环戊烷
化学
氢
水合物
笼状水合物
氢气储存
无机化学
四氢呋喃
制氢
动力学
钠
碳纤维
十二烷基硫酸钠
动能
氘
碳氢化合物
二氧化碳
氢燃料
吸附低温
作者
Harmit Kadu,LA Sudeeksha,Hari Prakash Veluswamy
标识
DOI:10.1021/acs.iecr.6c00966
摘要
Hydrogen is considered a clean energy source and an alternative to fossil fuels due to its high energy density and zero carbon emissions. Hydrate-based hydrogen storage offers a promising solution for storing hydrogen under moderate temperature and pressure conditions, but its sluggish kinetics and low storage capacity deter its application. Though individual thermodynamic promoters have been examined for their potential in promoting hydrogen hydrate formation, in this work, for the first time, a combination of THF and CP as thermodynamic promoters (sII structure) was used to study the kinetics of hydrogen hydrates. Kinetic and morphological effects of hydrogen hydrate formation at varying concentrations of THF and CP were studied at 278.2 K–280.2 K and in the range of 3–11 MPa. Presaturation of hydrogen gas before cooling significantly improved the induction time. It was found that a 2.8 mol % THF/2.8 mol % CP combination was the optimal concentration that showed the highest gas uptake of 18.8 mmol/mol H 2 O with a t 90 of 222 ± 33.2 min and a very short induction time of 1.8 ± 0.3 min. To improve the formation kinetics, l -valine, sodium dodecyl sulfate (SDS), and Tween 80 kinetic promoters were studied at a concentration of 0.3 wt %. It was observed that 0.3 wt % Tween 80 reduced the t 90 from 222 ± 33.2 min to 126.8 ± 0.2 min, corresponding to a 42.86% reduction, with the shortest induction time of 1 ± 0.7 min. Mixed hydrogen hydrate formation under much more moderate conditions (3 MPa and 278.2 K) was also demonstrated, with an observed hydrogen uptake of 6.08 mmol/mol H 2 O. The effect of driving force in terms of pressure and temperature on the mixed hydrogen hydrate was carried out to understand the behavior of the equimolar concentration of the promoter (2.8 mol % THF/2.8 mol % CP) system. By increasing the driving force by 3 MPa and decreasing Δ T by 2 K, an increase in gas consumption up to 22.39 mmol/mol H 2 O was observed.
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