Gaber A. M. Mersal

Air particulate matter with a diameter of 2.5 µm (PM_2.5) were assembled for a whole year from the historical Jeddah district. Additional PM_2.5 aerosols were collected during the autumn and winter seasons from another newly constructed district in Jeddah city (Alnaeem). The annual concentration of the total mass of the PM_2.5 aerosols from the historical Jeddah site was found to be 43 ± 6 µg/m³. In addition, the average of the total mass concentration at the Alnaeem site was 61 ± 14 µg/m³. These values were greater than the annual mass concentration of the air quality standards of the European Commission (25 µg/m³) and the World Health Organization (10 µg/m³). The elemental analysis of the collected fine atmospheric aerosols was achieved by energy dispersive X-ray fluorescence (EDXRF) with three secondary targets (CaF₂, Ge, and Mo). Quantitative elemental analyses of twenty-two (22) elements were achieved starting from the low atomic number element (Na) up to the high atomic number element (Pb). Although the historical Jeddah site is not well organized, the elemental concentrations and total mass concentrations were lower than those of the other site. The statistical analyses including enrichment factors, correlation analysis, and the principal component analysis revealed more information about the source identification of the PM_2.5 aerosols collected from both locations. It was recognized that the elements Al, Si, K, Ca, Ti, Mn, Fe, Rb, and Sr originated from a natural source. On the other hand, the elements Ta, Br, Pb, Sc, Ni, Cu, Zn, and S originated from anthropogenic sources. Finally, the elements Na, Cl, and Br came mainly from the sea spray source.

This article reports the synthesis of PbO doped MgZnO (PbO@MgZnO) by a co-precipitation method, followed by an ultrasonication process. PbO@MgZnO demonstrates a significant adsorption capability toward Magenta Dye (MD). The greatest adsorption capability was optimized by varying parameters such as pH, MD concentration, and adsorbent dose. The kinetics study illustrates that the adsorption of MD on PbO@MgZnO follows the pseudo-second-order. The isotherm study revealed that Langmuir is best fitted for the adsorption, but with little difference in the R² value of Langmuir and Freundlich, the adsorption process cloud be single or multi-layer. The maximum adsorption capacity was found to be 333.33 mg/g. The negative ΔG refers to the spontaneity of MD adsorption on PbO@MgZnO. The steric parameters from statistical physics models also favor the multi-layer adsorption mechanism. As a function of solution temperature, the parameter n pattern has values of n = 0.395, 0.290, and 0.280 for 298, 308, and 318 K, respectively (i.e., all values were below 1). Therefore, horizontal molecule positioning and multiple locking mechanisms were implicated during interactions between MD and PbO@MgZnO active sites.

Novel cyano-benzylidene xanthene derivatives were synthesized using one-pot and condensation reactions. A diprotic Brønsted acid (i.e., oxalic acid) was used as an effective catalyst for the promotion of the synthesis process of the new starting xanthene–aldehyde compound. Different xanthene concentrations (ca. 0.1–2.0 mM) were applied as corrosion inhibitors to control the alkaline uniform corrosion of aluminum. Measurements were conducted in 1.0 M NaOH solution using Tafel extrapolation and linear polarization resistance (LPR) methods. The investigated xanthenes acted as mixed-type inhibitors that primarily affect the anodic process. Their inhibition efficiency values were enhanced with inhibitor concentration, and varied according to their chemical structures. At a concentration of 2.0 mM, the best-performing studied xanthene derivative recorded maximum inhibition efficiency values of 98.9% (calculated via the Tafel extrapolation method) and 98.4% (estimated via the LPR method). Scanning electron microscopy (SEM) was used to examine the morphology of the corroded and inhibited aluminum surfaces, revealing strong inhibitory action of each studied compound. High-resolution X-ray photoelectron spectroscopy (XPS) profiles validated the inhibitor compounds’ adsorption on the Al surface. Density functional theory (DFT) and Monte Carlo simulations were applied to investigate the distinction of the anticorrosive behavior among the studied xanthenes toward the Al (111) surface. The non-planarity of xanthenes and the presence of the nitrile group were the key players in the adsorption process. A match between the experimental and theoretical findings was evidenced.

The strawberry has a very short postharvest life due to its fast softening and decomposition. The goal of this research is to see how well a starch-silver nanoparticle (St-AgNPs) coating affects the physical, chemical, and microbiological qualities of strawberries during postharvest life. Additionally, the effect of washing with running water on silver concentration in coated strawberry fruit was studied by an inductively coupled plasma-optical emission spectrometer (ICP-OES). Furthermore, the shelf-life period was calculated in relation to the temperature of storage. Fourier transform infrared-attenuated total reflectance (FTIR-ATR), UV-Visible, and Transmission Electron Microscopic (TEM) were used to investigate the structure of starch-silver materials, the size and shape of AgNPs, respectively. The AgNPs were spherical, with an average size range of 12.7 nm. The coated samples had the lowest weight loss, decay, and microbial counts as compared to the uncoated sample. They had higher total acidity and anthocyanin contents as well. The washing process led to the almost complete removal of silver particles by rates ranging from 98.86 to 99.10%. Finally, the coating maintained strawberry qualities and lengthened their shelf-life from 2 to 6 days at room storage and from 8 to 16 days in cold storage.

