Decolorization Efficiency Research Articles

Fabrication of Multifunctional Green-Synthesized Copper Oxide Nanoparticles Using Rumex vesicarius L. Leaves for Enhanced Photocatalytic and Biomedical Applications

Recently, the use of plant extracts has emerged as an innovative approach for the production of various nanoparticles. Enhancing green methods for synthesizing copper oxide (CuO) nanoparticles (NPs) is a key focus in the field of nanotechnology. This study presents a novel and eco-friendly synthesis of CuO NPs using Rumex vesicarius L. leaf extracts, offering a cost-effective and efficient method. The synthesized CuO NPs were evaluated for their cytotoxic effects against human cervical carcinoma (HeLa) cells, as well as their photocatalytic and antimicrobial activities. The morphology, size, and structural properties of the CuO NPs were characterized using various analytical techniques. X-ray diffraction (XRD) analysis confirmed the pure crystalline structure of the CuO NPs with a size of 19 nm, while transmission electron microscopy (TEM) showed particle sizes ranging from 5 to 200 nm. The photocatalytic performance of the CuO NPs was assessed through the photodegradation of crystal violet (CV) and methylene blue (MB) dyes under UV light. The NPs exhibited excellent decolorization efficiency, effectively degrading dyes in aqueous solutions under irradiation. Furthermore, the green-synthesized CuO NPs displayed strong antibacterial and antifungal activities against a variety of human pathogens. They also demonstrated significant dose-dependent cytotoxicity against the HeLa cancer cell line, with an IC50 value of 8 ± 0.54 μg/mL.

Synergistic enhancement of photocatalytic degradation performance in Cl-g-C3N4/Bi3Al0.06O10 through nitrogen vacancies and S-scheme heterojunctions

The ternary Aurivilius compound BixAlyOz was prepared via a solvothermal technique, with the specific composition determined to be Bi3Al0.06O10 using inductively coupled plasma optical emission spectroscopy. A Cl-g-C3N4/Bi3Al0.06O10 heterojunction was constructed using the solvothermal coprecipitation method. Notably, the introduction of Cl-g-C3N4 with Bi3Al0.06O10 significantly enhanced the decolorization efficiency of both Rhodamine B (RhB) and methylene blue (MB). Specifically, the Cl-g-C3N4/Bi3Al0.06O10 composite with a mass ratio of 1:4 achieved a removal rate of 96.81 % for RhB within 20 min and 96.70 % for MB within 180 min. This is mainly attributed to the synergistic effects of N vacancies and the formation of S-scheme heterojunction in Cl-g-C3N4/Bi3Al0.06O10. These features facilitate the effective separation of photogenerated electrons and holes while expanding the light absorption range. This study not only presents a novel method for synthesizing photocatalysts with N vacancies but also offers a new approach for treating dye-contaminated wastewater.

Exploring Aspergillus biomass for fast and effective Direct Black 22-dye removal

Azo dyes are widely used in the textile industry due to their stability and resistance. These properties also make them recalcitrant xenobiotics, toxic, mutagenic, and carcinogenic, even at low concentrations. Considered emerging pollutants, there is an urgency to address mechanisms capable of remediating these contaminants, with Aspergillus fungi standing out as an effective solution. Fifteen strains of Aspergillus were investigated for the decolorization of the tetra azo dye Direct Black 22. The influence of different culture media was evaluated on fungi biomass production, dye concentrations (50–300 mg/L), biomass concentrations (1–5g), and the reuse of biomass in continuous batches. The strains that stood out the most were Aspergillus japonicus URM 5620, Aspergillus niger URM 5741, and A. niger URM 5838. Obtaining biomass in less nutrient-rich medium favored decolorization by forming more organized pellets. The live biomass of these fungi was 59% more efficient than the dead biomass. The decolorization efficiency was not affected at lower dye concentrations, showing a decrease in decolorization only when the concentration reached 300 mg/L. Increasing the amount of biomass resulted in proportionally greater decolorization. Even with just 1 g of biomass, the three fungi could remove more than 90% of the dye in less than 60 minutes, and with 5 g, the dye was completely removed in 10 minutes. Thebiomass was reused in three consecutive decolorization cycles, and the fungus that best withstood the cycles was A. niger URM 5741. These results demonstrate the potential of the genus Aspergillus fungi tested in this study as sustainable and efficient biosorbents for the remediation of azo dyes such as Direct Black 22, with potential for colored industrial effluent treatment.

