Search Results (259)

This work shows a sustainable methodology for the synthesis of biogenic materials designed for the removal and photodegradation of rhodamine B (RhB), a highly dangerous environmental pollutant that induces reproductive toxicity. The classical synthesis of MCM-41-ordered mesoporous materials was modified using biocompatible rice husk as the silica template. Iron was incorporated and the so-prepared biogenic photocatalysts were characterized by X-ray diffraction, N₂ adsorption–desorption isotherms, transmission electron microscopy, diffuse reflectance UV-Vis, surface pH, cyclic voltammetry, and Fourier transform infrared spectral analysis of pyridine adsorption. The photocatalytic performance of the materials was evaluated following the removal by adsorption and the photon-driven degradation of RhB. The adsorption capacity and photocatalytic activity of the biogenic materials were correlated with their properties, including iron content, texture, surface content, and electrochemical properties. The best biogenic material boosted the degradation rates of RhB under UV irradiation up to 4.7 and 2.2 times greater than the direct photolysis and the benchmark semiconductor TiO₂-P25. It can be concluded that the use of rice husks for the synthesis of biogenic Fe-modified mesoporous materials is a promising strategy for wastewater treatment applications, particularly in the removal of highly toxic organic dyes. Full article

Hypericum perforatum L. (H.P.), a plant renowned for its wound-healing properties, was investigated for antioxidant/antimicrobial efficacy, toxicological safety, and in vivo wound-healing effects in this research to develop and characterize novel nanoemulsion hydrogel (NG) formulations. NG were prepared via emulsion diffusion–solvent evaporation and polymer hydration using Cremophor RH40 and Ultrez 21/30. A D-optimal design optimized oil/surfactant ratios, considering particle size, PDI, and drug loading. Antioxidant activity was tested via DPPH, ABTS⁺, and FRAP. Toxicological assessment followed HET-CAM (ICH-endorsed) and ICCVAM guidelines. The optimized NG-2 (NE-HPM-10 + U30 0.5%) demonstrated stable and pseudoplastic flow, with a particle size of 174.8 nm, PDI of 0.274, zeta potential of −23.3 mV, and 99.83% drug loading. Release followed the Korsmeyer–Peppas model. H.P. macerates/NEs showed potent antioxidant activity (DPPH IC₅₀: 28.4 µg/mL; FRAP: 1.8 mmol, Fe²⁺/g: 0.3703 ± 0.041 mM TE/g). Antimicrobial effects against methicillin-resistant S. aureus (MIC: 12.5 µg/mL) and E. coli (MIC: 25 µg/mL) were significant. Stability studies showed no degradation. HET-CAM tests confirmed biocompatibility. Histopathology revealed accelerated re-epithelialization/collagen synthesis, with upregulated TGF-β1. The NG-2 formulation demonstrated robust antioxidant, antimicrobial, and wound-healing efficacy. Enhanced antibacterial activity and biocompatibility highlight its therapeutic potential. Clinical/pathological evaluations validated tissue regeneration without adverse effects, positioning H.P.-based nanoemulsions as promising for advanced wound care. Full article

Detecting heavy metal ions is essential for maintaining environmental safety, ensuring industrial quality control, and protecting public health. In this study, we have synthesized a novel Rhodamine B-based fluorescent probe, RhB-DCT, which is functionalized with 2,4-dichloro-1,3,5-triazine (DCT) to enhance selectivity and sensitivity for metal ions detection. The probe functions through a “turn-on” fluorescence mechanism activated by the opening of the spiro-lactam ring induced by Fe³⁺ ions, resulting in a distinct color change from colorless to deep pink. The RhB-DCT probe demonstrated a rapid and robust fluorescence response within seconds, exhibited a broad pH stability from 4 to 13, showed excellent reversibility, and possessed a low detection limit of 0.0521 μM, surpassing numerous existing fluorescent probes. The RhB-DCT probe exhibited significant selectivity for Fe³⁺ than other competing metal ions. The integration of high sensitivity, rapid response, and strong stability positions RhB-DCT as a viable option for real-time detection of Fe³⁺ ions in aqueous settings. This study demonstrates the efficacy of the RhB-DCT probe in environmental monitoring, water quality assessment, and analytical sensing platforms, serving as an effective and dependable tool for detecting heavy metal ions. Full article

