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Water contamination is a serious issue that has an impact on the whole globe. In the current work, adsorption technique was used to remove synthetic Reactive Blue MEBF 222 textile dye utilizing Cd-doped Co (Co1 - xCd1.5xFeO3), Zn-doped Co (Co1 - xZn1.5xFeO3), Cr-doped Co (Co1 - xCr1.5xFeO3), Zn-doped Ni (Ni1 - xZn1.5xFeO3), and Cr-doped Ni (Ni1 - xCr1.5xFeO3) perovskites, synthesized by sol-gel auto-combustion approach. According to the findings of batch adsorption studies, maximum adsorption was observed at pH 3 (45.62 mg/g), 0.01 g/50 ml dosage (36.67 mg/g), 60 min (14.31 mg/g), 100 ppm dye concentration (47.41 mg/g), and 308 K (35.96 mg/g) for Co1 - xCd1.5xFeO3; at 3 pH (42.94 mg/g), 0.01 g/50 ml dosage (35.33 mg/g), 60 min (12.88 mg/g), 100 ppm dye concentration (40.52 mg/g), and 308 K (31.31 mg/g) for Co1 - xZn1.5xFeO3; at 2 pH (38.82 mg/g), 0.01 g/50 ml dosage (32.20 mg/g), 60 min (11.98 mg/g), 100 ppm dye concentration (33.54 mg/g), and 308 K (29.34 mg/g) for Co1 - xCr1.5xFeO3; at 2 pH (34.97 mg/g), 0.01 g/50 ml dosage (30.41 mg/g), 60 min (10.46 mg/g), 100 ppm dye concentration (27.19 mg/g), and 308 K (26.12 mg/g) for Ni1 - xZn1.5xFeO3; and at 2 pH (31.22 mg/g), 0.01 g/50 ml dosage (25.04 mg/g), 60 min (9.48 mg/g), 100 ppm dye concentration (21.73 mg/g), and 308 K (23.61 mg/g) for Ni1 - xCr1.5xFeO3. The pseudo-second-order model showed good fitness for adsorption kinetic data. Electrolytes, detergents/surfactants, and heavy metal ions had a substantial impact on the adsorption potential. The column adsorption experiments demonstrated optimal bed height, flow rate, and intake dye concentration to be 3 cm, 1.8 ml/min, and 70 mg/l, respectively, in the column experiment. With an adsorption capacity of 44.1 mg/g, reactive blue (RB) 222 dye was able to achieve its maximum adsorption. Detailed desorption of RB 222 dye was also achieved. The novelty of this adsorption method lies in its eco-friendliness, ease of handling, and cost-effectiveness.

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Silica-based scaffolds are promising in Tissue Engineering by enabling personalized scaffolds, boosting exceptional bioactivity and osteogenic characteristics. Moreover, silica materials are highly tunable, allowing for controlled drug release to enhance tissue regeneration. In this study, we developed a 3D printable silica material with controlled mesoporosity, achieved through the sol-gel reaction of tetraethyl orthosilicate (TEOS) at mild temperatures with the addition of different calcium concentrations. The resultant silica inks exhibited high printability and shape fidelity, while maintaining bioactivity and biocompatibility. Notably, the increased mesopore size enhanced the incorporation and release of large molecules, using cytochrome C as a drug model. Due to the varying surface charge of silica depending on the pH, a pH-dependent control release was obtained between pH 2.5 and 7.5, with maximum release in acidic conditions. Therefore, silica with controlled mesoporosity could be 3D printed, acting as a pH stimuli responsive platform with therapeutic potential.