Cationic waste hemp fibers-based membrane: Case study of anionic pollutants removal through environmentally friendly processes

In this study, waste hemp fibers were transformed into cationically modified lignocellulosic adsorbent through a three-step process. First, a delignification/defibrillation pretreatment was performed, followed by quaternization of fibers using the synthesized ionic liquid chlorocholine chloride-urea (CCC-U). Pressure-assisted cross-linking of modified fibres, using a citric acid, produced new membrane (CCC-UHM). The removal of anionic dyes (Acid Yellow 36 (AY36), Congo Red (CR), Acid Green 25 (AG25), and Acid Blue 92 (AB92)), and oxyanions (As(V) and Cr(VI)) was tested in batch and column system. The structural characteristics and chemical properties of the syntesised materials were investigated by SEM, FTIR, Raman, XPS, XRD, specific density, porosity and point of zero charges analysis. The endothermic and spontaneous equilibration of the system resulted in high capacity (qm), i.e., 302.9 mg g−1 (AY36), 456.8 mg g−1 (CR), 812.8 mg g−1 (AG25), 587.6 mg g−1 (AB92), 107.9 mg g−1 (As(V)), and 67.84 mg g−1 (Cr(VI)) at 25 °C, using the Langmuir model. The optimum pH for the adsorption process was 7. The multi-cycle adsorption/desorption process was followed by either decolorization, using laccase from M. thermophile expressed in Aspergillus oryzae (Novozym 51,003® laccase) immobilized on amino-modified fibers as biocatalyst, or photocatalytic degradation, in the presence of zinc oxide. The high decolorization efficiency (96%) observed for AG25 and AB92 underscores the considerable potential of laccase immobilized preparations as sustainable and eco-friendly approach for treating dye-contaminated wastewater. Photodegradation process provided low environmental threat of processed water, and biodegradabilty of exhausted membrane confirmed the circularity of the developed technology with implemented principles of sustainability.

Catalase-peroxidase StKatG2 from Salinicola tamaricis: a versatile Mn(II) oxidase that decolorizes malachite green.

Manganese (Mn) oxidation processes have garnered significant attention recently due to their potential for degrading organic pollutants. These processes are primarily catalyzed by Mn(II) oxidases. Salinicola tamaricis F01, an endophytic bacterium derived from wetland plants, has demonstrated Mn(II)-oxidizing capacity. In this study, a catalase-peroxidase, StKatG2, was cloned and overexpressed in Escherichia coli from the strain F01. The purified recombinant StKatG2 exhibited Mn(II)-oxidizing activity with K m and K cat values of 2.529 mmol/L and 2.82 min-1, respectively. Optimal catalytic conditions for StKatG2 were observed at pH 7.5 and 55°C, with 45.1% activity retention after an 8-h exposure to 80°C. The biogenic manganese oxides produced by StKatG2 exhibited mixed-valence states with Mn(II), including Mn(III), Mn(IV), and Mn(VII). Furthermore, StKatG2 demonstrated superior decolorization efficiency for malachite green (MG), achieving decolorization rates of 73.38% for 20 mg/L MG and 60.08% for 50 mg/L MG, while degrading MG into 4-(dimethylamino)benzophenone. Therefore, the catalase-peroxidase StKatG2 exhibits multifunctionality in Mn(II)-oxidizing activity and has the potential to serve as an environmentally friendly enzyme for MG removal.

