Metal Content Research Articles

Antifungal Activity of Some New Binuclear Complexes

Three complexes of copper(II) and iron(II) with mixed ligands acetylacetonebis(thio-semicarbazone)- ABTSH2 and benzaldazine- BA have been prepared and characterized using different physico-chemical techniques including the determination of metal contents, mole-cular weight, measurement of molar conductivity, magnetic moment, molar refraction, infrared and electronic spectra. Accordingly, octahedral complexes having general formulaes [Cu2(ABTSH2)2(BA)2Cl2]Cl2 and [M2(ABTSH2)2(BA)2(SO4)2] {M= Cu(II) or (Fe(II)} have been proposed. The resulted complexes screened for antifungal activity in vitro against the citrus pathogen Aspergillus niger and Fusarium sp. which caused root rot of sugar and the beans pathogen Alternaria sp. All the complexes exhibited significant antifungal activities against these pathogens. The antifungal activity of these complexes were comparable with the standard fungicides in ethanol. The complex [Cu2(ABTSH2)2(BA)2Cl2]Cl2 had the best antifungal activity against Alternaria sp.

Comparative pharmaceutical evaluation of different samples of Yellow orpiment (Haratala) and Ayurvedic mineral formulation (Rasamanikya)

Background: The present work aimed to study the Physical and Physico-chemical Properties of raw Haratala (Yellow Orpiment), processed Haratala, and its self-prepared formulation Rasamanikya with different market preparations of Rasamanikya by using advance methods such as ICP-AES (qualitative and quantitative analysis), XRD and FEGSEM so that the particle size and elemental content can be estimated and compared in all the samples. This is an attempt to study the classical method of preparation as well as effect of purification process on the constituents of the drug and their size. Methods: Raw Patra Haratala (Orpiment) and three different samples of Rasamanikya were procured from authentic sources. Shodhana (purification) of Haratala was conducted by two different methods. Rasamanikya was prepared from the Haratala processed by two different methods. All the eight samples were subjected to physicochemical analysis, ICPAES, XRD and FEGSEM. Results: Arsenic content is decreased in all the samples except CSH in comparison with ASH. In ICPAES, number of elements is reduced in CSH, KSH and RMCSH in comparison with ASH whereas it is increased in RMKSH, RMMSA, RMMSB, and RMMSC. XRD analysis reveals that Average Crystal Size is minimum in RMMSA and maximum in RMMSC. Average Lattice Strain is minimum in ASH and maximum in RMMSC. Orpiment was detected in all the samples except RMKSH, RMMSB and RMMSC. FEG SEM indicates that the gross particle size of all the samples varies from 1um to 100nm at resolution ranging from 200 to 100000 magnifications. The nanoparticles are visualized at 50000 to 100000 magnifications. Conclusion: Advanced techniques like ICPAES, XRD and FEGSEM are very helpful in estimating the heavy metal content and particle size in Ayurvedic medicine. It is necessary from safety point of view. Small size particles increase the absorption of the drug in the body which causes increase in the bioavailability and potency of the drug. Hence the dose of the formulation may be reduced. Thereby the untoward effects of the high doses can be avoided.

Production of hydroxyapatite utilizing calcium and phosphorus in sewage sludge incineration ash

Sewage sludge incineration ash (SSIA), enriching the most of phosphorus (P), could be named as promising P source for P recycling and management. The novel strategy including extraction of P from SSIA by acid (HCl), purification and separation to obtain Ca liquid and Al-P liquid that could produce hydroxyapatite was investigated in this study. The P acid leaching rate was 97.9 % from SSIA at 0.2 mol/L HCl for 2 h. In P purification, P combined with Fe and Al to form precipitation (Al-P and Fe-P) with the increase of pH (<4.0). At a pH of around 4.0, the separation of Ca in the liquid phase was maximized, while Al-P and Fe-P precipitated out. Then, the Al-P precipitation could be dissolved in NaOH solution (0.2 mol/L) to separate Fe-P precipitation, that obtaining the Al-P liquid. What’s more, the high P content (P2O5, 25.5 %) in P product could be produced directly under 1.5 Ca/P molar ratio, which could be used in P fertilizer. The heavy metal content in the P product were far below the Chinese, American and EU fertilizer regulation, indicating that its environment safety. The Ca and P elements leached out during the acid leaching process were eventually recombined to form hydroxyapatite by wet-chemical purification. The cost of P recovery from SSIA was $3.06/kg P product demonstrating commercial potential of this strategy.

