Methyl Orange Dye Research Articles

Effect of percentage of methanol on micellization position of mixed surfactant interaction in the absence and presence of dye

The interaction behavior of mixed surfactant-dye systems, i.e., anionic surfactant sodium dodecyl sulfate (SDS), cationic surfactant cetyl pyridinium chloride (CPC), and dye methyl orange (MO) was investigated through the allocation of micelles using conductivity measurements. Conductivity as a function of surfactant concentration was monitored to calculate the critical micelle concentration (CMC). The conductivity increased sharply as the surfactant content increased, according to the results. Moreover, the conductivity rises with temperature, whereas it falls with increased methanol (CH3OH). CH3OH-H2O mixed solvent media containing 0 %, 10 %, 20 %, and 30 % of CH3OH at 298.15, 308.15, and 318.15 K to work out the basic micelle fixation, gives significant understanding to the arrangement of the mixed surfactants. The CMC and degree of micellar dissociation (α) of SDS with CPC increase in the CH3OH and H2O mixture. The CMC and α values are increased by increasing the temperature. Various thermodynamic parameters, i.e. Standard free energy of micellization (ΔGmo), Standard enthalpy of micellization (ΔHmo), and Standard entropy of micellization (ΔSmo) were computed in SDS-CPC without MO. ΔGmo values for SDS-CPC in the presence of MO results in micellization more probable with MO.

Aspergillus versicolor mediated biofabrication of zinc phosphate nanosheets for exploring their antimycotic activity and development of alginate-based nanocomposite for enhanced dye degradation

The production of novel, suitable, and cost-effective nanocomposites are highly required for its prospective application in the remediation of environmental pollutants and as antimycotic agents. Zinc phosphate nanosheets (ZP-ns) were fabricated by harnessing the exometabolites of Aspergillus versicolor and then incorporated within an alginate biopolymer (ZP-ns@Alg) to improve the biosorptive removal of the methyl orange (MthO) dye from its aqueous solution. For the very first time, the antimycotic activity of the green synthesized ZP-ns was unveiled. The mycelial growth inhibition was obtained in a dose-dependent manner with significant (P < 0.05) behavior compared to the control plates. The biosorption conditions using ZP-ns@Alg microbeads were optimized using the response surface methodology-based central composite design (RSM-CCD) to maximize the biosorption efficiency. The highest biosorptive efficiency was achieved at pH 4.0, biosorption dosage 0.07 g, contact time 50 min, dye concentration 100 mg/l, and shaking speed 100 rpm. The equilibrium data were more tailored to the pseudo-second order (PS) model with an R2 of 0.9955 and a Langmuir isotherm (R2 = 0.9945) with a maximum biosorptive capacity (qmax) of 166.95 mg/g and an average RL value of 0.0003, indicating favorable biosorption. The removal capacity was reduced to ∼90 % after the 6th cycle, which is a robust signal that the developed biosorbent microbeads could be recycled and regenerated for a prolonged time. These results marked the application of ZP-ns as a novel antimycotic agent with excellent activities. Microbeads, made from low-cost biopolymers, can be applied to remediating environmental pollutants from wastewater.

Construction of Visible light Driven Z-Scheme 1D/1D p-CuBi2O4/n-CdWO4 Heterojunction Nanocomposite for Effective Degradation of Organic Pollutants

