High Poisonous Cd Ions Removal by Ru-ZnO-g-C₃N₄ Nanocomposite: Description and Adsorption Mechanism

Ru-ZnO-g-C3N4 nanocomposite was made using a straightforward ultrasonication method and evaluated for its potential to remove Cd ions from aqueous environments. X-ray diffraction analysis confirms composite production with an average crystalline size of 6.61 nm, while transmission electron microscopy results indicate nanosheet-like nanomaterials with uniform elements distribution. Measurements of N2 adsorption–desorption reveal the creation of a mesoporous structure with a BET surface area of approximately 257 m2/g. Fourier converted infrared reveals vibrational modes for O-H, amino groups, triazine, and Ru-ZnO. In contrast, X-ray photoelectron spectroscopy investigation reveals the presence of the elements Ru, Zn, O, N, and C. Ru-ZnO-g-C3N4 nanocomposite has remarkable adsorption efficiency for aqueous Cd ions, achieving 475.5 mg/g in 18 min. This study reveals that the Ru-ZnO-g-C3N4 nanocomposite may be used as an effective and reusable adsorbent for removing Cd ions during wastewater treatment and, possibly, for eliminating other toxic metal ions

Uptake of BF Dye from the Aqueous Phase by CaO-g-C₃N₄ Nanosorbent: Construction, Descriptions, and Recyclability

Removing organic dyes from contaminated wastewater resulting from industrial effluents with a cost-effective approach addresses a major global challenge. The adsorption technique onto carbon-based materials and metal oxide is one of the most effective dye removal procedures. The current work aimed to evaluate the application of calcium oxide-doped carbon nitride nanostructures (CaO-g-C3N4) to eliminate basic fuchsine dyes (BF) from wastewater. CaO-g-C3N4 nanosorbent were obtained via ultrasonication and characterized by scanning electron microscopy, X-ray diffraction, TEM, and BET. The TEM analysis reveals 2D nanosheet-like nanoparticle architectures with a high specific surface area (37.31 m2/g) for the as-fabricated CaO-g-C3N4 nanosorbent. The adsorption results demonstrated that the variation of the dye concentration impacted the elimination of BF by CaO-C3N4 while no effect of pH on the removal of BF was observed. Freundlich isotherm and Pseudo-First-order adsorption kinetics models best fitted BF adsorption onto CaO-g-C3N4. The highest adsorption capacity of CaO-g-C3N4 for BF was determined to be 813 mg. g−1. The adsorption mechanism of BF is related to the π-π stacking bridging and hydrogen bond, as demonstrated by the FTIR study. CaO-g-C3N4 nanostructures may be easily recovered from solution and were effectively employed for BF elimination in at least four continuous cycles. The fabricated CaO-g-C3N4 adsorbent display excellent BF adsorption capacity and can be used as a potential sorbent in wastewater purification

Fabrication of Mesoporous V₂O₅@g-C₃N₄ Nanocomposite as Photocatalyst for Dye Degradation

This study investigated the photocatalytic degradation of RB dye by V2O5@g-C3N4 nano-catalysts. The sonication method was utilized to create V2O5@g-C3N4 nano-catalysts. V2O5@g-C3N4 nano-catalysts were characterized using X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), high-resolution electron microscopy (TEM), BET-surface area analyzer, X-ray photoelectron spectroscopy (XPS), and ultraviolet spectroscopy. In the meantime, the photocatalytic activity, pH, and photocatalyst dosage are investigated in depth to account for RB dye decolorization. The rate constant for RB dye photodegradation was 0.0517 (min−1) and the decolorization rate was 93.4%. The degrading efficiency of RB dye by V2O5@g-C3N4 nanocatalysts is consistent with pseudo-first-order kinetics. The results of this study demonstrated that V2O5@g-C3N4 nanocatalysts are particularly effective at destroying dyes in water

Dependency of Crystal Violet Dye Removal Behaviors onto Mesoporous V₂O₅-g-C₃N₄ Constructed by Simplistic Ultrasonic Method

This research examined the production of a V2O5-g-C3N4 nanocomposite to remove organic dyes from wastewater. To generate the V2O5-g-C3N4 nanocomposite, the sonication method was applied. The testing of V2O5-g-C3N4 with various dyes (basic fuchsin (BF), malachite green (MG), crystal violet (CV), Congo red (CR), and methyl orange (MO)) revealed that the nanocomposite has a high adsorption ability towards BF, MG, CV, and CR dyes in comparison with MO dye. It was established that the modification of pH influenced the removal of CV by the V2O5-g-C3N4 nanocomposite and that under optimal operating conditions, efficiency of 664.65 mg g−1 could be attained. The best models for CV adsorption onto the V2O5-g-C3N4 nanocomposite were found to be those based on pseudo-second-order adsorption kinetics and the Langmuir isotherm. According to the FTIR analysis results, the CV adsorption mechanism was connected to π–π interactions and the hydrogen bond

