Activity For Degradation Of Dye Research Articles

Reduced Work Function in Anatase ⟨101⟩ TiO2 Films Self-Doped by O-Vacancy-Dependent Ti3+ Bonds Controlling the Photocatalytic Dye Degradation Performance.

TiO2 has the proven capability of catalytically decomposing pollutants under light illumination, thereby embracing potential applications in wastewater management. The photocatalytic dye degradation activity is largely controlled by the optical band gap that dictates the extent of electron-hole pair generation via photon absorption, and the recombination kinetics of charges. In this context, the material's work function governs how easily the charge carriers can be transferred at the dye-adsorbed photocatalytically active sites. Accordingly, nanocrystalline TiO2 thin films are grown in the anatase phase with ⟨101⟩ orientation, using RF magnetron sputtering at 200 °C. Besides studying the film's structural morphology, optical band gap, and elemental composition, the electronic properties are extensively investigated. The work function of the material was controlled by varying the O-vacancy-dependent Ti3+ bonding configuration in the network. It has been demonstrated how the photocatalytic methylene blue dye degradation activity of the nanocrystalline TiO2 films of predominantly the anatase phase improves on reducing the sputtering pressure during deposition. At a low deposition pressure of 20 mTorr, a low work function of ∼4.2 eV of the film, resulting from the formation of a Ti3+-bond through the O vacancies in the network, potentially increases its carrier lifetime and delivers the superior photocatalytic activity (∼82.7% dye degradation with a rate constant of k ∼ 0.0073 min-1) via silently facilitating fast electron transfer from the photocatalyst to the dye in the aqueous solution. The higher stoichiometric film prepared at p = 40 mTorr exhibits an inferior photocatalytic activity (∼20.4% dye degradation with a rate constant of k ∼ 0.0009 min-1), as retarded by its higher work function of ∼4.62 eV, despite retaining a relatively low band gap. Thus, without using any heterojunction or extrinsically doped photocatalyst, the dye degradation can be controlled simply by reducing the work function of nanocrystalline TiO2 thin films via controlling the O-vacancy-dependent Ti3+ bonding in its self-doped network.

Bio-capped multifunctional CuO nanoparticles via Knautia arvensis for dye removal, antibacterial and antifungal efficiency, and molecular docking

Copper oxide nanoparticles (CuONPs) synthesized using Knautia arvensis flower extract in an environmentally friendly and one-step procedure were characterized by UV–vis, FT-IR, SEM and DLS. The in vitro antibacterial and antifungal activities of CuONPs were determined using E. coli, S. aureus and A. niger. In silico antibacterial and antifungal evaluation of CuONPs were performed by molecular docking analysis using chitin deacetylase of A. niger, topoisomerase IV of E. coli and tyrosyl-tRNA synthetase of S. aureus. The best binding energy was determined using these microbial targets in molecular docking analyses and the antimicrobial mechanisms between the microorganism and the CuONP were elucidated. The degradation potential of Remazol brilliant blue R (RBBR) and Napthol blue black (NBB) dyes in the presence of CuONPs were investigated. The peak obtained at 289 nm as a result of UV–vis analysis revealed the presence of CuONPs. The spherical morphology of CuONPs and the particle size varying between 88–289 nm were visualized by SEM. DLS analysis pointed out the mean diameter of CuONPs was 189 nm along with the PDI value of 0.324. The 600 and 595 cm−1 vibrations attained in the FT-IR spectroscopy showed the presence of CuONPs. In addition, the presence of phenolic compounds found in the plant extract responsible for bio-capping of copper ions into CuONPs were enlightened by the FT-IR analysis. Dye degradation activity of CuONPs was found as 69% and 71% using NBB and RBBR at 50 °C in 90 min, respectively. Antifungal and antibacterial interactions of CuONPs with chitin deacetylase of A. niger, topoisomerase IV of E. coli and tyrosyl-tRNA synthetase of S. aureus were analyzed in order to reveal the antimicrobial mechanisms of CuONPs and it was found that CuONPs demonstrate significant interactions with those proteins with binding energies −7.25, −7.14 and −7.89 kcal mol−1, respectively.

Environmentally friendly silver nanoparticles synthesized from Verbascum nudatum var. extract and evaluation of its versatile biological properties and dye degradation activity.