A novel polyhedron-based anionic Er-MOF with three types of cages and abundant open metal sites (OMSs) and Lewis base sites (LBSs) has been successfully synthesized. The inorganic secondary unit possesses a rarely reported six-connected three-nucleated rare-earth cluster, and the overall framework shows a new (3,3,6)-connected topology. The Er-MOF has good fluorescence selectivity and anti-interference performance with Fe³⁺ and Cu²⁺. In addition, benefiting from the anionic framework, nanoscale cavity and small window size of the Er-MOF, the composite RhB@Er-MOF has been synthesized by in situ encapsulation of the cationic dye Rhodamine B (RhB). It can provide dual-emitting fluorescence that facilitates self-calibration in sensing. The RhB@Er-MOF has higher accuracy than the Er-MOF with regard to the fluorescence-selective and anti-interference performance of Fe³⁺ and quenching coefficient K_sv values of 1.97 × 10⁴ M⁻¹, which are attributed to its self-calibration function that can eliminate environmental interference. The fluorescence quenching mechanism was explained by our experiments and density functional theory (DFT) calculations. Furthermore, RhB@Er-MOF can achieve the visual and rapid selective detection of Fe³⁺ by a smartphone RGB color analysis application, resulting in the dual-signal output performance of the material. Full article

To degrade high-concentration and toxic organic effluents, we developed Fe-Cu active sites loaded on biomass-source carbon aerogel (CA) to produce a low-cost and high-efficiency magnetic Fenton-like catalyst for the catalytic oxidative decomposition of organic pollutants. It exhibits excellent performance in catalytic Fenton-like reactions for RhB removal at an ultrahigh initial concentration of up to 1000 ppm. To be specific, Fe₃O₄ and Cu nanoparticles are generated in situ on a mesoporous CA support, denoted as an Fe₃O₄-Cu/CA catalyst. Experimentally, factors including initial dye concentration, catalyst dosage, H₂O₂ dosage, pH, and temperature, which significantly influence the oxidative degradation rate of RhB, are carefully studied. The RhB (1000 ppm) degradation ratio reaches 93.7% within 60 min under low catalyst and H₂O₂ dosage. The catalyst also shows slight metal leaching (almost 1.4% of total Fe and 4.0% of total Cu leached after a complete degradation of 25 μmol RhB under conditions of 15 mg catalyst dosage, 20 mL RhB solution (600 ppm), and 200 μL 30 wt% H₂O₂ dosage, at pH of 2.5, at 40 °C), good catalytic activity for degrading organic pollutants, excellent reusability, and good catalytic stability (the degradation ratio is nearly 82.95% in the 8th cycle reaction). The synergistic effect between Fe and Cu species plays a vital role in promoting the redox cycle of Fe(III)/Fe(II) and enhancing the generation of ·OH. It is suitable for ultrahigh-concentration organic pollutant degradation in practical wastewater treatment applications. Full article

The molten salt reactor is a fourth-generation nuclear power plant considered a long-term eco-friendly energy source with high efficiency and the potential for green hydrogen production. The selection of alloys for such reactors, which can operate for more than 30 years, is a primary concern because of corrosion by high-temperature molten salt. In this study, three Fe- and Ni-based alloys were selected as structural material candidates. Corrosion immersion tests were conducted in NaCl–KCl molten salt for 48 h at 800 °C and 40% RH conditions in an air environment. In the absence of moisture and oxygen removal, ClNaK salt-induced damage was observed in the investigated alloys. The corrosion behavior of the alloys was characterized using various techniques, including scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and Auger electron spectroscopy. The results show that the corrosion process can be explained by salt-induced surface damage, internal ion migration, and depletion to the surface. The corrosion rate is high in SS316L (16Cr-Fe), N10003 (7Cr-Ni), and C-276 (16Cr-Ni), in decreasing order. Based on the corrosion penetration, ion elution, and interfacial diffusion results, C-276 and N10003 are good candidates for structural materials for MSRs. Therefore, Ni-based alloys with high Cr content minimize surface damage and ion depletion in unpurified molten salt environments. This indicates that Ni-based alloys with high Cr content exhibit highly corrosion resistance. Full article

