Here we compare the standard European benchmark of wood treatment by molecularly dissolved copper amine (Cu-amine), also referred to as aqueous copper amine (ACA), against two nanoenabled formulations: copper(II)oxide nanoparticles (CuO NPs) in an acrylic paint to concentrate Cu as a barrier on the wood surface, and a suspension of micronized basic copper carbonate (CuCO·Cu(OH)) for wood pressure treatment. After characterizing the properties of the (nano)materials and their formulations, we assessed their effects in vitro against three fungal species: Coniophora puteana, Gloeophyllum trabeum, and Trametes versicolor, finding them to be mediated only partially by ionic transformation. To assess the use phase, we quantify both release rate and form. Cu leaching rates for the two types of impregnated wood (conventional and nanoenabled) are not significantly different at 172 ± 6 mg/m, with Cu being released predominantly in ionic form. Various simulations of outdoor aging with release sampling by runoff, during condensation, by different levels of mechanical shear, all resulted in comparable form and rate of release from the nanoenabled or the molecular impregnated woods. Because of dissolving transformations, the nanoenabled impregnation does not introduce additional concern over and above that associated with the traditional impregnation. In contrast, Cu released from wood coated with the CuO acrylate contained particles, but the rate was at least 100-fold lower. In the same ranking, the effectiveness to protect against the wood-decaying basidiomycete Coniophora puteana was significant with both impregnation technologies but remained insignificant for untreated wood and wood coated by the acrylic CuO. Accordingly, a lifecycle-based sustainability analysis indicates that the CuO acrylic coating is less sustainable than the technological alternatives, and should not be developed into a commercial product.
The International Thermonuclear Experimental Reactor (ITER) is an international project aimed at the production of carbon-free energy through the use of thermonuclear fusion. During ITER operation, in case of a loss-of-vacuum-accident, tungsten nanoparticles (W-NPs) could potentially be released into the environment and induce occupational exposure via inhalation. W-NPs toxicity was evaluated on MucilAir™, a 3D in vitro cell model of the human airway epithelium. MucilAir™ was exposed for 24 h to metallic ITER-like milled W-NPs, tungstate (WO42−) and tungsten carbide cobalt particles alloy (WC-Co). Cytotoxicity and its reversibility were assessed using a kinetic mode up to 28 days after exposure. Epithelial tightness, metabolic activity and interleukin-8 release were also evaluated. Electron microscopy was performed to determine any morphological modification, while mass spectrometry allowed the quantification of W-NPs internalization and of W transfer through the MucilAir™. Our results underlined a decrease in barrier integrity, no effect on metabolic activity or cell viability and a transient increase in IL-8 secretion after exposure to ITER-like milled W-NPs. These effects were associated with W-transfer through the epithelium, but not with intracellular accumulation. We have shown that, under our experimental conditions, ITER-like milled W-NPs have a minor impact on the MucilAir™ in vitro model.
Tungsten was chosen as a wall component to interact with the plasma generated by the International Thermonuclear Experimental fusion Reactor (ITER). Nevertheless, during plasma operation tritiated tungsten nanoparticles (W-NPs) will be formed and potentially released into the environment following a Loss-Of-Vacuum-Accident, causing occupational or accidental exposure. We therefore investigated, in the bronchial human-derived BEAS-2B cell line, the cytotoxic and epigenotoxic effects of two types of ITER-like W-NPs (plasma sputtering or laser ablation), in their pristine, hydrogenated, and tritiated forms. Long exposures (24 h) induced significant cytotoxicity, especially for the hydrogenated ones. Plasma W-NPs impaired cytostasis more severely than the laser ones and both types and forms of W-NPs induced significant micronuclei formation, as shown by cytokinesis-block micronucleus assay. Single DNA strand breaks, potentially triggered by oxidative stress, occurred upon exposure to W-NPs and independently of their form, as observed by alkaline comet assay. After 24 h it was shown that more than 50% of W was dissolved via oxidative dissolution. Overall, our results indicate that W-NPs can affect the in vitro viability of BEAS-2B cells and induce epigenotoxic alterations. We could not observe significant differences between plasma and laser W-NPs so their toxicity might not be triggered by the synthesis method.
Oxidative transformation of Tungsten (W) nanoparticles potentially released in aqueous and biological media in case of Tokamak (nuclear fusion) Lost of Vacuum Accident (LOVA)
During International Thermonuclear Experimental Reactor operation, due to plasma–wall interaction, particles/dust will be created in sizes ranging from nanometers to tens of microns. The dust properties, especially their ability to be covered by a thin oxide electrostatic insulating layer, and surface topology deeply affect their tritium inventory. Consequently, physico-chemical properties specific to tritiated tungsten particles and consequence on particle behavior in the facility and environment must be carefully assessed. For size-relevant tungsten particles, the measured tritium inventory is ~10 GBq g−1. However, it varies with the particle specific surface area. Due to tritium beta decay and the oxide-insulating layer, dust exhibits a positive electrostatic self-charging. For a 5 µm particle in diameter with a 10 GBq g−1 tritium inventory, self-charging rate could lead to 5.5 104 elementary electric charges per day. These electrostatic properties could change the adhesion of dust on walls. In the case of a single particle, the adhesion will be reinforced due to image and dielectric forces. However, if the tritiated particle is part of an aggregate, the adhesion remains unknown. Due to the limited free path of the β emission in material, the tritium inventory carried by airborne particles cannot be measured in real time by conventional continuous radioactive aerosols monitors, and a new measurement strategy is needed for atmospheric surveillance in the workplace and of facility exhaust. Toxicity studies dealing with exposure to untritiated/tritiated tungsten particles of 100 nm have been undertaken. It was shown that these particles are rapidly dissolved in biologic media. Finally, after collection, dust must be confined to avoid its spreading into the environment. Different technical solutions are presented in this paper.
During ITER operation, it is expected that the large panel of plasma-wall interactions triggers the production of dust particles, potentially loaded with tritium present nearby. Tritium (T) inventory in the various materials, such as tungsten (W), is of prime importance for the safety assessment of a Tokamak machine, and it is even more crucial when considering dispersible matters like dusts: in case of a Loss Of Vacuum Accident (LOVA), dusts may form aerosols containing tritium and activation products that could escape the first confinement barrier and be released in the environment. The with tritium inventory in the described W dusts and their suspension in various liquid media for cell exposure for toxicity studies.
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