Removal of tritiated water molecules by isotope exchange reaction between H2O vapor and tritium water

被引:1
作者
Matsumoto, Takahiro [1 ,2 ]
Sakuragawa, Chiyori [1 ]
Mu, Tong [1 ]
Tachibana, Koki [1 ]
Ishihara, Masashi [3 ]
Tomita, Makoto [4 ]
Sugimoto, Hidehiko [5 ]
机构
[1] Nagoya City Univ, Grad Sch Design & Architecture, Nagoya 4640083, Japan
[2] Nagoya City Univ, Grad Sch Med Sci, Nagoya 4640083, Japan
[3] Nagoya City Univ, Lab Radioisotope Res, Nagoya 4678601, Japan
[4] Shizuoka Univ, Fac Sci, Dept Phys, Shizuoka 4228529, Japan
[5] Chuo Univ, Fac Sci & Engn, Dept Phys, Tokyo 1128551, Japan
关键词
Tritium water; Isotope; Exchange reaction; Purification; Nuclear fusion; Nuclear fission; EVAPORATION COEFFICIENT; CATALYTIC EXCHANGE; ELECTROLYSIS; SEPARATION; SURFACE;
D O I
10.1016/j.heliyon.2024.e33956
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Developing a cost-effective method for separating and concentrating tritium water (HTO) from light water (H2O) 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 H2O solution and H2O 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 degrees 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 H2O 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.
引用
收藏
页数:9
相关论文
共 50 条
[1]   Heavy water detritiation by combined electrolysis catalytic exchange at the experimental industrial plant [J].
Alekseev, IA ;
Bondarenko, SD ;
Fedorchenko, OA ;
Vasyanina, TV ;
Konoplev, KA ;
Arkhipov, EA ;
Voronina, TV ;
Grushko, AI ;
Tchijov, AS ;
Uborsky, VV .
FUSION ENGINEERING AND DESIGN, 2003, 69 (1-4) :33-37
[2]   Effects of additives and electrolytic treatment to remove tritium from contaminated water [J].
Ando, Shizutoshi ;
Komatsuzaki, Takashi ;
Okada, Mitsukiyo ;
Kataoka, Noriaki .
HELIYON, 2023, 9 (06)
[3]  
asn, Autorite de surete nucleaire, LIVRE BLANC TRITIUM, Groupes de reflexion menes de mai 2008 a avril 2010, sous l'egide de l'ASN et Bilan annuel des rejets de tritium pour les installations nucleaire de base de 2018 a 2022
[4]  
Benedict M., 1981, Nuclear Chemical Engineering
[5]  
Canadian Nuclear Safety Commission, Radioactive release data from Canadian Nuclear Power Plants 2001-10
[6]   Ratio of deuterium to hydrogen termination on silicon surface in aqueous electrolyte solutions [J].
Chikalova-Luzina, OP ;
Matsumoto, T .
APPLIED PHYSICS LETTERS, 2002, 80 (24) :4507-4509
[7]   The evaporation coefficient of water: A review [J].
Eames, IW ;
Marr, NJ ;
Sabir, H .
INTERNATIONAL JOURNAL OF HEAT AND MASS TRANSFER, 1997, 40 (12) :2963-2973
[8]   Tritium: Its relevance, sources and impacts on non-human biota [J].
Ferreira, Maria Florencia ;
Turner, Andrew ;
Vernon, Emily L. ;
Grisolia, Christian ;
Lebaron-Jacobs, Laurence ;
Malard, Veronique ;
Jha, Awadhesh N. .
SCIENCE OF THE TOTAL ENVIRONMENT, 2023, 876
[9]   Tritium isotope separation by water distillation column packed with silica-gel beads [J].
Fukada, S .
JOURNAL OF NUCLEAR SCIENCE AND TECHNOLOGY, 2004, 41 (05) :619-623
[10]   Screening of Metal-Organic Frameworks for Highly Effective Hydrogen Isotope Separation by Quantum Sieving [J].
Han, Guopeng ;
Gong, Yu ;
Huang, Hongliang ;
Cao, Dawei ;
Chen, Xiaojun ;
Liu, Dahuan ;
Zhong, Chongli .
ACS APPLIED MATERIALS & INTERFACES, 2018, 10 (38) :32128-32132