Effect of long-term application of pig slurry and NPK fertilizers on trace metal content in the soil.

One of the goals of sustainable agricultural production is to avoid soil contamination by elements defined as trace metals (TMs). The aim of this study was to assess the long-term impact of the use of pig slurry (PS) and NPK mineral fertilizers on the soil content of cadmium (Cd), copper (Cu), lead (Pb) and zinc (Zn). In a 9-year crop rotation, PS was used three times only before root crops. The same four levels of NPK doses (N0P0K0, N1P1K1, N3P2K2, N4P2K2) were applied to both plots with and without PS. Soil samples were collected in early spring from topsoil (0-0.3m) and subsoil (0.3-0.6m). Three forms of TMs were determined in the soil: pseudo-total (Aqua regia); bioavailable (Mehlich 3 method) and readily bioavailable (mobile) forms (1M NH4NO3). The tested factors did not have a significant impact on the Cd, Cu and Pb content, regardless of the form analyzed and the soil depth. PS application significantly increased the content of bioavailable forms of Zn regardless of the year, and the content of pseudo-total Zn only in the sugar beet year, i.e. after manure application. Increasing NPK doses increased the content of mobile Zn in the topsoil, especially in PS plots. A tendency to accumulate mobile forms of Cd and Pb was also observed on NPK-fertilized plots. Thus, long-term application of high NPK doses may increase the risk of contamination of the food chain with these metals. The content of mobile Cd and Zn was positively related to the content of total nitrogen in the soil and negatively related to pH.

Constraints on the early luminosity history of the Sun: applications to the Faint Young Sun problem

ABSTRACT Stellar evolution theory predicts that the Sun was fainter in the past, which can pose difficulties for understanding Earth’s climate history. One proposed solution to this Faint Young Sun (FYS) problem is a more luminous Sun in the past. In this paper, we address the robustness of the solar luminosity history using the yrec code to compute solar models including rotation, magnetized winds, and the associated mass-loss. We present detailed solar models, including their evolutionary history, which are in excellent agreement with solar observables. Consistent with prior standard models, we infer a high solar metal content. We provide predicted X-ray luminosities and rotation histories for usage in climate reconstructions and activity studies. We find that the Sun’s luminosity deviates from the standard solar model trajectory by at most 0.5 per cent during the Archean (corresponding to a radiative forcing of 0.849 W m$^{-2}$). The total mass-loss experienced by solar models is modest because of strong feedback between mass and angular momentum loss. We find a maximum mass-loss of $1.35 \times 10^{-3} \,{\rm M}_\odot$ since birth, at or below the level predicted by empirical estimates. The associated maximum luminosity increase falls well short of the level necessary to solve the FYS problem. We present compilations of paleotemperature and CO$_2$ reconstructions. One-dimensional ‘inverse’ climate models demonstrate a mismatch between the solar constant needed to reach high temperatures (e.g. 60–80 $^{\circ }$C) and the narrow range of plausible solar luminosities determined in this study. Maintaining a temperate Earth, however, is plausible given these conditions.

A comparative study between the efficacy of fertigation and spraying procedures in terms of the content of Cadmium (Cd) and Arsenic (As) in greenhouse cucumber.

A comparative study between fertigation and spraying procedures in terms of the status of Cadmium (Cd) and Arsenic (As) in greenhouse cucumber was conducted as a two-factor split plot based on a randomized complete block design with three replications at the Soil and Water Research Institute, Karaj, Iran in 2023. The main and sub-factors were respectively fertigation and spraying that were used in two levels [the maximum permissible concentration of Cd and As in granular triple super phosphate fertilizer (25ppm Cd and 50ppm As) and the minimum permissible concentration of these metals in granular triple super phosphate fertilizer (5ppm Cd and 5ppm As)]. Spraying was done in three modes (spraying of leaves, leaves and fruit, and fruit). On average, the results showed that the order of the concentration of Cd in plant tissues (DW) was as leaf (0.284mg/kg) > fruit peel (0.102mg/kg) > fruit peel + flesh (0.054mg/kg) > fruit flesh (0.044mg/kg). This order for As was as leaf (0.608mg/kg) > fruit flesh (0.127mg/kg) > fruit peel + flesh (0.109mg/kg) > fruit peel (0.072mg/kg). Based on the measurements, the spraying procedure accumulated more amounts of Cd and As in the fruit (i.e., peel + flesh) than the fertigation procedure. In general, it is concluded that under soilless culture, the status of heavy metals in plant tissues of greenhouse cucumber is related to the nature of the metal, the organ exposed to the metal, and the fertilization procedure. Because there is the risk of contamination of vegetables grown in the areas fertigated and sprayed with poor-quality nutrient solutions in terms of the content of heavy metals, the frequency of fertigation and spraying needs to be monitored continuously for the quality of the vegetables cultivated in greenhouses.