Three mononuclear 2-picolylamine-containing zinc(III) complexes viz [(2-PA)₂ZnCl]₂(ZnCl₄)] (Zn1), [(2-PA)₂Zn(H₂O)](NO₃)₂] (Zn2) and [Zn(2-PA)₂(OH)]NO₃] (Zn3) were synthesized and fully characterized. Spectral and X-ray structural characteristics showed that the Zn1 complex has a square-pyramidal coordination environment around a zinc(II) core. The hydroxide complex Zn3 was non-covalently functionalized with few layers of graphene oxide (GO) sheets, formed by exfoliation of GO in water. The resulting Zn3/GO hybrid material was characterized by FT-IR, TGA-DSC, SEM-EDX and X-ray powder diffraction. The way of interaction of Zn3 with GO has been established through density functional theory (DFT) calculations. Both experimental and theoretical findings indicate that, on the surface of GO, the complex Zn3 forms a complete double-sided adsorption layer. Zn3 and its hybrid form Zn3/GO have been individually investigated as electrocatalysts for the hydrogen evolution reaction. The hybrid heterogenized form Zn3/GO was supported on glassy carbon (GC) with variable loading densities of Zn3 (0.2, 0.4 and 0.8 mg cm⁻²) to form electrodes. These electrodes have been tested as molecular electrocatalysts for the hydrogen evolution reaction (HER) using linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS) in 0.1 M KOH. Results showed that both GC-Zn3 and GC-Zn3/GO catalysts for the HER are highly active, and with increase of the catalyst’s loading density, this catalytic activity enhances. The high catalytic activity of HER with a low onset potential of −140 mV vs. RHE and a high exchange current density of 0.22 mA cm⁻² is achieved with the highest loading density of Zn3 (0.8 mg cm⁻²). To achieve a current density of 10 mA cm⁻², an overpotential of 240 mV was needed.

The present study examines the role of leguminous compost (LC), humic acids (HA), and phosphate-solubilizing bacteria (P-SB) in alleviating the stress effects of high soil CaCO₃ content in Phaseolus vulgaris. Two pot trials for two consecutive seasons; fall 2019 and summer 2020 were implemented in an open greenhouse. A mixed three-way ANOVA, two independent factors (season and soil treatments) and one within factors (time) were used with four replicates. Residual maximum likelihood (REML) analysis was used for the mixed model of the studied traits. Inoculation of calcareous soil with P-SB (a 1:1 mixture of two Pseudomonas sp.; Ps. mallei and Ps. cepaceae) significantly exceeded LC, HA, or even LC+HA for the positive results obtained. P-SB facilitated nutrient solubility (e.g., N, K, Fe, and Mn), including conversion of insoluble phosphorous into a form available in the tested soil due to increased soil enzymatic activities (e.g., phosphatases and phytases). This mechanism, combined with a decrease in soil calcium carbonate content and an increase in cation exchange capacity (CEC) and organic matter (OM) content, increased the availability of various nutrients to plants, including P, in the soil, which contributed to the increased plant output. Adequate P content in plants led to a marked decrease in plant acid phosphatase activity under high content of CaCO₃. The study concluded that the use of P-SB promotes biological activities, nutrient availability, and thus the productivity of calcareous soils, enabling Phaseolus vulgaris plants to withstand stress produced by high CaCO₃ content through the development and/or adoption of potentially effective mechanisms. Strong highly significant interactions between the treatments and time were observed using the Wald’s statistics test, which indicates a positive correlation.

The molecular complexes between barbituric acid (BU) and chloranilic acid (ChA) over graphitic nitride (g-C₃N₄) are investigated. The molecular complexes and the nanocomposite were investigated both in solid state and in methanol. The solid complexes and the corresponding nanocomposite were investigated using FTIR, TGA, and UV-Vis spectroscopy. The structures were explored using DFT calculations using wB97XD/ and def2-TZVP basis set. The DFT calculations revealed the formation of hydrogen-bonded complexes, which initiate the proton transfer from ChA to BU. Immobilization of the BUChA complex over the g-C₃N₄ sheet was stabilized by weak non-covalent interactions, such as π–π interactions. g-C₃N₄ facilitated the charge transfer process, which is beneficial for different applications.

Type 2 diabetes mellitus (T2DM) and hypertension are common chronic diseases mainly associated with the development and progression of end-stage renal disease (ESRD) leading to morbidity and mortality. Gene polymorphisms linked to the renin–angiotensin (AGT)–aldosterone system (RAAS) were broadly inspected in patients with diabetic nephropathy (DN) and hypertension. This study aimed to investigate the association of AGT gene polymorphisms (rs699 and rs4762) with ESRD in T2DM hypertensive Egyptian patients. Genotyping of rs699 and rs4762 was conducted using the tetra-primers amplification refractory mutation system (ARMS-PCR). The allelic distribution analysis was performed on 103 healthy control subjects, 97 non-ESRD patients, and 104 patients with ESRD. The allelic frequencies of AGT gene polymorphisms (rs4762 and rs699) in all study participants were assessed. For the non-ESRD group, the frequencies of the alleles of AGT-rs4762 (χ² = 31.88, p < 0.001, OR = 5.17, CI 95%: 2.81–9.51) and AGT-rs699 (χ² = 4.85, p = 0.027, OR = 1.56, CI 95%: 1.05–2.33) were significantly associated with the non-ESRD group. However, for the ESRD group, the T allele was significantly higher than that in the controls (χ² = 24.97, p < 0.001, odds ratio (OR) = 4.35, CI 95%: 2.36–8.02). Moreover, AGT (rs699) genotypes showed no significant difference between the ESRD group and controls. In conclusion, AGT gene polymorphisms rs699 and rs4762 were associated with non-ESRD versus controls, without any significant risk observed in all patient groups. However, the AGT (rs4762) variant showed a significant risk in the ESRD group in comparison to controls in Egyptians.