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The abstract highlights the global issue of environmental contamination caused by organic compounds and the exploration of various methods for its resolution. One such approach involves the utilization of titanium dioxide (TiO2) as a photocatalyst in conjunction with natural adsorption materials like kaolin. The study employed a modeling-based approach to investigate the sustainable photocatalytic degradation of acidic dyes using a Jordanian nano-kaolin-TiO2 composite material and solar energy. Mechanistic insights were gained through the identification of the dominant reactive oxygen species (ROS) involved in the degradation process, as well as the synergetic effect between adsorption and photocatalysis. The Jordanian nano-kaolin-TiO2 composite was synthesized using the sol-gel method and characterized. The nanocomposite photocatalyst exhibited particle sizes ranging from 27 to 41 nm, with the TiO2 nanoparticles well-dispersed within the kaolin matrix. The efficacy of this nanocomposite in removing Congo-red dye was investigated under various conditions, including pH, initial dye concentration, and photocatalyst amount. The optimal conditions for dye removal were found to be at pH 5, with an initial dye concentration of 20 ppm, and using 0.1 g of photocatalyst, resulting in a 95 % removal efficiency. The mechanistic insights gained from this study indicate that the hydroxyl radicals (•OH) generated during the photocatalytic process play a dominant role in the degradation of the acidic dye. Furthermore, the synergetic effect between the adsorption of the dye molecules onto the photocatalyst surface and the subsequent photocatalytic degradation by the ROS was found to enhance the overall removal efficiency. These findings contribute to the fundamental understanding of the photodegradation mechanisms and guide the development of more efficient photocatalytic systems for the treatment of acidic dye-containing wastewater. The use of solar power during the purification procedure also leads to cost reduction and strengthens sustainability efforts.

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The Gd-doped ZnO/SnO2 nanocomposites with various atomic percentages (0, 0.5, 0.8, and 1.2 at%) of gadolinium (coded as GdZS0, GdZS1, GdZS2, and GdZS3) was synthesis via the sol-gel method and explored for photodegradation against dye solutions exposing solar light irradiation. The synthesized nanocomposites were characterized employing the XRD, FTIR, FE-SEM, Raman spectroscopy, BET analysis and UV-Vis spectrophotometer. The FE-SEM results indicated that the formation of nanoparticles to nanoflowers covered with Gd ions was observed with an increased doping concentration of Gd. The optical bandgap was evaluated and found in the range of 3.21-3.27 eV for GdZS nanocomposites. The GdZS nano-photocatalysts were investigated against the degradation of different organic dyes and GdZS3 shows the highest degradation efficiencies of 99.3%, 98.3% and 99.4% towards MO, MB and RhB dyes, respectively at neutral pH in aqueous media. Before and after photodegradation. Biological oxygen demand and chemical oxygen demand tests to make estimations of mineralization. The investigations are very promising for the degradation process in rare earth doped metal oxide nanocomposites. A plausible photodegradation mechanism of synthesized nanocomposites under investigation has also been proposed.

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Blue-emitting bismuth-doped lanthanum oxide (La2O3: Bi3+) with various concentrations of Bi was synthesized using the sol-gel combustion method and used for visualization of latent fingerprints (LFPs). An X-ray diffraction (XRD) study revealed the hexagonal structure of the phosphors and total incorporation of the bismuth in the La2O3 matrix. Field Emission Scanning Electron Microscopy (FE-SEM) and Fourier Transform Infrared Spectroscopy (FTIR) were used to study the morphology and the relative vibrations of the synthesized samples. Photoluminescence (PL) studies showed strong blue emission around 460 nm due to the 3P1 → 1S0 transition. Clear bright-blue fingerprint images were obtained with the powder dusting method on various surfaces like aluminum, compact discs, glass, wood and marble. A first evaluation of these images indicated a clear visualization of all three levels of details and a very high contrast ranging from 0.41 on marble to 0.90 on aluminum. As a further step, we used an algorithm for extracting fingerprint minutiae with which we succeeded in detecting all three levels of fingerprint details and even the most difficult ones, like open and closed pores. According to these analyses, La2O3: Bi phosphor is demonstrated to be an effective blue fluorescent powder for excellent visualization of latent fingerprints.

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In recent years, the demand for natural and synthetic zeolites has surged due to their distinctive properties and myriad industrial applications. This research aims to synthesise crystalline zeolites by co-recycling two industrial wastes: salt slag (SS) and rice husk ash (RHA). Salt slag, a problematic by-product of secondary aluminium smelting, is classified as hazardous waste due to its reactive and leachable nature, though it is rich in aluminium. Conversely, RHA, an abundant and cost-effective by-product of the agro-food sector, boasts a high silicon content. These wastes were utilised as aluminium and silicon sources for synthesising various zeolites. This study examined the effects of temperature, ageing time, and sodium concentration on the formation of different zeolite phases and their crystallinity. Results indicated that increased Na+ concentration favoured sodalite (SOD) zeolite formation, whereas Linde type-A (LTA) zeolite formation was promoted at higher temperatures and extended ageing times. The formation range of the different zeolites was defined and supported by crystallographic, microstructural, and morphological analyses. Additionally, the thermal behaviour of the zeolites was investigated. This work underscores the potential to transform industrial waste, including hazardous materials like salt slag, into sustainable, high-value materials, fostering efficient waste co-recycling and promoting clean, sustainable industrial production through cross-sectoral industrial symbiosis.

