Search Results (101)

Osteoporosis is a major public health concern, particularly among postmenopausal women. Environmental exposure to metals has been proposed as a potential contributor to osteoporosis, but human data remain limited and inconsistent. This study investigated changes in urinary concentrations of 20 metal(loid)s in patients with osteoporosis, as well as the association of these elements with bone mineral density (BMD), in a cohort of 380 postmenopausal women aged 50–70 years from Cascavel, Paraná, Brazil. Demographic, lifestyle, and clinical data were collected, and urinary concentrations of aluminum (Al), barium (Ba), cadmium (Cd), cobalt (Co), cesium (Cs), copper (Cu), mercury (Hg), lithium (Li), manganese (Mn), molybdenum (Mo), nickel (Ni), lead (Pb), rubidium (Rb), antimony (Sb), selenium (Se), tin (Sn), strontium (Sr), thallium (Tl), uranium (U), and zinc (Zn) were measured by inductively coupled plasma mass spectrometry. BMD was assessed at the lumbar spine, femoral neck, and total hip using dual-energy X-ray absorptiometry. Osteoporosis was diagnosed in 73 participants (19.2%). Osteoporotic women had significantly higher urinary concentrations of Cd, Mn, Pb, Sb, Sn, and Zn (p < 0.05). Statistically significant negative correlations were observed between BMD and urinary concentrations of Al, Cd, Hg, Mn, Sb, and U. After adjustment for confounders, elevated urinary concentrations of Cd, Mn, Pb, and Sb remained independently and significantly associated with higher odds of osteoporosis, with Cd (aOR = 1.495; p = 0.026) and Sb (aOR = 2.059; p = 0.030) showing the strongest associations. In addition, women with urinary concentrations above the 90th percentile for both Cd and Sb had a significantly higher prevalence of osteoporosis compared to those with lower levels (44.4% vs. 18.0%; p = 0.011). Longitudinal studies are needed to confirm causality and inform prevention strategies. Full article

Thin-film solar cells (TFSCs) represent a promising frontier in renewable energy technologies due to their potential for cost reduction, material efficiency, and adaptability. This literature review examines the key materials and advancements that make up TFSC technologies, with a focus on Cu(In,Ga)Se₂ (CIGS), cadmium telluride (CdTe), and Cu₂ZnSnS₄ (CZTS) and its sulfo-selenide counterpart Cu₂ZnSn(S,Se)₄ (CZTSSe). Each material’s unique properties—including tuneable bandgaps, high absorption coefficients, and low-cost scalability—make them viable candidates for a wide range of applications, from building-integrated photovoltaics (BIPV) to portable energy solutions. This review explores recent progress in the enhancement of power conversion efficiency (PCE), particularly through bandgap engineering, alkali metal doping, and interface optimization. Key innovations such as silver (Ag) alloying in CIGS, selenium (Se) alloying in CdTe, and sulfur (S) to Se ratio optimization in CZTSSe have driven PCE improvements and expanded the range of practical uses. Additionally, the adaptability of TFSCs for roll-to-roll manufacturing on flexible substrates has further cemented their role in advancing renewable energy adoption. Challenges remain, including environmental concerns, but ongoing research addresses these limitations, paving the way for TFSCs to become a crucial technology for transitioning to sustainable energy systems. Full article

