Engineering of hollow periodic mesoporous organosilica nanorods for augmented hydrogen clathrate formation

被引:3
|
作者
Watson, Geert [1 ]
Kummamuru, Nithin B. [2 ]
Verbruggen, Sammy W. [2 ,3 ]
Perreault, Patrice [4 ,5 ]
Houlleberghs, Maarten [6 ]
Martens, Johan [6 ]
Breynaert, Eric [6 ]
van der Voort, Pascal [1 ]
机构
[1] Univ Ghent, Ctr Ordered Mat Organometall & Catalysis COMOC, Dept Chem, Krijgslaan 281-S3, B-9000 Ghent, Belgium
[2] Univ Antwerp, Dept Biosci Engn, Sustainable Energy Air & Water Technol DuEL, Groenenborgerlaan 171, B-2020 Antwerp, Belgium
[3] Univ Antwerp, NANOlab Ctr Excellence, Groenenborgerlaan 171, B-2020 Antwerp, Belgium
[4] Univ Antwerp, Fac Sci, Inst Milieu & Duurzame Ontwikkeling IMDO, Campus Groenenborger Bldg V 612,Gronenborgerlaan 1, B-2020 Antwerp, Belgium
[5] Univ Antwerp, BlueApp, Olieweg 97, B-2020 Antwerp, Belgium
[6] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Dept Microbial & Mol Syst M2S, NMRCoRe NMR XRAY EM Platform Convergence Res, Celestijnenlaan 200F, B-3001 Leuven, Belgium
基金
欧洲研究理事会;
关键词
GAS HYDRATE FORMATION; THERMODYNAMIC STABILITY; STORAGE CAPACITY; METHANE HYDRATE; METAL-HYDRIDES; KINETICS; HYDROGEN/TETRAHYDROFURAN; NUCLEATION; SURFACES; CLUSTERS;
D O I
10.1039/d3ta05530b
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
Hydrogen (H2) storage, in the form of clathrate hydrates, has emerged as an attractive alternative to classical storage methods like compression or liquefaction. Nevertheless, the sluggish enclathration kinetics along with low gas storage capacities in bulk systems is currently impeding the progress of this technology. To this end, unstirred systems coupled with porous materials have been shown to tackle the aforementioned drawbacks. In line with this approach, the present study explores the use of hydrophobic periodic organosilica nanoparticles, later denoted as hollow ring-PMO (HRPMO), for H2 storage as clathrate hydrates under mild operating conditions (5.56 mol% THF, 7 MPa, and 265-273 K). The surface of the HRPMO nanoparticles was carefully decorated/functionalized with THF-like moieties, which are well-known promoter agents in clathrate formation when applied in classical, homogeneous systems. The study showed that, while the non-functionalized HRPMO can facilitate the formation of binary H2-THF clathrates, the incorporation of surface-bound promotor structures enhances this process. More intriguingly, tuning the concentration of these surface-bound promotor agents on the HRPMO led to a notable effect on solid-state H2 storage capacities. An increase of 3% in H2 storage capacity, equivalent to 0.26 wt%, along with a substantial increase of up to 28% in clathrate growth kinetics, was observed when an optimal loading of 0.14 mmol g-1 of promoter agent was integrated into the HRPMO framework. Overall, the findings from this study highlight that such tuning effects in the solid-state have the potential to significantly boost hydrate formation/growth kinetics and H2 storage capacities, thereby opening new avenues for the ongoing development of H2 clathrates in industrial applications. Careful engineering of the surface chemistries of porous additives for H2 clathrate formation could enhance the H2 storage capacities, a vital requirement for their use as alternative H2 storage medium.
引用
收藏
页码:26265 / 26276
页数:12
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