Preparation and hydrogen storage capacity of templated and activated carbons nanocast from commercially available zeolitic imidazolate framework

被引:159
作者
Almasoudi, A. [1 ]
Mokaya, R. [1 ]
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
关键词
METAL-ORGANIC FRAMEWORKS; ORDERED MESOPOROUS CARBONS; CHEMICAL-VAPOR-DEPOSITION; CARBIDE-DERIVED CARBONS; POROUS CARBONS; KOH ACTIVATION; SURFACE-AREA; NANOPOROUS CARBONS; PORE-SIZE; ADSORPTION;
D O I
10.1039/c1jm13314d
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
A commercially available zeolitic imidazolate framework (ZIF), namely Basolite Z1200 (BASF), has been used as template for nanocasting of highly microporous ZIF-templated carbon. The "hard template carbonization technique" consists of liquid impregnation of furfuryl alcohol into the pores of the ZIF followed by polymerization and then carbonization during which the ZIF template is removed to generate the microporous carbon (90-95% microporosity) with a surface area of 900-1100 m(2) g(-1) and a pore volume of ca. 0.7 cm(3) g(-1). Chemical activation (with KOH at a relatively low temperature of 700 degrees C for 1 h and a carbon/KOH weight ratio of 1 : 4) of the ZIF-templated carbons increases their porosity by between 30 and 240% depending on their carbonization temperature, to achieve a surface area of up to 3200 m(2) g(-1) and a pore volume of 1.94 cm(3) g(-1). Despite the drastic increase in porosity, the activated ZIF-templated carbons retain significant microporosity with micropores contributing 80-90% of surface area and 60-70% of pore volume. This occurs because the activation process mainly enhances existing porosity rather than creating new larger pores. The activation enhances the hydrogen uptake capacity of the ZIF-templated carbons by between 25 and 140% from 2.6-3.1 wt% to the range 3.9-6.2 wt% (at -196 degrees C and 20 bar). The increase in hydrogen uptake after activation is closely related to rises in the micropore surface area and micropore volume rather than overall increase in porosity. Due to their microporous nature, the carbons exhibit high hydrogen storage density in the range 13.0-15.5 mu mol H(2) m(-2), which is much higher than that of most high surface area activated carbons.
引用
收藏
页码:146 / 152
页数:7
相关论文
共 80 条
[1]   The effect of Al content of zeolite template on the properties and hydrogen storage capacity of zeolite templated carbons [J].
Alam, Nurul ;
Mokaya, Robert .
MICROPOROUS AND MESOPOROUS MATERIALS, 2011, 144 (1-3) :140-147
[2]   Characterisation and hydrogen storage of Pt-doped carbons templated by Pt-exchanged zeolite Y [J].
Alam, Nurul ;
Mokaya, Robert .
MICROPOROUS AND MESOPOROUS MATERIALS, 2011, 142 (2-3) :716-724
[3]   Evolution of optimal porosity for improved hydrogen storage in templated zeolite-like carbons [J].
Alam, Nurul ;
Mokaya, Robert .
ENERGY & ENVIRONMENTAL SCIENCE, 2010, 3 (11) :1773-1781
[4]  
Allen S.J., 1998, DEV CHEM ENG MINERAL, V6, P231, DOI [DOI 10.1002/apj.5500060501, 10.1002/apj.5500060501]
[5]   Role of microporosity in hydrogen adsorption on templated nanoporous carbons [J].
Armandi, M. ;
Bonelli, B. ;
Arean, C. Otero ;
Garrone, E. .
MICROPOROUS AND MESOPOROUS MATERIALS, 2008, 112 (1-3) :411-418
[6]   The optimum average nanopore size for hydrogen storage in carbon nanoporous materials [J].
Cabria, Ivan ;
Lopez, Maria J. ;
Alonso, Julio A. .
CARBON, 2007, 45 (13) :2649-2658
[7]   Synthesis, characterization and hydrogen storage properties of microporous carbons templated by cation exchanged forms of zeolite Y with propylene and butylene as carbon precursors [J].
Chen, Louis ;
Singh, Ranjeet K. ;
Webley, Paul .
MICROPOROUS AND MESOPOROUS MATERIALS, 2007, 102 (1-3) :159-170
[8]   Hydrogen storage in carbon nanotubes [J].
Cheng, HM ;
Yang, QH ;
Liu, C .
CARBON, 2001, 39 (10) :1447-1454
[9]   Mesoporous carbons with KOH activated framework and their hydrogen adsorption [J].
Choi, Minkee ;
Ryoo, Ryong .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (39) :4204-4209
[10]   Hydrogen storage in metal-organic frameworks [J].
Collins, David J. ;
Zhou, Hong-Cai .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (30) :3154-3160