Decomposition Kinetics and Recycle of Binary Hydrogen-Tetrahydrofuran Clathrate Hydrate

被引:22
作者
Yoshioka, Hiroki [1 ]
Ota, Masaki [1 ]
Sato, Yoshiyuki [1 ]
Watanabe, Masaru [1 ]
Inomata, Hiroshi [1 ]
Smith, Richard L., Jr. [1 ]
Peters, Cor J. [2 ,3 ]
机构
[1] Tohoku Univ, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, Japan
[2] Delft Univ Technol, Lab Proc Equipment, Dept Proc & Energy, Fac Mech Maritime & Mat Engn, NL-2628 CA Delft, Netherlands
[3] Petr Inst, Chem Engn Program, Abu Dhabi, U Arab Emirates
关键词
hydrogen storage; clathrate hydrate; formation kinetics; hydrogen hydrate phase diffusion model; MOLECULAR-HYDROGEN; STORAGE CAPACITY; DISSOCIATION; DYNAMICS; MODEL; H-2; CFD;
D O I
10.1002/aic.12241
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Decomposition kinetics and recycle of hydrogen-tetrahydrofuran (H-2-THF) clathrate hydrates were investigated with a pressure decay method at temperatures from 265.1 to 273.2 K, at initial pressures from 3.1 to 8.0 MPa, and at stoichiometric THF hydrate concentrations for particle sizes between 250 and 1000 mu m. The decomposition was modeled as a two-step process consisting of H-2 diffusion in the hydrate phase and desorption from the hydrate cage. The adsorption process occurred at roughly two to three times faster than the desorption process, whereas the diffusion process during formation was slightly higher (ca. 20%) than that during decomposition. Successive formation and decomposition cycles showed that occupancy seemed to decrease only slightly with cycling and that there were no large changes in hydrate structure due to cycling. Results provide evidence that the formation and decomposition of H-2 clathrate hydrates occur reversibly and that H-2 clathrate hydrates can be recycled with pressure. (C) 2010 American Institute of Chemical Engineers AIChE J, 57: 265-272, 2011
引用
收藏
页码:265 / 272
页数:8
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