Analysis of Fibropapillomatosis in Roe Deer (Capreolus capreolus) Confirms High Content of Heavy Metals.

In recent decades, there has been an increase in European wild ungulate populations, often associated with a decline in health and spread of disease. This is true for the roe deer (Capreolus capreolus), the most common European cervid, with populations apparently affected by fibropapillomatosis, an increasingly common cancer. To date, however, there has been little research into this disease, thus many interactions remain unclear and descriptions of tumour composition are poorly validated. The main aim of the present study was to evaluate the presence and concentration of toxic heavy metals in roe deer skin tumours. Our results confirmed the presence of virtually all the metals tested for, i.e., Pb, Hg, Cd, As, Cr, Mn, Al, Co, Cu, Ni, Se, Zn, and Fe, with the highest average concentrations found for Cr (0.99 mg/kg-1 ± 2.23 SD), Cd (0.03 mg/kg-1 ± 0.03 SD), and Hg (0.02 mg/kg-1 ± 0.02 SD), exceeding FAO limits for meat from slaughtered animals. We also observed a significant positive relationship between heavy metal concentration and age, especially for Pb, As, Hg, Mn, Se, Al, Zn, and Ni. Our findings provide a strong baseline for further research on the impact of fibropapillomatosis, not only on the welfare and health status of game but also on the final consumer of venison, which in many respects is regarded as a high-quality, ecological, and renewable wild resource. While deer with this disease are not considered qualitatively or medically defective, they could represent a potential reservoir of substances toxic to humans and could affect substance levels in adjacent tissues or the animal as a whole.

Cytotoxic Potencies of Zinc Oxide Nanoforms in A549 and J774 Cells.

Zinc oxide nanoparticles (NPs) are used in a wide range of consumer products and in biomedical applications, resulting in an increased production of these materials with potential for exposure, thus causing human health concerns. Although there are many reports on the size-related toxicity of ZnO NPs, the toxicity of different nanoforms of this chemical, toxicity mechanisms, and potency determinants need clarification to support health risk characterization. A set of well-characterized ZnO nanoforms (e.g., uncoated ca. 30, 45, and 53 nm; coated with silicon oil, stearic acid, and (3-aminopropyl) triethoxysilane) were screened for in vitro cytotoxicity in two cell types, human lung epithelial cells (A549), and mouse monocyte/macrophage (J774) cells. ZnO (bulk) and ZnCl2 served as reference particles. Cytotoxicity was examined 24 h post-exposure by measuring CTB (viability), ATP (energy metabolism), and %LDH released (membrane integrity). Cellular oxidative stress (GSH-GSSG) and secreted proteins (targeted multiplex assay) were analyzed. Zinc oxide nanoform type-, dose-, and cell type-specific cytotoxic responses were seen, along with cellular oxidative stress. Cell-secreted protein profiles suggested ZnO NP exposure-related perturbations in signaling pathways relevant to inflammation/cell injury and corresponding biological processes, namely reactive oxygen species generation and apoptosis/necrosis, for some nanoforms, consistent with cellular oxidative stress and ATP status. The size, surface area, agglomeration state and metal contents of these ZnO nanoforms appeared to be physicochemical determinants of particle potencies. These findings warrant further research on high-content "OMICs" to validate and resolve toxicity pathways related to exposure to nanoforms to advance health risk-assessment efforts and to inform on safer materials.