Fabrication of Mesoporous V2O5@g-C3N4 Nanocomposite as Photocatalyst for Dye Degradation

This study investigated the photocatalytic degradation of RB dye by V2O5@g-C3N4 nano-catalysts. The sonication method was utilized to create V2O5@g-C3N4 nano-catalysts. V2O5@g-C3N4 nano-catalysts were characterized using X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), high-resolution electron microscopy (TEM), BET-surface area analyzer, X-ray photoelectron spectroscopy (XPS), and ultraviolet spectroscopy. In the meantime, the photocatalytic activity, pH, and photocatalyst dosage are investigated in depth to account for RB dye decolorization. The rate constant for RB dye photodegradation was 0.0517 (min−1) and the decolorization rate was 93.4%. The degrading efficiency of RB dye by V2O5@g-C3N4 nanocatalysts is consistent with pseudo-first-order kinetics. The results of this study demonstrated that V2O5@g-C3N4 nanocatalysts are particularly effective at destroying dyes in water

Stripping of Cu Ion from Aquatic Media by Means of MgY2O4@g-C3N4 Nanomaterials

International audienceIn this study, quaternary MgY2O5@g-C3N4 nanomaterials were produced using a simplistic ultrasonic power technique in the presence of an organic solvent, and their capability to abolish Cu (II) from an aqueous solution was evaluated. As validated by powder X-ray diffraction, the synthesized nanomaterials possessed excellent crystallinity, purity, and tiny crystalline size. According to BET and TEM, the nanomaterials with high porosity nanosheets and perfect active sites made Cu (II) removal from water treatment feasible. At a pH of 3.0, the MgY2O5@g-C3N4 displayed good Cu (II) adsorption capability. The Cu (II) adsorption adhered to the Langmuir adsorption model, with an estimated theoretical maximum adsorption aptitude of 290 mg/g. According to the kinetics investigation, the adsorption pattern best fitted the pseudo-second-order kinetics model. Depending on the FTIR results of the nanocomposite prior to and after Cu (II) uptake, surface complexation and ion exchange of Cu (II) ions with surface hydroxyl groups dominated the adsorption of Cu (II). The MgY2O5@g-C3N4 nanomaterials have great potential as adsorbents for Cu (II) removal due to their easy manufacturing process and high adsorption capacity. Additionally, the reuse of MgY2O4@g-C3N4 nanomaterials was tested through the succession of four adsorption cycles using HNO3. The result showed the good stability of this material for mineral pollution removal

Ba2+ removal from aquatic medium via TiY2O5@g-C3N4 nanocomposites

International audienceThis research intends to produce TiY2O5@g-C3N4 nanocomposite that can be utilized to eliminate Ba+2 from aqueous solutions. The nanocomposite was studied with XRD, BET, EDX, and TEM investigation. The TiY2O5@g-C3N4 nanocomposite sorption effectiveness was studied by contact time, adsorbent dose, beginning pH, and initial barium ions concentration in batch kinetic and equilibrium tests. The barium ions adsorption was conducted using 10 mg of adsorbent, 60 mg. L−1 initial Ba+2 concentration at pH = 7 and equilibrium was reached in within 54.5 min. The Langmuir isotherm offered the highest correlation for Ba+2 adsorption to TiY2O5@g-C3N4 and demonstrated favorable adsorption; a maximum adsorption capacity of 295.52 mg. g−1 was achieved. The experimental data was utilized to study adsorption mechanisms and potential rate-controlling stages for mass transfer and kinetic models. External mass transfer and intra-particle diffusion influenced barium adsorption, and adsorption's kinetics followed a pseudo-second-order model with R2 = 0.9996, t1/2 = 38.8 min and h0 = 1.51 mg.g−1.min−1. The results indicate that Ba+2 are chemisorbed on TiY2O5@g-C3N4 nanocomposite. The results indicate that the nanocomposite has high aptitude and reusability for an effective metal ions adsorption

Identification of dual-target isoxazolidine-isatin hybrids with antidiabetic potential: Design, synthesis, in vitro and multiscale molecular modeling approaches

