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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 December 29, 2024
Revised February 14, 2025
Accepted March 5, 2025
Available online October 25, 2025
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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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Capturing a Specifi c Component from Mixed (SF 6 + N 2 ) Gasses Using Crystal Structure Change of Hydroquinone
https://doi.org/10.1007/s11814-025-00440-1
Abstract
During the reaction of the solid and the gas phases, solid hydroquinone (HQ) changes its crystal structure while a specifi c
component from mixed gasses is captured into the changed HQ crystal structure. To investigate the partitioning of mixed
gasses in the solid phase, the (SF 6 + N 2 ) gas mixtures having various compositions are used as a gas phase reactant at two
experimental pressures, 2.0 and 4.0 MPa. In addition, spectroscopic measurements are also performed to obtain qualitative
and quantitative information on partitioning of each gas component. From a series of experimental results, it was found that
N 2 is exclusively accommodated in the gas-loaded HQ crystal structure, while SF 6 is excluded from the solid crystal structure
due to its large molecular size. However, because such partitioning requires high partial pressures of N 2 in the gas mixtures
(higher N 2 composition at a given pressure or higher experimental pressure at a given gas composition), N 2 capture in the
HQ crystal structure is only observed at 80-mol% N 2 composition at the experimental pressure of 4.0 MPa among various
gas compositions. The captured amount of N 2 corresponds to 13.7 L at the STP condition per 1 kg of HQ. Although N 2 is
found to be selectively separated from the binary gas mixtures, further investigations focusing mainly on the reduction of
the experimental pressure and the increase of captured N 2 amount are necessary to apply to industrial fi elds.

