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Isotopes & Radiation
Members are devoted to applying nuclear science and engineering technologies involving isotopes, radiation applications, and associated equipment in scientific research, development, and industrial processes. Their interests lie primarily in education, industrial uses, biology, medicine, and health physics. Division committees include Analytical Applications of Isotopes and Radiation, Biology and Medicine, Radiation Applications, Radiation Sources and Detection, and Thermal Power Sources.
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ANS Student Conference 2025
April 3–5, 2025
Albuquerque, NM|The University of New Mexico
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The Standards Committee is responsible for the development and maintenance of voluntary consensus standards that address the design, analysis, and operation of components, systems, and facilities related to the application of nuclear science and technology. Find out What’s New, check out the Standards Store, or Get Involved today!
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Latest News
Disa seeks NRC license for its uranium mine waste remediation tech
The Nuclear Regulatory Commission has received a license application from Disa Technologies to use high-pressure slurry ablation (HPSA) technology for remediating abandoned uranium mine waste at inactive mining sites. Disa’s headquartersin are Casper, Wyo.
Kazuya Furuichi, Kazunari Katayama, Hiroyuki Date, Toshiharu Takeishi, Satoshi Fukada
Fusion Science and Technology | Volume 68 | Number 2 | September 2015 | Pages 458-464
Technical Note | Proceedings of TOFE-2014 | doi.org/10.13182/FST14-969
Articles are hosted by Taylor and Francis Online.
In this study, tritiated water was poured in a packed bed of natural soil and subsequently distilled water was poured in the bed to recover tritium retained in the soil at room temperature. From tritium balance, 22.5 % (7.1 MBq) of input tritium (31.5 MBq) was retained in the soil bed. By distilled water purge, 70 % (5 MBq) of retained tritium was recovered but 30% (2.1MBq) was left. To recover residual tritium, the soil was immersed in distilled water for 531 days but the amount of tritium released to distilled water was slight (0.04 MBq). A part of the soil immersed in the water was taken out and heated up to 300°C under humid oxygen atmosphere. Tritium release terminated at about 50 hours. 11 % (0.23 MBq) of retained tritium was released. By heating to 1000°C, the release amount of tritium increased proportionally to the time and additional 4% (0.09 MBq) was released at 5 hours. The desorption rates of tritium in each process was quantified.
Tritium is quite slowly released from the natural soil exposed to tritiated water in water at room temperature. However, a long time heating by 1000°C would be required to try to recover all tritium from the contaminated soil positively, although tritium recovery was not completed in this work.