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This article describes the synthesis of a hydrophobic protective coating for concrete based on a silane derivative of fatty acids. The coating was obtained through a thiol-ene click addition reaction using methyl oleate and 3-mercaptopropyltrimethoxysilane in the presence of the photoinitiator 2,2-dimethoxy-2-phenylacetophenone (DMPA). This reaction proved to be more efficient compared with other tested (photo)initiators, considering the double bond conversion of oleate. The coating was applied to concrete using two methods: immersion and brushing. Both methods exhibited similar consumption of methyl oleate-based silane (UVMeS) at approximately 20 g/m2. The hydrophobic properties of the coatings were evaluated based on the contact angle, which for the modified surfaces was above 93°, indicating their hydrophobic nature. The penetration depth of the silane solution into the concrete was also studied; it was 5-7 mm for the immersion method and 3-5 mm for the brushing method. The addition of tetraethoxysilane (TEOS) to the silane solution slightly improved the barrier properties of the coating.

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Semiconductor oxides are frequently used as active photocatalysts for the degradation of organic agents in water polluted by domestic industry. In this study, sol-gel ZnO thin films with a grain size in the range of 7.5-15.7 nm were prepared by applying a novel two-step drying procedure involving hot air treatment at 90-95 °C followed by conventional furnace drying at 140 °C. For comparison, layers were made by standard furnace drying. The effect of hot air treatment on the film surface morphology, transparency, and photocatalytic behavior during the degradation of Malachite Green azo dye in water under ultraviolet or visible light illumination is explored. The films treated with hot air demonstrate significantly better photocatalytic activity under ultraviolet irradiation than the furnace-dried films, which is comparable with the activity of unmodified ZnO nanocrystal powders. The achieved percentage of degradation is 78-82% under ultraviolet illumination and 85-90% under visible light illumination. Multiple usages of the hot air-treated films (up to six photocatalytic cycles) are demonstrated, indicating improved photo-corrosion resistance. The observed high photocatalytic activity and good photo-corrosion stability are related to the hot air treatment, which causes a reduction of oxygen vacancies and other defects and the formation of interstitial oxygen and/or zinc vacancies in the films.

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The use of heterogeneous catalysts to increase the development of green chemistry is a rapidly growing area of research to save industry money. In this paper, mesoporous SiO2-Al2O3 mixed oxide supports with various Si/Al ratios were prepared using two different sol-gel routes: hydrolytic sol-gel (HSG) and non-hydrolytic sol-gel (NHSG). The HSG route was investigated in both acidic and basic media, while the NHSG was explored in the presence of ethanol and diisopropyl ether as oxygen donors. The resulting SiO2-Al2O3 mixed oxide supports were characterized using EDX, N2 physisorption, powder XRD, 29Si, 27Al MAS-NMR and NH3-TPD. The mesoporous SiO2-Al2O3 supports prepared by NHSG seemed to be more regularly distributed and also more acidic. Consequently, a simple one-step NHSG (ether and alcohol routes) was selected to prepare mesoporous and acidic SiO2-Al2O3-NiO mixed oxide catalysts, which were then evaluated in ethylene oligomerization. The samples prepared by the NHSG ether route showed better activity than those prepared by the NHSG alcohol route in the oligomerization of ethylene at 150 °C.

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Protein therapeutics, vaccines, and other commercial products are often sensitive to environmental factors, such as temperature and long-term storage. In many cases, long-term protein stability is achieved by refrigeration or freezing. One alternative is the encapsulation of the protein cargo within an inert silica matrix (ensilication) and storage or transport at room temperature as a dry powder. In this paper, we test the effect of three commonly used biological buffers on the ensilication, storage, and desilication of the enzyme lysozyme. We show that ensilication protects lysozyme from heat (100 °C for 1 h) and during storage (18 months at room temperature). The choice of ensilication buffer has little effect on the activity of lysozyme after desilication. Our results provide confidence in the continued pursuit of ensilication as a methodology for protein stabilisation and in its compatibility with biological buffers.

