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The utilization of phosphorite deposits as an industrial resource is of paramount importance, and its sustainability largely depends on ensuring safe and responsible practices. This study aims to evaluate the suitability of phosphorite deposits for industrial applications such as the production of phosphoric acid and phosphatic fertilizers. To achieve this goal, the study meticulously examines the geochemical characteristics of the deposits, investigates the distribution of natural Radioactivity within them, and assesses the potential radiological risk associated with their use. The phosphorites are massive and collected from different beds within the Duwi Formation at the Hamadat mining area. They are grain-supported and composed of phosphatic pellets, bioclasts (bones), non-phosphatic minerals, and cement. Geochemically, phosphorites contain high concentrations of P 2 O 5 (23.59–28.36 wt.%) and CaO (40.85–44.35 wt.%), with low amounts of Al 2 O 3 (0.23–0.51 wt.%), TiO 2 (0.01–0.03 wt.%), Fe 2 O 3 (1.14–2.28 wt.%), Na 2 O (0.37–1.19 wt.%), K 2 O (0.03–0.12 wt.%), and MnO (0.08–0.18 wt.%), suggesting the low contribution of the detrital material during their deposition. Moreover, they belong to contain enhanced U concentration (55–128 ppm). They are also enriched with Sr, Ba, Cr, V, and Zn and depleted in Th, Zr, and Rb, which strongly supports the low detrital input during the formation of the Hamadat phosphorites. The high Radioactivity of the studied phosphorites is probably due to the widespread occurrence of phosphatic components (e.g., apatite) that accommodate U in high concentrations. Gamma spectrometry based on NaI (Tl) crystal 3×3 has been used to measure occurring radionuclides in the phosphorite samples. The results indicate that the radioactive concentrations’ average values of 226 Ra, 232 Th, and 40 K are 184.18±9.19, 125.82±6.29, and 63.82±3.19 Bq Kg -1 , respectively. Additionally, evaluations have been made of the radiological hazards. The calculated risk indicators exceeded the recommended national and world averages. The data obtained will serve as a reference for follow-up studies to evaluate the effectiveness of the Radioactivity of phosphatic materials collected from the Hamdat mine area.

In the current study, polyvinyl alcohol (PVA) films were doped with different concentrations of Caesium dichromate (Cs 2 Cr 2 O 7 ) nanoparticles (0, 2, 4, 6, and 8%). The PVA-Cs 2 Cr 2 O 7 films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and ultraviolet–visible (UV–Vis) spectrophotometry. XRD analysis showed that increasing Cs 2 Cr 2 O 7 significantly changed the crystalline structure of the PVA films. FT-IR spectroscopy confirmed the interaction between PVA and Cs 2 Cr 2 O 7 nanoparticles, which showed the appearance of Cr–O–Cr and Cr=O starching bonds at higher concentrations of Cs 2 Cr 2 O 7 in the PVA matrix. UV–Vis analysis revealed a remarkable increase in optical absorbance and redshift in the edge of the absorption of the PVA matrix to the visible region with increasing Cs 2 Cr 2 O 7 concentration. The optical indirect and direct bandgap energies were decreased to about 2.03 eV and 2.69 eV for the PVA film doped with 8% Cs 2 Cr 2 O 7 , respectively. Radiation shield properties were also studied using Phy-X/PSD software. The mass attenuation coefficient (G mac ) was calculated in the energy range of 0.015–15 MeV for gamma rays. The results showed that PCCO4 exhibited the highest mass attenuation coefficient of 0.295 cm 2 /g at 0.1 MeV, about 42% higher than that of PCCO0. The half value (G hvl ) decreased from 2.6 cm for PCCO0 to 1.5 cm for PCCO4, indicating increased radiation shielding effectiveness and higher Cs 2 Cr 2 O 7 concentration. Incorporating Cs 2 Cr 2 O 7 nanoparticles into PVA films significantly improves their optical and radiation shielding properties, making them promising materials for various applications, including protective coatings and photoelectronic devices.

For technical and radioprotection causes, it has become essential to find new trends of smart materials which used as protection from ionizing radiation. To overcome the undesirable properties in lead aprons and provide the proper or better shielding properties against ionizing radiation, the tendency is now going to use ferrite as a shielding material. The co-precipitation method was utilized to prevent any foreign phases in the investigated MZN nano-ferrite. X-ray diffraction (XRD) and Fourier transmission infrared spectroscopy (FTIR) methods were used to analyze the manufactured sample. As proven by XRD and FTIR, the studied materials have their unique spinel phase with cubic structure Fd3m space group. The DC resistivity of Mg–Zn ferrite was carried out in the temperature range (77–295 K), and its dependence on temperature indicates that there are different charge transport mechanisms. The Mössbauer spectra analysis confirmed that the ferrimagnetic to superparamagnetic phase transition behaviour depends on Zn concentration. The incorporation of Zn to MZF enhanced the nano-ferrite density, whereas the addition of different Zn-oxides reduced the density for nano-ferrite samples. This variation in density changed the radiation shielding results. The sample containing high Zn (MZF-0.5) gives us better results in radiation shielding properties at low gamma, so this sample is superior in shielding results for charged particles at low energy. Finally, the possibility to use MZN nano-ferrite with various content in different ionizing radiation shielding fields can be concluded.

