The objective of the present study was to prepare CuFe2O4 ferrite nanoparticles using the sol-gel combustion method, employing lemon juice as a surfactant and energy agent. This method is located within the green chemistry, representing an environmentally friendly and less expensive approach compared to other methods. The nanoparticles were subsequently evaluated as antibacterial agents against different pathogenic bacteria. Before the antibacterial assays, a cytotoxicity test was conducted to evaluate their safety when applied to organisms. The structural, morphological, elemental composition, and magnetic properties of the samples were analyzed using Fourier-Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), Field Emission-Scanning Electron Microscopy (FE-SEM), and Energy Dispersive X-Ray Detection (EDX). The X-ray diffraction patterns confirmed both the phase purity and the particle size to be 24.27 nm. The results demonstrated that the CuFe2O4 nanoparticles exhibited substantial antibacterial activity against both Gram-negative bacteria (Sphingomonas paucimobilis) and Gram-positive bacteria (Staphylococcus lentus and Bacillus subtilis). The antibacterial efficacy was more pronounced against Gram-negative bacteria, with inhibition diameter 5.46mm and 10.64mm at concentrations of 5000 ppm and 10000 ppm, respectively. When making a comparison, the effectiveness against Gram-positive bacteria displayed a slight reduction. Inhibition zones measured 2.76 mm and 8.33 mm for Staphylococcus lentus, while they were 3.58 mm and 5.35 mm for Bacillus subtilis. These measurements were observed at nanoparticle concentrations of 5000 ppm and 10000 ppm, respectively. Furthermore, the study confirmed the safety of the CuFe2O4 nanoparticles by assessing their toxicity on human red blood cell at different concentrations (50, 100,250,500,1000,5000, and 10000 ppm).

Preparation of an efficient hybrid structure photocatalyst for photocatalytic decomposition has been considered a great option to develop renewable technologies for environmental remediation. Herein, ternary magnetic Fe3O4/GQD/g-C3N4 nanocomposite (FGC) was prepared using the ball mill method. Binary nanocomposites Fe3O4/g-C3N4 (F/CN) and GQD/g-C3N4 (G/CN) were prepared to compare photocatalytic activity with FGC. The performance of photocatalysts for degradation of rhodamine B (RhB) was studied. EDX results showed that Fe3O4, GQD and g-C3N4 nanoparticles (NPs) are uniformly distributed in the FGC. The FGC nanocomposite shows superparamagnetic behaviour with a saturation magnetization of 12 emu. g-1, which makes it favourable compound for magnetic separation procedure. Photocatalytic activity of FGC (100%) was much higher than those of the G/CN (88%) and F/CN (77%) photocatalysts. The superior activity of FGC compared to binary composites was attributed to broader absorption in the visible light band and greater suppression of electron-hole recombination. The photocatalytic degradation of RhB using FGC was consistent with pseudo-first-order kinetics. The reusability of FGC was examined for four runs and no noticeable decrease was observed with the same irradiation time for each run. Finally, it can be argued that FGC photocatalyst can be an efficient semiconductor for the degradation of organic dyes from wastewater.

Antimicrobial nanomaterials provide numerous opportunities for the synthesis of next-generation sustainable water disinfectants. Using the keywords graphene and water disinfection and graphene antibacterial activity, a detailed search of the Scopus database yielded 198 and 1433 studies on using graphene for water disinfection applications and graphene antibacterial activity in the last ten years, respectively. Graphene family nanomaterials (GFNs) have emerged as effective antibacterial agents. The current innovations in graphene-, graphene oxide (GO)-, reduced graphene oxide (rGO)-, and graphene quantum dot (GQD)-based nanocomposites for water disinfection, including their functionalization with semiconductor photocatalysts and metal and metal oxide nanoparticles, have been thoroughly discussed in this review. Furthermore, their novel application in the fabrication of 3D porous hydrogels, thin films, and membranes has been emphasized. The physicochemical and structural properties affecting their antibacterial efficiency, such as sheet size, layer number, shape, edges, smoothness/roughness, arrangement mode, aggregation, dispersibility, and surface functionalization have been highlighted. The various mechanisms involved in GFN antibacterial action have been reviewed, including the mechanisms of membrane stress, ROS-dependent and -independent oxidative stress, cell wrapping/trapping, charge transfer, and interaction with cellular components. For safe applications, the potential biosafety and biocompatibility of GFNs in aquatic environments are emphasized. Finally, the current limitations and future perspectives are discussed. This review may provide ideas for developing efficient and practical solutions using graphene-, GO-, rGO-, and GQD-based nanocomposites in water disinfection by rationally employing their unique properties.