WO₃ has attracted great attention in the field of catalysts due to its excellent photocatalytic performance. However, the difficulty in recycling and low reuse percentage of nano WO₃ limit its application. This paper used the hydrothermal method to prepare an Fe₃O₄@SiO₂@WO₃ core–shell nanocatalyst. Its composition and structure were characterized by various techniques including XRD, FT-IR, and Raman analyses, which confirmed the successful preparation of a core–shell-structured catalyst with a strong response to an external magnetic field. In the degradation experiment of rhodamine B solution (RhB), the composite catalyst with a WO₃ doping amount of 0.8 g and catalyst dosage amount of 30 mg had the best catalytic degradation effect on 10 ppm RhB, with a degradation efficiency of 99.80%. Due to its high transparency and ion conductivity, SiO₂ did not affect the performance of the composite catalyst, but could effectively reduce the corrosion of WO₃ by the reaction solution. The presence of a SiO₂ interlayer prevented any deterioration in the catalytic efficiency of WO₃ nanocrystal shells and the chemical and thermal stability of Fe₃O₄ nuclei. By applying an external magnetic field, this nanocatalyst can be easily recovered from the solution. These features not only maximize the value of this new material, but also provide sustainable solutions for environmental protection, energy crises, and health issues. Full article

A model of a “smart” composite based on a thermosensitive PNIPAM polymer deposited on a FeRh substrate with a modified periodic microstructure was proposed. The initial parameters of the model were determined from the properties of the actual composite sample and its components. Cooling of the sample using a magnetic field was shown by two independent methods, and at ~37 °C, it was −5.5 °C when a magnetic field of 1.8 T was applied. Based on experimental data, models of traditional and modified PNIPAM/FeRh composites were constructed. Calculations show that surface modification allows for an increase in the activation time for a polymer layer that is 20 µm thick from ~20 ms for a conventional composite to ~60 ms for a modified composite. Modification of the surface in the form of wells can be used to more effectively implement the idea of loading and releasing drugs for potential biomedical applications. Full article

We present structural, morphological, optical and photocatalytic properties of multiferroic Bi_0.98Ba_0.02FeO₃ (BBFO2) perovskite thin films prepared by a combined sol–gel and spin-coating method. X-ray diffraction (XRD) analysis revealed that all the perovskite films consisted of the stable polycrystalline rhombohedral phase structure (space group R3c) with a tolerance factor of 0.892. By using Rietveld refinement of diffractogram XRD data, crystallographic parameters, such as bond angle, bond length, atom position, unit cell parameters, and electron density measurements were computed. Scanning electron microscopy (SEM) allowed us to assess the homogeneous and smooth surface morphology of the films with a small degree of porosity, while chemical surface composition characterization by X-ray photoelectron spectroscopy (XPS) showed the presence of Bi, Fe, O and the doping element Ba. Absorption measurements allowed us to determine the energy band gap of the films, while photoluminescence measurements have shown the presence of oxygen vacancies, which are responsible for the enhanced photocatalytic activity of the material. Photocatalytic degradation experiments of Methylene Blue (MB), Methyl orange (MO), orange G (OG), Violet and Rhodamine B (RhB) performed on top of BBFO2 thin films under solar light showed the degradation of all pollutants in varying discoloration efficiencies, ranging from 81% (RhB) to 54% (OG), 53% (Violet), 47% (MO) and 43% (MB). Full article

Metallic Pd/Ni gauzes, located downstream of the Pt/Rh ammonia oxidation catalyst nets in the Ostwald process, is the current technology for capturing volatile gas phase platinum and rhodium species lost from the Pt/Rh combustion catalyst through evaporation. In this screening study, we explore four oxide families, ABO₃ perovskites, (ABO₃)_n(AO) Ruddlesden–Popper (RP) phases, AO rock salt, and A₂O₃ sesquioxide type oxides, as alternative materials for platinum capture. It was found that all the tested nickelates, LaNiO₃, NdNiO₃, La₂NiO₄, and La₄Ni₃O₁₀, captured platinum well and formed A₂NiPtO₆. In contrast, La_0.85Sr_0.15FeO₃, LaFeO₃, and LaCoO₃ did not capture platinum. CaO, SrO, and Nd₂O₃ formed low-dimensional platinates such as Ca_xPt₃O₄, Sr₄PtO₆, and a newly discovered neodymium platinate, Nd_10.67Pt₄O₂₄. Gd₂O₃ did not capture platinum in bench-scale experiments in dry air, but did, however, seem to capture platinum under pilot plant conditions, likely due to the co-capture of Co lost from the N₂O abatement catalyst. The catalytic activity of both oxides and platinum-containing products were studied, toward NO_x and N₂O decomposition. None of the oxides showed significant activity toward NO_x decomposition, and all showed activity toward N₂O decomposition, but to different extents. An overall assessment of the screened oxides with respect to potential use in industrial Ostwald conditions is provided. All tested oxides except CaO and SrO withstood industrial conditions. From our assessments, the nickelates and A₂O₃ (A = Nd, Gd) stand out as superior oxides for platinum capture. Full article

