Journal of Environmental Science and Health Part A-toxic\/hazardous Substances & Environmental Engineering最新文献

In the present study the concentration of selected elements in tissues of domestic rabbits and of wild brown-hares (kidneys, liver, and muscle - m. quadriceps femoris) in Slovakian habitats were determined. After mineralization the elements examined were detected using flame atomic absorption spectrophotometry/graphite furnace atomic absorption spectrophotometry. For rabbits, Fe in the liver was correlated with essential (Mn, Cu) (R² = 0.94, p < 0.05; R² = 0.96, p < 0.05 respectively) or toxic (Pb) elements (R² = -0.93, p < 0.05). For hares, significant correlations were found between Cd and Cu or between Cd and Mn in the kidneys (R² = -0.96, p < 0.05; R² = 0.92, p < 0.05 respectively), which is the target organ for Cd. Higher concentrations of the elements were found in hare tissue, and this may be linked to pollution of their wild habitats. The xenobiotic elements as well as the essential elements were accumulated in the kidneys of the hares than rabbits. For liver, differences were less pronounced and significance was only for Fe and Cu. Muscle of hares was more contaminated than of rabbits for both biogenic and toxic elements. These results show that detectable concentrations of inorganic elements. These levels may be linked to contamination of the natural habitats of wild biota due to industry, traffic, agriculture, and urban sprawl.

This study investigates biochar as an attractive option for removing pharmaceuticals from wastewater streams utilizing data from various literature sources and also explores the sensitivity of the characteristics and implementation of biochar. ANN 1 was designed to determine the optimal biochar characteristics (Surface Area, Pore Volume) to achieve the maximum percentage removal of pharmaceuticals in wastewater streams. ANN 2 was developed to identify the optimal biomass feedstock composition, pyrolysis conditions (temperature and time), and chemical activation (acid or base) to produce the optimal biochar from ANN 1. ANN 3 was developed to investigate the effectiveness of the biochar produced in ANN 1 and 2 in removing dye from water. Biomass feedstock with a high lignin content and high volatile matter at a high pyrolysis temperature, whether using an acid or base, achieves a high mesopore volume and high surface area. The biochar with the highest surface area and mesopore volume achieved the highest removal percentage. Regardless of hydrophobicity conditions, at low dosages (0.2), a high surface area and pore volume are required for a high percent removal. And with a higher dosage, a lower surface area and pore volume is necessary to achieve a high percent removal.

This study proposes the use of diglycolamic acid-functionalized graphitic carbon nitride (HDGA-gCN) as an adsorbent for uranium removal. Our experiments showed that at pH 6.0, HDGA-gCN had a high adsorption capacity of 263.2 mg g^-1 and achieved equilibrium in 30 min. The adsorption isotherm was well-fitted by the Langmuir model, and the adsorption kinetics followed a pseudo-second-order equation. U(VI) adsorption on HDGA-gCN is due to electrostatic interactions between the amine, diglycolamic acid, and uranium species. The thermodynamic parameters indicate that adsorption is spontaneous and exothermic. The loaded U(VI) can be desorbed using 0.1 M Na₂CO₃, and HDGA-gCN exhibited an exceptional adsorption percentage for U(VI) compared to other coexisting ions. HDGA-gCN had faster kinetics, adsorption capacity, and reusability, making it suitable for U(VI) remediation.

Plant-mediated biosynthesis of nanoparticles is a green method that allows synthesis in one-pot process. Synthesis of gold nanoparticles with plant extracts has gained interest in the field of biomedicine due to its variety of applications. This study presents the synthesis via green chemistry of gold nanoparticles (AuNPs) using the methanol extract of Moringa oleifera seeds. The AuNPs were synthesized at room temperature. UV-Vis spectroscopy confirmed the formation of AuNPs by identifying the surface plasmon resonance located at 546 nm. TEM analysis shows spherical nanoparticles. FTIR analysis demonstrated the presence of specific bioactive molecules responsible for the Au³⁺ ion reduction process. The antioxidant activity of the nanoparticles was evaluated on the stabilization of the DPPH radical (1,1-diphenyl-2-picrylhydrazyl, 2,2-diphenyl-1-(2,4,6-trinitrophenyl) hydrazyl). The antimicrobial activity analysis was developed by broth microdilution method at different concentrations against Escherichia coli and Staphylococcus aureus. Minimum inhibitory concentration were 400 µg/mL and 200 µg/mL, respectively. A549 lung cancer cell proliferation was measured according to the MTT protocol, indicating a dose-dependent response and a IC₅₀ of 163.9 ± 13.27 µg/mL. The AuNPs synthesized using M. oleifera seeds showed promise as active materials for antimicrobial or anticancer products.

Removing hazardous organic pollutants, such as 4-nitrophenol (4-NP) and Congo red (CR) dyes from aqueous media and CO₂ from the atmospheric medium remains a significant challenge. Herein, we report a facile in-situ synthetic approach for fabricating CuO-ZnO heterostructure photocatalysts through the surfactant-assisted co-precipitation method. The catalytic results demonstrate that the Cu₁O-ZnO photocatalyst exhibits excellent activity under direct sunlight irradiation, owing to the heterostructure formation between the CuO and ZnO. The Cu₁O-ZnO photocatalyst showed higher reaction rate constant (k) values of 0.20 min^-1 for 4-NP and 0.09 min^-1 for CR compared to previous reports. Additionally, efficient CO₂ reduction was also achieved over Cu₁O-ZnO photocatalyst. The optical and structural characterization results indicate that the improved photocatalytic reduction and degradation observed for the Cu₁O-ZnO photocatalyst can be attributed to the strong synergistic interaction between p-type CuO and n-type ZnO and the construction of the p-n heterojunction. As a result, the absorption of visible light distinctly increased and inhibited the recombination rate of the photo-created electron-hole (e^-/h⁺). Furthermore, the Cu₁O-ZnO photocatalyst exhibited remarkable durability and recyclability, retaining high photoactivity (≥ 93%) after five cycles, demonstrating its potential for real-world applications in the photocatalytic reduction and degradation reactions under direct sunlight irradiation.

In indoor air the reaction of ozone (O₃) with terpenes may lead to the formation of irritating gas-phase products which may induce acute airway effects (i.e. sudden, short-term changes or symptoms related to the respiratory system). We aimed to perform an in vitro study on possible health effects of products from the O₃-initiated reaction of limonene with printer exhaust, representing real-life mixtures in offices. Human bronchial epithelial cells were exposed for 1 hour (h) to limonene and O₃, combined with printer exhaust. The resulting concentrations represented 34% and 6% of the generated initial concentrations of limonene (400 µg/m³) and O₃ (417 µg/cm³), respectively, which were in range of high end realistic indoor concentrations. We observed that the reaction of limonene with O₃ generated an increase of ultrafine particles within 1 h, with a significant increase of secondary reaction products 4-oxopentanal and 3-isopropenyl-6-oxo-heptanal at high end indoor air levels. Simultaneous printing activity caused the additional release of micron-sized particles and a further increase in reaction products. Relevant cellular endpoints to evaluate the possible induction of acute airway effects were measured. However, none of the test atmospheres representing office air was observed to induce these effects.