In this research work, silica nanoparticles and silica-gentamicin nanostructured solution were synthesized by using the microwave-assisted synthesis, in basic medium, using two silane precursors (tetraethylorthosilicate and octyltriethoxysilane) and the antibiotic (gentamicin sulfate). The prepared materials were characterized through Fourier transform infrared (FTIR) spectroscopy, TGA analysis, transmission electron microscopy (TEM), and atomic force microscopy (AFM) to investigate the morphology and structure. Antimicrobial studies of the silica-gentamicin nanostructured solution versus silica nanoparticles were performed against Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli. FTIR spectra showed that the gentamicin has been loaded to the silica nanoparticles. AFM analysis showed that the morphology of the silica-gentamicin nanostructured solution has changed, and agglomerations of particles are present at the surface. Antimicrobial testing, performed using the diffusion method through spot inoculation, indicates that the silica-gentamicin nanostructured solution exhibited activity against the resistant strain. The obtained silica-gentamicin solution can be used as biochemical agent for the prevention and treatment of microorganisms which are deposited on different surfaces (e.g., glass, plastic, ceramic).
The present paper synthesized, characterized, and evaluated the performance of the novel biopolymeric membrane enriched with cellulose acetate and chitosan (CHI)-silver (Ag) ions in order to remove iron ion from the synthetic wastewater using a new electrodialysis system. The prepared membranes were characterized by Fourier Transforms Infrared Spectroscopy-Attenuated Total Reflection (FTIR-ATR), Thermal Gravimetric Analysis (TGA) and Differential Thermal Analysis (DSC), contact angle measurements, microscopy studies, and electrochemical impedance spectroscopy (EIS). The electrodialysis experiments were performed at the different applied voltages (5, 10, and 15 V) for one hour, at room temperature. The treatment rate (TE) of iron ions, current efficiency (IE), and energy consumption (Wc) were calculated. FTIR-ATR spectra evidenced that incorporation of CHI-Ag ions into the polymer mixture led to a polymer-metal ion complex formation within the membrane. The TGA-DSC analysis for the obtained biopolymeric membranes showed excellent thermal stability (>350 °C). The contact angle measurements demonstrated the hydrophobic character of the polymeric membrane and a decrease of it by CHI-Ag adding. The EIS results indicated that the silver ions induced a higher ionic electrical conductivity. The highest value of the iron ions treatment rate (>60%) was obtained for the biopolymeric membrane with CHI-Ag ions at applied voltage of 15 V.
The goal of the present paper was to synthesize, characterize, and evaluate the performance of the modified composite based on magnetite (Fe3O4) and polyvinyl alcohol (PVA). The obtained composite was used to degrade Methyl Orange dye from synthetic wastewater by a laboratory photocatalytic reactor. Various parameters of the photodegradation process were tested: composite dosage, amount of hydrogen peroxide (H2O2), and pH. The composite was characterized by Fourier Transform Infrared (FTIR) Spectroscopy, X-ray Diffraction (XRD), and Scanning Electron Microscopy (SEM). The degradation experiments indicated that the complete dye decolorization depended on the amount of H2O2. In addition, the H2O2 could accelerate Methyl Orange degradation to more highly oxidized intermediates in the presence of UV light (99.35%). The results suggested that the obtained modified composite could be used to treat wastewater containing various types of dyes.
The heterojunction based on n-TiO2 nanolayer/p-CuMnO2 thin film was achieved using an efficient two-step synthesis process for the fabrication of a UV photodetector. The first step consisted of obtaining the TiO2 nanolayer, which was grown on titan foil by thermal oxidation (Ti-TiO2). The second step consisted of CuMnO2 thin film deposition onto the surface of Ti-TiO2 using the Doctor Blade method. Techniques such as X-ray diffraction, UV-VIS analysis, SEM, and AFM morphologies were used for the investigation of the structural and morphological characteristics of the as-synthesized heterostructures. The Mott–Schottky analysis was performed in order to prove the n-TiO2/p-CuMnO2 junction. The I-V measurements of the n-TiO2 nanolayer/p-CuMnO2 thin film heterostructure confirm its diode characteristics under dark state, UV and visible illumination conditions. The obtained heterojunction, which is based on two types of semiconductors with different energy band structures, improves the separating results of charges, which is very important for high-performance UV photodetectors.
The main goal of the present paper was to synthesize the polyvinyl alcohol-SiO2 nanoparticles polymeric membrane by wet-phase inversion method. The efficiency of prepared membranes (without and with SiO2) was investigated using a versatile laboratory electrodialysis system filled with simulated wastewaters that contain zinc ions. All experiments were performed at following conditions: the applied voltage at electrodes of 5, 10 and 15 V, a concentration of zinc ions solution of 2 g L−1, time for each test of 1 h and at room temperature. The demineralization rate, extraction percentage of zinc ions, current efficiency and energy consumption were determined. The polymeric membranes were characterized by Fourier Transforms Infrared Spectroscopy-Attenuated Total Reflection (FTIR-ATR), Scanning Electron Microscopy (SEM) and Electrochemical Impedance Spectroscopy (EIS). The higher value of percentage removal of zinc ions (over 65%) was obtained for the polymeric membrane with SiO2 nanoparticles, at 15 V. The FTIR-ATR spectra show a characteristic peak located at ~1078 cm−1 assigned to the Si-O-Si asymmetrical stretching. SEM images of the polymeric membrane with SiO2 nanoparticles show that the nanoparticles and polymer matrix were well compatible. The impedance results indicated that the SiO2 nanoparticles induced the higher proton conductivity. The final polymeric membranes can be used for the removal of various metallic ions, dyes, organic or inorganic colloids, bacteria or other microorganisms from different natural waters and wastewaters.
Transparent and antireflective coatings were prepared by deposition of modified silica materials onto polyvinyl chloride (PVC) substrates. These materials were obtained by the sol-gel route in acidic medium, at room temperature (25 °C), using different alkoxysilanes with various functional groups (methyl, vinyl, octyl or hexadecyl). Physicochemical and microstructural properties of resulted silica materials and of thin coatings were investigated through Fourier Transforms Infrared Spectroscopy (FTIR), UV-Vis spectroscopy, Thermal Gravimetric Analysis (TGA), Dynamic Mechanical Analysis (DMA), Atomic Force Microscopy (AFM) and ellipsometric measurements. Wetting behaviors of the silica coatings were evaluated by measurement of static contact angle against water. FTIR spectra of materials confirmed the high degree of cross-linking that result from the formation of the inorganic backbone through the hydrolysis and polycondensation reactions together with the formation of the organic network. These sol-gel silica coatings showed a reduction in the reflectance (10%) compared with uncoated PVC substrate. AFM reveals that the films are uniform, and adherent to the substrate, but their morphology is strongly influenced by the chemical composition of the coating matrices. These silica coatings can be useful for potential electronic and optical devices.