MgAl-Layered Double Hydroxide-Coated Bio-Silica as an Adsorbent for Anionic Pollutants Removal: A Case Study of the Implementation of Sustainable Technologies.

The adsorption efficiency of Cr(VI) and anionic textile dyes onto MgAl-layered double hydroxides (LDHs) and MgAl-LDH coated on bio-silica (b-SiO2) nanoparticles (MgAl-LDH@SiO2) derived from waste rice husks was studied in this work. The material was characterized using field-emission scanning electron microscopy (FE-SEM/EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopic (XPS) techniques. The adsorption capacities of MgAl-LDH@SiO2 were increased by 12.2%, 11.7%, 10.6%, and 10.0% in the processes of Cr(VI), Acid Blue 225 (AB-225), Acid Violet 109 (AV-109), and Acid Green 40 (AG-40) dye removal versus MgAl-LDH. The obtained results indicated the contribution of b-SiO2 to the development of active surface functionalities of MgAl-LDH. A kinetic study indicated lower intraparticle diffusional transport resistance. Physisorption is the dominant mechanism for dye removal, while surface complexation dominates in the processes of Cr(VI) removal. The disposal of effluent water after five adsorption/desorption cycles was attained using enzymatic decolorization, photocatalytic degradation of the dyes, and chromate reduction, satisfying the prescribed national legislation. Under optimal conditions and using immobilized horseradish peroxidase (HRP), efficient decolorization of effluent solutions containing AB-225 and AV-109 dyes was achieved. Exhausted MgAl-LDH@SiO2 was processed by dissolution/precipitation of Mg and Al hydroxides, while residual silica was used as a reinforcing filler in polyester composites. The fire-proofing properties of composites with Mg and Al hydroxides were also improved, which provides a closed loop with zero waste generation. The development of wastewater treatment technologies and the production of potentially marketable composites led to the successful achievement of both low environmental impacts and circular economy implementation.

Enhancement of the anaerobic biodegradation efficiency of azo dye by anthraquinone-loaded biochar biofilm: factors affecting biofilm formation and the enhancement mechanism

Carbon-based materials that serve as microbial carriers, and the role of surface-formed biofilms in anaerobic digestion, merit further investigation. This study explored the role and mechanism behind the biodegradation enhancement of biofilms formed onto anthraquinone-loaded biochar (AQS-BC) surfaces through the anaerobic decolorization process of azo dye Reactive Red 2, and optimized the conditions for AQS-BC biofilm formation. The results indicated that the AQS-BC biofilm system exhibited high treatment efficiency and stability in RR2 anaerobic decolorization. RR2 led to the accumulation of volatile fatty acids (VFAs) and inhibition of methane production, while the presence of AQS increased methane production. The effects of sludge concentration, contact time, carbon source concentration, and RR2 concentration on biofilm maturity were also analyzed. Combining biochemical characteristics, electrochemical properties, surface structure, and microbial community analysis, a mechanism for the anaerobic decolorization of RR2 via AQS-BC as a microbial carrier was proposed. This study provides insights into the roles of biofilms in the anaerobic wastewater treatment processes.Graphical

Enhancing biodecolorization of Malachite Green by Flavobacterium sp. through monothetic analysis

Malachite Green (MG) is a prevalent dye in the textile industry, known for its harmful environmental impacts. Addressing the urgent need for environmentally friendly and cost-effective methods to remove MG from wastewater, this study investigated the efficacy of Flavobacterium sp., isolated from Malaysian batik wastewater, in decolorizing MG. Under shaking conditions at 160 rpm, Flavobacterium sp. exhibited a notable decolorization efficiency, with 91 % removal of MG after a 3-day incubation time, surpassing the static mode efficiency of 39 %. Further optimization using a one-factor-at-a-time (OFAT) methodology at 37 °C, pH 10, 6 % (v/v) inoculum, banana peel as the carbon source and 250 mg/L MG resulted in a remarkable enhancement, achieving 95 % decolorization within a reduced incubation time of 12 h. Moreover, repeated addition of 250 mg/L MG showed consistent and complete decolorization after 6 h by Flavobacterium sp. for four successive cycles, suggesting its economic viability for treating actual Malaysian batik wastewater. Ultraviolet–visible (UV) analysis confirmed the biodegradation of MG, evidenced by the disappearance of characteristic peaks at 618 nm and the appearance of new peaks, indicating the formation of metabolites. Flavobacterium sp. reduced pH, temperature, color, TDS, TSS, BOD and COD in batik wastewater, showing 99 % color removal efficiency. This research highlights its potential as an eco-friendly, cost-effective treatment for batik wastewater. The capacity of Flavobacterium sp. to decolorize MG in an immobilized state will be the subject of future research endeavors, aimed at elucidating the adaptability and usefulness of the biocatalyst.

