Monitoring phase behavior of hydrogen confined in carbon nanopores by in-situ Small Angle Neutron Scattering technique

2012 ◽  
Vol 1440 ◽  
Author(s):  
Hongxin Zhang ◽  
Lilin He ◽  
Yuri B. Melnichenko ◽  
Cristian I. Contescu ◽  
Nidia C. Gallego

ABSTRACTWe report on the use of in-situ small angle neutron scattering (SANS) technique to study the phase behavior of hydrogen confined in narrow pores of ultramicroporous carbon (UMC) with a very large surface area (2630 m2/g) and pore volume (1.3 cm3/g). The effect of pore size and pressure on hydrogen adsorbed on UMC at room temperature and pressures up to ∼200 bar were investigated. In a previous experiment, we have measured the density of adsorbed H2 gas in the nanopores and mesopores of polyfurfuryl alcohol-derived activated carbon (PFAC) by SANS technique. Here, a comparative SANS study between the UMC and PFAC was conducted in order to further investigate the densification of H2 as a function of pore size and pressure. Initial results suggest that the density of confined H2 in both UMC and PFAC is considerably higher than that of the bulk hydrogen gas. The density is systematically higher in the narrow pores and decreases with increasing pore size. These results clearly demonstrate the advantage of adsorptive storage over compressed gas storage and emphasize the greater efficiency of micropores over mesopores in the adsorption process, which can be used to guide the development of new carbon adsorbents tailored for maximum H2 storage capacities at near-ambient temperatures.

2011 ◽  
Vol 1334 ◽  
Author(s):  
Dipendu Saha ◽  
Lilin He ◽  
Cristian I. Contescu ◽  
Nidia C. Gallego ◽  
Yuri B. Melnichenko

ABSTRACTEntrapping hydrogen molecules within the nanopores of solid adsorbents serves as a unique alternative for on-board storing of hydrogen for transportation purposes. The key advantage of the physisorption process for hydrogen storage is the higher density values achieved with the adsorbed gas, compared to that of the compressed phase, translating into higher storage capacities at lower pressures. The necessary condition for effective adsorption is the presence of narrow micropores of < 2 nm in width which provide the most suitable environment of hydrogen adsorption. Despite numerous theoretical calculations or indirect experimental estimations, there has not been a direct experimental measurement of the density of adsorbed hydrogen as a function of pressure and/or pore size. In the present study, we report on the use of in-situ small angle neutron scattering (SANS) to study the phase behavior of hydrogen confined in narrow micropores. We provide for the first time direct experimental measurements of the effect of pore size and pressure on hydrogen adsorbed on a polyfurfuryl alcohol-derived activated carbon (PFAC), at room temperature and pressures up to 207 bar. SANS studies were carried out at the General-Purpose Small-Angle Neutron Scattering spectrometer of the High Flux Isotope Reactor at Oak Ridge National Laboratory. The measurements covered the Q-range from 0.01 to 0.8 Å-1, covering the pores in the range of 9 to 34 Å of the PFAC material. Initial results suggest that the density of adsorbed hydrogen is higher than the density of bulk hydrogen gas and increases with decreasing pore size.


Carbon ◽  
2013 ◽  
Vol 57 ◽  
pp. 460-469 ◽  
Author(s):  
Félix Balima ◽  
Vittoria Pischedda ◽  
Sylvie Le Floch ◽  
Annie Brûlet ◽  
Peter Lindner ◽  
...  

Langmuir ◽  
2019 ◽  
Vol 35 (10) ◽  
pp. 3822-3831 ◽  
Author(s):  
Ignacio Martín-Fabiani ◽  
David K. Makepeace ◽  
Philip G. Richardson ◽  
Jennifer Lesage de la Haye ◽  
Diego Alba Venero ◽  
...  

1989 ◽  
Vol 166 ◽  
Author(s):  
Alan I. Nakatani ◽  
Hongdoo Kim ◽  
Charles C. Han

ABSTRACTThe phase behavior of polymer blends and solutions can be changed dramatically by a flow field using a variety of flow geometries. Unlike simple binary fluids which require extremely high shear rates to produce only small shifts in the phase boundary, polymer phase behavior may be influenced by as much as 10 degrees with the application of much lower shear rates. However, there is a large body of conflicting data concerning the nature of these shear effects in polymers.Here we report on the effects of shear on the phase behavior of polymer blends by small angle neutron scattering (SANS). Experiments were conducted using a specially constructed, concentric cylinder apparatus for in situ studies of concentrated polymer solutions and melts. Two separate systems will be discussed: 1) a blend of polystyrene and polybutadiene. 2) a blend of polystyrene and poly(vinylmethylether). Both systems exhibit shifts in the phase behavior which indicate shear induced mixing in agreement with previous results obtained by other techniques. These results will be interpreted within the context of existing theories of shear induced phase behavior.


1994 ◽  
Vol 27 (9) ◽  
pp. 2566-2573 ◽  
Author(s):  
N. P. Balsara ◽  
B. Hammouda ◽  
P. K. Kesani ◽  
S. V. Jonnalagadda ◽  
G. C. Straty

2013 ◽  
Vol 125 (17) ◽  
pp. 4716-4720 ◽  
Author(s):  
S. Boukhalfa ◽  
L. He ◽  
Y. B. Melnichenko ◽  
Gleb Yushin

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