgae configuration demonstrated a substantial performance improvement, yielding a significantly higher CD of 49.33 ± 0.36 mA/m³ and PD of 0.78 ± 0.01 mW/m³ at room temperature. This configuration also achieved a maximum decolorization of 93.57 ± 0.10% with a corresponding algal biomass recovery of 134.90 ± 2.69 mg/L. These findings highlighted the critical role of microbial composition in PMFC performance. The combination of bacteria and microalgae yielded superior results compared to other configurations under the investigated conditions.

Decolourization and detoxification of Reactive Red-195 azo dye by Staphylococcus caprae isolated from textile effluent.

Azo dyes are used as coloring agent in textile industries at larger scale. As a result, large quantity of dye-enriched waste water is generated which subsequently poses environmental problems. Biological tool involving bacteria having azoreductase enzyme has proved to be more effective and efficient in dye effluent treatment. Current work focuses on Staphylococcus caprae (S. caprae) for degradation and decolorization of Reactive Red-195 (RR-195) azo dye. For this purpose, factors such as pH, temperature, inoculums, carbon and nitrogen sources, and dye concentrations have been optimized for maximum decolorization and degradation. S. caprae (4mg/mL) efficiently resulted into 90% decolorization of RR-195 dye under static condition at 100µg/mL concentration, 30°C and pH 7.0 at a 12-h contact period. FTIR analysis has revealed the formation of new functional groups in the treated dye such as O-H stretch at 3370cm-1, C-H band stretching at 2928cm-1, and new band at 1608cm-1 which specify the degradation of aromatic ring, 1382 and 1118cm-1 represents desulfonated peaks. Biodegraded metabolites of RR-195 dye such as phenol, 3, 5-di-tert-butylphenol, and phthalic acid have been identified respectively that find industrial applications. Phytotoxicity test has shown non-toxic effects of treated dye on germination of Vigna radiata and Triticum aestivum seeds. Further, antibiotic diffusion assay has confirmed the biosafety of S. caprae.

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.

Optimization and modeling of solar photocatalytic degradation of raw textile wastewater dyes using green ZnO-ED NPs by RSM

ABSTRACT This study aims to use green ZnO-ED NPs produced from Eleocharis dulcis (E. dulcis) extract to maximize solar photocatalytic degradation of raw textile wastewater. The optimization of photocatalysis was decided using the response surface methodology (RSM) as a function of ZnO-ED NPs mass load (0.1–2 g), initial concentration (10–100%), pH (4–9), and contact time (60–200 min). The maximum decolorization (87.34%) and COD removal (100%) were recorded at pH 7, time (60 min), ZnO-ED NPs dosage (2 g/L), and 10% of color concentrations with R2 coefficient of 0.78 at p < 0.05. FESEM analysis showed the presence of granules with smaller diameters than the diameter of the ZnO-ED NPs granules before SPD. EDX analysis revealed the presence of impurities like copper (Cu). XRD analysis indicated the purity of ZnO-ED NPs after SPD, as the values were all quite similar to the XRD values before SPD. The results of an AFM analysis presented that agglomerations of ZnO-ED NPs, in contrast, were somewhat homogeneous in size, nature, and dispersion before SPD.

The potential biological activities of Aspergillus luchuensis-aided green synthesis of silver nanoparticles.

Biosynthetic metals have attracted global attention because of their safety, affordability, and environmental friendliness. As a consequence, the cell-free filtrate (CFF) of Dill leaf-derived endophytic fungus Aspergillus luchuensis was employed for the extracellularly synthesis silver nanoparticles (AgNPs). A reddish-brown color shift confirmed that AgNPs were successfully produced. The obtained AgNPs were characterized by UV-Vis (ultraviolet-visible spectroscopy), Transmission electron microscopy (TEM), FTIR, EDX, and zeta potential. Results demonstrated the creation of crystalline AgNPs with a spherical shape at 427.81 nm in the UV-Vis spectrum, and size ranged from 16 to 18 nm as observed by TEM. Additionally, the biogenic AgNPs had a promising antibacterial activity versus multidrug-resistant bacteria, notably, S. aureus, E. coli, and S. typhi. The highest growth reduction was recorded in the case of E. coli. Furthermore, the biosynthesized AgNPs demonstrated potent antifungal potential versus a variety of harmful fungi. The maximum growth inhibition was evaluated from A. brasinsilles, followed by C. albicans as compared to cell-free extract and AgNO3. In addition, data revealed that AgNPs possess powerful antioxidant activity, and their ability to scavenge radicals increased from 33.0 to 85.1% with an increment in their concentration from 3.9 to 1,000 μg/mL. Furthermore, data showed that AgNPs displayed high catalytic activity of safranin under light irradiation. The maximum decolorization percentage (100%) was observed after 6 h. Besides, the biosynthesized AgNPs showed high insecticidal potential against 3rd larval instar of Culex pipiens. Taken together, data suggested that endophytic fungus, A. luchuensis, is an attractive candidate as an environmentally sustainable and friendly fungal nanofactory.