Enhanced bioremediation of saline azo dye effluents using PersiLac3: A thermo-halotolerant laccase from a tannery metagenome

Large quantities of recalcitrant azo dye wastewater represent an important environmental issue, owing to their toxicity and the difficulty of their treatment under hypersaline conditions. By maintaining high activity under salt-rich conditions, salt-tolerant laccases offer a promising solution for the effective breakdown of toxic azo dyes, making them indispensable for the sustainable treatment of industrial wastewater. This study explored the identification and application of a thermo-halotolerant laccase, PersiLac3, for bioremediation of azo dye wastewater under high-salt conditions typical of textile effluents. The broad substrate oxidation potential of PersiLac3 was assessed across diverse temperatures, pH levels, and challenging conditions, such as high salt levels, and in the presence of organic solvents and inhibitors. Remarkably, PersiLac3 showed enhanced activity (112.25 %) in 3 M NaCl, highlighting its superior ability to adapt to saline conditions. Kinetic studies of PersiLac3 indicated high efficiency and affinity for its substrate at saline concentrations ranging from 1 to 6 M NaCl. PersiLac3 effectively decolorized the Congo red dye (82.9 %) in highly concentrated solutions (5000 mg/L) within 15 min, and its performance was further improved in the presence of wastewater-relevant ions, achieving 92.3 % dye removal. Monitoring real wastewater treatments, PersiLac3 reduced optical density, underscoring its potential for application in the bioremediation of dye-laden and saline wastewater streams. The adaptability of PersiLac3 to harsh, high-salinity environments, coupled with its rapid dye decolorization efficiency, is an innovative and powerful tool for addressing environmental pollution challenges and advancing waste treatment methodologies.

Efficient biodecolorization of direct black 22 Azo Dye by Aspergillus tamarii Kita UCP1279 isolated from caatinga soil

The textile industry is a major consumer of water, generating large volumes of wastewater contaminated with harmful substances, particularly azo dyes, which contain aromatic rings, amines, and sulfonic groups that contribute to their environmental toxicity. The use of microbial agents for wastewater treatment offers a cost-effective and sustainable solution, minimizing sludge production. Fungi from the Caatinga biome have demonstrated potential for bioremediation, especially under extreme environmental conditions. This study explores the ability of Aspergillus tamarii Kita to decolorize the azo dye Direct Black 22 (DB22) under varying conditions, including the use of both active and inactive fungal biomass, in static and agitated systems (120 rpm), at a controlled temperature of 30°C. Dye concentrations of 50, 125, and 250 mg/L were evaluated over time intervals of 75, 180, and 180 minutes, respectively. The influence of dissolved oxygen concentration and redox potential on the decolorization process was also investigated to identify optimal treatment conditions. Decolorization efficiency was quantified via spectrophotometric analysis. Results revealed decolorization rates of 100%, 97%, and 63% for the respective dye concentrations, with active biomass in agitated conditions achieving the highest removal rates. The study further demonstrated that dissolved oxygen levels and redox potential are critical factors in enhancing dye decolorization. These findings underscore the bioremediation potential of Aspergillus tamarii Kita in treating textile dye effluents, offering a promising approach to sustainable industrial wastewater management.

