Search Results (299)

As one of the world’s most widely used packaging materials, paper obtains its properties from its major component: wood. Variations in the species of wood result in variations in the paper’s mechanical properties. The pulp and paper production industry is known to be a polluting industry and a consumer of a large amount of energy but remains an essential heavy industry globally. Paper production, based largely on the kraft process, is mainly intended for the food packaging sector and, thus, is associated with contamination risks. The lack of standardized regulations and the different analytical techniques used make information on the subject complex, particularly for inorganic elements where little information is available in the literature. Most research in this field is based on sample preparation using mineralization via acid digestion to obtain a liquid and homogeneous matrix, mainly with a HNO₃/H₂O₂ mixture. The most commonly used techniques are Atomic Absorption Spectrometry (AAS), Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES), and Inductively Coupled Plasma Mass Spectrometry (ICP-MS), each with its advantages and disadvantages, which complicates the use of these tech-niques for routine analyses on an industrial site. In the same field of inorganic compound analysis, Microwave Plasma Atomic Emission Spectrometry (MP-AES) has become a real alternative to techniques such as AAS or ICP-AES. This technique has been used in several studies in the food and environmental fields. This publication aims to examine, for the first time, the state of the art regarding the analysis of inorganic elements in food packaging and different matrices using MP-AES. The entire manufacturing process is studied to identify possible sources of inorganic contaminants. Various analytical techniques used in the field are also presented, as well as research conducted with MP-AES to highlight the potential benefits of this technique in the field. Full article

Detailed description of phase composition and geochemistry of the Muschelkalk carbonate rocks of the Upper Silesian Province in Poland were presented in this article. The tests were carried out to determine mineralogical features and geochemical properties. The samples were collected from the formations of the Lower Muschelkalk (Gogolin Unit), Middle Muschelkalk (Diplopore Dolomite Unit) and Upper Muschelkalk (Tarnowice Unit, Boruszowice Unit). The following research methods were used: macroscopic description, X-Ray Diffraction, Fourier transform infrared spectroscopy, X-Ray Fluorescence and Atomic spectrometry with plasma intensification. The following carbonate phases were identified: a low-Mg calcite, a high-Mg calcite, a proto-dolomite, an ordered dolomite and a huntite. The results of XRD analysis allowed the determination of the chemical formulas of the mineral phases. XRF and ICP AES analyses allowed to establish the content of following trace elements: Sr, Ba, Al, Si, Fe, Mn, K, Na, S, Cl, Ti, Cr, Ni, Zn, Rb, Zr, Pb, As, V, Be, B, Co, Cu, Br, Mo and Cd. Apart from Sr and Ba, they are not fundamental components of carbonate rocks. They indicate the presence of minerals such as silicates, aluminosilicates, oxides and sulfides. Full article

Despite its many important health benefits, fish consumption is associated with a growing risk of toxicity due to increasing levels of environmental pollution. Therefore, this study compared the potential risks to human health associated with the consumption of imported fish and locally produced fish, which may be contaminated with toxic elements. A selection of the most commonly consumed fish in Poland, imported and domestic, was assayed for 11 trace elements in muscle tissue using ICP-AES, CV-AAS and GF-AAS. In general, the levels of toxic elements decreased according to the following sequence: As > Hg > Cd > Pb; however, the values of lead were slightly higher than those of cadmium in cod. All imported fish contained significantly more cadmium than the Polish species. Our assessment of EDI, THQ, TTHQ, TWI, PTMI and BMDL₀₁ indicates that typical levels of consumption of fish do not pose a risk based on the assumed intake. The highest TTHQ was observed in tilapia, but it did not exceed 0.169. This was well below the acceptable value. Hence, the consumption of these fish does not appear to entail any non-carcinogenic or carcinogenic health risks. In addition, the estimated consumer risk parameters indicate no risk to consumer health in the short term; however, the presence of these elements may present a long-term hazard due to the potential for bioaccumulation. Continuous monitoring of trace element concentrations, especially toxic ones, is recommended for the protection of communities in both local and global contexts. Our findings provide a clearer picture of the health risk associated with the consumption of fish in the Polish market. Full article