In the present study, green synthesis of silver nanoparticles (VNE-AgNPs) via Verbascum nudatum extract was carried out for the first time. The synthesized AgNPs were characterized by different spectral methods such as UV-vis, FTIR, XRD, TEM, and EDAX. According to TEM analyses, the average size range of AgNPs was 17-21nm, and the dominant peaks in the 111°, 200°, 221°, and 311° planes in the XRD pattern indicated the Ag-NPs FCC crystal structure. FTIR data showed that VNE-AgNPs interacted with many reducing, capping, and stabilizing phytochemicals during green synthesis. VNE-AgNPs had higher antibacterial activity against S. aureus and E. coli bacterial strains with a maximum inhibition zone of 21 and 18mm, respectively, than penicillin 5IU, used as a positive control in the study. The cytotoxic effect of VNE-AgNPs appeared at a concentration of 50µg/mL in L929 cells and 5µg/mL in cancer (A549) cells. When the impact of VNE-AgNPs and C-AgNPs on inflammation was compared, it was found that VNE-AgNPs increased TNF-α levels (333.45 ± 67.20ng/mg-protein) statistically (p < 0.05) more than TNF-α levels (256.92 ± 27.88ng/mg-protein) in cells treated with C-AgNPs. VNE-Ag-NPs were found to have a degradation efficiency of 65% against methylene blue (MB) dye within 3h.

Gum karaya polymer-based biodegradable silver nanocomposite hydrogel through green approach for photocatalytic dye degradation and antimicrobial activity

The rise in industrialization and population growth has elevated water pollution to a critical environmental concern. This study introduces a novel polymer-mediated silver nanocomposite hydrogel for antibacterial activity and photocatalytic dye degradation for environmental remediation. In this study, silver nanocomposite hydrogels were developed using Karaya gum (KG), acrylamide, N-isopropyl acrylamide (NI), and 2-Bismethacryloyloxy ethyl phosphate (BMEP) as a crosslinker through a radical polymerization process. These hydrogels were utilized as templates for the eco-friendly synthesis of silver nanoparticles by employing an aqueous Canthium leaf extract as a reducing and stabilizing agent. Various analytical methods, including FTIR, UV–Vis, XPS, FESEM, EDX, XRD, AFM, and HRTEM, are characterized by the green synthesized KG-NIB-Ag nanocomposite hydrogel. Evaluation of the KG-NIB-Ag hydrogel involved examining its chemical composition, morphology, size, crystallinity, surface properties, bandgap, and chemical purity. TEM analysis validated an average crystallite size 33.2 nm. Moreover, the photocatalytic performance of the green-synthesized KG-NIB-Ag nanocomposite hydrogel was utilized to examine the degradation of Congo red dye under visible light irradiation. The findings of this study demonstrate that the degradation efficiency of CR reached approximately 73.25 % within 90 min, with a corresponding kinetic rate constant of 0.032 min−1. Furthermore, the antibacterial efficacy of the Ag nanocomposite hydrogel was evaluated against both Staphylococcus aureus and Escherichia coli. The disc diffusion method was employed to assess its antibacterial activity, and the diameter of the inhibition zones was measured. This study introduces an innovative and influential strategy for environmental remediation, emphasizing the potential of KG-NIB-Ag nanocomposite hydrogel in tackling ecological challenges associated with wastewater treatment across various industries.

Green Synthesis of Reduced Graphene Oxide Using the Tinospora cordifolia Plant Extract: Exploring Its Potential for Methylene Blue Dye Degradation and Antibacterial Activity.

Graphene has attracted significant attention recently due to its unique mechanical, electrical, thermal, and optical properties. The present study focuses on synthesizing green rGO using the Tinospora cordifolia plant extract by mixing it in a suspension of graphene oxide. The plant extract of T. cordifolia acts as a reducing agent and is cost-effective, renewable, and eco-friendly. Green-synthesized rGO (G-rGO) was characterized using FTIR, HR-SEM, EDX, and HR-XRD analyses. G-rGO consists of nanosheets with an average width of approximately 30 nm. G-rGO has a range of hydrodynamic radius (270-470) nm and an average ζ potential of -29.9 mV. Further, G-rGO was used as a nanoadsorbent for optimal exclusion of methylene blue (MB) dye using the response surface methodology (RSM). Adsorption results confirmed 94.85% MB dye removal with 58.81 mg g-1 adsorption capacity at optimum conditions. The G-rGO's antibacterial activity was also tested against Staphylococcus aureus (Gram-positive) and Escherichia coli (Gram-negative) bacteria, finding the exhibited zone of inhibition of 10, 11, and 15 mm and 10, 13, and 17 mm at 20, 40, and 80 μg mL-1 concentrations of G-rGO, respectively.