In the development of novel antidiabetic agents, a novel series of isoxazolidine-isatin hybrids were designed, synthesized, and evaluated as dual α‐amylase and α-glucosidase inhibitors. The precise structures of the synthesized scaffolds were characterized using different spectroscopic techniques and elemental analysis. The obtained results were compared to those of the reference drug, acarbose (IC50 = 296.6 ± 0.825 μM for α‐amylase & IC50 = 780.4 ± 0.346 μM for α-glucosidase). Among the title compounds, 5d exhibited impressive α-amylase and α-glucosidase inhibitory activity with IC50 values of 30.39 ± 1.52 μM and 65.1 ± 3.11 μM, respectively, followed by 5h (IC50 = 46.65 ± 2.3 μM; IC50 = 85.16 ± 4.25 μM) and 5f (IC50 = 55.71 ± 2.78 μM; IC50 = 106.77 ± 5.31 μM). Mechanistic studies revealed that the most potent derivative 5d bearing the chloro substituent attached to the oxoindolin-3-ylidene core, and acarbose, are a competitive inhibitors of α-amylase and α-glucosidase, respectively. Structure activity relationship (SAR) was examined to guide further structural optimization of the most appropriate substituent(s). Moreover, drug-likeness qualities and ADMET prediction of the most active analogue, 5d was also performed. Subsequently, 5d was subjected to molecular docking and dynamic simulation during the progression of 120 ns analysis to check the essential ligand-receptor patterns, and to estimate its stability. In silico studies were found in good agreement with the in vitro enzymatic inhibitions results. In conclusion, we demonstrated that most potent compound 5d could be exploited as dual potential inhibitor of α-amylase and α-glucosidase for possible management of diabetes

Excellent Adsorption of Dyes via MgTiO3@g-C3N4 Nanohybrid: Construction, Description and Adsorption Mechanism

This report investigates the elimination of hazardous Rhodamine B dye (RhB) from an aqueous medium utilizing MgTiO3@g-C3N4 nanohybrids manufactured using a facile method. The nanohybrid MgTiO3@g-C3N4 was generated using an ultrasonic approach in the alcoholic solvent. Various techniques, including HRTEM, EDX, XRD, BET, and FTIR, were employed to describe the fabricated MgTiO3@g-C3N4 nanohybrids. RhB elimination was investigated utilizing batch mode studies, and the maximum removal was attained at pH 7.0. The RhB adsorption process is more consistent with the Langmuir isotherm model. The highest adsorption capacity of MgTiO3@g-C3N4 nanohybrids for RhB was determined to be 232 mg/g. The dye adsorption followed a pseudo-second-order model, and the parameters calculated indicated that the kinetic adsorption process was spontaneous. Using ethanol and water, the reusability of the nanomaterial was investigated, and based on the results; it can be concluded that the MgTiO3@g-C3N4 nanohybrids are easily regenerated for dye removal. The removal mechanism for the removal of RhB dye into MgTiO3@g-C3N4 nanohybrids was also investigated

Preparation, Characterization, DFT Calculations, Antibacterial and Molecular Docking Study of Co(II), Cu(II), and Zn(II) Mixed Ligand Complexes

In the present work, complexes of cobalt(II), copper(II), and zinc(II), 2-amino-4-methylpyrimidineand, and 2,3-diaminopyridine were successfully prepared and characterized using elemental analysis, UV-visible, and FTIR spectroscopy, as well as magnetic susceptibility measurements, molar conductance, TGA analysis, and X-ray diffraction. From elemental and spectral data, the formulae [M(L1)(L2)Cl2(H2O)] (where L1 = AMPY (2-amino-4-methylpyrimidine) and L2 = DAPY(2,3-diaminopyridine)) and M = Co(II) (2), Cu(II) (2), and Zn(II)) for the metal complexes have been proposed. The geometric structures of the mixed-ligand complexes were found to be octahedral around the metal ions, and the XRD patterns showed monoclinic crystal systems with space group P21. The mode of bonding was pentacoordinate for Cu and hexacoordinate for Zn and Co. Different features may result from the fact that not all molecules have the same electron distribution. For example, Zn and Co have larger electron densities in at least one of the chlorides in the HOMO compared with pentacoordinate Cu, which has a small electron distribution on the chloride. Thermal analysis indicated that all metal complexes are stable up to about 88 °C with thermodynamically favored overlapped chemical reactions. Excellent antibacterial and antifungal activity was shown by the three synthesized forms of the complexes. The Zn(II) complex had a high level of antioxidant activity with a DPPH scavenging of 91.5%, whereas the Cu(II) complex had a low level of antioxidant potential (16.5%). The docking tests also showed that all compounds had good binding energy levels (7.2–7.9 kcal mol−1). For this reason, all molecules can easily fit in the receptor protein’s catalytic sites. However, the Co(II) complex is shown to be more active