Green biocatalyst for decolorization of azo dyes from industrial wastewater: Coriolopsis trogii 2SMKN laccase immobilized on recycled brewer's spent grain.

This study presents an innovative approach for the reuse and recycling of waste material, brewer's spent grain (BSG) for creating a novel green biocatalyst. The same BSG was utilized in several consecutive steps: initially, it served as a substrate for the cultivation and production of laccase by a novel isolated fungal strain, Coriolopsis trogii 2SMKN, then, it was reused as a carrier for laccase immobilization, aiding in the process of azo dye decolorization and finally, reused as recycled BSG for the second successful laccase immobilization for six guaiacol oxidation, contributing to a zero-waste strategy. The novel fungal strain produced laccase with a maximum activity of 171.4 U/g after 6 days of solid-state fermentation using BSG as a substrate. The obtained laccase exhibited excellent performance in the decolorization of azo dyes, both as a free and immobilized, at high temperatures, without addition of harmful mediators, achieving maximum decolorization efficiencies of 99.0%, 71.2%, and 61.0% for Orange G (OG), Congo Red, and Eriochrome Black T (EBT), respectively. The immobilized laccase on BSG was successfully reused across five cycles of azo dye decolorization process. Notably, new green biocatalyst outperformed commercial laccase from Aspergillus spp. in the decolorization of OG and EBT. GC-MS and LC-MS revealed azo-dye degradation products and decomposition pathway. This analysis was complemented by antimicrobial and phytotoxicity tests, which confirmed the non-toxic nature of the degradation products, indicating the potential for safe environmental disposal.

Synthesis and characterization of the Cu(II)-quinoxaline, 3,3-thiodipropionate mixed ligand coordination polymer for the removal of methylene blue from aqueous solution

Herein, we report the removal of methylene blue (MB) dye from water by Cu(II)-quinoxaline, 3,3-thiodipropionate mixed ligand coordination polymer synthesized as [Cu2(TDPH)4(QNX)]·DMF. Characterization of the synthesized material was carried out by elemental analysis, thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), BET surface area analysis, X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), and UV–visible spectroscopy. ν(C = O) and ν(C–O) absorption bands were detected at 1735 and 1093 cm−1, respectively, while ν(C = N) was observed at 1608 cm−1 in the synthesized compound. The synthesized material was used as adsorbent for the removal of MB dye from aqueous solution using batch adsorption technique. The maximum adsorption capacity was found to be 7.9745 mg/g, while the maximum decolorization efficiency for the adsorbent was observed to be 99.04%. Adsorption data from the study fitted the Langmuir isotherm with an R 2 value of 0.9815, while the adsorption kinetics followed the pseudo-second-order kinetic model with an R 2 value of 0.9953. The results obtained from the study, therefore showed that the synthesized materials could be used as adsorbents in wastewater treatment.