The effective separation and harnessing of photoinduced charge carriers in photocatalysis are significant challenges. The present study aims to overcome this obstacle by developing a Z-Scheme heterojunction between a p-type CuBi2O4 (CBO) and a n-type CdWO4 (CWO) through a straightforward heat treatment method. The powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and High-resolution transmission electron microscopy (HRTEM) results revealed the successful formation of heterostructures. The photocatalytic efficiency of the materials was assessed by selecting an anionic methyl orange (MO) and cationic Rhodamine-B (Rh-B) dyes under visible light irradiation. Among all the materials, 85 wt.% CBO+ 15 wt.% CWO (CBO/CWO-15) heterostructure exhibited superior photocatalytic activity (90%) corresponding to 90 and 45 times higher than the pristine CBO and CWO, respectively. The positively charged photocatalyst surface attracts a greater number of MO dye molecules than Rh-B, thereby enhancing the degradation of MO over Rh-B. The scavenger results confirmed the involvement of hydroxy ( and superoxide () radicals in the degradation of MO. The rate constant of CBO/CWO-15 (0.01061 min-1) was 64 and 39 times higher than those of CBO (0.00016 min-1) and CWO (0.00027 min-1), respectively. The photoluminescence (PL) and electrochemical impedance spectroscopy (EIS) analyses substantiated the improved charge separation in the CBO/CWO-15 composite, establishing the Z-scheme mechanism. Cycling experiments over four cycles demonstrated consistent stability of the CBO/CWO-15 composite. The study provides an in-detail plausible mechanism of MO degradation. This type of Z-scheme composite material has potential applications in environmental remediation for the effective removal of organic pollutants and antibiotics from wastewater.

Enhanced photocatalytic removal of methyl orange dye employing SiO2/Mn2O3 based nanocatalyst under visible light

Surface water contamination by dye pollutants is a global environmental concern. The treatment of effluent from textile waste using metal oxide-based photocatalysts is a widely employed approach owing to its efficacy and simplicity. Herein, the synthesis and fabrication of novel visible radiation receptive manganese oxide and mesoporous silica nanocomposites (Mn2O3/SiO2) is described. Surface morphology of nanocomposites using scanning electron microscopy (SEM) displayed spherical shaped agglomerated structure. The chemical composition of nanocomposites was examined by using energy dispersive x-ray (EDX) analysis respectively indicating the presence of respective elements. Structural analysis was carried out by using XRD spectroscopy, while optical properties were evaluated by employing UV–visible spectroscopy. The photocatalytic activity of pure Mn2O3 and SiO2 nanoparticles as well as their nanocomposites with two different ratios Mn2O3/SiO2 (1:3) and Mn2O3/SiO2 (3:1) were evaluated by using methyl orange (MO) as a model dye. The band gap energy of Mn2O3/SiO2 (1:3) and Mn2O3/SiO2 (3:1) nanocomposite was 2.39 eV and 1.69 eV respectively. The nanocomposites exhibited improved photocatalytic efficiency as compared to pure nanoparticles as a function of pH and mixing ratio. For instance, at pH 7.0, Mn2O3/SiO2 (1:3) nanocomposite has depicted maximum degradation efficiency of 68 % for degradation of MO as compared to Mn3O4/SiO2 (3:1) nanocomposite, Mn3O4 and SiO2 nanoparticles. However, at pH 2.0 Mn2O3/SiO2 (3:1) nanocomposite had shown maximum degradation efficiency of 99 % as compared to Mn2O3/SiO2 (1:3), Mn2O3 and SiO2 nanoparticles. The degradation reaction followed pseudo first order kinetics. At pH 7.0, the rate constant values of nanocomposites i.e. Mn2O3/SiO2(1:3) and Mn2O3/SiO2(3:1) comes out to be 4.68 × 10−3 min−1 and 2.49 × 10−3 min−1 respectively. At pH 2.0, the rate constant values calculated for Mn2O3/SiO2(1:3) nanocomposite and Mn2O3/SiO2(3:1) nanocomposite was 4.91 × 10−3 min−1 and 1.24 × 10−2 min−1 respectively. The easy fabrication of these nanocomposites coupled with facile tuning of their properties make them suitable contenders for efficient dye degradation in wastewater treatment.

