Novel Cellulose Derivatives Containing Metal (Cu, Fe, Ni) Oxide Nanoparticles as Eco-Friendly Corrosion Inhibitors for C-Steel in Acidic Chloride Solutions

Novel environmentally-friendly corrosion inhibitors based on primary aminated modified cellulose (PAC) containing nano-oxide of some metals (MONPs), for instance iron oxide nanoparticles (Fe3O4NPs), copper oxide nanoparticles (CuONPs), and nickel oxide nanoparticles (NiONPs), were successfully synthesized. The as-prepared PAC/MONPs nanocomposites were categorized using Fourier transform infrared spectroscopy (FT-IR), transmission electron microscope (TEM), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and selected area diffraction pattern (SAED) techniques. The data from spectroscopy indicated that successful formation of PAC/MONPs nanocomposites, as well as the TEM images, declared the synthesized PAC/Fe3O4NPs, PAC/CuONPs, and PAC/NiONPs with regular distribution with particle size diameters of 10, 23 and 43 nm, respectively. The protection performance of the as-prepared PAC and PAC/MONPs nanocomposites on the corrosion of C-steel in molar HCl was studied by the electrochemical and weight-loss approaches. The outcomes confirmed that the protection power increased with a rise in the [inhibitor]. The protection efficiency reached 88.1, 93.2, 96.1 and 98.6% with 250 ppm of PAC/CuONP, PAC/Fe3O4NPs, and PAC/NiONPs, respectively. PAC and all PAC/MONPs nanocomposites worked as mixed-kind inhibitors and their adsorption on the C-steel interface followed the isotherm Langmuir model. The findings were reinforced by FT-IR, FE-SEM and EDX analyses.

Self-Assembly of Au-Fe3O4 Hybrid Nanoparticles Using a Sol–Gel Pechini Method

The Pechini method has been used as a synthetic route for obtaining self-assembling magnetic and plasmonic nanoparticles in hybrid silica nanostructures. This manuscript evaluates the influence of shaking conditions, reaction time, and pH on the size and morphology of the nanostructures produced. The characterization of the nanomaterials was carried out by transmission electron microscopy (TEM) to evaluate the coating and size of the nanomaterials, Fourier-transform infrared spectroscopy (FT-IR) transmission spectra to evaluate the presence of the different coatings, and thermogravimetric analysis (TGA) curves to determine the amount of coating. The results obtained show that the best conditions to obtain core–satellite nanostructures with homogeneous silica shells and controlled sizes (<200 nm) include the use of slightly alkaline media, the ultrasound activation of silica condensation, and reaction times of around 2 hours. These findings represent an important framework to establish a new general approach for the click chemistry assembling of inorganic nanostructures.

Reactions of MoCl5 with 4-Methylpyridine, 2-Methylpyridine and 1-Methylimidazole in Tetrahydrofuran

MoCl5 reactions with 4-methylpyridine/2-methylpyridine/1-methylimidazole in THF in 1:1/1:2 stoichiometric ratios, at room temperature were carried out. The following products were synthesized: MoO2Cl(C6H7N), 1;Mo2O2Cl5(C6H7N)2(C4H8O)2,2; Mo4O4Cl4(C6H7N)3(C4H8O)2, 3 and Mo2O4Cl4(C4H6N)2(C4H8O), 4. These compounds have been investigated by FT-IR (transmission mode), FT-1H NMR, FT -13C NMR, microbiological, LC-MS and elemental (C, H, N, Mo, Cl) studies. In view of the sensitivity of all the reactants and products towards oxidation/hydrolysis by air/moisture, all the reactions and products were handled using dry nitrogen atmosphere in vacuum line. LC-MS and elemental studies agree with the formulae of compounds.

