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Based on the selectivity study, it was confirmed that the selectivity of doped NSs phase was the most towards Fe(III) ion. The static adsorption capacity for Fe(III) was calculated to be 110.06 mgg-1. Results from adsorption isotherm also verified that the adsorption process was mainly monolayer-adsorption onto a surface containing a finite number of CuO-TiO2 NSs adsorption sites.
This study presents a sustainable, green synthesis of silver-coated magnetite nanocomposites (Ag-Fe3O4) using Brachychiton populneus leaf extract, aiming to develop an efficient and reusable photocatalyst for wastewater treatment. The nanocomposites combine the visible-light plasmonic activity of silver nanoparticles (AgNPs) with the magnetic recovery capability of Fe3O4, resulting in a multifunctional hybrid material. Comprehensive characterization using XRD, SEM, EDX, FTIR, UV–Vis spectroscopy, BET surface area analysis, and VSM confirmed successful formation of Ag-Fe3O4 with a mesoporous structure, uniform particle distribution, reduced bandgap (1.95 eV), and strong magnetic properties. The photocatalytic performance was evaluated by the degradation of methylene blue (MB) and Congo red (CR) under visible light. The composite demonstrated superior photocatalytic efficiency, achieving 97% and 92% degradation of MB and CR (20 ppm), respectively, within 30 min, significantly outperforming individual AgNPs and Fe3O4. Kinetic studies confirmed pseudo-first-order reaction behavior. The enhanced activity was attributed to the synergistic effect of Ag and Fe3O4, which improved light absorption, interfacial charge separation, and reactive oxygen species (ROS) generation. This work highlights the potential of green-synthesized Ag-Fe3O4 as a highly efficient, magnetically recoverable, and environmentally friendly photocatalyst for wastewater remediation applications.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
In the title compound, C(12)H(11)BrN(2)O, the 4-bromo-benzaldehyde and 5-amino-3,4-dimethyl-isoxazole units are oriented at a dihedral angle of 4.89 (8)°. In the crystal, weak π-π inter-actions are present between the benzene rings at a centroid-centroid distance of 3.7862 (14) Å.
A PEG/MCM-41 composite was synthesized by a simple solution method with polyethylene glycol (PEG) and mesoporous MCM-41. The thermal behavior of the composite was studied using thermogravimetric analysis (TGA) and an in situ electrical conductivity measurement. The results showed that polymer degradation occurs in the temperature range of 300 to 550 °C, and is accompanied by a decrease in the electrical conductivity. Thus, to elucidate the influence of polymer elimination on the structural, textural and electrical conductivity properties of MCM-41, a sample was prepared by calcining the PEG/MCM-41 composite for 3 h at 550 °C in air. Various physico-chemical techniques such as XRD, FT-IR, FE-SEM and N2 physisorption, were used for characterization. It was shown that the calcined solid still exhibits the mesoporous MCM-41 framework with poor ordering. A texture analysis revealed that the PEG/MCM-41 composite formation and the subsequent PEG elimination are accompanied by a loss of the type IV character of the MCM-41 and a sharp decrease in the textural parameters. The observed meso-porosity loss of the MCM-41 as a result of adding and then eliminating the PEG molecules was accompanied by a reduction of the conductivity.
Pollution problem increases with the same face as the industrial development. One of the toxic ingredients of these industrial effluents is the organic dyes. Zinc oxide/Graphene oxide nanocomposite (ZnO-GNc) was synthesized in aqueous solution by mixing ultrasonically various compositions. The prepared ZnO-GNc nanocomposite was characterized by XRD, FTIR, FE-SEM, EDX and TEM. XRD of Graphene oxide (GO) showed their crystalline nature and the average size was 3.54, 18.98 and 15.47 nm for GO, ZnO, and ZnO-GNc respectively. An active toxic and stable dye, Methyl red (MR) was employed as the target pollutant to evaluate the photocatalytic activity of ZnO-GNc. The photocatalytic performance of ZnO-GNc nanocomposite was compared with that of zinc oxide (ZnO) and GO. The effect of some parameters, dye concentration, pH and temperature of dye solution were studied. The kinetic studies show that the process of MR photocatalytic discoloration by ZnO-GNc followed first-order reaction kinetics under different conditions with the rate constant of 2.2 × 10−2 s−1. The possible reasons for the high values of photocatalytic efficiency of the ZnO-GNc may be due to the improved charge passage and separation.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
The title compound, C(23)H(17)N(3)O, has been previously described in a monoclinic P2(1)/c polymorph with Z = 4 [Asiri, Al-Youbi, Faidallah, Ng & Tiekink (2011). Acta Cryst. E67, o2449]. In the new monoclinic P2(1)/n form, with Z = 8, there are two independent mol-ecules, A and B, in the asymmetric unit. In both mol-ecules, the cyclo-hexa-1,3-diene ring has a screw-boat conformation, whereas it is a distorted half-chair in the original polymorph. There is a fold in each mol-ecule, as indicated by the dihedral angle between the benzene rings of the 1,2-dihydro-naphthalene and aniline residues of 33.19 (10)° (mol-ecule A) and 30.6 (10)° (mol-ecule B). The meth-oxy-benzene ring is twisted out of the plane of the aniline residue to which it is connected [dihedral angles = 49.22 (10) and 73.27 (10)°, in A and B respectively]. In the crystal, the two independent mol-ecules self-associate via N-H⋯N hydrogen bonds, generating a 12-membered {⋯HNC(3)N}(2) synthon. These are connected into a supra-molecular tape in the (-101) plane by N-H⋯O(meth-oxy) inter-actions. In the P2(1)/c polymorph, supra-molecular layers are formed by N-H⋯N and N-H⋯O inter-actions.