In this work, new samples of PVA-TiO₂/Cu nanocomposites were prepared via the casting method. The prepared samples were examined using different analytical methods. An XRD analysis showed the semi-crystalline nature of the PVA polymer, as well as showing a decrease in the degree of the crystallinity of the PVA structure as a result of the addition of the mixed nanoparticles. TEM images indicate the spherical shape of the Cu NPs, with a size ranging from 2 to 22 nm, and the rectangular shape of the TiO₂ NPs, with a size ranging from 5 to 25 nm. It was evident via FTIR measurements that there were interactions between the functional groups of the PVA and the TiO₂/Cu NPs. The optical properties of the PVA nanocomposites were improved with an increase in the content of the TiO₂/Cu nanoparticles, as shown via a UV/Vis analysis. DSC curves showed an improvement in the thermal stability of the PVA-TiO₂/Cu nanocomposites after the embedding of the TiO₂/Cu nanoparticles. It was evident using impedance spectroscopy that the AC conductivity was improved by adding the TiO₂ and Cu nanoparticles to the polymeric matrix. The maximum AC conductivity was found at 1.60 wt.% of TiO₂/Cu nanoparticles in the PVA polymer, and this was 13.80 × 10⁻⁶ S/cm at room temperature. Relaxation occurred as a result of the charge carrier hopping between the localized state and the correlated barriers hopping model, describing the dominant mechanism, as presented in an electrical modulus analysis. These results indicate that the PVA-TiO₂/Cu nanocomposite samples can be used in energy storage capacitor applications and in the alternative separator-rechargeable lithium-ion battery industry.

In this article, the synthesis, optical, and electrical properties of composites consisting of polyethylene oxide (PEO), carboxymethyl cellulose (CMC), and titanium dioxide nanoparticles are examined. Flexible nanocomposite samples comprising PEO, CMC, and TiO₂ nanoparticles were produced swiftly via using the cast synthesis method. In addition, XRD and FT-IR analysis were performed in order to analyze the structures of the prepared samples. Our results demonstrate the PEO/CMC blend’s effectiveness in interacting with TiO₂ nanoparticles. The optical properties of the PEO/CMC and nanocomposite samples, such as the energy band gap, were studied using the UV/Vis optical absorbance. It was found that as TiO₂ NP weight fraction increases, the energy gap narrows. Moreover, TiO₂ nanoparticles with an average size of 16 nm were formed in spherical and rod shapes, according to a TEM image. The SEM images demonstrate how the distribution of TiO₂ NPs increased upon the surfaces of the prepared films. The antibacterial activity in the nanocomposites was shown to be enhanced by the TiO₂ NP concentrations. Finally, we proposed that PEO/CMC-0.8 wt. % TiO₂ nanocomposites with enhanced optical, electrical, and dielectric properties should be used in electrochemical devices.

In this work, a three-component reaction of 3-acetyl-4-hydroxycoumarine, malononitrile, or cyanoacetate in the presence of ammonium acetate was used to form coumarin derivatives. The chemical structures of new compounds were identified by ¹H, ¹³C NMR and an elemental analysis. These compounds were examined in vitro for their antimicrobial activity against a panel of bacterial strains. In addition, these compounds were investigated for antioxidant activities by superoxideradical, DPPH (2,2-Diphenyl-1-picrylhydrazyl), and hydroxyl radical scavenging assays, in which most of them displayed significant antioxidant activities. Furthermore, these compounds were evaluated for anti-inflammatory activity by indirect hemolytic and lipoxygenase inhibition assays and revealed good activity. In addition, screening of the selected compounds 2–4 against colon carcinoma cell lines (HCT-116) and hepatocellular carcinoma cell lines (HepG-2) showed that that 2-amino-4-hydroxy-6-(4-hydroxy-2-oxo-2H-chromen-3-yl)nicotinonitrile 4 exhibited good cytotoxic activity against standard Vinblastine, while the other compounds exhibited moderate cytotoxic activity. Docking simulation showed that2-amino-4-hydroxy-6-(4-hydroxy-2-oxo-2H-chromen-3-yl)nicotinonitrile 4 is an effective inhibitor of the tumor protein HCT-116. A large fluorescence enhancement in a highly acidic medium was observed, and large fluorescence quenching by the addition of traces of Cu²⁺ and Ni²⁺ was also remarked.

A closed-vessel microwave digestion method was developed for the simultaneous determination of macro, micro, and toxic elements (Mg, K, Ca, Al, Mn, Fe, Cu, Zn, Se, Rb, V, Cd, and As) in wheat by inductively coupled plasma mass spectrometry (ICP-MS). A two-level factorial design with four variables was employed to determine the optimal conditions for the significant parameters. The optimal conditions for microwave digestion of ground wheat samples were found to be 0.5g of the sample, 9mL of 8mol/L HNO₃, and 3mL of 33 H₂O₂ at 210°C. The analytical method was validated, and the accuracy of the method was then evaluated through analysis of wheat flour-certified standard reference materials (NIST SRM 1567b). The validated procedure was subsequently applied to the analysis of 12 wheat samples sourced from local farms in the Al-Qassim region and a further six samples purchased from the Al-Qassim markets, covering six imported brands common in Saudi Arabia. The results of the study showed that the level of minerals in wheat grown in desert areas is higher than in other areas. The concentrations of macroelements and microelements in the Al-Qassim samples exceeded those of the imported samples by 12.41 and those of the samples from other countries by 33.90. The results were also evaluated using multivariate analysis techniques: principal component analysis (PCA) and hierarchical cluster analysis (HCA).

Micellar catalysis exhibited by mixed surfactant systems and gemini surfactants was reviewed. The review focused on mixed surfactant systems and tried to correlate the changes in the physico-chemical properties of these systems to the variations of their catalytic activities. Mixed surfactant systems are promising as the catalytic efficiency of some single surfactants was significantly enhanced in the presence of other critically selected surfactants. The selection should consider the charge, size, and structures of the head group as well as an appropriate length of hydrocarbon tail. The overall conclusion has arrived the mixed surfactant systems could be a tool by which the reaction rate can be tuned by changing the composition and/or the components’ structures. The higher catalytic activity of gemini surfactants compared to conventional ones, their facile synthesis and liability for structure control made them of superior choice for micellar catalysis.