Heterogenous Nanocomposite Catalysts With Rhenium Nanostructures for the Catalytic Reduction of 4-nitrophenol

Stable and efficient heterogenous nanocatalysts for the reduction of 4-nitrophenol (4-NP) has attracted much attention in recent years. In this context, a unique and efficient in-situ approach is used for the production of new polymeric nanocomposites (pNCs) containing rhenium nanostructures (ReNSs). These rare materials should facilitate the catalytic decomposition of 4-NP, in turn ensuring increased catalytic activity and stability. These nanomaterials were analyzed using Fourier-Transformation Infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), and X-Ray powder diffraction (XRD). The efficiency of the catalytic reaction was estimated based on the acquired UV-Vis spectra, which enabled the estimation of the catalytic activity using pseud-first order modelling. The applied method resulted in the successful production and efficient loading of ReNSs in the polymeric matrices. Amino functionalities played a primary role in the reduction process. Moreover, the functionality that is derived from 1.1’-carbonyl imidazole improved the availability of the ReNSs, which resulted in 90% conversion of 4-NP with a maximum rate constant of 0.28 min-1 over 11 subsequent catalytic cycles. This effect was observed despite the trace amount of Re in the pNCs (~5%), suggesting a synergistic effect between the polymeric base and the ReNSs-based catalyst.

Synthesis and Properties of Inositol Nanocapsules

Sugar alcohols are phase−change materials with various advantages but may suffer from leakage during applications. In this study, inositol nanocapsules were synthesized at various conditions, including the amount of precursors and the time for adding the precursors. The effects of synthesis conditions on the properties of the nanocapsules were studied. The morphology, chemical composition, microstructure, phase−change characteristics and size distribution of the nanocapsules were investigated by scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FT−IR), transmission electron microscope (TEM), differential scanning calorimeter (DSC) and a zeta potential analyzer. The results confirm that inositol was well−encapsulated by an SiO2 shell. The shell thickness increased, while the supercooling degree of the nanocapsules decreased with increasing time for adding the precursors. In order to obtain nanocapsules with good morphology and phase−change characteristics, the time for adding the precursors should increase with the amount of precursors. The nanocapsules with the best properties exhibited high melting enthalpy, encapsulation ratio and energy storage efficiency of 216.0 kJ/kg, 83.1% and 82.1%, respectively. The size of the nanocapsules was remarkably affected by the triethoxysilane (TES) amount.

One pot three component synthesis of substituted 3,4,6,7-tetrahydro-3,3,6,6-tetramethyl-9,10-diphenylacridine-1,8(2H,5H,9H,10H)-diones catalyzed by efficient In2O3-SiO2

A convenient, One pot synthesis of heterocyclic nucleous acridine derivative compound has been achieved those are having very much attention in medicinal chemistry because of their extensive application in biology. The mixture of dimedone, substituted benzaldehyde and aniline were catalyzed by efficient In2O3-SiO2 heterogeneous reusable catalyst in ethanol to obtain the desired acridine derivatives with good yield. Hydrothermal method used to synthesize In2O3-SiO2 catalytic material. This catalytic material were characterized by using X-ray diffraction spectroscopy (XRD), scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR), Transmission electron microscope (TEM), Temperature-programmed desorption (NH3-TPD) and Brunauer-Emmett-Teller (BET). Our synthetic strategy features high yield, simple work up procedure, non-toxic, clean, and easy recovery and reusability of the catalytic system.

Synthesis and Characterization of Solid-state Fe-exchanged Nano-bentonite and Evaluation of Methyl Orange Adsorption

A new adsorbent was synthesized using ion-exchange between iron salts and bentonite modified with acetyl trimethylammonium bromide (CTAB) in the solid phase. Ion exchange was performed in the solid-state at a temperature of 100 ° C for 2 min. Various analyzes such as X-ray diffraction (XRD), scanning electron microscopy (SEM), porosity measurement (BET), infrared Fourier transform (FT-IR), transmission electron microscopy (TEM), X-ray energy diffraction (EDX), and thermal weighing (TGA) were used to characterize the synthesized nano-adsorbents. Under optimal conditions (pH = 7, time 60 min, concentration of dye solution 150 ppm, and amount of nano-adsorbent 0.75 g / l), the modified nano-adsorbent absorbed 73% of the methyl orange (MO) dye. Adsorption isotherm studies and kinetic model showed that the pseudo-second-order model and Langmuir equation agree with the obtained results. After three reductions of the modified nano-adsorbent in the photo-Fenton process, the dye absorption percentage was 69.50%.