Tannery industries are one of the extensive industrial activities which are the major source of chromium contamination in the environment. Chromium contamination has been an increasing threat to the environment and human health. Therefore, the removal of chromium ions is necessary to save human society. This study is oriented toward the preparation of a new triazole Schiff base derivatives for the remediation of chromium ions. 4,4′-((1E)-1,2-bis ((1H-1,2,4-triazol-3-yl) imino)ethane-1,2-diyl) diphenol was prepared by the interaction between 3-Amino-1H-1,2,4-triazole and 4,4′-Dihydroxybenzil. Then, the produced Schiff base underwent a phosphorylation reaction to produce the adsorbent (TIHP), which confirmed its structure via the different tools FTIR, TGA, 1HNMR, 13CNMR, GC-MS, and Phosphorus-31 nuclear magnetic resonance (31P-NMR). The newly synthesized adsorbent (TIHP) was used to remove chromium oxyanions (Cr(VI)) from an aqueous solution. The batch technique was used to test many controlling factors, including the pH of the working aqueous solution, the amount of adsorbent dose, the initial concentration of Cr(VI), the interaction time, and the temperature. The desorption behaviour of Cr(VI) changes when it is exposed to the suggested foreign ions. The maximum adsorption capacity for Cr(VI) adsorption on the new adsorbent was 307.07 mg/g at room temperature. Freundlich’s isotherm model fits the adsorption isotherms perfectly. The kinetic results were well-constrained by the pseudo-second-order equation. The thermodynamic studies establish that the adsorption type was exothermic and naturally spontaneous.

This study aims to evaluate the suitability of subsurface layers for infrastructure development using geophysical and geotechnical studies. Six seismic refraction and six 2D geoelectic profiles were conducted in the study area to analyze the geotechnical characteristics of the subsoil in order to assess its suitability for construction projects. According to the geophysical investigation, there are two main geoelectric strata, each with a different lithology and thickness. The first layer has high resistivity values of more than 200 (Ωm) and its thickness is between 3.5 and 6.3 m. The second layer's resistivity ranges from 0.3 to 200 (Ωm). The findings indicate that the near-surface area of the study site is composed of two layers in addition to the surface layer, which consists of semi-consolidated wadi fill deposits of gravel, sand, and silt with rock fragments. The first layer comprises fractured limestone with clay intercalation, followed by a second layer of marly limestone, which transitions into marl and clay. Both compressional (P) and shear (S) waves were detected and analyzed. The shallow seismic refraction technique indicates that the velocity waves (Vp) in the first and second layers range from 133 to 770 and 790 to 3100 m/s respectively. Various engineering parameters for the second layer were determined, including elastic moduli (bulk modulus, Poisson’s ratio, rigidity modulus, and Young’s modulus), competence scales (stress ratio, concentration index, material index and density gradient), and bearing capacity (ultimate and allowable). The average Poisson ratio for the first and second layers is 0.235. The ultimate bearing capacity (Qu) of the first layer ranges from 379.1 to 1031.2 gm/cm 2 and between 1040.8 and 1548.5 gm/cm 2 of the second layer. Allowable bearing capacity (Qall) for the first layer is between 126.4 and 343.7 gm/cm 2 , and for the second layer, it is between 346.9 and 516.2 gm/cm 2 . According to the geotechnical investigation's findings, the range of liquid limit (LL) values is between 41.20 and 86.30%, the range of plastic limit (PL) values is between 18 and 35.25%, the range of plasticity index (PI) values is between 14.17 and 51.45%, and the range of free swelling values is between 60 and 170%. However, the study identified high-risk areas in the study area. These zones are located in the first and second layers represented by strongly swelling clay layers and strongly fractured limestone, which will have a major impact on the road and buildings. Therefore, this study recommends addressing these problems before any development to protect these areas from subsidence and collapse.

AbstractThis study focuses on the consequences of the COVID-19 pandemic on annual effective doses and excess lifetime cancer risk values due to ionizing radiation and radon which has been reported UNSCEAR 2000. The random data collection questionnaire method was applied to assess the indoor and outdoor occupancy factor for three age groups during the epidemic in Turkey. The results indicated age group C (Age > 65 y) has more influence from pandemic indoor and outdoor occupancy factor. As compared to before pandemic data in study area and global average exposure to natural radioactive sources.Graphic abstract

This paper presents a new approach of energy management for a fuel cell electric vehicle traction system. This system includes a supercapacitor, a traction battery of valve-regulated sealed lead–acid type, a high-performance permanent magnet traction system, and a power electronics converter. Special attention was placed on the coordination for managing the flow of energy from several sources to treat the concerns of prolonged electric vehicle mileage and battery lifetime for drivetrains of electric vehicles. Connection to a supercapacitor in parallel with the electric vehicle’s battery affects electric vehicle battery lifetime and its range. The paper used a study case of an all-electric train, but the used methods can be applied on hybrid or electric train cases. Fuzzy logic control and proportional integral control methods were used to control the electric vehicle system. The results of these two control methods were examined and compared. The simulation results were compared between the proposed electric vehicle system and the traditional system to show the effectiveness of the proposed method. Comparison of waveforms was made with and without the supercapacitor. The proposed optimized energy management strategy could improve the overall performance of the hybrid system and reduce the power consumption.