Evaluation of blue textile dye decolorization by immobilized polyphenol oxidase using pumice stone under optimum conditions

Industrial dyes are major pollutants in wastewater and river water with an initial visible concentration of 1 mg/L. Recent studies have shown the possibility of using polyphenol oxidase in catalytic biological treatment due to its ability to oxidize a large number of dyes and pollutants in wastewater and the flexibility to work in wide ranges of temperature, pH and salinity. It is easy availability as well as the low economic cost resulting from its use in biological treatments, this enzyme polyphenol oxidase was used. The findings in this study showed that the extraction of polyphenol oxidase (PPO) from potato peel was homogenized with potassium phosphate buffer (0.1 M, pH 7) at a ratio of 1:10 (weight: volume) for two min. The result of enzyme purification by ion exchange chromatography showed that the yield of this step was 64 % and the specific activity was 6541.67 U/mg. The polyphenol oxidase was immobilized covalently on the functionalized pumice stone (25.2 U/gm) compared with other methods. The characterization results demonstrated that the optimum pH for immobilized and free enzyme activity was 6.0 while the pH range of free and immobilized polyphenol oxidase stability was from 4.5 -7.0 and 3.5 - 8.5 respectively. The better temperature for free and immobilized polyphenol oxidase activity was 25 ºC, whereas the free and immobilized polyphenol oxidase was stable at 15-35 and 15-50 °C respectively. The outcomes showed that the decolorization efficiency of blue textile dye employing immobilized polyphenol oxidase reached 99.85 % after 24 hr. for 100 mg/L concentration while for other concentrations 200, 300, 400, 500 and 1000 mg/L the decolorization efficiencies were 85.96, 76.15, 72.54, 66.94 and 63.5 % respectively. Based on the results, the immobilized polyphenol oxidase on pumice stone is highly efficient in removing textile dyes at large concentrations and in different environmental conditions.

Enhancing Azo Dye Mineralization and Bioelectricity Generation through Biocathode-Microbial Fuel Cell Integration with Aerobic Bioreactor

This study explores the efficient decolorization and complete mineralization of the diazo dye Evans blue, using an integrated aerobic bioreactor system coupled with a double-chamber microbial fuel cell (DCMFC) including a bio-cathode and acetate as a cosubstrate. The research addresses the environmental challenges posed by dye-laden industrial effluents, focusing on achieving high decolorization efficiency and understanding the microbial communities involved. The study utilized mixed strains of actinomycetes, isolated from garden compost, to treat initial dye concentrations of 100 mg/L and 200 mg/L. Decolorization efficiency and microbial community composition were evaluated using 16S rRNA sequencing, and electrochemical impedance spectroscopy (EIS) was used to assess anode and DCMFC resistance. The results demonstrated decolorization efficiencies ranging from 90 ± 2% to 98 ± 1.9% for 100 mg/L and from 79 ± 2% to 87% ± 1% for 200 mg/L. An anode resistance of 12.48 Ω indicated a well-developed biofilm and enhanced electron transfer. The microbial community analysis revealed a significant presence of Pseudomonadota (45.5% in dye-acclimated cultures and 32% in inoculum cultures), with key genera including Actinomarinicola (13.75%), Thermochromatium (4.82%), and Geobacter (4.52%). This study highlights the potential of the integrated DCMFC–aerobic system, utilizing mixed actinomycetes strains, for the effective treatment of industrial dye effluents, offering both environmental and bioenergy benefits.