Elimination of Methyl Orange Dye with Three Dimensional Electro-Fenton and Sono-Electro-Fenton Systems Utilizing Copper Foam and Activated Carbon

Elimination of Methyl Orange Dye with Three Dimensional Electro-Fenton and Sono-Electro-Fenton Systems Utilizing Copper Foam and Activated Carbon

Methyl Orange Dye Removal by Dimethylamine Functionalized Graphene Oxide

Graphene oxide (GO) functionalized with dimethylamine (DMA) was successfully prepared using a facile technique. GO was first synthesized using the modified Hummers method, followed by chemical functionalization with DMA in the presence of an electrophilic linker, i.e., epichlorohydrin (ECH). FTIR analysis of the end product ascertains the successful synthesis of GO as well as its functionalization with DMA. Typical characteristic peaks attributed to GO and DMA are clearly discernible in the spectrum. The effect of pH, adsorbent dosage, dye concentration, and contact time towards methyl orange (MO) dye removal was studied and reported herein. In summary, enhanced adsorption of methyl orange was observed for DMA functionalized GO compared to GO alone. 90% removal was observed with 10 mg/L of MO concentration, pH = 2 at temperature 25 °C and 5 mg of adsorbent. Modelling study shows that the pseudo-second-order kinetic model and Freundlich isotherm model provide better fitness to the experimental data.

One-step hydrothermal synthesis of ternary heterostructure stannic sulfide - bismuth sulfide - bismuth oxychloride (SnS2-Bi2S3-BiOCl) composite loaded on carbon felt for highly efficient piezocatalytic degradation of organic dyes and antibiotics

The piezoelectric catalysis technique harnesses naturally occurring vibrational energy to remove organic pollutants from water in an environmentally friendly manner. In this study, a ternary heterostructure SnS2-Bi2S3-BiOCl (S-B-B) composite was successfully synthesized via a one-step hydrothermal method and simultaneously deposited on the surface of carbon felt. The S-B-B heterojunction exhibits significantly enhanced piezoelectric catalytic activity compared to SnS2, Bi2S3, and BiOCl, achieving a k value of 2.26 × 10⁻² min⁻¹ and a degradation efficiency of 89.9 % towards methyl orange (MO) dye after 100 min of ultrasonic degradation. This performance is markedly superior to the individual components, with k values of 3.80 × 10⁻⁴ min⁻¹ for SnS2, 1.16 × 10⁻² min⁻¹ for BiOCl, and 1.31 × 10⁻² min⁻¹ for Bi2S3. Moreover, in addition to levofloxacin (LV), it demonstrates high removal efficiency for Congo red (CR), methylene blue (MB), tetracycline hydrochloride (TC-HCl), and sulfanilamide (SN). Furthermore, it can be loaded onto carbon felt for use in piezoelectric catalytic degradation of dyeing wastewater, highlighting its potential for practical applications. Trapping experiments suggest that singlet oxygen non-radicals and hydroxyl radicals play a critical role in the piezocatalytic degradation of organic contaminants. Based on LC-MS results, a possible degradation pathway for MO dye is proposed. Furthermore, DFT calculations confirm electron transfer from Bi2S3 to SnS2 and BiOCl at the interfaces between SnS2/Bi2S3 and BiOCl/Bi2S3. The piezoelectric mechanism of the S-B-B composite is also elucidated, highlighting the interaction and electron dynamics within the heterostructure.

Morphology controlled fabrication of porous magnesium oxide nanostructures for the efficient elimination of methyl orange

Abstract Magnesium oxide-based adsorbents (MGO-A) with different morphologies were synthesized via the hexamethylene tetramine-assisted hydrothermal method. The role of four anions in the reaction system, chloride (Cl⁻), nitrate (NO3 ⁻), sulfate (SO4 2⁻), and acetate (C2H3O2 2⁻) was systematically investigated to determine the properties of the MgO. Standard characterization techniques were used, such as X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and surface area and pore size interpretations. The kinetics and adsorption isotherm were studied for removal of the dye methyl orange. The dye’s rapid removal led to equilibrium being reached within 5 min. The correlation coefficient values indicate more applicability of pseudo-second-order kinetics than the pseudo-first-order kinetics. Both physisorption and chemisorption can be a pathway towards successfully removing methyl orange. The adsorption isotherm shows that the maximum capacity of the material is very high, 1,062 mg/g for MGO-A. In light of these results, it appears this material holds promise as a dye removal material.

