Interfacial study of clathrates confined in reversed silica pores

被引:12
|
作者
Mileo, Paulo G. M. [1 ]
Rogge, Sven M. J. [1 ]
Houlleberghs, Maarten [2 ]
Breynaert, Eric [2 ]
Martens, Johan A. [2 ]
Van Speybroeck, Veronique [1 ]
机构
[1] Univ Ghent, Ctr Mol Modeling CMM, Technol Pk 46, B-9052 Zwijnaarde, Belgium
[2] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Celestijnenlaan 200F, B-3001 Heverlee, Belgium
基金
欧洲研究理事会; 比利时弗兰德研究基金会;
关键词
METHANE HYDRATE FORMATION; MOLECULAR-DYNAMICS SIMULATIONS; GAS-STORAGE; CARBON-DIOXIDE; PHASE-EQUILIBRIA; ORBITAL METHODS; DRY WATER; BASIS-SET; CAPTURE; CYCLOPENTANE;
D O I
10.1039/d1ta03105h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Storing methane in clathrates is one of the most promising alternatives for transporting natural gas (NG) as it offers similar gas densities to liquefied and compressed NG while offering lower safety risks. However, the practical use of clathrates is limited given the extremely low temperatures and high pressures necessary to form these structures. Therefore, it has been suggested to confine clathrates in nanoporous materials, as this can facilitate clathrate's formation conditions while preserving its CH4 volumetric storage. Yet, the choice of nanoporous materials to be employed as the clathrate growing platform is still rather arbitrary. Herein, we tackle this challenge in a systematic way by computationally exploring the stability of clathrates confined in alkyl-grafted silica materials with different pore sizes, ligand densities and ligand types. Based on our findings, we are able to propose key design criteria for nanoporous materials favoring the stability of a neighbouring clathrate phase, namely large pore sizes, high ligand densities, and smooth pore walls. We hope that the atomistic insight provided in this work will guide and facilitate the development of new nanomaterials designed to promote the formation of clathrates.
引用
收藏
页码:21835 / 21844
页数:10
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