ABSTRACT
In this study, a magnetic perovskite nanohybrid based on g-C3N4 (gCN) nanosheets was synthesized and developed for the efficient photodegradation of toxic environmental pollutants under short-time visible irradiation. The synthesis of this nanohybrid involved the incorporation of SrTiO3:N (STO:N) and ZnFe2O4 (ZnF) onto the g-C3N4 nanosheets through a simple reflux method. Our investigation encompassed a comprehensive suite of analytical techniques, including BET, TGA, TEM, SEM, EDX, DRS, VSM, XRD, photocurrent, and FT-IR, to elucidate the physicochemical characteristics of this nanocomposite in the context of its application in photodegradation processes. The nanohybrid displayed significantly enhanced photocatalytic activity compared to its individual components, achieving a degradation efficiency of over 90% for various pollutants, including organic dyes like Rhodamine B (Rh-B), within a short irradiation time. This enhanced activity can be attributed to the synergistic effect between gCN, STO:N, and ZnF, which promotes the generation of reactive oxygen species and facilitates the degradation process. Notably, the nanocomposite containing 20 wt% STO:N perovskite and 20 wt% ZnF demonstrated the highest Rh-B degradation rate under visible light irradiation within just 30 min. Furthermore, the nanohybrid displayed excellent stability and reusability over seven consecutive runs, retaining its high photocatalytic activity even after multiple cycles of degradation. This remarkable performance can be attributed to the strong interaction between the gCN nanosheets and the magnetic perovskite components, which prevents their aggregation and ensures their efficient utilization. Additionally, the nanohybrid exhibited excellent visible light absorption, enabling the utilization of a wider range of light for degradation. This feature is particularly advantageous, as visible light is more abundant in sunlight compared to UV light, rendering the nanohybrid suitable for practical applications under natural sunlight. In conclusion, the ternary gCN-STO:N@ZnF nanocomposite represents a promising candidate for the treatment of organic pollutants in aqueous environments, offering a versatile and efficient solution.
ABSTRACT
In this research, the amoxicillin (AMX) removal was studied on a prepared nanosorbent from MOFs. The aim of this research work is to prepare nanohybrids based on metal-organic frameworks (MOFs) as an efficient nanosorbent for the absorption of amoxicillin drug. In this study, UIO-66 nanoparticles (UIO-66 NPs) were prepared from Zirconium (Zr) metal and 1,4-benzene dicarboxylic acid (BDC). Then UIO-66@Cr-MIL-101 nanohybrid was synthesized by hydrothermal method. Structural and physicochemical properties of nanohybrid UIO-66@Cr-MIL-101 were characterized by different analyses such as X-ray diffraction analysis (XRD), fourier transform infrared spectrometer (FT-IR), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), transmission electron microscopy (TEM), therapeutic goods administration (TGA), and Brunauer-Emmett-Teller (BET). The effect of four fundamental variables effective on adsorption was optimized by the central composite response surface methodology (CCRSM). This parameters including loading percentage of Cr-MIL-101 NPs (10-30%), initial concentration of AMX (20-140 mg L-1), contact time (20-60 min), and pH (20-10). The removal percentage (Re%) of AMX equal to 99.50% was obtained under the following conditions: The loading value of 20% Wt%, the initial concentration of AMX 80 mg L-1, contact time 20 min, and pH = 6. Also, the experimental data were investigated with famous kinetic models and isotherms, and it was observed that AMX removal by nanohybrid is correlated with the PSO kinetic model and Langmuir isotherm.
ABSTRACT
The major part of water pollutants includes of organic such as phenolic pollutant, thus there are every hazardous to environment. Present work is a comparative onto surface chemistry and adsorptive characteristics of coordinate organic polymer (Cop-150) and nanoporous carbon (NPC) prepared using solvothermal method. New NPC was successfully synthesized to remove of phenol. FT-IR, XRD, XPS, SEM, TGA, and BET techniques have been used to characterization and confirm physicochemical variation during preparing Cop-150 and NPC. Box-Behnken response surface methodology (BBRSM) was used to optimize four important factors of the pH (2-10), contact time (1-40 min), temperature (25-60 °C), and initial concentration of phenol (5-50 mg L-1). To analyze the data obtained from the adsorption of phenol by synthesized adsorbents, four linear, 2FI, quadratic and cubic models were examined, which the quadratic model was recognized as the best model. To the NPC the equal adsorption capacity 500 mg g-1 is achieved at the initial concentration of phenol = 49.252 mg L-1, contact time = 15.738 min, temperature = 28.3 °C, and pH 7.042. On the other hand, the adsorption capacity for Cop-150 in pH 4.638, the contact time = 19.695 min, the temperature = 56.8 °C, and the initial concentration of phenol = 6.902 mg L-1 was equal to 50 mg g-1. The experimental data at different conditions were investigated by some famous kinetic and isotherm models, which among them, were corresponded to the pseudo-second-order kinetic model and the Langmuir isotherm. Moreover, based to result of thermodynamics to the both Cop-150 and NPC, the adsorption process is exothermic and spontaneous. According to results the Cop-150 and NPC could be used for up to four and five cycles without significantly reducing their performance, respectively.
ABSTRACT
PURPOSE: Today, the development of wounds and their side effects has become a problematic issue in medical science research. Hydrogel-based dressings are some of the best candidates for this purpose due to their ability to keep the wound bed clean, as well as provide proper moisture, tissue compatibility and an antimicrobial effect for wound healing. On the other hand, copper and its compounds have been used experimentally for many years in studies as an antimicrobial substance. Various studies have been performed determining the antimicrobial properties of this element, during which significant effects on infection have been shown. METHODS: Chitosan/polyvinyl alcohol/copper nanofibers were successfully prepared by incorporating Cu onto a polymer electrospun using an electrospinning technique. A double-layer nanofiber composed of poly(vinyl alcohol) and chitosan incorporated with Cu nanoparticles as a protective layer and a second layer composed of polyvinylpyrrolidone (PVP) nanofibers which was adjacent to the damaged cells was prepared. The prepared nanofiber was characterized by TGA, FT-IR, TEM, SEM-EDS, and X-ray powder diffraction. The antimicrobial efficiency of the nanofibers was demonstrated through biological tests on some Gram-positive and Gram-negative bacteria. Finally, the prepared hydrogel formulations were prepared to evaluate their effect on the healing process of rat open wounds. RESULTS: In this study, data from SEM, TEM, EDS, and XRD confirmed the formation of uniform fibers with nanodiameters and the presence of Cu nanoparticles onto the electrospun nanofibers. The antibacterial activity of copper was observed against all of the selected bacteria, but the Gram-positive bacteria were more sensitive compared to Gram-negative bacteria. CONCLUSION: According to the obtained results, the hydrogel wound dressing prepared in this research can be effective in caring for open wounds in the early stages of wound healing and preventing the occurrence of prolonged open wounds.