Poly(methyl methacrylate) functionalized graphene oxide/CuO as nanocomposite for efficient removal of dye pollutants

In this research, the use of a three-component nanocomposite of graphene oxide-methyl methacrylate and copper(II) oxide (PMMA-GO-CuO) was investigated. The aim of synthesizing this nanocomposite is to removal dye pollutants, specifically methylene blue (MB) and methyl orange (MO), which are commonly used in dyeing industries, through adsorption. The study focuses on creating GO-CuO and PMMA-GO-CuO nanocomposites as effective adsorbents. A simple and quick method led to the development of the PMMA-GO-CuO nanocomposite, which shows enhanced physical and chemical properties. Key materials include graphene oxide, methyl methacrylate, and copper(II) oxide nanoparticles. Characterization techniques such as FT-IR, XRD, SEM, and TGA were used to analyze the nanocomposite. Results indicate that dye adsorption is more effective at lower pH levels, suggesting that the PMMA-GO-CuO nanocomposite can efficiently remove dyes from industrial wastewater. The experimental data showed that the Langmuir isotherm model accurately represented the equilibrium adsorption, with maximum capacities of 285.71 mg g−1 for methylene blue and 256.41 mg g−1 for methyl orange, indicating a single layer of adsorption. The kinetics followed a pseudo-second order model, suggesting that the adsorption process involves chemical bonding. Additionally, thermodynamic parameters (ΔG°, ΔH°, and ΔS°) indicated that the adsorption is spontaneous. The adsorption mechanism involves hydrogen bonding, π-π interactions, and electrostatic interactions. This study investigates how factors like pH, temperature, contact time, and dye concentration affect the adsorption of methyl orange and methylene blue dyes. A PMMA-GO-CuO nanocomposite was used, achieving 84% removal of MB and 35% removal of MO from industrial wastewater. This study highlights the promising potential of PMMA-GO-CuO nanocomposite as an effective material for the removal of dye pollutants from industrial wastewater. The results showed that the graphene oxide in the composite is effective for removing cationic dyes due to its negative charge. Further research will focus on the optimization of the synthesis process with the aim of achieving competitive performance of this nanocomposite on a large scale. These findings not only advance the field of nanocomposite materials but also provide a practical solution to an important environmental issue, demonstrating the innovation of the present study in the literature.

Influence of Pd, Pt and Au nanoparticles in the photocatalytic performance of N-TiO2 support under visible light.

In this article, we report the modification and photocatalytic evaluation of commercial TiO2-P25 under visible light for methyl orange (MO) dye degradation under visible light. The activity of materials doped with N, Pd, Pt and Au on to the TiO2-P25 was evaluated, with optimal photocatalytic performance achieved using Au nanoparticles doped on an N-functionalized titania surface. X-ray diffraction (XRD), physical nitrogen adsorption/desorption isotherm curves, transmission electron microscopy (TEM), diffuse reflectance spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) were used to study the structural and textural properties of the samples. The chemical species present in the bulk and surface of the catalysts were identified using X-ray photoelectron spectroscopy (XPS) and microwave plasma-atomic emission spectroscopy. The results show that Au/N-TiO2 photocatalyst presents a remarkable enhanced activity for MO dye degradation, under visible light illumination, reaching 100% after 4 h. The enhanced photocatalytic activity using this composite is attributable to the well-dispersed and small size of Au nanoparticles, large surface area, reduction of band-gap energy and the interaction between nitrogen and Au which promoted a synergistic effect. This article is part of the discussion meeting issue 'Green carbon for the chemical industry of the future'.