Flexible supercapacitors (FS) are ideal as power backups for upcoming stretchable electronics due to their high power density and good mechanical compliance. However, lacking technology for FS mass manufacturing is still a significant obstacle. The present study describes a novel method for preparing FS based on reduced graphene oxide (RGO) using the N + plasma technique, in which N + reduces graphene oxide on the surface of a cotton/polyester substrate. The effect of aloe vera (AV) as a natural reducing & capping agent and carbon nanotubes (CNT) as nanoconductors on the electrochemical performance of the electrodes is studied. FESEM and XPS were employed to investigate the electrodes' structural and chemical composition of electrodes. The galvanostatic charge–discharge curves of electrodes revealed the enhancement of the electrochemical activity of the as-prepared electrode upon additions of AV and CNT. The areal capacitance of the RGO, RGO/AV, and RGO/AV/CNT supercapacitors at 5 mV/s was 511, 1244.5, and 1879 mF/cm 2 , respectively. The RGO electrode showed capacitive retention of 80.9% after 2000 cycles enhanced to 89.7% and 92% for RGO/AV and RGO/AV/CNT electrodes, respectively. The equivalent series resistance of the RGO electrode was 126.28 Ω, decreased to 56.62 and 40.06 Ω for RGO/AV and RGO/AV/CNT electrodes, respectively.

The widely distributed granitic intrusions in the Nubian Shield can provide comprehensive data for understanding its crustal evolution. We present new bulk-rock geochemistry and isotopic (zircon U-Pb and Lu-Hf) data from the Haweit granodiorites in the Gabgaba Terrane (NE Sudan). The dated zircons presented a 206Pb/238U Concordia age of 718.5 ± 2.2 Ma, indicating that they crystallized during the Cryogenian. The granodiorites contain both biotite and amphibole as the main mafic constituents. The samples exhibit metaluminous (A/CNK = 0.84–0.94) and calc-alkaline signatures. Their mineralogical composition and remarkable low P2O5, Zr, Ce, and Nb concentrations confirm that they belong to I-type granites. They exhibit subduction-related magma geochemical characters such as enrichment in LILEs and LREEs and depletion in HFSEs and HREEs, with a low (La/Yb)N ratio (3.0–5.9) and apparent negative Nb anomaly. The positive Hf(t) values (+7.34 to +11.21) and young crustal model age (TDMC = 734–985 Ma) indicates a juvenile composition of the granodiorites. The data suggest that the Haweit granodiorites may have formed from partially melting a juvenile low-K mafic source. During subduction, the ascending asthenosphere melts might heat and partially melt the pre-existing lower crust mafic materials to generate the Haweit granodiorites in the middle segment of the Nubian Shield.

The main objective of this work is to recycle unwanted industrial waste in order to produce innovative nanocomposites with improved mechanical, tribological, and thermal properties for use in various industrial purposes. In this context, powder metallurgy (PM) technique was used to fabricate iron (Fe)/copper (Cu)/niobium carbide (NbC)/granite nanocomposites having outstanding mechanical, wear and thermal properties. Transmission electron microscopy (TEM) and X-ray diffraction (XRD) examinations were used to investigate the particle size, crystal size, and phase composition of the milled samples. Additionally, it was investigated how different volume percentages of the NbC and granite affected the sintered specimens in terms of density, microstructure, mechanical and wear properties, and coefficient of thermal expansion (CTE). According to the findings, the milled powders included particles that were around 55 nm in size and clearly contained agglomerates. The results showed that the addition of 4 vol.% NbC and 8 vol.% granite nanoparticles caused a reduction in the Fe–Cu alloy matrix particle sizes up to 47.8 nm and served as a barrier to the migration of dislocations. In addition, the successive increase in the hybrid concentrations led to a significant decrease in the crystal size of the samples prepared as follows: 29.73, 27.58, 22.69, 19.95 and 15.8 nm. Furthermore, compared with the base Fe–Cu alloy, the nanocomposite having 12 vol.% of hybrid reinforcement demonstrated a significant improvement in the microhardness, ultimate strength, Young’s modulus, longitudinal modulus, shear modulus, bulk modulus, CTE and wear rate by 94.3, 96.4, 61.1, 78.2, 57.1, 73.6, 25.6 and 61.9%, respectively. This indicates that both NbC and granite can actually act as excellent reinforcements in the Fe alloy.