At present, lead halide PVSKSCs are promising photovoltaic cells but have some limitations, including their low stability in ambient conditions and the toxicity of lead. Thus, it will be of great significance to explore lead-free perovskite materials as an alternative absorber layer. In recent years, the numerical simulation of perovskite solar cells (PVSKSCs) via the solar cell capacitance simulation (SCAPS) method has attracted the attention of the scientific community. In this work, we adopted SCAPS for the theoretical study of lead (Pb)-free PVSKSCs. A cesium bismuth iodide (CsBi₃I₁₀; CBI) perovskite-like material was used as an absorber layer. The thickness of the CBI layer was optimized. In addition, different electron transport layers (ETLs), such as titanium dioxide (TiO₂), tin oxide (SnO₂), zinc oxide (ZnO), and zinc selenide (ZnSe), and different hole transport layers, such as spiro-OMeTAD (2,2,7,7-tetrakis(N,N-di(4-methoxyphenylamine)-9,9′-spirobifluorene), poly(3-hexylthiophene-2,5-diyl) (P₃HT), poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine (PTAA), and copper oxide (Cu₂O), were explored for the simulation of CBI-based PVSKSCs. A device structure of FTO/ETL/CBI/HTL/Au was adopted for simulation studies. The simulation studies showed the improved photovoltaic performance of CBI-based PVSKSCs using spiro-OMeTAD and TiO₂ as the HTL and ETL, respectively. An acceptable PCE of 11.98% with a photocurrent density (J_sc) of 17.360258 mA/cm², a fill factor (FF) of 67.10%, and an open-circuit voltage (V_oc) of 1.0282 V were achieved under the optimized conditions. It is expected that the present study will be beneficial for researchers working towards the development of CBI-based PVSKSCs. Full article

The chemical transport method is a process that occurs naturally; however, it is also very useful in the chemical laboratory environment for the synthesis of inorganic crystals. It was successfully used for the syntheses of simple and complex inorganic compounds, from binary (e.g., ZnS, CdSe) to quaternary (e.g., Cu₂ZnSnS₄) compounds. Many experimental parameters influence the quality of products of chemical transport reactions, and among them, one may distinguish the used precursors and applied temperature gradient. The careful selection of experimental conditions is crucial for the production of high-quality crystals. Mathematical descriptions of the chemical transport phenomena, however, may potentially help in the design of proper conditions. Full article

Minor and trace elements in soil play a crucial role in regulating ecological processes that sustain the functionality of forest ecosystems. In this study, we have selected three conifer forests (Pinus sylvestris, Picea asperata, Larix principis-rupprechtii), one broadleaf forest (Betula Platyfilla) and one mixed forest of Betula Platyfilla and Larix principis-rupprechtii in the Winter Olympic core area and determined the pattern of 12 typical elements (B, Fe, V, Cr, Ni, Co, Mn, As, Cu, Zn, Sn and Se) in soils and their main drivers in the three different soil layers (A, B and C horizon) in each soil profile. Our results showed that the concentrations of B, Fe, Cr, Cu, Ni and Sn were mainly enriched in the broadleaf forest and mixed broadleaf–conifer forest zones, and the average concentrations of Co, Mn, V, Zn, As and Se were mainly enriched in coniferous forest zones in contrast. We have observed that the mean concentrations of Fe, Cr, Ni, Zn, As, Sn and Co increase with soil depth in the BP forest. The concentrations of Se and Cu were higher in the A layer than the C layer. The piecewise structural equation modeling (piecewiseSEM) results visualized a direct and negative effect on B, Fe, V, Cr and Ni concentrations due to soil temperature, while the concentrations of Se is mainly influenced by soil temperature and soil properties. Full article

Energy generation and storage are critical challenges for developing economies due to rising populations and limited access to clean energy resources. Fossil fuels, commonly used for energy production, are costly and contribute to environmental pollution through greenhouse gas emissions. Quantum dot-sensitized solar cells (QDSSCs) offer a promising alternative due to their stability, low cost, and high-power conversion efficiency (PCE) compared to other third-generation solar cells. Kesterite materials, known for their excellent optoelectronic properties and chemical stability, have gained attention for their potential as hole transport layer (HTL) materials in solar cells. In this study, the SCAPS-1D numerical simulator was used to analyze a solar cell with the configuration FTO/TiO₂/MoS₂/HTL/Ag. The electron transport layer (ETL) used was titanium dioxide (TiO₂), while Cu₂FeSnS₄ (CFTS), Cu₂ZnSnS₄ (CZTSe), Cu₂NiSnS₄ (CNTS), and Cu₂ZnSnSe₄ (CZTSSe) kesterite materials were evaluated as HTLs. MoS₂ quantum dot served as the absorber, with FTO as the anode and silver as the back metal contact. The CFTS material outperformed the others, yielding a PCE of 25.86%, a fill factor (FF) of 38.79%, a short-circuit current density (J_SC) of 34.52 mA cm⁻², and an open-circuit voltage (V_OC) of 1.93 V. This study contributes to the advancement of high-performance QDSSCs. Full article