Thermodynamic Insights into the Influence of Welding Current on Oxygen Levels in the Submerged Arc Welding Process

Welding current is an essential parameter for submerged arc welding process. In submerged arc welding, the enormous heat generated by the current promotes the decomposition of the oxides in the flux, releasing oxygen and increasing the oxygen level in the metal, which further affects the microstructure and mechanical properties of the weld joint. Although previous studies have developed various models to evaluate oxygen content, the thermodynamic mechanism by which current influences oxygen levels in metal remains inadequately understood. This study integrates CALPHAD technology with welding thermodynamics to predict and simulate the impact of the welding current on oxygen content in metals. By combining experimental data with thermodynamic modeling, the research investigates how different current settings affect oxygen content in the metal across various welding zones, specifically when using CaO-Al2O3 fluxes with low and high basicity indices for the welding of typical carbon steel. This study selected two current values, 300 A and 600 A, for modeling analyses of the welding process, along with two typical fluxes with basicity indices of 1.6 and 0.4. The results indicate that the proposed method outperforms the BI model and can predict the metallurgical effects of current on oxygen content in the droplet and molten pool zones. The thermodynamic mechanisms that govern the metal oxygen level are also evaluated. These findings aim to enhance the understanding of the thermodynamic mechanism that governs oxygen behavior under different current conditions, thereby contributing to the optimization of submerged arc welding process.

Differences in quality between canned and pouched tuna packed with various media

Canned and pouched tuna products may be present in different liquid media such as brine, different types of oil and sauces in the markets. Limited reported information about the pouched tuna products and the differences between them in different liquid media available in Turkish markets. pH values of CW and PW were lower than the others. TBA values of all groups were found to be below the limits for development of an objectionable odor/taste. Omega 6/omega3 ratio was determined very high in CS and PS. On the other hand, higher content of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) were found in CW and PW when compared with others (CO, CS, PO, PS). Heavy metal contents of tuna products, they were found to be safe according to limits for arsenic, mercury, lead and cadmium levels. L* values of all canned tunas (CO, CS, CW) were significantly higher than the pouched tunas (PO, PS, PW). b* values of both CW and PW were lower than the other groups. CW got the significantly lowest overall quality, color and taste scores when compared with the others. As a matter of fact, pouched tuna products especially PW were recommended for health purposes.

Seasonal nitrogen removal in an outdoor microalgal polyculture at Nordic conditions.

Microalgal solutions to clean waste streams and produce biomass were evaluated in Nordic conditions during winter, spring, and autumn in Southeast Sweden. The study investigated nitrogen (N) removal, biomass quality, and safety by treating industrial leachate water with a polyculture of local microalgae and bacteria in open raceway ponds, supplied with industrial CO2 effluent. Total N (TN) removal was higher in spring (1.5 g-2d-1), due to beneficial light conditions compared to winter and autumn (0.1 and 0.09 g-2d-1). Light, TN, and N species influenced the microalgal community (dominated by Chlorophyta), while the bacterial community remained stable throughout seasons with a large proportion of cyanobacteria. Winter conditions promoted biomass protein (19.6-26.7%) whereas lipids and carbohydrates were highest during spring (11.4-18.4 and 15.4-19.8%). Biomass toxin and metal content were below safety levels for fodder, but due to the potential presence of toxic strains, biofuels or fertilizer could be suitable applications for the algal biomass. PRACTITIONER POINTS: Microalgal removal of nitrogen from leachate water was evaluated in Nordic conditions during winter, spring, and autumn. Total nitrogen removal was highest in spring (1.5 g-2d-1), due to beneficial light conditions for autotrophic growth. Use of local polyculture made the cultivation more stable on a seasonal (light) and short-term (N-species changes) scale. Toxic elements in produced algal biomass were below legal thresholds for upcycling.

