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- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
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Received September 14, 2025
Revised October 31, 2025
Accepted November 10, 2025
Available online June 26, 2026
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This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits
unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Metal Incorporated Mesoporous Silica for Hydrogen Isotope Gas Separation Application in Heavy Water Nuclear Power Plant
https://doi.org/10.1007/s11814-025-00606-x
Abstract
The separation of hydrogen isotopologues, such as protium (H2), deuterium (D2) and tritium (T2), is necessary for the
stable and consistent operation of heavy water nuclear power plants, where deuterium oxide (D2O) is used as both a
moderator and coolant. As conventional processes, cryogenic distillation and catalytic exchange are widely applied for
hydrogen isotopologues separation. However, those techniques encounter intrinsic limitations including high energy consumption,
slow reaction rates and large operational costs. As an alternative, separation techniques based on the mechanism
of chemical affinity quantum sieving have been studied to separate isotopes at liquid nitrogen (N2, 77 K) to upwards
through differences in adsorption. In this study, mesoporous silica modified with silver (Ag) or copper (Cu) was prepared
and applied for hydrogen isotopologues separation at 77 and 87 K. The structural, morphological and surface chemical
properties of the metal incorporated mesoporous silica were analyzed using X-ray diffraction, scanning electron microscopy,
transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy, N2 physisorption, X-ray photoelectron
spectroscopy and solid-state silicon-29 magic angle spinning nuclear magnetic resonance spectroscopy. Single
gas adsorption isotherms of H2 and D2 were measured. The isosteric heats of adsorption were calculated to compare
how strongly each hydrogen isotopologues interact with the adsorbents and binary separation performance was evaluated
using equilibrium modeling. The Cu incorporated mesoporous silica showed the highest D2 over H2 selectivity, reaching
5.52 under the D2 diluted conditions (1:99). This is attributed to the dispersed Cu oxide species in the silica framework
as well as the silanol rich domains of mesoporous silica which both enhance interaction with D2. These results suggest
that isotope selectivity (D2/H2) can be tuned by adjusting the surface structure, property and pore network of mesoporous
silica, offering a practical approach for hydrogen isotopologues separation in nuclear facility