The oxime group is important in organic and inorganic chemistry. In most cases, this group is part of an organic molecule possessing one or more donor sites capable of forming bonds to metal ions. One family of such compounds is the group of 2-pyridyl (aldo)ketoximes. Metal complexes of 2-pyridyl oximes continue to attract the intense interest of many inorganic chemistry groups around the world for a variety of reasons, including their interesting structures, physical and biological properties, and applications. A unique member of 2-pyridyl ketoximes is di-2-pyridyl ketoxime (dpkoxH), which contains two 2-pyridyl groups and an oxime functionality that can be easily deprotonated giving the deprotonated ligand (dpkox⁻). The extra 2-pyridyl site confers a remarkable flexibility resulting in metal complexes with exciting structural and reactivity features. Our and other research groups have prepared and characterized many metal complexes of dpkoxH and dpkox⁻ over the past 30 years or so. This work is an attempt to build a “periodic table” of dpkoxH, which is near completion. The filled spaces of this “periodic table” contain metal ions whose dpkoxH/dpkox⁻ complexes have been structurally characterized. This work reviews comprehensively the to-date published coordination chemistry of dpkoxH with emphasis on the syntheses, reactivity, relationship to metallacrown chemistry, structures, and properties of the metal complexes; selected unpublished results from our group are also reported. The sixteen coordination modes adopted by dpkoxH and dpkox⁻ have provided access to monomeric and dimeric complexes, trinuclear, tetranuclear, pentanuclear, hexanuclear, heptanuclear, enneanuclear, and decanuclear clusters, as well as to a small number of 1D coordination polymers. With few exceptions ({M^IILn^III₂} and {Ni^II₂Mn^III₂}; M = Ni, Cu, Pd, and Ln = lanthanoid), most complexes are homometallic. The metals whose ions have yielded complexes with dpkoxH and dpkox⁻ are Cr, Mn, Fe, Co, Ni, Cu, Zn, Ru, Rh, Pd, Ag, Cd, Re, Os, Ir, Au, Hg, lanthanoids (mainly Pr and Nd), and U. Most metal complexes are homovalent, but some mixed-valence Mn, Fe, and Co compounds have been studied. Metal ion-assisted/promoted transformations of dpkoxH, i.e., reactivity patterns of the coordinated ligand, are also critically discussed. Some perspectives concerning the coordination chemistry of dpkoxH and research work for the future are outlined. Full article

A novel sequential one-pot bimetallic catalytic system combining Fe(III)-catalyzed alkynylation and a Rh(I)-catalyzed [2+2+2] reaction was successfully developed. The σ-Lewis acid properties of iron (III) and the π-Lewis acid properties of rhodium (I) catalysts were unified in an unprecedented intermolecular alkynylation/cyclotrimerization one-pot process. Using this unique Fe/Rh bimetallic relay catalytic system, a variety of benzo and pyrridinoisoindolinone derivatives were obtained under mild conditions from easily available N-(propargyl) hydroxy aminals, as the simplest N-acyliminium ion precursors, and several alkynes. Full article

This study investigates the humidity-sensing properties of two semiconductor metal oxide (SMO)-reduced graphene oxide (RGO) nanocomposites: TiO₂/RGO and α-Fe₂O₃/RGO, at room temperature. Both nanocomposites are synthesized via hydrothermal methods and coated onto printed circuit board (PCB) interdigital electrodes to construct humidity sensors. The surface morphology and crystallographic structure of the materials are characterized using field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD). The sensors are tested across a humidity range of 11%RH to 97%RH, and the impedance is measured over a frequency range of 1 Hz to 1 MHz. The results show that both TiO₂/RGO and α-Fe₂O₃/RGO exhibit favorable humidity-sensing performance at room temperature. The sensitivity and humidity hysteresis of TiO₂/RGO are 12.2 MΩ/%RH and 3.811%RH, respectively, while those of α-Fe₂O₃/RGO are 0.826 MΩ/%RH and 8.229%RH. The response and recovery times of TiO₂/RGO are 72 s and 99 s, respectively, while those of α-Fe₂O₃/RGO are 48 s and 54 s. Both sensors demonstrate good repeatability and stability. These findings suggest that SMO/RGO nanocomposites are promising materials for the development of low-cost, high-sensitivity, and stable humidity sensors. Full article