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In this work, Co0.5Zn0.5LaxFe2-xO4 (0.00 ≤ x ≤ 0.10) spinel ferrites were synthesized using the sol-gel auto-combustion method. X-ray diffraction (XRD) analysis and Rietveld refinement confirmed the presence of a cubic spinel structure. The crystallite size was estimated to be between 17.5 nm and 26.5 nm using Scherrer's method and 31.27 nm-54.52 nm using the Williamson-Hall (W-H) method. Lattice constants determined from XRD and Rietveld refinement ranged from (8.440 to 8.433 Å and 8.442 to 8.431 Å), respectively. Scanning electron microscopy (SEM) revealed a non-uniform distribution of morphology with a decrease in particle size. The bandgap values decreased from 2.0 eV to 1.68 eV with increasing rare earth (La3+) doping concentration. Fourier-transform infrared (FT-IR) spectroscopy confirmed the presence of functional groups and M-O vibrations. The dielectric constant and dielectric loss exhibited similar behavior across all samples. The maximum tan δ value obtained at lower frequencies. Regarding magnetic behavior, there was a decrease in magnetization from 55.84 emu/g to 22.08 emu/g and an increase in coercivity from 25.63 Oe to 33.88 Oe with higher doping concentrations. Based on these results, these materials exhibit promising properties for applications in microwave and energy storage devices.

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This study presents a novel approach for the fabrication of a Co,Ni/MoS2-derived nanohybrid material using wheat straw extract. The facile synthesis method involves a sol-gel process, followed by calcination, showcasing the potential of agricultural waste as a sustainable reducing and chelating reagent. The as-prepared nanohybrid has been characterized using different techniques to analyse its physicochemical properties. X-ray diffraction analysis confirmed the successful synthesis of the nanohybrid material, identifying the presence of NiMoO4, CoSO4 and Mo17O47 as its components. Fourier-transform infrared spectroscopy differentiated the functional groups present in the wheat straw biomass and those in the nanohybrid material, highlighting the formation of metal-oxide and sulphide bonds. Scanning electron microscopy revealed a heterogeneous morphology with agglomerated structures and a grain size of around 70 nm in the nanohybrid. Energy-dispersive X-ray spectroscopy analysis shows the composition of elements with weight percentages of (Mo) 9.17%, (S) 6.21%, (Co) 12.48%, (Ni) 12.18% and (O) 50.46% contributing to its composition. Electrochemical analysis performed through cyclic voltammetry showcased the exceptional performance of the nanohybrid material as compared with MoS2, suggesting its possible applications for designing biosensors and related technologies. Thus, the research study presented herein underscores the efficient utilization of natural resources for the development of functional nanomaterials with promising applications in various fields. This study paves a way for manufacturing innovation along with advancement of novel synthesis method for sustainable nanomaterial for future technological developments.

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Purpose: The aim of this study was to evaluate the antibacterial efficacy of surface-treated hernia implants modified by a hybrid nanolayer with incorporated Ag, Cu, and Zn cations using the sol-gel method. Methods: The materials (polypropylene, polyester, and polyvinylidene difluoride) were activated by vacuum plasma treatment or UV C radiation, then modified and tested for bacterial strains of Escherichia coli (gram-negative) and Staphylococcus aureus (gram-positive). The AATCC 100 (2019) method for quantitative and the ISO 20645 agar plate propagation method for qualitative evaluation of microbiological efficacy were used. The gradual release of incorporated ions was monitored over time in simulated body fluids (blood plasma, peritoneal fluid) and physiological saline using an inductively coupled plasma mass spectrometer. The thickness and the homogeneity of the layers were measured for individual random samples with scanning electron microscope analysis (SEMA) and evaluated with an elemental analysis. Results: Qualitative and quantitative microbiological tests clearly show the great suitability of vacuum plasma and UV C with sol AD30 (dilution 1:1) surface treatment of the implants. The absolute concentration of Ag, Cu, and Zn cations in leachates was very low. SEMA showed a high degree of homogeneity of the layer and only very rare nanocracks by all tested materials appear after mechanical stress. Conclusion: This study confirms that surface treatment of meshes using the sol-gel method significantly increases the antibacterial properties. The nanolayers are sufficiently mechanically resistant and stable and pose no threat to health.