Almost 81% of nitrogen fertilizers are applied in form of urea but most of it is lost due to volatilization and leaching leading to environmental pollution. In this regard, slow-release nano fertilizers can be an effective solution. Here, we have synthesized different Fe₃O₄-urea nanocomposites with Fe₃O₄ NPs: urea ratio (1:1, 1:2, 1:3) ie. NC-1, 2, and 3 respectively, and checked their efficacy for growth and yield enhancement. Oryza sativa L. cv. Swarna seedlings were treated with different NCs for 14 days in hydroponic conditions and significant up-regulation of photosynthetic efficiency and nitrogen metabolism were observed due to increased availability of nitrogen and iron. The discriminant functional analysis confirmed that the NC3 treatment yielded the best results so further gene expression studies were performed for NC-3 treated seedlings. Significant changes in expression profiles of ammonia and nitrate transporters indicated that NC-3 treatment enhanced nitrogen utilization efficiency (NUE) due to sustained slow release of urea. From pot experiments, we found significant enhancement of growth, grain nutrient content, and NUE in NC supplemented sets. 1.45 fold increase in crop yield was achieved when 50% N was supplemented in form of NC-3 and the rest in form of ammonium nitrate. NC supplementation can also play a vital role in minimizing the use of bulk N fertilizers because, when 75% of the recommended N dose was supplied in form of NC-3, 1.18 fold yield enhancement was found. Thus our results highlight that, slow-release NC-3 can play a major role in increasing the NUE of rice.

Volatile organic compounds (VOCs) represent a considerable threat to humans and ecosystems. Strategic remediation techniques for the abatement of VOCs are immensely important and immediately needed. Given a unique set of optical, mechanical, electrical, and thermal characteristics, inimitable surface functionalities, porous structure, and substantial specific surface area, graphene and derived nanohybrid composites have emerged as exciting candidates for abating environmental pollutants through photocatalytic degradation and adsorptive removal. Graphene oxide (GO) and reduced graphene oxide (rGO) containing oxygenated function entities, i.e., carbonyl, hydroxyl, and carboxylic groups, provide anchor and dispersibility of their surface photocatalytic nanoscale particles and adsorptive sites for VOCs. Therefore, it is meaningful to recapitulate current state-of-the-art research advancements in graphene-derived nanostructures as prospective platforms for VOCs degradation. Considering this necessity, this work provides a comprehensive and valuable insight into research progress on applying graphene-based nanohybrid composites for adsorptive and photocatalytic abatement of VOCs in the aqueous media. First, we present a portrayal of graphene-based nanohybrid based on their structural attributes (i.e., pore size, specific surface area, and other surface features to adsorb VOCs) and structure-assisted performance for VOCs abatement by graphene-based nanocomposites. The adsorptive and photocatalytic potentialities of graphene-based nanohybrids for VOCs are discussed with suitable examples. In addition to regeneration, reusability, and environmental toxicity aspects, the challenges and possible future directions of graphene-based nanostructures are also outlined towards the end of the review to promote large-scale applications of this fascinating technology.

Multiwalled carbon nanotubes (MWCNTs) were oxidized using a mixture of H₂SO₄ and HNO₃, and the oxidized MWCNTS were decorated with magnetite (Fe₃O₄). Finally, poly-N-isopropyl acrylamide-co-butyl acrylate (P-NIPAM) was added to obtain P-NIPAM/Fe/MWCNT nanocomposites. The nanosorbents were characterized by various techniques, including X-ray diffraction, transmission electron microscopy, scanning electron microscopy, thermogravimetric analysis, and Brunauer–Emmett–Teller analysis. The P-NIPAM/Fe/MWCNT nanocomposites exhibited increased surface hydrophobicity. Owing to their higher adsorption capacity, their kerosene removal efficiency was 95%; by contrast, the as-prepared, oxidized, and magnetite-decorated MWCNTs had removal efficiencies of 45%, 55%, and 68%, respectively. The P-NIPAM/Fe/MWCNT nanocomposites exhibited a sorbent capacity of 8.1 g/g for kerosene removal from water. The highest kerosene removal efficiency from water was obtained at a process time of 45 min, sorbent dose of 0.005 g, solution temperature of 40 °C, and pH 3.5. The P-NIPAM/Fe/MWCNTs showed excellent stability after four cycles of kerosene removal from water followed by regeneration. The reason may be the increase in the positive charge of the polymer at pH 3.5 and the increased adsorption affinity of the adsorbent toward the kerosene contaminant. The pseudo second-order model was found to be the most suitable model for studying the kinetics of the adsorption reaction.