Flower-like nickel oxide nanostructures: Superior ammonia gas sensing and efficient dye removal behavior under UV–visible light illumination

In this study, we fabricated the NiO nanostructures using a straightforward solvothermal technique. The NiO nanoparticles were characterized using various analytical techniques. The FESEM images clearly show the flower-like structure of NiO nanoparticles. These nanostructures were then employed as a sensor to detect the presence of highly toxic ammonia (NH3) gas. The flower-shaped nanostructures of NiO played a vital role in improving sensing performance. Moreover, the NiO sensor displayed rapid response to 100 ppm ammonia at room temperature, with responses/recovery times of 40 s/44 s. This research holds promise as a viable approach for effectively sensing and detecting NH3 gas. The NiO exhibited excellent photocatalytic activity and degradation rates of 80% and 84.75% for Methyl orange (MO) and methylene blue dye (MB) respectively under UV-visible light irradiation. The NiO nanoflower remains unaffected after recycling MB dye degradation. This effective photocatalytic performance might be due to the formation of flower-like morphology. This underscores the potential of NiO as a promising candidate for applications in environmental and healthcare safety applications.

Exploration of laser-assisted chemical bath for enhancing synthesis of undoped and nickel-doped zinc oxide and its potential applications in water purification and mitigating antimicrobial resistance

This study aims to explore the antimicrobial and photocatalytic efficiencies of pure and Ni-doped ZnO nanostructures produced via Laser-assisted Chemical Bath Synthesis (LACBS) to develop sustainable solutions for water treatment and pathogen control amid the global water crisis exacerbated by climate change and environmental pollution. Utilizing zinc acetate dihydrate and hexamethylenetetramine, the nanostructures were synthesized with Ni doping levels of 0.0 %, 1.5 %, 3.0 %, and 4.5 %, targeting their promising photocatalytic and antimicrobial properties to combat contaminants from pharmaceuticals, agriculture, and industries. Morphological analyses using Scanning Electron Microscopy showed a transition from hexagonal particles to nanoflowers, enhancing photocatalytic activity due to increased surface-to-volume ratio. X-ray Diffraction confirmed the hexagonal wurtzite structure, with variations in peak intensities indicating improved crystallinity with Ni doping. Energy Dispersive X-ray analysis verified the purity and successful incorporation of Ni. Photocatalytic assessments indicated up to 99.24 % degradation of Methylene Orange dye under blue laser irradiation within 60 minutes, correlating with Ni content. Antimicrobial tests demonstrated effective inhibition of pathogens such as Escherichia coli, Staphylococcus aureus, and additional strains like Candida albicans and Klebsiella pneumonia, with increasing zones of inhibition corresponding to higher Ni levels, extending up to 37 mm. The results underscore the dual functionality of ZnO nanostructures for applications in sustainable water treatment and antimicrobial controls, highlighting the need for future studies to examine the impacts of further increased doping concentrations on the material properties and efficacy.

A novel organic-inorganic hybrid hollow polymer capsule with rich amino/imino groups for anionic contaminant removal in wastewater: Synthesis, performance and mechanism

Herein, we developed a new organic-inorganic hybrid polymer adsorbent, termed PECP, by one-step precipitation polycondensation between polyethyene polyamine and hexachlorocyclotriphosphazene. The morphology and microstructure of PECP were investigated by FTIR, SEM, TEM, XPS, XRD and N2 adsorption. Results show PECP owned a hollow capsule structure and lots of amino/imino groups. The adsorption capacity of PECP for anionic dye methyl orange (MO) was up to 1031.9 mg g-1. The adsorption process was very fast. After five cycles, the adsorption capacity of PECP for MO still remained at 89 % of the initial adsorption capacity. Meanwhile, PECP delivered a high adsorption capacity for other anionic contaminants like acid chrome blue K (1003.5 mg g-1), congo red (1152.2 mg g-1) and diclofenac sodium (914.2 mg g-1). In the binary systems contaminated with double dyes, the separation factors of MO for methylene blue, Rhodamine B and crystal violet were up to 450.8, 55.4 and 355.9, respectively. The experimental data unveiled that the MO removal by PECP was very consistent with the pseudo-second-order kinetic model and the Langmuir isotherm model. The removal process was spontaneous and endothermic. FTIR spectroscopy and XPS analysis confirmed the role of electrostatic force and hydrogen bond on the adsorption of MO on PECP.