Fundamental research, exploration, extraction, and metallurgical studies of rare earth elements (REEs) require the use of analytical techniques. Recently, emerging developments of analytical instrumentation for REEs have taken place, with some of them having shrunk in size, becoming handheld devices. The Flame and Graphite Furnace AAS, ICP-OES, and MP-AES are standard laboratory techniques used for the analysis of REEs. ICP-MS, ICP-MS/MS, ICP-TOF-MS, HR-ICP-MS, MH-ICP-MS, and MC-ICP-MS are popular techniques for REE analysis thanks to their ultrahigh sensitivity, minimal interference effects, and broad applicability. The INAA, XRF, LIBS, and LA-based ICP-MS techniques are widely employed for the direct analysis of solid samples. The TIMS, SIMS, and SHRIMP are common techniques used for dating isotopic REE deposits. The portable XRF, LIBS, and Raman spectrometer devices can perform on-the-spot in situ analysis, which may help make speedy decisions in the exploration study of REEs. Currently, hyperspectral remote sensing platforms, such as handheld, drone, and satellite-based devices, are preferred for the exploration of REEs due to their cost-effectiveness, which enables the coverage of large areas in a limited amount of time. The use of microanalytical sensors installed on remotely operated vehicles has been successfully applied in analyzing rich REE-bearing deposits in the deep sea. In general, this review provides in-depth information on all essential aspects, from analytical instruments to cutting-edge developments in the analysis of REE-bearing resources. Full article

This study systematically investigates soil and stream sediment along the 165 km Ibar River to examine the origin and transfer of pollutants. The research focuses on the environmental impact of long-term mining and irregular waste management, as well as natural enrichment related to weathering processes. A comprehensive sampling campaign was conducted, collecting 70 samples from 14 locations. At each location, samples of river sediment, floodplain soil (0–5 cm and 20–30 cm depths), and river terrace soil (same depths) were collected. The contents of 21 elements (Ag, Al, As, B, Ba, Ca, Cd, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, P, Pb, Sr, V, and Zn) were determined using inductively coupled plasma atomic emission spectrometry (ICP-AES). Analysis of Variance (ANOVA) was performed to identify statistically significant differences in element contents between defined zones, sampled materials (river sediments, floodplain soils, and river terrace soils), and sampled soil horizons (topsoil, 0–5 cm, and subsoil, 20–30 cm). Multivariate analysis, including correlation coefficient, cluster analysis, and principal component analysis, revealed two distinct groups of elements with highly significant correlation coefficients (r > 0.7). The first group, comprising Ag, As, Cd, Cu, Mn, and Zn, indicates anthropogenic enrichment, likely resulting from mining and smelting activities in the middle flow of the Ibar River (The Mining and Metallurgical Complex Trepča). The second group, consisting of Cr, Mg, and Ni, suggests enrichment related to the weathering of elements from the ophiolite zone in the lower Ibar River. The study found high enrichment ratios of toxic elements like arsenic, cadmium, lead, and zinc, particularly in stream sediments and floodplains. Notably, arsenic contents exceeded European averages by up to 57 times in stream sediments, posing a significant environmental concern due to its high content. Full article

