LAPSE:2025.0351
Published Article

LAPSE:2025.0351
Simulation and Optimisation of Cryogenic Distillation and Isotopic Equilibrator Cascades for Hydrogen Isotope Separation Processes in the Fusion Fuel Cycle
June 27, 2025
Abstract
Hydrogen isotope separation is a critical component of the fusion fuel cycle, particularly for achieving the desired purity levels of deuterium and tritium while minimising tritium inventory. This study investigates the cryogenic distillation of hydrogen isotopes, with a focus on the effects of isotopic equilibrium reactions at reduced temperatures and different system configurations. A one-column architecture was analysed to evaluate the impact of feed and side stream equilibrator temperatures and flowrates on separation performance and tritium inventory. Additionally, a two-column architecture was studied, incorporating multiple isotopic equilibrators in interconnecting streams, to further reduce unwanted heteronuclear isotopologues and improve system efficiency. Comparative analysis of the proposed configurations highlights significant operational advantages of optimising equilibrator temperatures, including reduced tritium contamination and inventory. Results indicate that reducing equilibrator temperatures to 77.4 K not only improves separation efficiency but also enables reductions in the number of theoretical stages required, minimising tritium inventory. A case study of the ITER Isotope Separation System demonstrates that reducing equilibrator temperatures achieves comparable performance with fewer stages in key columns, validating the benefits of optimised equilibrator operation for practical application. These findings contribute to the development of more efficient, cost-effective designs for fusion fuel cycle isotope separation systems.
Hydrogen isotope separation is a critical component of the fusion fuel cycle, particularly for achieving the desired purity levels of deuterium and tritium while minimising tritium inventory. This study investigates the cryogenic distillation of hydrogen isotopes, with a focus on the effects of isotopic equilibrium reactions at reduced temperatures and different system configurations. A one-column architecture was analysed to evaluate the impact of feed and side stream equilibrator temperatures and flowrates on separation performance and tritium inventory. Additionally, a two-column architecture was studied, incorporating multiple isotopic equilibrators in interconnecting streams, to further reduce unwanted heteronuclear isotopologues and improve system efficiency. Comparative analysis of the proposed configurations highlights significant operational advantages of optimising equilibrator temperatures, including reduced tritium contamination and inventory. Results indicate that reducing equilibrator temperatures to 77.4 K not only improves separation efficiency but also enables reductions in the number of theoretical stages required, minimising tritium inventory. A case study of the ITER Isotope Separation System demonstrates that reducing equilibrator temperatures achieves comparable performance with fewer stages in key columns, validating the benefits of optimised equilibrator operation for practical application. These findings contribute to the development of more efficient, cost-effective designs for fusion fuel cycle isotope separation systems.
Record ID
Keywords
Aspen Plus, Fusion Fuel Cycle, Modelling and Simulations, Nuclear, Optimization, Process Design, Tritium Inventory Minimisation
Subject
Suggested Citation
Barrow EA, Bennett I, Cecelja F, Garciadiego-Ortega E, Thompson M, Tsaoulidis D. Simulation and Optimisation of Cryogenic Distillation and Isotopic Equilibrator Cascades for Hydrogen Isotope Separation Processes in the Fusion Fuel Cycle. Systems and Control Transactions 4:1244-1250 (2025) https://doi.org/10.69997/sct.124889
Author Affiliations
Barrow EA: School of Chemistry and Chemical Engineering, University of Surrey, Guildford, Surrey, United Kingdom
Bennett I: United Kingdom Atomic Energy Authority, Culham Science Centre, Abingdon, Oxfordshire, United Kingdom
Cecelja F: School of Chemistry and Chemical Engineering, University of Surrey, Guildford, Surrey, United Kingdom
Garciadiego-Ortega E: United Kingdom Atomic Energy Authority, Culham Science Centre, Abingdon, Oxfordshire, United Kingdom
Thompson M: United Kingdom Atomic Energy Authority, Culham Science Centre, Abingdon, Oxfordshire, United Kingdom
Tsaoulidis D: School of Chemistry and Chemical Engineering, University of Surrey, Guildford, Surrey, United Kingdom
Bennett I: United Kingdom Atomic Energy Authority, Culham Science Centre, Abingdon, Oxfordshire, United Kingdom
Cecelja F: School of Chemistry and Chemical Engineering, University of Surrey, Guildford, Surrey, United Kingdom
Garciadiego-Ortega E: United Kingdom Atomic Energy Authority, Culham Science Centre, Abingdon, Oxfordshire, United Kingdom
Thompson M: United Kingdom Atomic Energy Authority, Culham Science Centre, Abingdon, Oxfordshire, United Kingdom
Tsaoulidis D: School of Chemistry and Chemical Engineering, University of Surrey, Guildford, Surrey, United Kingdom
Journal Name
Systems and Control Transactions
Volume
4
First Page
1244
Last Page
1250
Year
2025
Publication Date
2025-07-01
Version Comments
Original Submission
Other Meta
PII: 1244-1250-1705-SCT-4-2025, Publication Type: Journal Article
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LAPSE:2025.0351
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References Cited
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