Sodium alginate-supported AgSr nanoparticles for catalytic degradation of malachite green and methyl orange in aqueous medium

Abstract In the last few years, metal nanoparticles (NPs) have become one of the major components in the field of nanotechnology. NPs with fascinating and tunable properties (size and shape) have provided solutions for many problems including water pollution which has now become alarming in the current era. Herein, natural polymer-supported AgSr bimetallic NPs have been synthesized. For this purpose, sodium alginate (Na-Alg) was used as a stabilizer along with sodium borohydride (NaBH4) as a reducing agent. The synthesized Na-Alg-supported AgSr NPs were characterized employing UV–Vis, FTIR, SEM, and XRD techniques. The spectrophotometric analysis confirmed the formation and SEM and XRD confirmed the size of NPs up to 24.18 and 12.95 nm, respectively. These NPs were tested for catalytic degradation potential against malachite green (MG) and methyl orange (MO) dyes in the aqueous medium. The catalytic activity of NPs was evaluated in terms of kinetics and percent removal of the dyes. The results revealed that the MO dye was degraded in 21 min with a removal efficiency of 86.45% and MG dye in 24 min with 91.74%. Catalytic degradation of MO and MG dyes was also monitored in the absence of AgSr NPs which showed no catalytic degradation of dyes even after half an hour. The study has confirmed that biopolymer-supported NPs can be synthesized with suitable morphology for catalytic applications and these NPs can be further used for the removal of dyes from aqueous medium.

Development of a novel lightweight brick-activated carbon based BiVO4 photocatalyst and its adsorption-photocatalytic behavior for toxic dye removal in wastewater

The purpose of this research was to develop a novel photocatalyst by loading BiVO4 (BVO) particles on lightweight brick-activated carbon (LWB-AC). The characterizations of as-prepare samples were studied using X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV–VIS –NIR spectrophotometer (UV-VIS-NIR) techniques. The adsorption-photocatalytic methylene blue (MB) removal, methyl orange (MO) removal and rhodamine B (RhB) removal of the as-prepared LWB-AC based BVO photocatalyst were tested by irradiating visible light. The results showed that the LWB-AC based BVO photocatalyst exhibited the highest adsorption-photocatalytic efficiency for the removal of MB, MO and RhB dyes under visible light irradiation as compared to the other samples. This might be due to the synergistic effect between AC and BVO on the surface of LWB. Moreover, the presence of both AC and BVO on the surface of LWB helped in preventing the electron-hole recombination, resulting in the enhanced adsorption-photocatalytic activity. For reusability tests, the LWB-AC based BVO photocatalyst did not show the loss of adsorption-photodegradation ability of MB, MO and RhB dyes after five runs. A probable adsorption-photodegradation mechanism of LWB-AC based BVO photocatalyst was also proposed.

Rational design of Zn4O(BDC)3 metal organic framework incorporated with NiCr2O4 nanoparticles: An affordable photocatalyst for the degradation of hazardous dyes