Interaction between the electrochemical properties of powdered activated carbon and the biochemical processes within bacteria in Azo dye biodecolorization: An explanatory mechanism

Drawing on prior reports highlighting the redox mediator properties of powdered activated carbon (PAC), this study was designed to evaluate these properties to enhance the decolorization of azo dye by Klebsiella quasipneumoniae GT7. It was found that the presence of 0.5 % PAC in the medium increased the biodecolorization rate early in incubation. Chemical analysis revealed that dye conversion into aromatic amines occurred in microbial systems both with and without PAC. However, at initial dye concentrations (Cid) of 2 mM or higher, some dye remained on the PAC surface and in the medium. In contrast, the PAC-free system achieved nearly 100 % biodecolorization at all initial dye concentrations. The negative impact of PAC on decolorization efficiency in microbial systems with high initial dye concentrations cannot be solely explained by its redox mediator function. This study used the amphoteric-Donnan model for PAC's electrical double layer (EDL) and Mitchell's chemiosmotic model for bacterial proton motive force (PMF) to explore this. It found that charge storage in PAC's EDL regulates electron transfer fluxes, and proton species enhance the proton motive force across the bacterial membrane. These observations improve the understanding of PAC's role in microbial decolorization and its potential future applications.

Fe78Si9B13/MnO2 composite: a magnetic and efficient Fenton-like catalyst in degradation of methyl orange under activation of H2O2

Abstract A magnetic and efficient Fe78Si9B13/MnO2 composite was successfully fabricated by a facile hydrothermal method. This composite was employed as a Fenton-like catalyst for the degradation of methyl orange (MO) under activation of H2O2. The phase and morphology of the composite were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The experimental results reveal that the theoretical mass loading of Fe78Si9B13/MnO2 composite and H2O2 dosage have a significant effect on MO degradation. Fe78Si9B13/MnO2 composite effectively improved MO oxidation ability and could quickly decolorize the MO to 99.7 %. Decolorization efficiency increased with increasing H2O2 concentration from 0 % to 1.15 %. Additionally, a possible reaction mechanism of the coupling system was proposed.

Nanoparticle-Mediated remediation of wastewater contaminants: An inclusive analysis of glyphosate, Congo red and methyl orange

New techniques in purification are called for because, currently pollutants found within the wastewater sources are known to have adverse effects of man health, agricultural productivity and industrial applications. The purpose of this research was to assess the efficiency of different synthesized NPs in the rteutal of glyphosate, Congo red and MO from aqueous solution using a glass column. To determine the concentration of these contaminants, two analytical techniques namely High-Performance Liquid Chromatography (HPLC) and UV–Visible spectrophotometry were used. The findings revealed that the community removal rates differed depending on nanoparticle type, treatment time and light intensity. Zinc oxide nanoparticles (ZONPs) were found to reduce the glyphosate concentration by 56.81 % under 100-watt light after 120 minutes. Iron oxide nanoparticles (IONPs) on the other hand were found to eliminate 62.63 % of glyphosate without the application of light for the same length of time, this figure rose to 87 % when 100-watt light was applied. ZONPs also decolourized 59 % Congo red after 4 h and the decolorization efficiency increased to 86 % when exposed to 30 watt light. Further, magnetic iron oxide nanoparticles (MIONPs) reduced MO by 23.81 % under 100-watt light for 120 minutes. This research demonstrates that NPs may have a future in regard to water treatment as agents which are efficient to high degree; and in part, the ZONPs are more effective in elimination of glyphosate while the IONPs may be better suited for the removal of Congo red. The evidence suggest that more attention should be paid to the characteristic of NPs, the treatment time, and the light intensity in case of employing the technology in water treatment.

Screening different solid supports for Pseudomonas aeruginosa biofilm formation and determining its efficiency for decolorization and degradation of congo red.