Cu-chelated polydopamine nanozymes with laccase-like activity for photothermal catalytic degradation of dyes

The industrial applications of enzymes are usually hindered by the high production cost, intricate reusability, and low stability in terms of thermal, pH, salt, and storage. Therefore, the de novo design of nanozymes that possess the enzyme mimicking biocatalytic functions sheds new light on this field. Here, we propose a facile one-pot synthesis approach to construct Cu-chelated polydopamine nanozymes (PDA-Cu NPs) that can not only catalyze the chromogenic reaction of 2,4-dichlorophenol (2,4-DP) and 4-aminoantipyrine (4-AP), but also present enhanced photothermal catalytic degradation for typical textile dyes. Compared with natural laccase, the designed mimic has higher affinity to the substrate of 2,4-DP with Km of 0.13 mM. Interestingly, PDA-Cu nanoparticles are stable under extreme conditions (temperature, ionic strength, storage), are reusable for 6 cycles with 97 % activity, and exhibit superior substrate universality. Furthermore, PDA-Cu nanozymes show a remarkable acceleration of the catalytic degradation of dyes, malachite green (MG) and methylene blue (MB), under near-infrared (NIR) laser irradiation. These findings offer a promising paradigm on developing novel nanozymes for biomedicine, catalysis, and environmental engineering.

Immobilized lipase enzyme on green synthesized magnetic nanoparticles using Psidium guava leaves for dye degradation and antimicrobial activities.

Zinc ferrite nanoparticles (ZnF NPs) were synthesized by a green method using Psidium guava Leaves extract and characterized via structural and optical properties. The surface of ZnF NPs was stabilized with citric acid (CA) by a direct addition method to obtain (ZnF-CA NPs), and then lipase (LP) enzyme was immobilized on ZnF-CA NPs to obtain a modified ZnF-CA-LP nanocomposite (NCs). The prepared sample's photocatalytic activity against Methylene blue dye (MB) was determined. The antioxidant activity of ZnF-CA-LP NCs was measured using 1,1-diphenyl-2-picryl hydrazyl (DPPH) as a source of free radicals. In addition, the antibacterial and antibiofilm capabilities of these substances were investigated by testing them against gram-positive Staphylococcus aureus (S. aureus ATCC 25923) and gram-negative Escherichia coli (E. coli ATCC 25922) bacterial strains. The synthesized ZnF NPs were discovered to be situated at the core of the material, as determined by XRD, HRTEM, and SEM investigations, while the CA and lipase enzymes were coated in this core. The ZnF-CA-LP NCs crystallite size was around 35.0nm at the (311) plane. Results obtained suggested that 0.01g of ZnF-CA-LP NCs achieved 96.0% removal of 5.0ppm of MB at pH 9.0. In-vitro zone of inhibition (ZOI) and minimum inhibitory concentration (MIC) results verified that ZnF-CA-LP NCs exhibited its encouraged antimicrobial activity against S. aureus and E. coli (20.0 ± 0.512, and 27.0 ± 0.651mm ZOI, respectively) & (1.25, and 0.625μg/ml MIC, respectively). ZnF-CA-LP NPs showed antibiofilm percentage against S. aureus (88.4%) and E. coli (96.6%). Hence, ZnF-CA-LP NCs are promising for potential applications in environmental and biomedical uses.