The present study provides a comprehensive characterization of soil elemental composition in the Nile Delta, Egypt. The soil samples were analyzed using Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES), highly appropriative for the major element determination and Inductively Coupled Plasma Mass Spectrometry (ICP–MS), outstanding for the trace element analysis. A total of 55 elements were measured across 53 soil samples. A variety of statistical and analytical techniques, including both descriptive and inferential methods, were employed to assess the elemental composition of the soil. Bivariate and multivariate statistical analyses, discriminative ternary diagrams, ratio biplots, and unsupervised machine learning algorithms—such as Principal Component Analysis (PCA), t-Distributed Stochastic Neighbour Embedding (t-SNE), and Hierarchical Agglomerative Clustering (HAC)—were utilized to explore the geochemical similarities between elements in the soil. The application of t-SNE for soil geochemistry is still emerging and is characterized by the fact that it preserves the local distribution of elements and reveals non-linear relationships in geochemical research compared to PCA. Geochemical background levels were estimated using Bayesian inference, and the impact of outliers was analyzed. Pollution indices were subsequently calculated to assess potential contamination. The findings suggest that the studied areas do not exhibit significant pollution. Variations in background levels were primarily attributed to the presence of outliers. The clustering results from PCA and t-SNE were consistent in terms of accuracy and the number of identified groups. Four distinct groups were identified, with soil samples in each group sharing similar geochemical properties. While PCA is effective for linear data, t-SNE proved more suitable for nonlinear dimensionality reduction. These results provide valuable baseline data for future research on the studied areas and for evaluating their environmental situation. Full article

Mining activities have long-term impacts on the environment even after the active stage. Historical mines developed in the 19th and 20th centuries for tin, copper, and mainly iron ore are located in the Pitkäranta area (Karelia, Russia). These objects are considered in our research as natural–anthropogenic sites of long-term water–rock interaction. Waters from flooded mines are the subject of this research. Redox conditions, pH, dissolved oxygen content, conductivity, and water temperature were determined during field work. The chemical composition of natural waters was determined by ICP-MS, ICP-AES, ion chromatography, potentiometric titration, and spectrophotometry. Our investigation showed that the mine waters are fresh and predominantly calcium–magnesium hydrocarbonate; most samples showed elevated sulfate ion contents. Circumneutral pH values and the absence of extremely high concentrations of heavy metals indicate neutral mine drainage. However the calculation of the accumulation coefficient showed the highest levels for siderophile elements relative to the corresponding data of the geochemical regional background. Moreover, zinc has the highest content in the series of heavy metal(loid)s considered. The maximum concentration of zinc was determined in the water of one of the shafts of the Lupikko mine, i.e., 5205 µg/L. The accumulation of heavy metals occurs in the process of long-term interaction of water–rock–organic matter under conductive redox conditions. Overall, the research highlighted the relevance of investigating the geochemistry of historical mines in the Pitkäranta area both from the perspective of environmental safety and the preservation of mining sites for scientific and educational purposes. Full article

Anemia remains a widespread public health concern, and the search for interventions demonstrating potent anti-anemic activity is critical for reducing its impact among high-risk populations. Conventional iron therapies are associated with several complications and potential adverse effects. This study explored a polyherbal approach to develop a safer and more effective alternative treatment for anemia. A molecular docking study was initially performed to screen and evaluate alizarin, catechin, kaempferol, recesmol, rubiadin, and rutin, which are known for their antioxidant and hematinic potential. Using AutoDock Vina, these compounds were docked against the target protein (PDB ID: 6MOE) with EPE and ferrous ions as controls. Rutin demonstrated the highest binding affinity of −6.4 kcal/moL, whereas alizarin and rubiadin both followed closely with −6.3 kcal/moL, while kaempferol and ellagic acid exhibited a binding affinity of −6.2 kcal/moL. In comparison, the reference compounds tested ferrous ions, and native ligand EPE (−5.0 kcal/moL) and iron (−4.8 kcal/moL), showed mild affinities. Moreover, the tested compounds demonstrated stable binding, suggesting their potential relevance in modulating anemia-related pathways. Based on the docking results and traditional therapeutic values, a polyherbal formulation (PHF) was developed using methanolic extracts of Trigonella foenum-graecum, Emblica officinalis, Pterocarpus marsupium, Withania somnifera, Asparagus racemosus, Zingiber officinale, Rubia cordifolia, Boerhavia diffusa, and Adhatoda vasica. Phytochemical screening via HPTLC analysis was used to quantify the presence of gallic and ellagic acids. In addition, PHF showed significant antioxidant potential (DPPH IC₅₀: 14.29 µg/mL; FRAP IC₅₀: 58.57 µg/mL) and iron content (98.47 ppm) values. Furthermore, in vivo evaluation using a phenylhydrazine-induced hemolytic anemia model in Sprague Dawley rats revealed that the PHF achieved complete restoration of RBCs (6.15 ± 0.04), hemoglobin (14.82 ± 0.03 g/dL), and hematocrit (43.08 ± 0.28%) in anemic rats and improved histopathological features in the liver, spleen, and bone marrow. These results demonstrate that combined molecular and pharmacological evidence support the efficacy of PHF as a promising candidate for the management of anemia by enhancing erythropoiesis, improving iron metabolism, and reducing oxidative stress. Full article