Synergistic effects of tree-herb intercropping on the phytoremediation efficiency of cadmium and lead contaminated soil

Tree-herb intercropping has emerged as an effective strategy for the remediation of soil contamination. In this study, the effects of intercropping willow with herbaceous plants Lolium perenne L., Iris lactea Pall. and Bidens pilosa L. were investigated on the phytoremediation of Cd- and Pb-contaminated soil. After a 90-day of cultivation, the results showed that intercropping stimulated the phytoremediation efficiency through increased metal accumulation in plants. Intercropping caused a significant (p < 0.05) increase in willow biomass ranging from 48.07 % to 95.58 % by promoting photosynthesis activities and antioxidant responses. Metal contents in willow leaves and roots were also observably (p < 0.05) enhanced, indicating a beneficial effect in tree-herb intercropping systems. The biomass and metal accumulation of I. lactea Pall. and B. pilosa L. decreased due to competitive interactions with willow in the intercropping treatments. However, intercropping with willow (p < 0.05) significantly increased the Pb contents of L. perenne L. Intercropping improved the absorption of bioavailable fractions of Cd and Pb by willow and herbs in comparison to the monoculture. The decrease in soil Cd contents was partly due to the chemical changes induced by root exudates, which enhanced the transfer of Cd from the soil to the plants. Willow showed a tendency for Cd accumulation, whereas herbs exhibited Pb accumulation, reflecting the complementarity of metal accumulation in tree-herb intercropping patterns. Intercropping willow with B. pilosa L. was found to be an effective method for the remediation of Cd-contaminated soil, whereas the combination of willow with L. perenne L. proved suitable for the Pb-contaminated soil. These findings might support the potential of tree-herb intercropping as an effective strategy for enhancing the phytoremediation of contaminated soils.

Surface Properties of the Kalliope–Linus System from ALMA and VLA Data

The abundance and distribution of metal in asteroid surfaces can be constrained from thermal emission measurements at radio wavelengths, informing our understanding of planetesimal differentiation processes. We observed the M-type asteroid (22) Kalliope and its moon Linus in thermal emission at 1.3, 9, and 20 mm with the Atacama Large Millimeter/submillimeter Array and the Karl G. Jansky Very Large Array over most of Kalliope's rotation period. The 1.3 mm data provide ∼30 km resolution on the surface of Kalliope, while both the 1.3 and 9 mm data resolve Linus from Kalliope. We find a thermal inertia for Kalliope of 116−91+326 J m−2 s−0.5 K−1 and emissivities of 0.65 ± 0.02 at 1.3 mm, 0.56 ± 0.03 at 9 mm, and 0.77 ± 0.02 at 20 mm. Kalliope's millimeter wavelength emission is suppressed compared to its centimeter wavelength emission, and is also depolarized. We measure emissivities for Linus of 0.73 ± 0.04 and 0.85 ± 0.17 at 1.3 and 9 mm, respectively, indicating a less metal-rich surface composition for Linus. Spatial variability in Kalliope’s emissivity reveals a region in the northern hemisphere with a high dielectric constant, suggestive of enhanced metal content. These results are together consistent with a scenario in which Linus formed from reaggregated ejecta from an impact onto a differentiated Kalliope, leaving Kalliope with a higher surface metal content than Linus, which is distributed heterogeneously across its surface. The low emissivity and lack of polarization suggest a reduced regolith composition where iron is in the form of metallic grains and constitutes ∼25% of the surface composition.

Stay with the green: New insights into ancient copper smelting in the Tonglüshan site, China

This paper presents new archaeometallurgical analyses from the Tonglüshan site, a famous ancient mining and smelting site in China. Results show that the primary phases in slag samples from two sites (Sifangtang and Lujia’nao) are all of a vitreous matrix, interspersed with fayalite crystals, wüstite, and hercynite. The trapped metallic particles in the slag are mainly raw copper with few sulfides present, which indicates a direct reduction process of oxidic ore. Iron-rich minerals were likely to be added as flux implied by the few unreacted inclusions in the slag samples. The extremely low copper content in the slag samples demonstrates a high rate of copper recovery, indicating that the copper smelting technology in the region had reached a considerably advanced level. In the meantime, the variations in metal content in slag samples from different periods reveal the diachronic changes in this copper smelting technology. The Tonglüshan site, with its millennia of ancient mining and metallurgical activities, provides an excellent material base for detailed studies on technological evolution.

