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The determination of the total concentration of selenium does not provide sufficient information about its toxicity and its bioavailability. The determination of its chemical forms is the basis for understanding the biogeochemical cycle in terrestrial and aquatic ecosystems and for detecting the species which might be toxic to biota. In this work we describe an analytical procedure to carry out the redox speciation of selenium present at ultratrace levels in rainwater from sites of Valparaiso region in Chile, impacted by mining activities of copper ores. A simple preconcentration step of the rainwater sample on a rotavapor system, in vacuum at low temperature permits the concentration of the different redox selenium species until levels quantifiable by sensitive techniques such as differential pulse cathodic stripping voltammetry or by spectrometric techniques, based on the hydride generation and detection by atomic absorption or atomic fluorescence spectrometry. These techniques coupled to redox chemical reactions allow the redox speciation of selenium. The results show that the open evaporation system can be used to concentrate water samples when the aim of the analysis is the determination of the total selenium concentration. On the contrary, to carry out its redox speciation only the preconcentration performed on rotavapor system, in vacuum can be used. When synthetic solutions containing different redox species of selenium, at ultratrace levels, were slowly evaporated on open system, Se(II) and Se(IV) were oxidized. The optimized procedure was then applied to the selenium determination and its redox speciation in rainwater samples collected in sites impacted by mining activities of copper ores. It was found that the amounts of total selenium in rainwater, as copper, from Puchuncavi valley decrease exponentially with the distance from the source, indicating that these elements in this region arise from the industrial complex Las Ventanas. In the redox speciation of selenium, Se(IV) and Se(VI) were the species found in all rainwater samples analyzed, providing selenium in species which are most favorable for their uptake by the vegetation grown in these soils.
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http://dx.doi.org/10.1016/s0043-1354(01)00240-8 | DOI Listing |
Environ Sci Technol
August 2025
State Key Laboratory of Lake and Watershed Science for Water Security, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences, Nanjing 210008, China.
Organic phosphorus (OP), a major phosphorus pool in sediments, can be converted into bioavailable phosphate. Although biological activity is considered the primary driver of OP dephosphorylation, the abiotic mechanism under redox oscillations remains unexplained. Here, we show that hydrological perturbation-driven redox fluctuations can mediate abiotic phosphate release from OP.
View Article and Find Full Text PDFRSC Adv
August 2025
Nuclear Materials Authority P.O. Box 530, El-Maadi Cairo Egypt
Carbon-free nuclear energy meets growing energy demand; uranium recycling enhances sustainability, economic, and environmental benefits. Herein, efficient three α-aminophosphonates-based sorbents were previously synthesized a one-pot method using distinct amine precursors (aniline, -phenylenediamine, anthranilic acid), yielding S-H, S-NH aminated, and S-COOH carboxylated, respectively enhanced aminophosphonate. Elemental analysis confirms three α-aminophosphonate sorbents (S-H, S-COOH, S-NH) with amine-dependent structures.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, P.O. Box 14117, Tehran 13116, Islamic Republic of Iran.
Here, a series of functionalized zirconium-based metal-organic frameworks (Zr-MOFs) were synthesized by using ZrCl and l-aspartic acid (ASP), 3-mercapto succinic acid (MSA), and succinic acid (SUC) as organic linkers for direct As(III) removal from contaminated water. The Zr-MOFs are nonfunctional Zr-SUC, amine-decorated Zr-ASP, and thiol-decorated Zr-MSA. Mechanistic studies reveal that the introduction of thiol and especially amine functional groups has significantly increased the adsorption capacity and affinity toward As(III) species.
View Article and Find Full Text PDFEnviron Geochem Health
August 2025
Department of Earth Sciences, University of Yaoundé I, BP 812, Yaoundé, Cameroun.
Contamination by potentially toxic elements (PTEs) is a major environmental concern, especially in mining sites, given the often-increasing concentrations in soil and sediments. Under certain conditions, such contamination may expand beyond the mining area, posing risks to human health. This study investigates the environmental hazard associated with PTEs in soils and river sediments from the Meiganga gold district by evaluating their speciation and mobility.
View Article and Find Full Text PDFEnviron Geochem Health
August 2025
Shandong Key Laboratory of Coastal Environmental Processes, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, 264003, Shandong, People's Republic of China.
Dissolved oxygen (DO) critically regulates biogeochemical processes in mariculture sediments, yet its integrated effects on sulfur-metal interactions during sediment aging remain poorly understood. This study investigated the migration and transformation of reduced inorganic sulfur (RIS) and heavy metals in mariculture sediments under varying DO levels. Lower DO accelerated the dominance of acid-volatile sulfide (AVS) within the reduced inorganic sulfur pool (AVS/RIS = 56.
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