Unlike municipal solid waste bottom ash (MSWBA), fly ash (MSWFA) is landfilled due to its toxicity. However, MSWFA may also be a source of elements. Ash samples collected from a Portuguese MSW incinerator from different locations and over six months were analyzed. Their geochemical composition was normalized to the upper continental crust (UCC) and compared since metal enrichment may be used as an indicator for potential recovery. The potential recovery economic viability was also assessed for metals K, Sb, Cu, Pb, and Zn, considering the ore cut-off grade and minimum industrial grade (MIG) from Chinese geological and mineral industry standards. Compared to the global samples, only the Baghouse 1 FA size fraction’s coarse fraction showed a slight enrichment (1- to 5-fold) in Bi, Nb, and Zr. After wet sieving, most trace elements were enriched in all fractions, but Sb, Bi, Pb, Zn, Ag, As, Cd, Sn, Se, and Hg were depleted in the coarse fractions and enriched in the fine ones. For Baghouse 1 samples collected over 6 months, the normalization to the UCC showed enrichment of Zn and Pb between 10× and 50×, Zr, Cu, In, and Se between 50× and 100×, and Ag, Mn, Cd, Sb, and Bi at more than 100×. Over six months, the Baghouse 1 FA soluble fraction ranged between 21 wt.% and 30 wt.%, and its precipitates comprised 27% CaO, 6% Na₂O, and 9% K₂O. The K concentration in the MSWFA was above the cut-off and the MIG, and K could be concentrated in precipitates via simple washing. Full article

Knowledge about determinants of addiction in people taking addictive substances is poor and needs to be supplemented. The novelty of this paper consists in the analysis of innovative aspects of current research about relationships between determinants of addiction in Polish patients taking addictive substances and rare available data regarding the relationships between these factors from studies from recent years from other environments, mainly in Europe, and on the development of genetic determinants of physiological responses. We try to explain the role of the microelements Mn, Fe, Cu, Co, Zn, Cr, Ni, Tl, Se, Al, B, Mo, V, Sn, Sb, Ag, Sr, and Ba, the toxic metals Cd, Hg, As, and Pb, and the rare earth elements Sc, La, Ce, Pr, Eu, Gd, and Nd as factors that may shape the development of addiction to addictive substances or drugs. The interactions between factors (gene polymorphism, especially ANKK1 (TaqI A), ANKK1 (Taq1 A-CT), DRD2 (TaqI B, DRD2 Taq1 B-GA, DRD2 Taq1 B-AA, DRD2-141C Ins/Del), and OPRM1 (A118G)) in patients addicted to addictive substances and consumption of vegetables, consumption of dairy products, exposure to harmful factors, and their relationships with physiological responses, which confirm the importance of internal factors as determinants of addiction, are analyzed, taking into account gender and region. The innovation of this review is to show that the homozygous TT mutant of the ANKK1 TaqI A polymorphism rs 1800497 may be a factor in increased risk of opioid dependence. We identify a variation in the functioning of the immune system in addicted patients from different environments as a result of the interaction of polymorphisms. Full article

Posidonia oceanica significantly contributes to the health of oceans and coastal areas; however, its progressive decline is becoming an increasing source of concern. The present preliminary study aims to assess the chemical parameters that describe the state of preservation of the aforementioned plant meadows located in the Tremiti Islands archipelago. To better understand the plants’ response to external factors, the emission of biogenic volatile organic compounds (BVOCs) was investigated using Posidonia oceanica as a biological indicator. Subsequently, the heavy metal concentrations (Ag, Al, As, Ba, Be, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Sb, Se, Sn, Ti, Tl, V, Zn) in sediments, leaves, and seawater were determined and pollution indicators were calculated to assess the deviation from the natural background levels of sediments. The dimethyl sulfoniopropionate (DMSP) to dimethyl sulfoxide (DMSO) ratio was calculated to evaluate the oxidative stress levels in the meadows because the DMSP naturally present in Posidonia oceanica is oxidized to DMSO and decreases the ratio of DMSP/DMSO. BVOC analysis revealed dimethyl sulphide (DMS) as the most abundant molecule. Morphological features led to variations in metal concentrations across sampling sites, with sheltered bays displaying a higher metal content. Degradation is indicated by a greater DMSO content in the outer leaves. In accordance with the metal content, the bioindicator ratio confirms greater degradation on the south side, which aligns with increased oxidative stress. Full article

