This study presents the pattern of exposure to uranium and other occupational pollutants known to be potentially carcinogenic, mutagenic or toxic and used at the main uranium conversion plant in France. For different uranium compounds specified according to their solubility and purity, and 16 other categories of pollutants: chemicals, fibres, vapours, dust, and heat a time- and plant-specific job exposure matrix (JEM) was created covering the period 1960-2006. For 73 jobs and for each pollutant the amount and frequency of exposure were assessed on a four-level scale by different time periods. The JEM shows 73% sensitivity and 83% specificity. Although exposure assessment was semi-quantitative, the JEM allows computing of individual cumulative exposure score for each pollutant across time. Despite the predominant natural uranium compounds exposure, the amount of exposure to other pollutants such as TCE and other chlorinated products, asbestos, and fibres, is important at the plant. Numerous correlations detected between uranium compounds exposure and exposure to chemicals warrants improving biological monitoring of exposed workers and accounting for associated exposures in epidemiological studies. Results of this study will be used for further investigation of association between exposure and mortality among uranium conversion workers cohort.
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http://dx.doi.org/10.1016/j.ijheh.2008.09.002 | DOI Listing |
Environ Sci Technol
December 2024
CAS Key Laboratory of Urban Pollutant Conversion, Department of Environmental Science and Engineering, University of Science and Technology of China, Hefei 230026, China.
Uranium is the primary fuel for nuclear energy, critical for sustainable, carbon-neutral energy transitions. However, limited terrestrial resources and environmental risks from uranium contamination require innovative immobilization and recovery solutions. In this work, we present a novel uranium recovery method using programmable electroactive living materials (ELMs).
View Article and Find Full Text PDFJ Hazard Mater
December 2024
Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, State Key Laboratory of Materials Processing and Die & Mould Technology, Hubei Engineering Research Center for Biomaterials and Medical Protective Materials, Huazhong University of Science and Technology, Wuhan 430074, China. Electronic address:
As the fundamental resource in nuclear energy, uranium is a sword of two sides, due to its radioactive character that could cause severe impact to the environment and living creatures once released by accident. However, limited by the passive ion transport, the currently available uranium adsorbents still suffer from low adsorption kinetics and capacity. Here, we report a self-driven modular micro-reactor composed of magnetizable ion-exchange resin and adsorbents that can be used to dynamically remove uranium from nonmarine waters.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan University, Haikou, 570228, P. R. China.
Highly efficient separation of dispersed uranium is important for the sustainable development of nuclear industry, and adsorption is the most recognized approach. However, there are many coexisting interfering metal ions that compete with uranyl ion for the chelating ligands in the adsorbents and lead to low separation selectivity and efficiency. Herein, a coordination-induced magnetism strategy is presented for the separation of uranium based on the conversion of diamagnetic cyanoferrocene (Fc-CN) nanocrystals to uranium-containing magnetic recoverable ferromagnetic aggregates.
View Article and Find Full Text PDFChem Sci
October 2024
Department of Chemistry, Southern University of Science and Technology Shenzhen 518055 China
Recycling uranium (U) adsorption and controlled conversion is crucial for the sustainable development of nuclear energy, in which photocatalytic reduction of U(vi) from aqueous solutions is considered one of the most effective strategies. The primary challenge in the photocatalytic elimination of U(vi) resides in the demand for photocatalysts with exceptional properties for effective U(vi) adsorption and charge separation. Herein, we developed the hybrids of polyoxometalate@Cu-metal-organic frameworks (POM@Cu-MOFs) through a self-assembly strategy and demonstrated the efficient removal of U(vi) synergistic adsorption and photocatalysis.
View Article and Find Full Text PDFDalton Trans
November 2024
Institute of Applied Physics and Computational Mathematics, Beijing 100088, China.
Solvation is a crucial task in developing efficient and selective extractants for actinide elements, but an understanding and perspective of solvent effects on the extraction of uranyl are still lacking. Herein, we present investigations into solvent effects on the geometry, stability and bonding properties of five uranyl porphyrin derivative complexes (UO(L)) in four solvents relativistic quantum chemical calculations, and reveal some trends in the influence of solvent polarity on uranyl compounds. All five [L] ligands equatorially coordinate [UO] in a hexa-dentate (κ) fashion.
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