A CHS-to-CFRHS Y-joint that consists of a circular hollow section (CHS) brace and a concrete-filled rectangular hollow section (CFRHS) chord by welding has a simple and smooth weld profile that saves time and cost for the fabrication of CHS-to-CFRHS Y-joints and leads to a superior fatigue performance, compared with other welded tubular joints. This investigation presented an analysis of the stress concentration factors (SCFs) of CHS-to-CFRHS Y-joints subjected to axial tension loading of the brace. First, a finite element (FE) modelling method, which was validated with the experimental results cited in the reference, was utilised to establish the FE models of CHS-to-CFRHS Y-joints. Then, a parametric analysis was conducted to investigate the influences of the significant non-dimensional geometric parameters on the SCFs of CHS-to-CFRHS Y-joints. It is found that the intersection angle of the brace and chord has an important influence on the magnitudes of the SCF values. An increase in the intersection angle of the brace and chord will increase the values of the SCFs at the 60° location and saddle. The values of the SCFs at the 60° location and saddle reach the maximum value when the intersection angle of the brace and chord reaches 90°. Furthermore, on the basis of the large database of the SCF results, empirical design equations were established to calculate the SCFs at the crown toe, 60° location and saddle via multiple regression analysis. A safety factor was applied to the empirical design equations to ensure safe and reliable results of SCF calculations for the fatigue design of CHS-to-CFRHS Y-joints in a composite truss structure. Ultimately, a comparative analysis of SCFs was conducted with the FE models of welded tubular joints with rectangular hollow section (RHS) chords and CFRHS chords. The results reveal that infilling concrete in the chord leads to a reduction in SCFs along the weld profile of more than 11% on average, and the peak SCF decreases by more than 15%. Full article

Biopolymer-based nanocomposite film is an efficient material for addressing the increasing levels of pollutants in the environment and also for the production of antimicrobial packing material due to its good film-forming properties, biodegradability, and minimal environmental impact. In particular, chitosan/polyvinyl alcohol/g-C₃N₄ (CS/PVA/g-C₃N₄) nanocomposite films with different weight percentages of PVA were prepared using simple methodologies and characterized using XRD, TGA, FT-IR, DSC, FE-SEM, EDX, and elemental mapping analysis. The XRD and FT-IR results validated the nanocomposite film formation. The FE-SEM images showed the smooth surface of the composite films without any wrinkles; the smoothness of the film increased with increases in the PVA loading, and the surface morphologies of the films were largely unchanged. The EDX and elemental mapping analysis validated the presence and uniform dispersion of g-C₃N₄ within the nanocomposite film. The photocatalytic activity of the CS/PVA/g-C₃N₄ composite films was assessed by the degradation of rhodamine B dye (RhB) and acetophenone under direct sunlight irradiation. The CS/PVA/g-C₃N₄ nanocomposite films exhibited superior degradation efficiency toward the RhB dye and acetophenone compared to the bare polymeric film and the g-C₃N₄ material. The order of degradation for the RhB dye and acetophenone was CS/PVA (1.0) g-C₃N₄ (95.34%, 33.33%) > CS/PVA (1.5) g-C₃N₄ (93.18%, 31.31%) > CS/PVA (0.5) g-C₃N₄ (93.02%, 29.29%) > CS/PVA (90.69%, 26.26%) > g-C₃N₄ (87.56%, 24%), respectively. Furthermore, the antimicrobial activity of the nanocomposite films was tested against E. coli, Pseudomonas sps., Klesiella sps., and Enterococcus sps., and the CS/PVA (1.5)/g-C₃N₄ nanocomposite film offered better antimicrobial properties than the other composite films and bare materials. In conclusion, these biopolymer-based nanocomposites are highly efficient and provide a promising path for the development of various biodegradable polymeric nanocomposites for environmental remediation and antibacterial packing applications. Full article