Cu₂(ZnSn)(S)₄ (copper, zinc, tin, and sulfide (CZTS)) provides possible advantages over CuInGaSe2 for thin-film photovoltaic devices because it has a higher band gap. Preparing CZTS by electrodeposition because of its high productivity and lower processing costs, electroplating is appealing. Recently published studies reported that the electrodeposition process of CZTS still faces significant obstacles, such as the sulfur atomic ratio (about half of the whole alloy), deposits’ adhesion, film quality, and optical properties. This work introduces an improved bath that facilitates the direct electroplating of CZTS from one processing step. The precursors used were significantly more diluted than the typical baths mentioned in the last few years. An extensive analysis of the electrochemical behavior at various rotation speeds is presented at room temperature (~22 °C). The deposited alloy’s composition and adherence to the molybdenum back contact are examined with agitation. The annealing process was carried out in an environment containing sulfur, and the metal was not added at this stage. The ultimate sulfur composition was adjusted to 50.2%, about the desired atomic ratio. The compound’s final composition was investigated using the Energy-Dispersive X-ray Spectroscopy technique. Finally, X-ray diffraction analysis was applied to analyze CZTS crystallography and to measure thickness. Full article

The Iberian Pyrite Belt (IPB) represents one of the largest districts of volcanogenic massive sulfide (VMS) deposits in the world, and is a critical source of base metals (Cu, Pb, and Zn) for Europe. Confirmed resources exceed 1700 Mt of massive sulfides with grades of around 1.2% Cu, 1% Pb, and 3% Zn as well as more than 300 Mt of stockwork-type copper mineralization. Significant resources of Sn, precious metals (Au and Ag), and critical metals (Co, Bi, Sb, In, and Se) have also been evaluated. The genesis of these deposits is related to a complex geological evolution during the late Devonian and Mississippian periods. The geological record of such evolution is represented by three main lithological units: Phyllite–Quartzite Group, the volcano–sedimentary Complex (VSC), and the so-called Culm Group. The sulfide deposits are located in the VSC, associated with felsic volcanic rocks or sedimentary rocks such as black shales. The massive sulfide deposits occur as tabular bodies and replacement masses associated with both volcanic and sedimentary rocks. Their mineralogical composition is relatively simple, dominated by pyrite, chalcopyrite, sphalerite, and galena. Their origin is related to three evolutionary stages at increasing temperatures, and a subsequent stage associated with the Variscan deformation. The present paper summarizes the latest developments in the IPB and revises research areas requiring further investigation. Full article

Various copper-related defects in the absorption layer have been a key factor impeding the enhancement of the efficiency of Cu₂ZnSn(S,Se)₄ (CZTSSe) solar cells. Alkali metal doping is considered to be a good strategy to ameliorate this problem. In this article, Rb-doped CZTSSe (RCZTSSe) thin films were synthesized using the sol–gel technique. The results show that the Rb atom could successfully enter into the CZTSSe lattice and replace the Cu atom. According to SEM results, a moderate amount of Rb doping aided in enhancing the growth of grains in CZTSSe thin films. It was proven that the RCZTSSe thin film had the densest surface morphology and the fewest holes when the doping content of Rb was 2%. In addition, Rb doping successfully inhibited the formation of Cu_Zn defects and correlative defect clusters and promoted the electrical properties of RCZTSSe thin films. Finally, a remarkable power conversion efficiency of 7.32% was attained by the champion RCZTSSe device with a Rb content of 2%. Compared with that of un-doped CZTSSe, the efficiency improved by over 30%. This study offers new insights into the influence of alkali metal doping on suppressing copper-related defects and also presents a viable approach for improving the efficiency of CZTSSe devices. Full article