Enhanced Visible Light Photocatalytic Activity of Exfoliated Boron‐TiO2 Composite for Degradation of Rhodamine B and Nitrogen Fixation

AbstractThe design of an efficient, recyclable, visible light photocatalytic system was examined as a viable new green way to address environmental challenges such as removal of pollutants from wastewater and N2 fixation. The exfoliated boron (Bexf)‐Titanium oxide (TiO2) composite visible light active photocatalysts were successfully constructed via a simple wet chemical method by utilizing acetone as a solvent. The composite was evaluated for the photodegradation of Rhodamine B (RhB) dye and reduction of N2, which exhibits improved photocatalytic activity for degradation of RhB as well as for reduction of N2. Experiments with different quenchers indicate that the photogenerated superoxide radical anion (O2⋅−) plays a significant role in the degradation of RhB as well as for N2 reduction reactions. The composite catalyst shows good photostability and there is no significant reduction of the catalyst activity for dye degradation up to 4 cycles of reaction. This work affords a significant view into the design of reusable TiO2 composite materials for photocatalytic RhB degradation and nitrogen fixation.

Antioxidant and dye degradation activity of green synthesized silver-iron oxide (Ag-Fe2O3) bimetallic nanoparticles

This research introduces an eco-friendly method for synthesizing silver-iron oxide bimetallic nanoparticles using cabbage peel extract, serving as both reducing and stabilizing agents. The successful production of nanoparticles is comprehensively analyzed through UV-Vis spectroscopy, Fourier transformation infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). The UV, XRD and EDS results indicated the elemental composition of Ag and Fe, suggesting the formation of a silver-core iron-shell bimetallic nanoparticles with a size of 22.3 nm, which was followed by an assessment of their antioxidant and catalytic properties. The findings revealed notable antioxidant capabilities, along with the efficient degradation of methyl red and phenol red dye. Remarkably, the Ag-Fe2O3 bimetallic nanoparticles exhibited good scavenging activity, reaching 63.87% at a concentration of 1000 µg/mL. The most significant dye degradation is observed for phenol red, achieving a remarkable 78% degradation within just 8 minutes. These results indicate the potential of Ag-Fe2O3 bimetallic nanoparticles derived from cabbage peels as promising agents for antioxidant and catalytic applications, especially in addressing dye-contaminated wastewater concerns.

Green synthesis of silver nanoparticles from Hibiscus tiliaceus L. Leaves and their applications in dye degradation, antioxidant, antimicrobial, and anticancer activities

The present study reports the green synthesis of silver nanoparticles (AgNPs) from aqueous extract of Hibiscus tiliaceus L. leaves and their application in dye degradation, antioxidant, antimicrobial, and anticancer activities. Analysis using Fourier transform infrared (FT-IR) spectroscopy revealed that plant metabolite functional groups had a role in the reduction and stability of AgNPs, and X-ray crystallography (XRD) demonstrated that the AgNPs were in crystal form. The UV–vis spectroscopy, dynamic light scattering (DLS), and zeta potential investigations revealed that the AgNPs were formed with an average size of 88.10 nm in colloidal form and were stable (-49 mV). The field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM) confirmed the shape and size of the AgNPs as spherical with a particle size of 30 - 35 nm, respectively. The AgNPs exhibited potential antioxidant activity by total antioxidant, DPPH, and reducing power assays. The biosynthesized AgNPs displayed a wide range of antibacterial activity on Gram-ve and Gram+ve bacteria by the zone of inhibition assay. AgNPs showed good anticancer activity on MCF-7 cells with an IC50 value of 65.83 µg/mL. Furthermore, AgNPs acted as potential catalysts in combination with the reducing agent sodium borohydride (NaBH4) for the degradation of methylene blue (MB), methylene orange (MO), and methylene green (MG) dyes. The degradation efficiency of catalyst AgNPs in the attendance of NaBH4 for 15 min was noted to be 12.8 %, 26.92 %, and 47.56 % for MO, MB, and MG, respectively. The study concluded that green synthesized AgNPs could be highly applicable as an antioxidant, antimicrobial, and anticancer agents in the biomedical field. Furthermore, AgNPs could be helpful in the remediation of dye effluents.

