The potential of organic polymer-based hydrogen storage materials

被引:171
作者
Budd, Peter M. [1 ]
Butler, Anna
Selbie, James
Mahmood, Khalid
McKeown, Neil B.
Ghanem, Bader
Msayib, Kadhum
Book, David
Walton, Allan
机构
[1] Univ Manchester, Sch Chem, Organ Mat Innovat Ctr, Manchester M13 9PL, Lancs, England
[2] Univ Wales Coll Cardiff, Sch Chem, Cardiff CF10 3AT, S Glam, Wales
[3] Univ Birmingham, Sch Engn, Dept Met & Mat, Birmingham B15 2TT, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1039/b618053a
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
The challenge of storing hydrogen at high volumetric and gravimetric density for automotive applications has prompted investigations into the potential of cryo-adsorption on the internal surface area of microporous organic polymers. A range of Polymers of Intrinsic Microporosity (PIMs) has been studied, the best PIM to date (a network-PIM incorporating a triptycene subunit) taking up 2.7% H-2 by mass at 10 bar/77 K. HyperCrosslinked Polymers (HCPs) also show promising performance as H-2 storage materials, particularly at pressures 410 bar. The N-2 and H-2 adsorption behaviour at 77 K of six PIMs and a HCP are compared. Surface areas based on Langmuir plots of H2 adsorption at high pressure are shown to provide a useful guide to hydrogen capacity, but Langmuir plots based on low pressure data underestimate the potential H2 uptake. The micropore distribution influences the form of the H2 isotherm, a higher concentration of ultramicropores (pore size < 0.7 nm) being associated with enhanced low pressure adsorption.
引用
收藏
页码:1802 / 1808
页数:7
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