An analysis was conducted on the influence of advancements in smelting technology at the copper smelter in Bor, Serbia, and seasonal changes on the level and chemical composition of PM₁₀ inside and outside a classroom at the Technical Faculty in Bor in 2015 and 2019. The results of chemical analyses revealed that the average level of arsenic in PM₁₀ within the classroom reached 11.9 ng/m³, nearly double the annual target value. In comparison, the average level of arsenic (As) in PM₁₀ in ambient air stood at 15 ng/m³. A notable enrichment factor was observed for elements present in copper concentrates (Se > Ag > Bi > Pb > Cd > As > Sb > S > Cu > Sn > Zn) in both the classroom and outdoor air, underscoring their predominantly anthropogenic origin. Higher concentrations of As in PM₁₀ were recorded during the non-heating season and the operation of the copper smelter with outdated smelting technology (2015). These findings hold significant implications for health protection for all citizens in the investigated area surrounding the Technical Faculty in Bor. The study highlights the need for additional measures to reduce As content in PM₁₀ in ambient air and prevent the infiltration of suspended particles from outdoor air into classrooms. Full article

The development of kesterite (Cu₂ZnSn(S,Se)₄, CZTSSe) thin films for photovoltaic applications is highly necessary, given their composition of Earth-abundant, environmentally friendly elements and their compatibility with established photovoltaic technologies. This study presents a novel synthesis approach for CZTSSe films with varied S/(S+Se) ratios, ranging from 0.83 to 0.44, by a two-step magnetron sputtering deposition/annealing process. The first step consists in an initial deposition of stacked Mo/SnS₂/Cu layers, which, upon thermal treatment in a sulfur atmosphere, were transformed into Cu₂SnS₃ (CTS) films. In the second step, further deposition of ZnSe and subsequent annealing in a tin and selenium atmosphere resulted in the formation of a CZTSSe phase. These processes were optimized to fabricate high-quality and single-phase CZTSSe films, thereby mitigating the formation of secondary phases. Characterization techniques, including scanning electron microscopy, demonstrated a clear correlation between decreased S/(S+Se) ratios and enhanced film densification and grain size. Moreover, grazing incidence X-ray diffraction and Raman spectroscopy confirmed a compositional and structural transition from close to CZTS to nearly a CZTSe phase as the S/(S+Se) ratios decreased. This study advances kesterite-based solar cell technology by enhancing the structural properties and crystallinity of the absorber layer, necessary for improving photovoltaic performance. Full article

Wildfires significantly influence the environmental distribution of various elements through their fire-induced input and mobilization, yet little is known about their effects on the forest floor in Siberian forests. The present study evaluated the effects of spring wildfires of various severities on the levels of major and minor (Ca, Al, Fe, S, Mg, K, Na, Mn, P, Ti, Ba, and Sr) trace and ultra-trace (B, Co, Cr, Cu, Ni, Se, V, Zn, Pb, As, La, Sn, Sc, Sb, Be, Bi, Hg, Li, Mo, and Cd) elements in the forest floors of Siberian forests. The forest floor (Oi layer) samples were collected immediately following wildfires in Scots pine (Pinus sylvestris L.), larch (Larix sibirica Ledeb.), spruce (Picea obovata Ledeb.), and birch (Betula pendula Roth) forests. Total concentrations of elements were determined using inductively coupled plasma–optical emission spectroscopy. All fires resulted in a decrease in organic matter content and an increase in mineral material content and pH values in the forest floor. The concentrations of most elements studied in a burned layer of forest floor were statistically significantly higher than in unburned precursors. Sb and Sn showed no statistically significant changes. The forest floor in the birch forest showed a higher increase in mineral material content after the fire and higher levels of most elements studied than the burned coniferous forest floors. Ca was a predominant element in both unburned and burned samples in all forests studied. Our study highlighted the role of wildfires in Siberia in enhancing the levels of geochemical elements in forest floor and the effect of forest type and fire severity on ash characteristics. The increased concentrations of elements represent a potential source of surface water contamination with toxic and eutrophying elements if wildfire ash is transported with overland flow. Full article