High density hydrogen storage in superactivated carbons from hydrothermally carbonized renewable organic materials

被引:407
作者
Sevilla, M. [1 ,2 ]
Fuertes, A. B. [1 ]
Mokaya, R. [2 ]
机构
[1] Inst Nacl Carbon CSIC, Oviedo 33080, Spain
[2] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
关键词
OXIDE HOLLOW SPHERES; ACTIVATED CARBONS; CHEMICAL ACTIVATION; POROUS CARBONS; SURFACE-AREA; METHANOL ELECTROOXIDATION; KOH ACTIVATION; GAS SENSORS; PORE-SIZE; ADSORPTION;
D O I
10.1039/c0ee00347f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrothermally carbonized organic materials (furfural, glucose, starch, cellulose and eucalyptus sawdust) have been used as precursors to produce high-surface area carbons. The synthesis methodology comprises two steps: (i) hydrothermal carbonization of organic materials and (ii) chemical activation with KOH as activating agent. In this way, activated carbon materials with a high surface area (up to 2700 m(2) g(-1)) and narrow micropore size distribution in the supermicropore range (0.7-2 nm) are produced. The textural properties of the activated carbon products can be easily tuned by modifying the activating conditions (i. e., the activation temperature and the amount of KOH used). The activated carbon materials exhibit high hydrogen uptakes, up to 6.4 wt%, and large isosteric heats of adsorption, up to 8.5 kJ mol(-1). In particular, the hydrogen storage density of the carbons is high and ranges between 12 and 16.4 mu mol H-2 m(-2). The hydrogen storage density is closely related to the pore size of the carbons, with small micropores (ca. 1 nm) favouring a high density. Taking into account the high hydrogen storage capacities of these materials, as well as the simplicity of their synthesis procedure and the ready availability and low-cost of the raw precursors, it can be concluded that these activated carbons constitute a promising adsorbent for hydrogen storage.
引用
收藏
页码:1400 / 1410
页数:11
相关论文
共 55 条
[1]   Hydrogen adsorption studies on single wall carbon nanotubes [J].
Ansón, A ;
Callejas, MA ;
Benito, AM ;
Maser, WK ;
Izquierdo, MT ;
Rubio, B ;
Jagiello, J ;
Thommes, M ;
Parra, JB ;
Martínez, MT .
CARBON, 2004, 42 (07) :1243-1248
[2]   Determination of the adsorption isotherms of hydrogen on activated carbons above the Critical Temperature of the adsorbate over wide temperature and pressure ranges [J].
Bénard, P ;
Chahine, R .
LANGMUIR, 2001, 17 (06) :1950-1955
[3]   Optimum conditions for adsorptive storage [J].
Bhatia, SK ;
Myers, AL .
LANGMUIR, 2006, 22 (04) :1688-1700
[4]   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
[6]   CARBONIZATION OF COALS IN THE PRESENCE OF ALKALINE HYDROXIDES AND CARBONATES - FORMATION OF ACTIVATED CARBONS [J].
EHRBURGER, P ;
ADDOUN, A ;
ADDOUN, F ;
DONNET, JB .
FUEL, 1986, 65 (10) :1447-1449
[7]   Importance of pore size in high-pressure hydrogen storage by porous carbons [J].
Gogotsi, Yury ;
Portet, Cristelle ;
Osswald, Sebastian ;
Simmons, Jason M. ;
Yidirim, Taner ;
Laudisio, Giovanna ;
Fischer, John E. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2009, 34 (15) :6314-6319
[8]   The preparation and mechanism studies of rice husk based porous carbon [J].
Guo, YP ;
Yang, SF ;
Yu, KF ;
Zhao, JZ ;
Wang, ZC ;
Xu, HD .
MATERIALS CHEMISTRY AND PHYSICS, 2002, 74 (03) :320-323
[9]   Activated carbons from Spanish coals .2. Chemical activation [J].
IllanGomez, MJ ;
GarciaGarcia, A ;
deLecea, CSM ;
LinaresSolano, A .
ENERGY & FUELS, 1996, 10 (05) :1108-1114
[10]   Simple synthesis of graphitic porous carbon by hydrothermal method for use as a catalyst support in methanol electro-oxidation [J].
Joo, Ji Bong ;
Kim, You Jung ;
Kim, Wooyoung ;
Kim, Pil ;
Yi, Jongheop .
CATALYSIS COMMUNICATIONS, 2008, 10 (03) :267-271