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      Removal of tritiated water molecules by isotope exchange reaction between H 2O vapor and tritium water

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          Abstract

          Developing a cost-effective method for separating and concentrating tritium water (HTO) from light water (H 2O) without consuming additional energy is crucial for achieving reliable and safe nuclear fission and fusion energy technologies. However, this presents a significant challenge because of the difficulties in obtaining basic information, such as the chemical and physical properties of HTO molecules. Here, we investigate the isotope exchange reaction (IER) between HTO molecules in H 2O solution and H 2O vapor in the atmosphere. The reduction and purification rates of HTO-containing water were measured by varying the system conditions, such as temperature (20−50 °C) and humidity (50 %–90 %), under an equilibrium state between the liquid phase (water) and vapor phase (air). Our findings indicate that the concentration of HTO in the solution can be significantly reduced by increasing H 2O vapor in the atmosphere. This result can be quantitatively explained by considering the entropy of mixing between the solution and vapor phases. The results obtained here provide both basic understanding on the exchange process between liquid- and vapor-water molecules and a passive technology for treating HTO-containing water.

          Highlights

          • Isotope exchange reaction found as a viable method to purify HTO-containing water.

          • Concentration of HTO can be reduced by increasing H 2O vapor in the atmosphere.

          • Our passive method consumes lower energy and time compared to traditional methods.

          • Airtightness of the storage tank controls HTO concentration reduction rate.

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          Most cited references37

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          Zur Lehre von der Wirkung der Salze

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            Raman thermometry measurements of free evaporation from liquid water droplets.

            Recent theoretical and experimental studies of evaporation have suggested that on average, molecules in the higher-energy tail of the Boltzmann distribution are more readily transferred into the vapor during evaporation. To test these conclusions, the evaporative cooling rates of a droplet train of liquid water injected into vacuum have been studied via Raman thermometry. The resulting cooling rates are fit to an evaporative cooling model based on Knudsen's maximum rate of evaporation, in which we explicitly account for surface cooling. We have determined that the value of the evaporation coefficient (gamma(e)) of liquid water is 0.62 +/- 0.09, confirming that a rate-limiting barrier impedes the evaporation rate. Such insight will facilitate the formulation of a microscopic mechanism for the evaporation of liquid water.
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              The evaporation coefficient of water: a review

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                Author and article information

                Contributors
                Journal
                Heliyon
                Heliyon
                Heliyon
                Elsevier
                2405-8440
                03 July 2024
                15 August 2024
                03 July 2024
                : 10
                : 15
                : e33956
                Affiliations
                [a ]Graduate School of Design and Architecture, Nagoya City University, Nagoya, 464-0083, Japan
                [b ]Graduate School of Medical Sciences, Nagoya City University, Nagoya, 464-0083, Japan
                [c ]Laboratory of Radioisotope Research, Nagoya City University, Nagoya, 467-8601, Japan
                [d ]Department of Physics, Faculty of Science, Shizuoka University, Shizuoka, 422-8529, Japan
                [e ]Department of Physics, Faculty of Science and Engineering, Chuo University, Tokyo, 112-8551, Japan
                Author notes
                [* ]Corresponding author. Graduate School of Design and Architecture, Nagoya City University, Nagoya, 464-0083, Japan. matsumoto@ 123456sda.nagoya-cu.ac.jp
                Article
                S2405-8440(24)09987-0 e33956
                10.1016/j.heliyon.2024.e33956
                11320128
                39144924
                f01b3ef5-ffd2-4e4d-be92-0ec9a9fe6195
                © 2024 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 5 April 2024
                : 30 June 2024
                : 1 July 2024
                Categories
                Research Article

                tritium water,isotope,exchange reaction,purification,nuclear fusion,nuclear fission

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