Multigene phylogeny, bioactive properties, enzymatic and dye decolorization potential of selected marine fungi from brown algae and sponges of Mauritius

Marine fungi represent an important proportion of the microbial diversity in the oceans. They are attractive candidates for biotechnological purposes and industrial applications. Despite an increasing interest in mycology, marine fungi associated with sponges and algae have been poorly studied in Mauritius. The objectives of this study were to: 1) use multigene phylogenetic analyses to identify isolated marine fungi; 2) determine the differences in the antimicrobial and antioxidant properties of the fungal extracts; and 3) assess their enzyme activities and dye decolorization potential. Five fungal isolates viz Aspergillus chevalieri, Aspergillus iizukae, Aspergillus ochraceus, Exserohilum rostratum and Biatriospora sp. were identified based on phylogenetic analyses. There was no significant difference in the antimicrobial properties of the liquid and solid media extracts unlike the antioxidant properties (p < 0.05). The solid media extract of Aspergillus chevalieri (F2-SF) had a minimum inhibitory concentration of 0.156 mg/ml against Staphylococcus aureus while Aspergillus ochraceus (F25-SF) had a minimum inhibitory concentration of 0.313 and 2.5 mg/ml against Enterococcus faecalis and Salmonella typhi. The solid media extract of Biatriospora sp. (F34-SF) had a minimum inhibitory concentration of 0.195 and 1.563 mg/ml against Bacillus cereus, Escherichia coli and Enterobacter cloacae. An IC50 of 78.92 ± 4.71 μg/ml in the 2,2-Diphenyl-1-picrylhydrazyl (DPPH) scavenging assay, ferric reducing antioxidant power (FRAP) value of 11.17 ± 0.20 mM Fe2+/g dry weight extract (DWE) and total phenolic content 360.35 ± 10.31 mg GAE/g DWE was obtained with the solid media extract of Aspergillus chevalieri (F2-SF). Aspergillus ochraceus (F25-SF) and Biatriospora sp. (F34-SF) solid media extracts showed lower IC50 values in the DPPH assay and higher total phenolic content as compared to the liquid media extracts. Aspergillus chevalieri was a good producer of the enzymes DNAse and lipase and had maximum percentage dye decolorization of 79.40 ± 17.72% on Congo red. An enzymatic index ≥ 2 was found for the DNAse and lipase and the maximum percentage dye decolorization of 87.18 ± 3.80% was observed with Aspergillus ochraceus on Methylene blue. Regarding Biatriospora sp., it was a moderate producer of the three enzymes amylase, DNAse and protease and had a maximum dye decolorization potential of 56.29 ± 6.51% on Crystal violet. This study demonstrates that Mauritian marine fungi possess good bioactive properties, enzymatic and dye decolorization potentials, that can potentially be considered for use in pharmaceutical and industrial applications.

Green synthesis of nanocomposite based on magnetic hydroxyapatite using Falcaria vulgaris Bernh leaf extract to remove tartrazine dye from aqueous solution

To mitigate the adverse impacts of water pollution, the application of nanotechnology in dye removal and by-product reduction has the potential to establish a sustainable potable water supply. For these methodologies, the materials must involve exhibit qualities such as simplicity, high efficiency, eco-friendliness, reusability, and affordability. This study presents a novel porous magnetic hydroxyapatite nanocomposite coated with zinc oxide (Fe3O4@HAP@ZnO). Initially, zinc oxide nanoparticles were generated via a green synthesis method, where a zinc nitrate solution was combined with an aqueous extract from the Falcaria Vulgaris Bernh plant, serving as a reducing and stabilizing agent. These were then coated onto the magnetic hydroxyapatite.Verification of successful nanocomposite synthesis was obtained through X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray spectroscopy (EDS), vibrating-sample magnetometer (VSM), High-resolution transmission electron microscopy (HRTEM) and scanning electron microscopy (SEM) images further substantiated these results. The synthesized nanocomposite exhibited a normal particle size distribution of approximately 89 nm. To achieve maximal decolorization efficiency, pertinent parameters were scrutinized and optimized through a detailed experimental design. Under optimal conditions, the nanocomposite's ability to decolorize tartrazine dye in an aqueous solution was evaluated. Remarkably, the highest observed efficiency approached 98 %, employing 0.07 g of the nanocomposite at 90 degrees Celsius, pH 6.4, over a span of 30 min. Further exploration of the nanocomposite's reusability revealed it could sustain an efficiency exceeding 90 % across 11 successive cycles, boasting an impressive capacity of 1398 (mgg-1).