Twenty-nine sediment samples were collected from Hurghada Bay, a highly impacted coastal area along the Northern Red Sea of Egypt, to evaluate environmental quality and human-induced effects on benthic ostracods. As potential bioindicators, benthic ostracods are highly responsive to environmental disturbances, with pollution leading to reduced abundance, lower diversity, and increased opportunistic taxa. To investigate the link between ostracod assemblages and sediment contamination, we measured the concentrations of eight heavy metals (Cu, Cd, Zn, Pb, As, Cr, Ni, and Mn) using inductively coupled plasma–atomic emission spectrometry (ICP-AES). Multivariate statistical analyses identified three distinct ostracod assemblages distributed across three station groups with varying pollution levels. Group I, associated with offshore stations, exhibited low to moderate heavy metal (HM) concentrations and high ostracod abundance and was dominated by Moosella striata, Hiltermannicythere rubrimaris, Ruggieria danielopoli, Neonesidea schulzi, and Paranesidea fracticorallcola, where the water depth and sand content are the main controlling factors. In contrast, Group II, corresponding to stations with the highest HMs and total organic matter (TOM), was dominated by pollution-tolerant species Jugosocythereis borchersi, Cyprideis torosa, Alocopocythere reticulata, and, to a lesser extent, Ghardaglaia triebeli, with reduced ostracod density and diversity. Group III, characterized by stations influenced by the mud-controlling factor, had the lowest HMs and was dominated by pollution-sensitive species Xestoleberis rhomboidei, Paranesidea fortificata, and Loxocorniculum ghardaquensis. These findings highlight the ecological risks posed by HM pollution and emphasize the urgent need for pollution mitigation strategies and continued monitoring to preserve the Red Sea’s benthic biodiversity. Full article

Groundwater quality in arid and semi-arid regions of Morocco is under increasing pressure due to both anthropogenic influences and climatic variability. This study investigates the physicochemical and heavy metal characteristics of groundwater across four Moroccan regions (Tangier-Tetouan-Al Hoceima, Oriental, Souss-Massa, and Marrakech-Safi) known for being argan tree habitats. Thirteen groundwater samples were analyzed for twenty-five parameters, including major ions, nutrients, and trace metals. Elevated levels of ammonium, turbidity, electrical conductivity, and dissolved oxygen were observed in multiple samples, surpassing Moroccan water quality standards and indicating significant quality deterioration. Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) detected arsenic concentrations exceeding permissible limits in sample AW11 alongside widespread lead contamination in most samples except AW5 and AW9. Spatial patterns of contamination were characterized using Principal Component Analysis (PCA), Hierarchical Cluster Analysis (HCA), K-means clustering, and GIS-based Inverse Distance Weighted (IDW) interpolation. These multivariate approaches revealed marked spatial heterogeneity and highlighted the dual influence of geogenic processes and anthropogenic activities on groundwater quality. To assess consumption suitability, a Water Quality Index (WQI) and Human Health Risk Assessment were applied. As a result, 31% of samples were rated “Fair” and 69% as “Good”, but with notable non-carcinogenic risks, particularly to children, attributable to nitrate, lead, and arsenic. The findings underscore the urgent need for systematic groundwater monitoring and management strategies to safeguard water resources in Morocco’s vulnerable dryland ecosystems, particularly in regions where groundwater sustains vital socio-ecological species such as argan forests. Full article