Design, fabrication, and analysis of Bi2O3/MnO2 hybrid nanomaterials for advanced photocatalytic applications

This research work describes a novel strategy for fabricating Bi2O3/MnO2 hybrid nanomaterials using a sonication synthesis method. Extensive characterization techniques, such as UV–Vis, PL, FTIR, SEM, XRD, photocatalytic activity of dye degradation, indicate the successful decorating of MnO2 nanoparticles on the surface of Bi2O3, resulting in well-defined Bi2O3/MnO2 hybrid nanocomposites. The photocatalytic performance of the synthesized materials in degrading methylene blue (MB) and tetracycline (TC) under visible light irradiation was investigated. The results show a considerable increase in photocatalytic activity when compared to pristine Bi2O3. Because of the special heterojunction structure of the optimized sample Bi2O3/MnO2-5, which further enables efficient separation of photogenerated electron-hole pairs as well as enhancing visible-light absorption, the hybrid nanocomposites have demonstrated remarkable photocatalytic effectiveness, with the optimized sample achieving maximum degradation of 83% for MB and 78% for TC within 120 min. Photocatalytic recycling experiments, Scavenger tests and XRD analysis are used to identify the reactive oxygen species (ROS) involved in photocatalytic activity and to confirm the stability of the optimized sample. Recyclability studies further revealed that the catalyst may be reused up to five cycles, indicating that it has the potential to be a long-term environmental cleanup solution. In summary, our work highlights the great promise of Bi2O3/MnO2 hybrid nanomaterials for enhanced photocatalytic applications, while also contributing to our knowledge of these materials. The study's comprehensive characterization and optimization techniques provide a substantial contribution to the area and open up the possibility for further advancements in energy conversion, ecological environmental remediation technologies and paves a way for manufacturing innovation.

Biosynthesis of zirconia nanoparticles (ZrO2) by water hyacinth: characterization and its photocatalytic dye degradation activity

Biosynthesis of zirconia nanoparticles (ZrO2) by water hyacinth: characterization and its photocatalytic dye degradation activity

Biogenic synthesis, characterization and photocatalytic activity of cerium nanoparticles for treatment of dyes contaminated water

In this study, Murraya Koenigii leaf extract mediated cerium oxide nanoparticles (Ce-NPs) were synthesized using an eco-friendly approach. The surface morphology, elemental composition, surface functional groups, crystal structure and thermal stability of the synthesized Ce-NPs were examined using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-Ray diffraction (XRD) and thermogravimetric (TGA) analysis. The synthesized Ce-NPs were evaluated for their photocatalytic activity with respect to degradation of methylene blue dye (MBD) and acid orange-7 dye (AO7D) aqueous solution in the presence of sunlight. The dye degradation activity of the developed Ce-NPs was analyzed by the analysis of absorbance in treated and untreated aqueous dyes solution using UV–Vis spectrophotometer. The result of the study inferred that Ce-NPs have promising photocatalytic degradation ability (>98 %) for both AO7D and MBD (concentration = 10 mg L−1 of each dye) within 100 min exposure to sunlight.

Improved photocatalytic activity for degradation of methylene blue dye using ZnO NPs

We present a plant-mediated green synthesized bare ZnO and Ni–ZnO NPs (nanoparticles) employing soursop leaf extract. The plant extract was treated with 0.1 M of Zn (NO3)2·6H2O The ZnO NPs have a wurtzite structure, according to XRD measurements. The mean size of the ZnO and Ni–ZnO NPs was examined to be 47.64 and 48.18 nm using an X-ray diffraction (XRD) pattern. The UV–visible spectrum displays absorbance maxima at 335 and 340 nm, which corresponds to an energy band gap of 3.28 and 3.24 eV for ZnO and Ni–ZnO NPs. Morphology studies show that the NPs are very permeable. The PL spectra of NPs revealed extremely intriguing blue, green, and red emissions following excitation at 391, 491 and 545 nm for ZnO and Ni–ZnO NPs, respectively. When exposed to UV light, the NPs exhibit photocatalytic efficacy for the reduction of methylene blue (MB) dye.