Mineral formation and element migration in fractures and pores of hydrogenetic ferromanganese nodules

Ferromanganese (FeMn) nodules composed of nano-sized FeMn (oxyhydr)oxides are significant mineral resources rich in multiple critical metals (e.g., Co, Ni, Cu, and REY). The ubiquitous high porosity, large pore size, and pore connectivity in hydrogenetic nodules enable the constant influx of seawater and/or porewater driving widespread diagenetic processes (i.e., mineral dissolution and recrystallization) in the abundant fractures and pores. These diagenetic processes are critical to understanding the migration, partitioning, and distribution of the critical metals, but remain unclear yet. In this study, high-resolution in-situ analyses were conducted to investigate the mineralogical and geochemical characteristics of diagenetic precipitates in fractures and pores of a hydrogenetic FeMn nodule (MP5D33) from the central Pacific. Both oxic and suboxic processes were found in the fracture. The oxidized diagenetic products exhibit geochemical and mineralogical characteristics similar to thoese of hydrogenetic precipitates (e.g., vernadite), while the suboxic diagenetic processes primarily produced large-size 10 Å phyllomanganate. The diagenetic conditions within this studied fracture gradually shifted from oxic to suboxic, causing changes in the contents of multiple critical metals. The minerals in pores are mainly composed of 10 Å phyllomanganate that crystallized forms through heterogeneous nucleation on small-size vernadite in a suboxic environment. Additionally, minor todorokite likely transformed from 10 Å phyllomanganate undergoing long-term diagenesis. These findings shed some insights into the diagenetic process in the interior fractures and/or pores of FeMn nodules and enhance the understanding of the migration of critical elements associated with FeMn (oxyhydr)oxides during diagenesis in FeMn deposits.

Mechanism of ozone catalysis by transition metal hydroxyl oxides: From reactive oxygen species to surface structural hydroxyl

Transition metal hydroxyl oxides have been used widely as ozone catalysts for water purification. However, the fabrication methods selected and the pollutants treated vary, making it difficult to compare their performance. In this study, ZnOOH, FeOOH, CoOOH, and MnOOH were synthesized by the same method to remove multiple structurally similar targets. Results showed that the ZnOOH performed the best, removing over 90% of all targets within 40min, and presenting the highest ozone utilization rate of 0.081min-1. Multiple ROS quantification and contribution experiments jointly demonstrated that ZnOOH had an advantage over the other catalysts only in ·OH generation, but the ·OH contributed 93% of target removal in the ZnOOH/O3 process. Structure analysis of ZnOOH suggested that its ·OH generation had little connection with the contents of surface metal and adsorbed water, but was dependent on the surface structural hydroxyl that would undergo loss at 100-300℃. This concentration of ZnOOH was 10.1mM/g, which was 1.7, 5.3, and 6.3 times higher than that of FeOOH, CoOOH, and MnOOH, respectively. Heat treatment further revealed that these surface hydroxyl mainly originated from the hydroxyl ions from water dissociation and could regenerate timely during reuse. Finally, a possible catalysis pathway was proposed.

Hydrogenation of CO2 to light olefins over Ga2O3-ZIF-8 tandem catalyst

Tandem catalysts composed of metal oxides and zeolites have demonstrated significant potential for the hydrogenation of CO2 to light olefins. However, their development is hindered by the competing reverse water–gas shift reaction and carbon accumulation on the zeolite surface. To address these challenges, we developed a series of innovative tandem catalysts by substituting conventional zeolites with ZIF-8. Our research primarily focused on examining the effects of metal species and content, as well as the particle size of ZIF-8, on catalytic performance. Notably, we achieved a CO2 conversion of 20.2 % and a light olefins selectivity of 73.6 % using a catalyst with 20 % Ga2O3 content and a ZIF-8 particle size of 100 nm at a reaction temperature of 340 °C and pressure of 3.0 MPa. In order to improve the stability of the catalyst, ZIF-8 was modified with La to improve its thermal stability. A CO2 conversion of 23.5 % and a light olefins selectivity of 66.5 % were maintained after 50 h of continuous reaction. While the catalytic activity of La-modified catalysts is slightly lower than that of unmodified ones, their superior stability makes them more suitable for thermal catalytic hydrogenation of CO2. Various characterizations and theoretical calculations revealed that La modification not only enhanced the thermal stability of catalyst but also improved its adsorption and activation capabilities for the reacting gases. Furthermore, the reaction mechanism of CO2 hydrogenation to light olefins was investigated by in-situ diffuse reflectance Fourier transform infrared spectroscopy. This study provides a technical foundation for designing efficient catalysts based on metal–organic frameworks in the field of carbon dioxide thermal catalytic conversion.