Mining activity in Peru generates environmental liabilities with the potential to release toxic metals into the environment. This study conducted a comprehensive physical, chemical, mineralogical, and toxicological characterization of ten active and inactive tailings samples from the Arequipa region in southern Peru. Particle size distribution analysis, inductively coupled plasma atomic emission spectroscopy (ICP-AES), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), and the Toxicity Characteristic Leaching Procedure (TCLP) followed by ICP-MS were employed. The results revealed variable particle size distributions, with the sample of Secocha exhibiting the finest granulometry. Chemically, 8 out of 10 samples exhibited concentrations of at least two metals surpassing the Peruvian Environmental Quality Standards (EQS) for soils with values reaching >6000 mg/kg of arsenic (Paraiso), 193.1 mg/kg of mercury (Mollehuaca), and 2309 mg/kg of zinc (Paraiso). Mineralogical analysis revealed the presence of sulfides such as arsenopyrite, cinnabar, galena, and sphalerite, along with uraninite in the Otapara sample. In the TCLP tests, 5 out of 10 samples released at least two metals exceeding the environmental standards on water quality, with concentrations up to 0.401 mg/L for mercury (Paraiso), 0.590 mg/L for lead (Paraiso), and 9.286 mg/L for zinc (Kiowa Cobre). These results demonstrate elevated levels of Potentially Toxic Elements (PTEs) in both solid and dissolved states, reflecting a critical geochemical risk in the evaluated areas. Full article

We report an investigation on the cobalt(II) chelation mechanism by a modified α-maltoside ligand 9 decorated with two iminodiacetate (IDA) residues on C6,C6′ positions. Herein we uncovered the capacity of this biodegradable ligand to chelate cobalt(II), an ionic metal contaminant in the environment that is used, in particular, in lithium-ion batteries. The interactions between cobalt(II) and synthesized ligand 9 were systematically studied using different analytical methods such as ¹H and ¹³C NMR, potentiometry, spectrophotometry, ITC, and ICP-AES. We observed a high affinity for the 1:1 complex, one cobalt(II) associated with two iminodiacetate groups, which is 10-fold higher than the 2:1 complex, where each of the two IDA groups interacts alone with a cobalt(II). Taking into account the log β_CoL value obtained (≈12.3) with the stoichiometry 1:1, the strength of this complexation with cobalt(II) can be ranked as follows for the most common ligands: IDA < MIDA < NTA < 9 < EDTA < TTHA < DTPA. We further completed a preliminary remediation test with water contaminated with cobalt(II) and recovered cobalt(II) metal using Chelex^® resin, which allowed a recycling of the synthetic ligand for future recovering experiments. The results shed light on the great potential of using this synthetic ligand as an effective and green remediation tool. Full article

Phytoremediation is based on the use of plants to decontaminate water and soil. In this work, the capacity of high Andean vegetation in the absorption and translocation of heavy metals was analyzed. Species were identified to analyze the presence of metals in roots, stems, and leaves by spectrometry. The translocation factor was determined and analyzed by means of pattern clusters. Based on the floristic inventory, the dominance of the Poaceae and Asteraceae families was determined, and 12 plant species with a high importance value were selected. According to the ICP-AES, mercury (951.07 mg/kg) was determined in the roots of Lachemilla orbiculata, and chromium (21.88 mg/kg) in Carex bonplandii. Arsenic (2.79 mg/kg) was detected as being significantly higher than the values recorded in lowland plants. Cadmium mobility was high in all species, reaching higher values in Baccharis salicifolia (86.28%) and Calamagrostis intermedia (37.16%). Rumex acetocella accumulated lead in leaves (9.27%), while Taraxacum officinale (1.20%) and Calamagrostis intermedia (1.20%) accumulated silicon. Stabilization of chromium, mercury, and sodium was determined in the roots without translocation to higher organs. Finally, cluster analysis showed physiological interactions between metals as a toxicity mitigation mechanism affecting mobility. These findings suggest that they are hyperaccumulator species. Full article