Au9 clusters deposited as co-catalysts on S-modified mesoporous TiO2 for photocatalytic degradation of methyl orange

Au9 nanoclusters (Au9 NCs) were deposited onto S-functionalized mesoporous TiO2 (SMTiO2) to produce efficient photocatalysts for Methyl Orange (MO) dye degradation with UV light. The morphology, the surface composition and the size of the deposited Au9 NCs of the catalyst was analysed. SMTiO2 could adsorb more clusters with lesser Au9 cluster agglomeration than unmodified MTiO2. This finding is attributed to the capability of the thiol groups to form strong bonds with the Au9 clusters. To study Au9 NCs effect on dye degradation activity, the MO degradation reaction constants under UV-light irradiation for SMTiO2 nanoparticles (NPs) and Au9 NCs decorated SMTiO2 photocatalysts were studied, which were 0.07 min−1 and 0.149 min−1, respectively. Hence, it takes almost half the time to completely degrade MO using Au9 NCs decorated SMTiO2 photocatalysts compared to SMTiO2 substrate. Results were analysed using the response surface methodology (RSM) to study the interaction between the reaction parameters.

Retraction Note: A New Porous Metal–Organic Framework Constructed from 2, 5-Thiophenedicarboxylate and Melamine Ligands: Catalysis Dye Degradation and Anti-tumor Activity in Myocardioma

Retraction Note: A New Porous Metal–Organic Framework Constructed from 2, 5-Thiophenedicarboxylate and Melamine Ligands: Catalysis Dye Degradation and Anti-tumor Activity in Myocardioma

Ferrocene carboxylic acid-doped copper MOFs as a nanozyme with high peroxidase-mimicking activity for catalytic dye degradation

A ferrocene carboxylic acid-doped copper–p-phthalic acid metal–organic framework material (Fc–Cu PTA) as a nanozyme exhibited high peroxidase-mimicking activity for catalytic dye degradation, while Cu PTA showed nearly no peroxidase-mimicking activity.

Shaddock peel-loaded CeO2 composites with peroxidase-like activity for dye degradation and trace detection of ascorbic acid

A new strategy was proposed to prepare the peroxide mimicase Ce@CSP by growing CeO2 in pomelo peel, which was used to degrade dye and detect ascorbic acid.

Nanoparticle synthesis advancements and their application in wastewater treatment: A comprehensive review

The global water crisis requires effective wastewater treatment methods where conventional approaches often face challenges related to cost, recyclability, efficiency, and overall effectiveness. In this regard, the significantly small size, large surface area, and enhanced photocatalytic properties of recently developed nanoparticles have opened new avenues for wastewater treatment. This comprehensive review focuses on recent advancements in the synthesis methods for different types of nanoparticles and nanocomposites based on metals, carbon, polymers, waste materials, and zeolites which have highly sustainable and innovative results in wastewater treatment. The introduction of silver and gold nanoparticles has enhanced photocatalytic and biological activities. Similarly, zeolite and seaweed composites have exhibited efficient dye degradation capabilities. Eco-friendly carbon soot nanoparticles have shown promising biological activities, while nitrogen-doped carbon quantum dots have exhibited long-term stability for various applications. Additionally, waste material-based calcium oxide nanoparticles and carbon quantum dot-carbon nanotube nanocomposites have also shown enhanced dye degradation activities.

Simple co-precipitation synthesis of activated carbon-cobalt ferrite (AC-CoFe2O4) nanocomposites: enhanced photocatalytic dye degradation and antimicrobial activity

Abstract In this present work, spinel cobalt ferrite nanoparticles (CoFe2O4 NPs) and activated carbon-CoFe2O4 nanocomposites (AC-CoFeO4 NCs) were synthesized by simple co-precipitation method and used for photocatalytic dye degradation (PCD) of rhodamine-B (Rh-B) dye. The antimicrobial study of the as-synthesized CoFe2O4 NPs was also performed. The as-synthesized CoFe2O4 NPs and AC-CoFe2O4 NCs were analyzed by ultraviolet spectroscopy (UV), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) studies, scanning electron spectroscopy (FE-SEM) techniques. Powder XRD analysis showed that the as-synthesized CoFeO4 NPs and AC-CoFeO4 NCs had average particle size of 18 nm and 46 nm, respectively. The FE-SEM showed that the CoFe2O4 samples have sphere like morphology and were well decorated on activated carbon in order to provide high surface area. AC-CoFe2O4 NCs have effectively used for the PCD of Rh-B dye with high efficiency. Furthermore, spinel CoFe2O4 NPs acted as a more effective antimicrobial agent against Gram-negative and Gram-positive bacterial strains. Moreover, AC-CoFe2O4 NCs can be used as the precursor materials for supercapacitor, sensors etc.