Seasonal assessment of surface water and sediments pollution in Rachiine River, Northern Lebanon, using multivariate statistical analysis

Urbanization has caused severe negative impacts on intra-urban river water worldwide. In this study, the WHO drinking water standards (2024) were used as reference to assess the physicochemical properties, heavy metals (HMs) content and microbial load in water and sediment samples collected from 25 locations along Rachiine River, located in Northern Lebanon, during wet and dry periods. Multivariate statistical analysis was applied to evaluate the seasonal variations in water and sediment quality, and determine the pollution sources. The microbial load assessment indicated high pollution levels by Escherichia coli, fecal enterococci, total coliform and fecal coliform, which generally increased as the river progressed downstream. Cluster analysis (CA) provided three major clusters in the study region, representing the northern, central, and southern sectors of the river. Principal components analysis (PCA) of water samples generated four principal components (PCs) accounting for 64.3, 11.4, 7.6 and 4.1 % of the total variance, whereas PCA of sediment samples explained 59.1, 16.9 and 11.1 % of the data set variance. These PCs revealed that the quality of water and sediments is significantly impacted by point and diffuse sources, including geological and anthropogenic factors. These findings call for urgent management strategies to limit future deterioration of the aquatic bodies.

Small extracellular vesicles contain metals and transfer metal intercellularly.

Cells have developed a highly regulated system for the uptake, transport, utilization, storage, and export of metals, ensuring the maintenance of cellular homeostasis. Small extracellular vesicles (sEVs) function as a mechanism through which a cell can export its cargo and transfer it to recipient cells. However, in contrast to the other molecular cargo associated with sEVs, the metal content of sEVs is not well characterized. To address this gap in knowledge, we measured the levels of nine essential metals (copper, iron, zinc, manganese, magnesium, potassium, calcium, chromium, cobalt) and six non-essential metals (nickel, rubidium, titanium, aluminium, lithium, lead) in sEVs originating from multiple in vitro and ex vivo sources. Our findings reveal that, beyond containing redox-active essential metals and those involved in redox reactions, sEVs also exhibit the capability to export and transfer non-physiological, potentially toxic metals.

Comparative study of Ni nanoparticles synthetized using electroless Ni plating waste and an analytical Ni reagent. Characterization and possible application in magnetic fluids

Wastewater from the electroless industry represents a potential danger to the environment and health, mainly due to its heavy metal content. In this study, nickel nanoparticles were synthesized through chemical reduction precipitation by using an electroless nickel plating waste and hydrazine sulfate as reducing agent. The aim of the present work is twofold. First we want to extract the metal from the aqueous medium, minimizing its content to levels allowed by environmental regulations. Second, we aim to valorize the residue by recovering the precipitated nickel to be applied as a solid phase in a magnetic fluid (MF). It is found that the present synthesis method using N2H4 as reducing agent, allowed us to minimize the Ni concentration in the aqueous waste in 97.49 %. The properties of the recovered Ni precipitate is compared with the Ni nanoparticles (NPs) obtained from a solution prepared with analytical grade nickel sulfate. The synthesized materials from both the waste (Ni-R) and analytical reagent (Ni-A) were characterized by comparing their chemical, physical, and morphological properties. In both cases, the Ni-R and Ni-A precipitates, spherical Ni NPs of 8–10 nm crystallite sizes are obtained, agglomerated in a bimodal size distribution centered at 174.6 and 383.4 nm, and a monomodal size distribution centered at 63.6 nm, respectively. Both Ni precipitated samples are ferromagnetic, but the Ni-R sample has a higher magnetic saturation of 40 emu/g compared to 8 emu/g of the Ni-A sample. The difference in the rheological behavior of both precipitates could be attributed to the presence of surface oxidation having a relatively less contribution in the case of the Ni-R particles due to the higher average size of the particles. The Fe content, probably coming from the nickel-plated parts in spent baths, is slightly higher in the Ni-R sample. Thus, the present work shows that it is possible to valorize an industrial Ni-based residue, by obtaining Ni precipitates that in magnetic fluids give even better results than those expected under more rigorous experimental conditions, i.e., in cases where the quality of the chemical precursors is usually a determining factor.