A global water crisis is emerging due to increasing levels of contaminated water and decreasing clean water supply on Earth. This study aims to address the removal of azo dye from wastewater to enable its reuse. Recently, utilizing microorganisms has been proven to be a practical choice for the remediation of azo dyes in wastewater. Hence, in this study, we employed a preformed biofilm of Pseudomonas aeruginosa on a solid support (called substrate) to degrade azo dyes. This process offers several advantages, such as stability, substrate portability, more biofilm production in less time, and efficient utilization of enzymes for remediation. From 50 ppm of initial Congo Red concentration, 75.74% decolorization was achieved within ten h using a preformed biofilm on a coverslip. A maximum of 52.27% decolorization was achieved using biofilm during its formation after 72h of incubation. The Fourier-transform infrared (FTIR) spectroscopic analysis of Congo Red dye before and after remediation revealed a significant change in peak intensity, indicating dye degradation. Phytotoxicity studies performed by seed germination with Vigna radiata revealed that, after 5-7 days, almost 40% more seeds with longer root and shoot lengths were germinated in the presence of treated dye compared to the untreated one. This data indicated that the harmful Congo Red was successfully degraded to a non-toxic product by Pseudomonas aeruginosa biofilm grown on a glass substrate.

Eco-benevolent synthesis of ZnO-NPs and ZnO-MFs from Inula oculus-christi L. (Asteraceae) with effective antioxidant, antimicrobial, DNA cleavage, and decolorization efficiencies.

As a result of the changes occurring globally in recent years, millions of people are facing challenging and even life-threatening diseases such as cancer and the COVID-19 pandemic, among others. This phenomenon has spurred researchers towards developing and implementing innovative and environmentally friendly scientific methods, merging disciplines with significant technological potential, such as nanotechnology with medicinal plants. Therefore, the focus of this research is to synthesize zinc nanoparticles (ZnO-NPs) and microflowers (ZnO-MFs) using extracts of the medicinal plant I. oculus christi prepared in n-hexane and methanol as new bioreduction and capping agents through a simple and environmentally friendly chemical approach. Optical, thermal, and morphological structural analyses of ZnO-NPs and ZnO-MFs were conducted using Ultraviolet-Visible (UV-Vis) spectroscopy, Fourier Transform Infrared (FT-IR) spectroscopy, Thermogravimetric Analysis (TGA), and Field Emission Scanning Electron Microscopy (FE-SEM). Metabolic profiles of extracts from different plant parts were analyzed using Gas Chromatography-Mass Spectrometry (GC-MS) and supported by visualization of contents through Principal Component Analysis (PCA), hierarchical cluster analysis heatmaps, and Pearson correlation graphs. Interestingly, ZnO-NPs and ZnO-MFs exhibited strong antioxidant properties and demonstrated particularly potent antimicrobial activity against Micrococcus luteus NRRL B-4375, Escherichia coli ATCC 25922, and Candida albicans ATCC 10231 strains compared to standard antibiotics. Furthermore, ZnO-NPs and ZnO-MFs showed excellent plasmid DNA-cleavage activity of pBR322 with increasing doses. The photocatalytic performance of the synthesized ZnO-NPs and ZnO-MFs was evaluated for methylene blue (MB), congo red (CR), and safranin-O(SO) dyes, demonstrating remarkable color removal efficiency. Overall, the results provide a promising avenue for the green synthesis of ZnO-NPs and ZnO-MFs using I. oculus-christi L. inflorescence and pappus extracts, potentially revolutionizing biopharmaceutical and catalytic applications in these fields.

Standardization of silver nanoparticle synthesis: Photocatalytic application (immobilized with chitosan complex) with textile dyes and antibacterial activity against Staphylococcus aureus using banana pseudo stem