Screening of azo dye biosorption efficacy of free, immobilized, indigenous bacterial strains associated with azo dye contaminated river water—An in vitro study

AbstractAzo dye degradation utilizing microorganisms has acquired significance over the last decades, owing to its beneficial properties such as rapid degradation, economic feasibility, and eco‐friendly. In this work, azo dyes (Methyl red and methylene blue) degradation efficacy using indigenous bacterial strains Pseudomonas sp. and Bacillus sp. as free and immobilized cells were investigated under in vitro batch decolorization setup was carried. Most importantly, the bacterial cells of both strains were immobilized with sodium alginate and the immobilized cells were evaluated for dye decolorization efficacy under laboratory conditions. An eco‐toxic assessment of the degraded products was done using in vitro phytotoxicity tests and in silico analyses. Among the free and immobilized cells, maximum decolorization efficacy was observed in the Pseudomonas sp. immobilized cells which exhibited 74.5% decolorization efficacy, and the maximum decolorization efficacy of free cells was 63% of was observed. Ecotoxicity of the dye‐degraded products was screened by determination of phytotoxicity. Seedlings emergence of groundnut seeds exposed to degraded dye products revealed phytotoxicity. Results indicated that degraded dye products of methyl red derived from Pseudomonas sp. showed 93.0% seedling emergence, and methylene blue‐degraded products Pseudomonas sp. degraded dye products supported 92.0% seedling emergence, respectively. Bacterial cells immobilized with biocompatible polymers can be effectively utilized in wastewater treatment without affecting the ecological components. The findings highlight the value of this work in contributing to the domain of sustainable and eco‐friendly wastewater treatment technology.

Optimized decolorization of two poly azo dyes Sirius Red and Sirius Blue using laccase-mediator system.

Factors, namely pH, laccase-like activity, dyes concentration as well as 1-Hydroxybenzotriazole (HBT) concentration was examined. The results indicated that the maximum decolorization yield and rate reached 98.30 ± 0.10% and 5.84 ± 0.01%/min, respectively for Sirius Blue, and 99.34 ± 0.47% and 5.85 ± 0.12%/min, respectively for Sirius Red after 4h. The presence of the redox mediator 1-hydroxybenzotriazole (HBT) greatly improved the decolorization levels. The optimum concentrations of HBT, dyes, and laccase were 0.62mM, 50mg/L, and 0.89 U/mL respectively at pH 4.58 for both dyes. Phytotoxicity tests using treated and untreated dyes proved that the applied treatment slightly decreased the toxicity of the by-products. However, the germination index (GI) increased from 14.6 to 36.08% and from 31.6 to 36.96% for Sirius Red and Sirius Blue, respectively. The present study focused on the treatment of two recalcitrant azo dyes, namely: Sirius Blue (Direct Blue 71) and Sirius Red (Direct Red 80). The decolorization was performed using cell-free supernatant from Coriolopsis gallica culture with high laccase activity. Response surface methodology (RSM) and Box-Behnken design were applied to optimize the decolorization of the two tested dyes. The effect of four.

Response surface methodology for low-energy consumption electro-Fenton process for xanthene dye electrochemical degradation

Erythrosine B (EB) is a dye widely used in the food and textile industries. Despite many studies that have been proposed in the literature about the electrochemical oxidation of dyes, few studies considered such recalcitrant xanthene compound, although it has been recognized as a threat to health and the environment. Then, this study investigates the oxidation of EB by a homogeneous electro-Fenton process using iron (II) sulfate heptahydrate as a catalyst, carbon felt cathode, and Ti/RuO2 anode. The treated synthetic wastewater contains 100 mg L−1 of EB and has a pH = 3. The effects of three independent variables have been considered for process optimization, such as applied current intensity (0.1–0.5 A), iron concentration (1–10 mM), and stirring rate (100–1000 rpm). Their interactions were investigated considering response surface methodology (RSM) based on Doehlert design as optimization method. EB removal efficiency and energy consumption were considered as model responses after 30 min of electrolysis. Analysis of variance (ANOVA) revealed that the quadratic model was adequately fitted to the experimental data with R2 (0.9819), adj-R2 (0.9276), and low Fisher probability (< 0.0181) for the EB removal model, and R2 (0.9968), adj-R2 (0.9872) and low Fisher probability (< 0.0014) relative to the energy consumption model, suggesting a robust statistical significance. The energy consumption model significantly depends on current density, as expected. The foregoing results obtained by RSM led to the following optimal conditions for EB degradation: current intensity of 0.2 A, iron concentration of 9.397 mM, and stirring rate of 500 rpm, which gave a maximum decolorization rate of 98.15% with a minimum energy consumption of 0.74 kWh m−3 after 30 min of electrolysis. The competitiveness of the electro-Fenton process has been confirmed by the literature analysis proposed as well as by the preliminary economic analysis proposed in the second section of the study.Graphical abstract