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This study investigates the synthesis and electrocatalytic performance of cobalt oxide (Co3O4) nanoparticles for the oxygen evolution reaction (OER) and their role in water treatment as contaminant removal agents. Cobalt oxide nanoparticles are recognized as promising materials in electrocatalysis due to their tunable properties and nanoscale engineering potential. Here, fine cobalt oxide nanoparticles are synthesized using the sol-gel method followed by various sintering temperatures to achieve precise control over surface morphology, size, and shape. Characterization via high-resolution scanning electron microscopy (HRSEM) and high-resolution transmission electron microscopy (HRTEM) elucidates the impact of sintering temperature on nanoparticle properties. Thin film electrodes of cobalt oxide are fabricated using the doctor blade method and evaluated using linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). Among the tested sintering temperatures, cobalt oxide electrodes sintered at 600 °C exhibit superior catalytic activity, demonstrating an overpotential of 258 mV (vs RHE) at 10 mA cm-2 current density and a Tafel slope of 17.33 mV dec-1. Furthermore, these electrodes demonstrate excellent stability, maintaining OER performance for 10 h in 1 M NaOH electrolyte. Additionally, the role of cobalt oxide nanoparticles in water treatment is explored using inductively coupled plasma atomic emission spectrometry (ICP-AES). Experimental results reveal that lower sintering temperatures enhance the electrocatalytic properties of cobalt oxide nanoparticles, highlighting their potential contribution to sustainable energy and water treatment technologies. This work underscores the significance of cobalt oxide nanoparticles as dual-functional materials for advancing electrocatalysis and water purification applications, thus paving the way for the development of efficient and environmentally friendly technologies.

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Molecularly imprinted polymers (MIPs) are promising for precise protein separation and purification. However, challenges persist due to their large size, variable configuration, and instability during preparation. Here, a simple silicon self-assembly program was designed to synthesize MIPs without any organic reagents and acid-base catalysis, avoiding the structural damage of protein under severe conditions. In this method, employing hemoglobin (Hb) as a model protein, with tween-20 in emulsification, and tetraethyl orthosilicate (TEOS) as the cross-linking agent, along with co-functional monomers 3-aminopropyltriethoxysilane (APTES) and benzyl(triethoxy)silane (BnTES), enhanced binding efficacy was achieved. Successful imprinting was evidenced through surface morphology observation and physical/chemical property evaluations of the synthesized MIPs. A series of adsorption experiments were performed to investigate the recognition performance of Hb-MIPs. The Hb-MIPs not only exhibited large adsorption capacity (400 µg/mg) and good imprinting factor (6.09) toward template protein, but also showed satisfactory selectivity for reference proteins. Five cycles of adsorption proved that the Hb-MIPs had good reusability. In addition, the successful isolation of HB from bovine blood indicated that Hb-MIPs were an excellent separation and purification material. The mild preparation conditions and good adsorption capacity demonstrated the potential value of this method in separation and purification research.

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A fixed Nd3+ and varied Yb3+ ion concentration were incorporated in a Zinc-Silicate (SZNYX) composite solution using ex-situ sol-gel solution to fabricate a novel thin film (TF) on Si (100)-substrate. The upconversion luminescence (UCL) spectra of the thin films were measured under 980 nm laser excitation, with the most optimized result for Yb3+ ion concentration of 1.5 mol%. Additionally, a 2-D photoluminescence (PL) confocal mapping of the SZNY15-TF material confirmed uniform PL distribution throughout the space under the same excitation wavelength. Structural characterization via XRD revealed the tetragonal Zn2SiO4 nano-crystalline nature of the film at three distinct annealing temperatures. Morphological characterization using the Field-emission scanning electron Microscope (FESEM) coupled with energy dispersion spectrometer (EDS) affirmed the nanoflower structure and the purity of doping purity in the samples, respectively. These findings collectively confirm the promising UCL properties of the SZNYX-TF samples, suggesting potential applications in photonic.