In this work, a simple hydrothermal approach was used to make Zn4O(BDC)3-NiCr2O4 nanocomposite. The structural, morphological and photophysical properties of the prepared samples were used to evaluate various characterization approaches. The Zn4O(BDC)3-NiCr2O4 nanocomposite appears to have a large surface area and increased absorption of visible light. When compared to pure Zn4O(BDC)3 and NiCr2O4, the Zn4O(BDC)3-NiCr2O4 nanocomposite displayed more effective catalytic activity for degradation of methyl orange (MO) and Rhodamine (Rh B) dye from aqueous solution when exposed to visible light. The Zn₄O(BDC)₃-NiCr₂O₄ nanocomposite achieved degradation efficiencies of 93.75 % and 89.91 % for MO and Rh B dyes, respectively, after 210 and 150 minutes of visible light irradiation. The degradation rate for MO was 0.016 min⁻¹, which is approximately 6.66 times and 3.13 times higher than that of pure Zn₄O(BDC)₃ or NiCr₂O₄ nanoparticles, respectively. In addition, the Zn4O(BDC)3-NiCr2O4 nanocomposite showed high structural stability after the degradation test, and most of its photocatalytic activity was retained even after the recycling examination. Moreover, the radical trapping experiments demonstrated that the major active species including superoxide and hydroxyl radicals played main roles in the photocatalytic process. Additionally, the photocatalytic mechanism of Zn4O(BDC)3-NiCr2O4 nanocomposite has been examined, and a more plausible path of hazardous dye degradation has been provided.

Facile synthesis of novel cobalt molybdenum sulfide-graphitic carbon nitride (CoMoS4/g-C3N4) nanocomposite electrode for improved supercapacitor and photocatalytic applications

Supercapacitors have gained significant attention from scientists due to their wide range of applications in energy storage devices. However, searching for abundant and eco-friendly materials on earth is still necessary while preserving their outstanding performance. Herein, cobalt molybdenum sulfide-graphitic carbon nitride (CoMoS4/g-C3N4) nanocomposite was synthesized to explore an exceptional electrode material for energy and photocatalytic applications. The structural analysis, vibrational modes, and porosity within the CoMoS4/g-C3N4 nanocomposite were studied by XRD, Raman, and SEM. The direct energy band gap decreased from 2.54 to 2.44 eV along with the increased ratio of CoMoS4 in the nanocomposite. The electrochemical measurements of CoMoS4/g-C3N4 nanocomposite exhibited an excellent specific capacitance (Cp) of 3675 F/g at 1 mV/s and 3150 F/g at 2.5 A/g with noticeable specific energy density (Eg) of 109.4 Wh/kg, high power density (Pd) of 625 W/kg and retain high capacitance (88 % of its initial value) even after 4000 cycles. Furthermore, the photocatalytic results revealed that high photodegradation efficiency (97.85 %) was attained against methyl orange (MO) dye under UV light irradiation. Prepared electrode materials are promising materials for next-generation energy storage and environmental applications.

Chemical and green synthesized Co/Ni-doped hematite nanoparticles for enhancing the photocatalytic and antioxidant properties

This research focuses on developing environmentally friendly and economically viable Co/Ni-doped hematite nanoparticles (HNPs) through both chemical and green synthesis methods and evaluated their potential for biomedical and environmental applications. The chemical synthesis employs polyvinylpyrrolidone (PVP), while the green approach utilizes Azadirachta indica (A. indica) leaf extract as a stabilizing agent. Co/Ni-doped HNPs are crystalline size ranging from 14 to 21 nm, morphology analysis revealed that the NPs exhibited a quasi-spherical, with an average particle size ranging from 15.98 to 25.91 nm, and dopants confirmed to contain by the XPS spectra. VSM study explains magnetic parameters, coactivity, residual magnetism, and magnetization. A. indica plants contain quinones, saponins, glycosides, alkaloids, and flavonoids. Characterization of the nanoparticles reveals optimized Co/Ni-doped HNPs with enhanced photocatalytic activity. These nanoparticles exhibit a remarkable 93%–95% degradation of UV-reactive dyes (methyl orange and methylene blue) within 90 min, attributed to structural and surface modifications that improve light absorption and enhance charge separation. The study concludes that green-synthesized Co/Ni-doped HNPs outperform chemically synthesized counterparts as superior photocatalysts. Additionally, antioxidant evaluations using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and nitric oxide (NO) assays suggest significant antioxidant capabilities. A high scavenging activity percentage, ranging from 83% to 88%, was observed, which increased with higher concentrations of the synthesized Co/Ni-doped HNPs making these nanoparticles suitable for biomedical and environmental applications that require a magnetic system. In this study, the IC50 values for the antioxidant activity of chemically and green synthesized Co/Ni-doped hematite nanoparticles against the DPPH/NO assay were calculated to be 18.33 μg ml−1 and 16.09 μg ml−1, respectively. The research highlights the multifunctional properties of Co/Ni-doped HNPs, addressing the demand for tailored inorganic magnetic nanoparticles with minimal ecological impact.