Chicken poultry industry produces a vast amount of feather waste and is often disposed into landfills, creating environmental pollution. Therefore, we explored the valorization of chicken feather waste into lipids and keratinous sludge biomass. This study demonstrates the successful utilization of keratinous sludge biomass as a unique precursor for the facile preparation of novel keratinous sludge biomass-derived carbon-based molybdenum oxide (KSC@MoO₃) nanocomposite material using two-step (hydrothermal and co-pyrolysis) processes. The surface morphology and electrochemical properties of as-prepared nanocomposite material were analyzed using HR-SEM, XRD, XPS, and cyclic voltammetric techniques. KSC@MoO₃ nanocomposite exhibited prominent electrocatalytic behavior to simultaneously determine hydroquinone (HQ) and catechol (CC) in environmental waters. The as-prepared electrochemical sensor showed excellent performance towards the detection of HQ and CC with broad concentration ranges between 0.5–176.5 μM (HQ and CC), and the detection limits achieved were 0.063 μM (HQ) and 0.059 μM (CC). Furthermore, the developed modified electrode has exhibited excellent stability and reproducibility and was also applied to analyze HQ and CC in environmental water samples. Results revealed that chicken feather waste valorization could result in sustainable biomass conversion into a high-value nanomaterial to develop a cost-effective electrochemical environmental monitoring sensor and lipids for biofuel.

In this work, we prepared nanocomposites of nickel-decorated manganese oxynitride on graphene nanosheets and demonstrated them as photocatalysts for degradation of acetylsalicylic acid (ASA). The catalyst exhibited a high degradation efficiency over ASA under visible light irradiation and an excellent structural stability after multiple uses. Compared to manganese oxide (MnO) and manganese oxynitride (MnON) nanoparticles, larger specific surface area and smaller band gap were observed for the nanocomposite accounting for the enhanced photocatalytic efficiency. Besides the compositional effect of the catalyst, we also examined the influence of various experimental parameters on the degradation of ASA such as initial concentration, catalyst dose, initial pH and additives. The best performance was obtained for the nanocomposite when the catalyst dose was 10 mg/mL and the initial pH 3. Detection of intermediates during photocatalysis showed that ASA undergoes hydroxylation, demethylation, aromatization, ring opening, and finally complete mineralization into CO₂ and H₂O by reactive species. For practical applications as a photocatalyst, cytotoxicity of the nanocomposite was also evaluated, which revealed its insignificant impact on the cell viability. These results suggest the nanocomposite of nickel-decorated manganese oxynitride on graphene nanosheets as a promising photocatalyst for the remediation of ASA-contaminated water.

Pieces of glass as solid wastes were recycled in the synthesis of highly order MCM-41 that decorated by green fabricated Co₃O₄ nanoparticles using the green extract of green tea leaves forming novel green nano-composite. The synthetic Co₃O₄/MCM-41 exhibit high surface area, low bandgap energy (1.63 eV), and typical spherical morphology decorated by Co₃O₄ nanoparticles. The composite was evaluated as green photocatalyst in effective oxidation of methyl parathion pesticide in the presence of a visible light source. The degradation results revealed complete removal of 50 mg/L and 100 mg/L after 60 min and 90 min, respectively using 0.25 of the catalyst at pH 8. The detection of the TOC in the treated methyl parathion solution gives strong indications about the formation of organic intermediate compounds during the oxidation steps. The main detected intermediate compound are C₆H₅OH(NO₂), C₆H₅OH, (CH₃O)₃P(S), C₆H₄(OH)₂, C₆H₃(OH)₃, C₆H₄(NH₂)OP(O)(OCH₃)₂, (CH₃O)₂P(O)OH, (CH₂)₂C(OH)OH(CHO)OC(O), and HO₂C(CH₂)₂C(O)CHO. The detected intermediate compounds converted into SO₄²⁻, PO₄³⁻, NO₃⁻, and CO₂ under the extensive photocatalytic of them over Co₃O₄/MCM-41. The oxidizing species trapping test verified the controlling of the methyl parathion degradation pathway by the hydroxyl radicals. Finally, the composite showed significant reusability properties and applied five times in the oxidation of methyl parathion with considerable degradation percentages.

A high-energy ball milling of magnetite nanoparticles with amino-phosphonic functionalized poly(glycidyl methacrylate) polymer is used for manufacturing a highly efficient magnetic sorbent for U(VI) sorption from aqueous solutions. The Uranyl ions were adsorbed through the binding with amine and phosphonic groups as confirmed by Fourier Transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) analyses. The maximum sorption capacity (up to 270 mg U g⁻¹) occurred at pH = 3–4; Langmuir isotherm well describes the sorption process. Small-size particles allow achieving fast uptake (within ≈90 min of contact); and the kinetic profiles are modeled by the pseudo-second order rate equation. Uranium is successfully desorbed from loaded sorbent using 0.25 M NaHCO₃ solution: Sorbent can be recycled with minimal decrease in sorption and desorption efficiency for at least 6 cycles. The sorbent is efficiently used for U(VI) recovery from the acidic leachates of U-bearing ores (after precipitation pre-treatment). Sorption capacity approaches 190 mg U g⁻¹ despite the presence of high concentrations of Fe and Si: the sorbent has a marked preference for U(VI) (confirmed by distribution ratios and selectivity coefficients).