Microwave‐assisted synthesis, characterization, and application of tragacanth gum grafted copolymer as bioflocculant for the treatment of textile wastewater using coagulation‐flocculation technique: Swelling behavior and biodegradation studies

AbstractThis study presents, the synthesis of microwave‐assisted biodegradable polyacrylamide grafted tragacanth gum (Tr‐g‐PAM), which was utilized as a bioflocculant to treat textile effluent and compared against the conventional flocculant. The reaction parameters for maximal grafting were optimized by varying the reaction factors. The grafting of acrylamide onto the backbone of Tragacanth gum was confirmed by FTIR, XRD, TGA, and SEM–EDX studies. Swelling studies were performed in deionized water and different salts. Tr‐g‐PAM exhibited pH and temperature‐dependent swelling behavior. Biodegradation studies of the graft copolymer were carried out by the soil composting method. Tr‐g‐PAM showed 91.54% degradation within 60 days, compared to Tragacanth, which degraded within 15 days. SEM techniques were used to describe various phases of biodegradation. Flocculation performances of the graft copolymers were evaluated in simulated colloidal wastewater. Influencing variables such as bioflocculant dosage, pH, and flocculation mixing speed were examined. The maximum decolorization at the optimum pH of 6 and 120 mg/L dosage was found to be 91.8% and 88.5% for Tr‐g‐PAM and Tragacanth. In conclusion, a biodegradable Tr‐g‐PAM with better flocculation efficiency than that of Tragacanth and other commercial flocculants would be a promising choice as an eco‐friendly adsorbent for the removal of contaminants from water resources.

Improved application of immobilized Enterobacter cloacae into a bio-based polymer for Reactive Blue 19 removal, an eco-friendly advancement in potential decolorizing systems.

The widespread use of highly complex synthetic dyes like reactive dyes in the textile industry has some adverse environmental impacts and deserves close attention. Biological treatment of these effluents utilizing various species of bacteria with remarkable efficiency in dye removal is still considered promising. Our current study deals with immobilizing an isolated bacterial strain into calcium alginate (Ca/Alg) gel beads and using it to treat pernicious pollutants like synthetic dyes. A potential Reactive Blue 19 (RB19)-degrading Enterobacter cloacae strain A1 was isolated from the Kashan textile industry and was characterized by 16S rDNA gene sequencing. The decolorization ability of strain A1 was assessed by time-based studies using free bacterial cells/immobilized in Ca/Alg. Based on the results of the 16S rDNA gene sequencing, it appears that strain A1 belonged to E.cloacae, with a 99.74% similarity. The findings suggest that immobilized strain A1 accomplished maximum decolorization activity compared with the free cells. The immobilized strain could utterly decompose and decolorize 0.05 mg/mL of RB19 within 48 h, while the free bacterial strain decolorized RB19 within 5 days. Moreover, Ca/Alg gel beads can maintain their efficiency for over three decolorization cycles. Further infrared spectroscopy (FTIR) and gas chromatograph mass spectrometer (GC/MS) investigation declared complete RB19 decomposition on reaction products. Artemia salina was used to investigate the toxicity of dye and its degraded metabolites. The LC50 values signified the pure dye as very toxic with 0.01 mg/mL concentration, while after-treatment products showed no toxic effect on larvae. This immobilization technique increased the applicability of bacterial strain for dye removal. It was beneficial for the decolorization of RB19 from textile wastewater due to a remarkable reduction in time. Notably, strain A1-immobilized beads can maintain their activity for three consecutive decolorization cycles without a considerable decrease in efficiency. PRACTITIONER POINTS: The remarkable capacity of immobilized Enterobacter cloacae strain A1 for Reactive Blue 19 (RB19) removal Immobilized A1 strain showed two-fold higher removal than free one over 48 h A promising method for enhancing RB19 decolorization Decolorization was due to degradation based on UV-Vis, FTIR, and GC/MS analysis Non-toxic posttreatment products for Artemia.