Self-Assembled Nanostructure of Ionic Sn(IV)porphyrin Complex Based on Multivalent Interactions for Photocatalytic Degradation of Water Contaminants.

[Sn(H2PO4)2(TPyHP)](H2PO4)4∙6H2O (2), an ionic tin porphyrin complex, was synthesized from the reaction of [Sn(OH)2TPyP] (1) with a dilute aqueous solution of a polyprotic acid (H3PO4). Complex 2 was fully characterized using various spectroscopic methods, such as X-ray single-crystal crystallography, 1H NMR spectroscopy, elemental analysis, FTIR spectroscopy, UV-vis spectroscopy, emission spectroscopy, EIS mass spectrometry, PXRD, and TGA analysis. The crystal structure of 2 reveals that the intermolecular hydrogen bonds between the peripheral pyridinium groups and the axially coordinated dihydrogen phosphate ligands are the main driving force for the supramolecular assembly. Simultaneously, the overall association of these chains in 2 leads to an open framework with porous channels. The photocatalytic degradation efficiency of methyl orange dye and tetracycline antibiotic by 2 was 83% within 75 min (rate constant = 0.023 min-1) and 75% within 60 min (rate constant = 0.018 min-1), respectively. The self-assembly of 2 resulted in a nanostructure with a huge surface area, elevated thermodynamic stability, interesting surface morphology, and excellent catalytic photodegradation performance for water pollutants, making these porphyrin-based photocatalytic systems promising for wastewater treatment.

Enhanced photocatalytic and antimicrobial properties of nickel-doped barium M-type hexaferrites synthesized via citrate sol-gel method

Industrial activities release waste into aquatic sources, which is hazardous because of the pathogenic and cytotoxic behaviour of the contaminants present in the effluent. To address this issue, the citrate sol-gel auto-combustion method synthesized nickel-substituted barium M-type hexaferrites BaNixFe12−xO19 (x = 0.0, 0.1, 0.2) nanoparticles. The nanoparticles show the single-phase hexaferrite structure having a crystallite size of 52.47 to 49.30 nm with the space group P63/mmc. Magnetic study of nanoparticles indicates that increased nickel ions give rise to saturation magnetization, whereas coercivity decreases. The band gap values of the pure and Ni-doped barium hexaferrites determined by Tauc plots have been noticed to range from 1.42 eV to 1.26 eV. The photocatalytic activity of nanoparticles for methyl orange (MO) dye has been investigated. The nanoparticles have shown a dye degradation efficiency of 84.5 % within 100 min. The antimicrobial properties of the synthesized nanoparticles have also been studied. The effectiveness of synthesized nanoparticles against two types of bacteria, gram-positive Staphylococcus aureus and gram-negative Escherichia coli, as well as against two pathogenic fungi, Candida albicans and Aspergillus niger, has been investigated. The antibacterial effect has been demonstrated by all samples at all concentrations, with MIC values ranging from 1 to 4 mg/ml. Therefore, this study investigates the potential applications of nickel-doped barium M-type hexaferrites nanoparticles in real-world biological settings, suggesting their promising role in fighting against bacterial and fungal infections.