The purpose of the study is to standardize the silver nanoparticle (BP-AgNPs) synthesis and its antibacterial activity and photocatalytic application with the selected dyes using the banana pseudo stem extract. “One-factor analysis (OFTA)” was carried out for the standardization of silver nanoparticle synthesis and nanoparticle-chitosan complex immobilization. The parameters were identified with plant quantity (20 g), silver nitrate concentration (1 mM), the ratio of plant extract and silver nitrate solution (2:8), pH (12), temperature (37 °C), dispersed light conditions, shaking conditions (120 rpm), and time (6 h) were analysed. The photocatalytic decolorization efficiency of the standardized BP-AgNPs (immobilized with chitosan complex) has shown 96.92% for methylene blue (10 ppm) at 3 h and 97.55% for safranin (100 ppm) at 15 h. The antibacterial activity for the synthesised BP-AgNPs was determined. MIC value of the BP-AgNPs was determined to be 15.62 μg. mL−1 for S. aureus. The synthesised BP-AgNPs treated with 0.5×, 1× and 2× MIC concentration (x = 15.62 μg. mL−1) showed decreased viable counts of S. aureus (99.6% at 2× concentration having viable count of 22.6 × 102 CFU. mL−1) at 24 h incubation when compared with the control culture. The structural characteristics of the BP-AgNPs were identified as spherical with SEM and the size was identified as 12.19 ± 1.62 nm with TEM and as 37.23 ± 17.89 nm with XRD. The parameters such as FTIR, Zeta potential, EDS further supports the nanoparticle synthesis with banana pseudostem extract. The current result suggested that, the silver nanoparticles (BP-AgNPs) synthesised using the extract of the banana pseudo stem could be used as an alternative source for dye decolorization and antibacterial activities.

Activation of Peroxymonosulfate using a novel heterogeneous catalyst SO-gCN@ZIF-67 for excellent degradation of Brilliant Green dye

This work presents a design of a novel heterogeneous catalyst, SO-gCN@ZIF-67, comprising Co-based MOF, ZIF-67, over a two-dimensional S and O co-doped graphitic carbon nitride nanosheet is reported. This novel heterogeneous SO-gCN@ZIF-67 catalyst is used to degrade organic polluting dyes by activating Peroxymonosulfate (PMS) at room temperature. Various analytical and spectroscopic techniques, such as PXRD, FT-IR, FE-SEM, EDS, HR-TEM, XPS, and UV-DRS, were employed to characterize the as-synthesized nano-catalyst. The as-prepared catalyst can activate PMS effectively to rapidly decolorize the Brilliant Green dye (BG dye) solution at room temperature. The catalyst SO-gCN@ZIF-67 showed high efficiency for PMS activation and decolorization of approximately 96.7 % BG dye with a catalyst concentration of 80.0 mg/L, which was achieved in 15 min. The degradation of the dye obeyed pseudo-first-order kinetics with a reaction rate constant of 0.2262 min−1. Further, the parameters that could influence the activation of PMS, such as the role of different catalysts, catalyst dosage, PMS dosage, and initial dye concentration, were also investigated. Radical trapping experiments revealed that O2− radicals and non-radical singlet oxygen, 1O2, were involved in the degradation of BG dye. A plausible mechanism for the degradation has been proposed using SO-gCN@ZIF-67 and the PMS system.

Carbon-Based Materials in Combined Adsorption/Ozonation for Indigo Dye Decolorization in Constrain Contact Time.

This study presents a comprehensive evaluation of catalytic ozonation as an effective strategy for indigo dye bleaching, particularly examining the performance of four carbon-based catalysts, activated carbon (AC), multi-walled carbon nanotubes (MWCNT), graphitic carbon nitride (g-C3N4), and thermally etched nanosheets (C3N4-TE). The study investigates the efficiency of catalytic ozonation in degrading Potassium indigotrisulfonate (ITS) dye within the constraints of short contact times, aiming to simulate real-world industrial wastewater treatment conditions. The results reveal that all catalysts demonstrated remarkable decolorization efficiency, with over 99% of indigo dye removed within just 120 s of mixing time. Besides, the study delves into the mechanisms underlying catalytic ozonation reactions, elucidating the intricate interactions between the catalysts, ozone, and indigo dye molecules with the processes being influenced by factors such as PZC, pKa, and pH. Furthermore, experiments were conducted to analyze the adsorption characteristics of indigo dye on the surfaces of the materials and its impact on the catalytic ozonation process. MWCNT demonstrated the highest adsorption efficiency, effectively removing 43.4% of the indigo dye color over 60 s. Although the efficiency achieved with C3N4-TE was 21.4%, which is approximately half of that achieved with MWCNT and less than half of that with AC, it is noteworthy given the significantly lower surface area of C3N4-TE.