Nickel aluminum bronze (NAB) and manganese aluminum bronze (MAB) are widely used in propulsion and seawater handling systems in naval platforms due to their attractive combination of mechanical strength, toughness, and very low susceptibility to marine corrosion. Nevertheless, it is well known that they can suffer from selective phase corrosion and erosion–corrosion, primarily caused by cavitation and sand erosion. Both alloys have a multiphase microstructure that governs their mechanical and chemical behavior. The tribocorrosion behavior of cast NAB and MAB alloys was studied in artificial seawater to analyze the effect on microstructure. The microstructure and nanohardness were evaluated and correlated with tribocorrosion test results conducted under two different loads (10 and 40 N) in a unidirectional sliding mode using a 1 M NaCl solution as the electrolyte. A significant increase in the corrosion rate due to the wear effect was observed in both alloys. MAB exhibited a slightly better tribocorrosion performance than NAB, which was attributed to significant differences in the shape, distribution, and size of the intermetallic kappa phases—rich in iron, aluminum, and nickel—within the microstructure. Pitting corrosion was observed in NAB, while selective corrosion of kappa phases occurred in MAB, highlighting the role of the protective layer in the tribocorrosion behavior of both alloys. These findings were supported by post-test solution analysis using ICP-AES and corrosion product characterization by EDX. A synergistic effect between wear and corrosion was confirmed for both alloys, as erosion removes the protective layer, exposing fresh material to continuous friction and favoring a progressive material loss over time. The practical impact of this study lies in improving the control and design of highly alloyed bronze microstructures under in-service corrosion–erosion conditions. Full article

Nickel’s durability and catalytic properties make it essential in the aerospace, automotive, electronics, and fuel cell technology industries. Wastewater analysis typically relies on sensitive but costly techniques such as ICP-MS, AAS, and ICP-AES, which require complex equipment and are unsuitable for on-site testing. This study introduces a novel screen-printed electrode array with 16 chemically and, optionally, electrochemically coated Au electrodes. Its electrochemical response to Ni²⁺ was tested using Na₂SO₃ and ChCl-EG deep eutectic solvents as electrolytes. Ni²⁺ solutions were prepared from NiCl₂·6H₂O, NiSO₄·6H₂O, and dry NiCl₂. In Na₂SO₃, the linear detection ranges were 20–196 mM for NiCl₂·6H₂O and 89–329 mM for NiSO₄·6H₂O. High Ni²⁺ concentrations (10–500 mM) were used to simulate industrial conditions. Two linear ranges were observed, likely due to differences in electrochemical behaviour between NiCl₂·6H₂O and NiSO₄·6H₂O, despite the identical Na₂SO₃ electrolyte. Anion effects (Cl⁻ vs. SO₄²⁻) may influence response via complexation or ion pairing. In ChCl-EG, a linear range of 0.5–10 mM (R² = 0.9995) and a detection limit of 1.6 µM were achieved. With a small electrolyte volume (100–200 µL), nickel detection in the nanomole range is possible. A key advantage is the array’s ability to analyze multiple analytes simultaneously via customizable electrode configurations. Future research will focus on nickel detection in industrial wastewater and its potential in the multiplexed analysis of toxic metals. The array also holds promise for medical diagnostics and food safety applications using thiol/Au-based capture molecules. Full article