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      Development of a Novel Passive Monitoring Technique to Showcase the 3D Distribution of Tritiated Water (HTO) Vapor in Indoor Air of a Nuclear Facility

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          Abstract

          Tritiated water (HTO), a ubiquitous byproduct of the nuclear industry, is a radioactive contaminant of major concern for environmental authorities. Although understanding spatiotemporal heterogeneity of airborne HTO vapor holds great importance for radiological safety as well as diagnosing a reactor’s status, comprehensive HTO distribution dynamics inside nuclear facilities has not been studied routinely yet due to a lack of appropriate monitoring techniques. For current systems, it is difficult to simultaneously achieve high representativeness, sensitivity, and spatial resolution. Here, we developed a passive monitoring scheme, including a newly designed passive sampler and a tailored analytical protocol for the first comprehensive 3D distribution characterization of HTO inside a nuclear reactor facility. The technique enables linear sampling in any environment at a one-day resolution and simultaneous preparation of hundreds of samples within 1 day. Validation experiments confirmed the method’s good metrological properties and sensitivity to the HTO’s spatial dynamics. The air in TU Wien’s reactor hall exhibits a range of 3H concentrations from 75–946 mBq m –3 in the entire 3D matrix. The HTO release rate estimated by the mass-balance model (3199 ± 306 Bq h –1) matches the theoretical calculation (2947 ± 254 Bq h –1), suggesting evaporation as the dominant HTO source in the hall. The proposed method provides reliable and quality-controlled 3D monitoring at low cost, which can be adopted not only for HTO and may also inspire monitoring schemes of other indoor pollutants.

          Abstract

          A novel passive monitoring technique was developed, validated, and applied to characterize the 3D spatiotemporal heterogeneity of airborne HTO in a nuclear facility.

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          Most cited references63

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          On the Computation of Saturation Vapor Pressure

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            Comparison of the Chernobyl and Fukushima nuclear accidents: a review of the environmental impacts.

            The environmental impacts of the nuclear accidents of Chernobyl and Fukushima are compared. In almost every respect, the consequences of the Chernobyl accident clearly exceeded those of the Fukushima accident. In both accidents, most of the radioactivity released was due to volatile radionuclides (noble gases, iodine, cesium, tellurium). However, the amount of refractory elements (including actinides) emitted in the course of the Chernobyl accident was approximately four orders of magnitude higher than during the Fukushima accident. For Chernobyl, a total release of 5,300 PBq (excluding noble gases) has been established as the most cited source term. For Fukushima, we estimated a total source term of 520 (340-800) PBq. In the course of the Fukushima accident, the majority of the radionuclides (more than 80%) was transported offshore and deposited in the Pacific Ocean. Monitoring campaigns after both accidents reveal that the environmental impact of the Chernobyl accident was much greater than of the Fukushima accident. Both the highly contaminated areas and the evacuated areas are smaller around Fukushima and the projected health effects in Japan are significantly lower than after the Chernobyl accident. This is mainly due to the fact that food safety campaigns and evacuations worked quickly and efficiently after the Fukushima accident. In contrast to Chernobyl, no fatalities due to acute radiation effects occurred in Fukushima. © 2013.
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              Tracking of airborne radionuclides from the damaged Fukushima Dai-ichi nuclear reactors by European networks.

              Radioactive emissions into the atmosphere from the damaged reactors of the Fukushima Dai-ichi nuclear power plant (NPP) started on March 12th, 2011. Among the various radionuclides released, iodine-131 ((131)I) and cesium isotopes ((137)Cs and (134)Cs) were transported across the Pacific toward the North American continent and reached Europe despite dispersion and washout along the route of the contaminated air masses. In Europe, the first signs of the releases were detected 7 days later while the first peak of activity level was observed between March 28th and March 30th. Time variations over a 20-day period and spatial variations across more than 150 sampling locations in Europe made it possible to characterize the contaminated air masses. After the Chernobyl accident, only a few measurements of the gaseous (131)I fraction were conducted compared to the number of measurements for the particulate fraction. Several studies had already pointed out the importance of the gaseous (131)I and the large underestimation of the total (131)I airborne activity level, and subsequent calculations of inhalation dose, if neglected. The measurements made across Europe following the releases from the Fukushima NPP reactors have provided a significant amount of new data on the ratio of the gaseous (131)I fraction to total (131)I, both on a spatial scale and its temporal variation. It can be pointed out that during the Fukushima event, the (134)Cs to (137)Cs ratio proved to be different from that observed after the Chernobyl accident. The data set provided in this paper is the most comprehensive survey of the main relevant airborne radionuclides from the Fukushima reactors, measured across Europe. A rough estimate of the total (131)I inventory that has passed over Europe during this period was <1% of the released amount. According to the measurements, airborne activity levels remain of no concern for public health in Europe.
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                Author and article information

                Journal
                Environ Sci Technol
                Environ Sci Technol
                es
                esthag
                Environmental Science & Technology
                American Chemical Society
                0013-936X
                1520-5851
                15 November 2023
                05 December 2023
                : 57
                : 48
                : 20024-20033
                Affiliations
                []Institute of Applied Synthetic Chemistry & TRIGA Center Atominstitut, TU Wien , 1060 Vienna, Austria
                []Institute of Inorganic Chemistry, Leibniz Universität Hannover , 30167 Hannover, Germany
                [§ ]TRIGA Center Atominstitut, TU Wien , 1020 Vienna, Austria
                Author notes
                [* ]Georg Steinhauser ( georg.steinhauser@ 123456tuwien.ac.at ).
                Author information
                https://orcid.org/0000-0003-3585-7517
                https://orcid.org/0000-0003-1494-1242
                https://orcid.org/0000-0002-6114-5890
                Article
                10.1021/acs.est.3c05783
                10702432
                37964532
                654f99c5-a982-4496-82f1-f07ebc584127
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 20 July 2023
                : 30 October 2023
                : 27 October 2023
                Funding
                Funded by: Alexander von Humboldt-Stiftung, doi 10.13039/100005156;
                Award ID: NA
                Funded by: Technische Universität Wien, doi 10.13039/501100004729;
                Award ID: NA
                Categories
                Article
                Custom metadata
                es3c05783
                es3c05783

                General environmental science
                tritium,passive sampler,indoor air pollution,nuclear industry,3d spatial distribution,environmental radioactivity

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