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In the present study, both short-range and long-range structural features of an ionic bridged silsesquioxane, specifically one containing the 1,4-diazoniabicyclo[2.2.2]octane chloride group (ISSQ), were elucidated. This ionic silsesquioxane was synthesized via direct polycondensation of a bridged organosilane precursor, without any additional functionalization step. Si-O-Si cage structures typical of Polyhedral Oligomeric Silsesquioxanes (POSS) were identified. The average interatomic distances of the POSS cages, including the open T8 cage and the T12 cage for the ISSQ, as well as the T8 cage for a commercially available pendant POSS were determined. It is the first report of the interatomic distance determination of POSS cage; achieved by using total pair distribution function G(r) values obtained through high-resolution synchrotron X-ray diffraction combined with density functional theory (DFT) calculations. The application of DFT was crucial for accurately assigning X-ray peaks and verifying structural details. Furthermore, the analysis of X-ray diffraction peaks and the examination of crystalline domains via transmission electron microscopy enabled the proposal of a hexagonal arrangement of Si-O-Si cages over long ranges within the ionic bridged silsesquioxane. This proposed arrangement highlights a distinctive structural organization that could impact the material's properties and applications.

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Various copper-related defects in the absorption layer have been a key factor impeding the enhancement of the efficiency of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells. Alkali metal doping is considered to be a good strategy to ameliorate this problem. In this article, Rb-doped CZTSSe (RCZTSSe) thin films were synthesized using the sol-gel technique. The results show that the Rb atom could successfully enter into the CZTSSe lattice and replace the Cu atom. According to SEM results, a moderate amount of Rb doping aided in enhancing the growth of grains in CZTSSe thin films. It was proven that the RCZTSSe thin film had the densest surface morphology and the fewest holes when the doping content of Rb was 2%. In addition, Rb doping successfully inhibited the formation of CuZn defects and correlative defect clusters and promoted the electrical properties of RCZTSSe thin films. Finally, a remarkable power conversion efficiency of 7.32% was attained by the champion RCZTSSe device with a Rb content of 2%. Compared with that of un-doped CZTSSe, the efficiency improved by over 30%. This study offers new insights into the influence of alkali metal doping on suppressing copper-related defects and also presents a viable approach for improving the efficiency of CZTSSe devices.

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The calcium ferrite nanoparticles were made by the sol-gel process. X-ray diffraction, a scanning electron microscope, and UV-vis spectroscopy were used to analyze the material. There is an orthorhombic phase in the space group Pnma. There were four techniques used to calculate the average crystallite size. Using ImageJ software, the particles were aggregated and their size was ascertained. Using energy-dispersive X-ray (EDX) analysis, the composition of the material was ascertained. 2.29 eV was determined to be the band gap. Vibrating test magnetometer (VSM) provided an explanation for the materials' magnetic property. A decreased band gap energy is responsible for the 90% degradation of malachite green dye at a concentration of 15 mg/L in 150 min, with a four-cycle reusability.

Calcium ferrite nanoparticles were successfully synthesized by sol­gel assisted combustion method using leaf extract of Brassica oleracea as fuel.To the best of the author's knowledge, no such case study that reports the synthesis of calcium ferrite nanoparticles by using leaf extract of Brassica oleracea is previously reported in academic literature.The method is cost-effective and convenient without the use of any chemical fuel agents.The synthesized prepared material efficiently removes malachite green dye, commonly used in industries for dyeing silk and nylon, from the solution.More than 90 % removal efficiency for MB.The material displayed excellent stability and reusability for dyes adsorption.Results were validated with pseudo-first-order kinetic model.

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In this article, the sol-gel method was used as a synthesis method, which shows the physicochemical nature of the synthesis of a new complex material, ferrite Li0.5MnFe1.5O4. The structure and composition of the synthesized ferrite were determined by X-ray phase analysis. According to analysis indicators, it was found that our compound is a single-phase, spinel-structured, and syngony-cubic type of compound. The microstructure of the compound and the quantitative composition of the elements contained within it were analyzed under a scanning electron microscope (SEM). Under a scanning electron microscope, microsystems were taken from different parts of Li0.5MnFe1.5O4-type crystallite; the elemental composition of crystals was analyzed; and the general type of surface layer of complex ferrite was shown. As a result, given the fact that the compound consists of a single phase, the clarity of its construction was determined by the topography and chemical composition of the compound. As a result, it was found that the newly synthesized complex ferrites correspond to the formula Li0.5MnFe1.5O4. The particles of the formed compounds have a large size (between 50.0 µm or 20.0 µm and 10.0 µm). Electrophysical measurements were carried out on an LCR-800 unit at intervals of 293-483 K and at frequencies of 1.5 and 10 kHz. An increase in frequency to 10 kHz led to a decrease in the value ε in the range of the studied temperature (293-483 K).