A INFLUENCE OF OPERATING PARAMETERS ON DECOLORATION OF INDIGO CARMINE SOLUTIONS USING GAMMA RADIATIONS

Abstract: It has been observed that the process parameters influence the extent of decoloration of synthetic dyes during gamma radiolysis in aqueous solutions. The influence of some factors viz. concentration of dye, dye solution pH, addition of H2O2 on the colour bleaching of Indigo Carmine dye in aqueous medium was studied using 60Co gamma radiation source (dose rate was 0.386 kGy/hr). The dose required for the thorough decoloration was observed to be the direct function of the dye concentration in the solution. Further, when pH of solution was increased, the extent of decoloration reduced, for all the concentrations. H2O2 addition had the accelerating effect on the overall decoloration. The addition of H2O2 was governed by the critical value which corresponds to optimum dose of H2O2 that is required for maximum decoloration.

Electricity generation and oxidoreductase potential during dye discoloration by laccase-producing Ganoderma gibbosum in fungal fuel cell

Color chemicals contaminate pure water constantly discharged from different points and non-point sources. Physical and chemical techniques have certain limitations and complexities for bioenergy production, which motivated the search for a novel sustainable production approaches during dye wastewater treatment. The emerging environmental problem of dye decolorization has attracted scientist's attention to a new, cheap, and economical way to treat dye wastewater and power production via fungal fuel cells. Ganoderma gibbosum was fitted in the cathodic region with laccase secretion in the fuel cell. At the same time, dye water was placed in the anodic region to move electrons and produce power. This study treated wastewater using the oxidoreductase enzymes released extracellularly from Ganoderma gibbosum for dye Remazol Brilliant Blue R (RBBR) degradation via fungal-based fuel cell. The maximum power density of 14.18 mW/m2 and the maximum current density of 35 mA/m2 were shown by the concentration of 5 ppm during maximum laccase activity and decolorization of RBBR. The laccase catalysts have gained considerable attention because of eco-friendly and alternative easy handling approaches to chemical methods. Fungal Fuel Cells (FFCs) are efficiently used in dye treatment and electricity production. This article also highlighted the construction of fungal catalytic cells and the enzymatic performance of fungal species in energy production during dye water treatment.

Biodegradation Assay of Heavy Metals and Dyes Decolorization in Textile Industrial Effluent using Laccase Isolated from Pleurotus ostreatus

This study focused on the isolation of laccase enzyme from the fungus Pleurotus ostreatus and its application in the biodegradation of various pollutants present in textile industrial effluent, including chemicals, ions, salts, heavy metals, brittle metals, total suspended solids, total dissolved solids, chemical oxygen demand, biological oxygen demand, minerals, total hardness, total alkalinity, turbidity, electrical conductivity, and dyes. Textile industrial effluent poses a significant threat to the environment, contaminating water bodies and posing risks to human, animal, and plant life. This study employed an economical and ecofriendly biological approach for wastewater treatment, distinguishing it from traditional physical and chemical methods. The optimum temperature of laccase is found to be 30 degree Celsius and pH is 3. Enzyme activity of laccase is 7.25 U/ml. This fugal laccase decolorizes textile Industrial dye effluent containing various dyes, such as Turquoise VG, Black B, Yellow R, Methyl red, Trypan blue, and Acid Orange 7. Laccase depicts maximum decolorization efficacy on Black B dye. Similarly, Laccase from P.ostreatus shows higher decolorization efficacy when compared to other fungal laccase. Additionally, the study assessed the biodegradation of various wastewater quality parameters, including physical and chemical parameters like toxic heavy metals and ions. This research of isolation, characterization, and utilizing laccase from P. ostreatus for the bioremediation of textile industrial effluent wastewater containing dyes, toxic chemicals, ions and metals is effective, economical and ecofriendly.