Behavior of Adsorbed Hydrogen Molecules on Zeolites

2009 ◽  
Vol 25 (03) ◽  
pp. 549-554
Author(s):  
DU Xiao-Ming ◽  
◽  
2003 ◽  
Vol 19 (02) ◽  
pp. 139-143
Author(s):  
Zheng Qing-Rong ◽  
◽  
Gu An-Zhong ◽  
Lin Wen-Sheng ◽  
Li Ming ◽  
...  

1989 ◽  
Vol 165 ◽  
Author(s):  
W. E. Quinn ◽  
B. G. Bagley ◽  
B. J. Wilkens ◽  
B. M. Gallois

AbstractSilicon nitride films deposited from silane-nitrogen and silane-ammonia mixtures by PECVD contain large amounts of hydrogen. We have determined that adding argon to the gas mixture reduces the amount of hydrogen in the resulting films. Differences in film composition are obviously due to changes in the chemistry of the discharge which was characterized by line-of-sight mass spectrometry, optical emission spectroscopy and plasma double probe measurements. Substrate temperature was fixed at 325°C, pressure was 500 mtorr, the RF power was 0.25 watts cm−2, the silane to nitrogen ratio was varied from 0.003 to 0.02, the silane to ammonia ratio was varied from 0.01 to 0.5, and the argon additions were 10% of the total gas flow. Argon additions to the discharge increased the plasma density in both nitrogen and ammonia plasmas. Optical emission from N2 and Si-H species increased upon the addition of 10% argon to the silane-nitrogen discharge, whereas the N-H emission decreased upon addition of argon to the silane-ammonia discharge. Infrared transmission spectra of films deposited with and without argon show no change in peak position or intensity of Si-H and N-H absorption bands in the spectral range studied, despite a large (over 20%) reduction in hydrogen content, as determined by nuclear profiling, upon the addition of argon. These results suggest that a substantial fraction of the hydrogen in the films is not infrared active. We propose that the reduction in hydrogen content is due to bombardment of the growing film by argon ions, which sputter the adsorbed hydrogen molecules.


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.


2006 ◽  
Vol 971 ◽  
Author(s):  
Dong Hyun Jung ◽  
Tae Bum Lee ◽  
Daejin Kim ◽  
Kangsung Park ◽  
Jaheon Kim ◽  
...  

ABSTRACTIn order to investigate the reason for the higher capacity of the interpenetrating isoreticular metal-organic frameworks (IRMOFs) at lower temperatures, we performed grand canonical Monte Carlo (GCMC) simulations and molecular dynamics simulations at 77 K for a set of the interpenetrating IRMOF-11 and the non-interpenetrating counterpart IRMOF-12. From the GCMC simulations, we found universal force field (UFF) is better for describing the hydrogen adsorption behavior than DREIDING force field. The results from the molecular dynamics simulations showed the density of adsorbed hydrogen molecules was increased in the various pores created by the catenation of IRMOF comparing to that of the pores in IRMOF-12. Moreover, the adsorbed hydrogen molecules in IRMOF-11 have the smaller diffusion coefficients. It means that their dynamic behavior is more restricted because of the complexity of the interpenetrating network of IRMOF-11. These results of molecular simulations show the small pores created by the catenation are important for the increase of hydrogen adsorption on IRMOF-11 at lower temperatures.


2014 ◽  
Vol 51 (3) ◽  
pp. 35-41
Author(s):  
P. Lesnicenoks ◽  
L. Grinberga ◽  
J. Kleperis

Abstract Large surface aluminosilicate compounds such as zeolites are not the best option for hydrogen storage due to their low hydrogen sorption capacity above cryogenic temperatures. However, the known crystal structure and easy ion exchange allows considering zeolites as easily tuneable media that with a little effort can be changed to suitable porous media for hydrogen sorption. Metal (Li, Mg) and ammonia ion exchange is performed in natural clinoptilolite samples with the aim to increase the amount of adsorbed hydrogen. The Fourier transform infrared spectroscopy of the prepared samples is used to study sorption of hydrogen molecules in the vicinity of light metal ions. An original thermogravimetric method is applied to characterise the amount of sorbed hydrogen. Our experiments show that the highest hydrogen uptake (~ 6.2 wt%) is for a clinoptilolite sample treated in acid. The cation exchange did not provide the expected hydrogen sorption capability; however, the amount of sorbed hydrogen exceeded that for the initial material.


1983 ◽  
Vol 61 (6) ◽  
pp. 1153-1157 ◽  
Author(s):  
John F. J. Read ◽  
Sandra J. Amirault ◽  
Yuk Tong Chan ◽  
Alan C. Higgins ◽  
Daphne G. Irvine ◽  
...  

The stoichiometric hydrogen–oxygen reaction has been studied in a static system over lanthanum oxide and europium oxide at an initial hydrogen pressure of approximately 200 N m−2 from 480 to 775 K, and at different initial hydrogen pressures from 70 to 750 N m−2 over the same temperature range. Nonstoichiometric reactions were conducted at five different temperatures over lanthanum oxide and four different temperatures over europium oxide, at hydrogen–oxygen ratios in the range 0.1 to 10. After detailed kinetic analysis it is shown that the results fit an equation of the form:[Formula: see text]where k is a proportionality constant, [Formula: see text] and [Formula: see text] are the adsorption coefficients for hydrogen and oxygen, respectively, PT is the total pressure of hydrogen plus oxygen, [Formula: see text] and [Formula: see text] are the partial pressures of hydrogen and oxygen, respectively, and x equals 2 for lanthanum oxide and 1 for europium oxide. The mechanism involves the competitive adsorption of molecular hydrogen and oxygen, with the rate-determining step involving the interaction between adsorbed hydrogen molecules and adsorbed oxygen or hydrogen peroxide (double hydroxide groups).


2017 ◽  
Vol 66 (10) ◽  
pp. 103601
Author(s):  
Wang Xiao-Xia ◽  
Liu Xin ◽  
Zhang Qiong ◽  
Chen Hong-Shan

1989 ◽  
Vol 135 (3) ◽  
pp. 457-466 ◽  
Author(s):  
P.R. Hirst ◽  
L.M. Needham ◽  
A.D. Taylor ◽  
Z.A. Bowden ◽  
J.W. White

2011 ◽  
Vol 187 ◽  
pp. 797-802 ◽  
Author(s):  
Xiao Ming Du ◽  
Yong Huang ◽  
Er Dong Wu

A general model based on Ono-Kondo lattice theory for hydrogen adsorption, nearest neighbor interaction energy among adsorbate molecules were derived according to thermodynamic principle. A linear form of the above general model was applied to determine the interaction energies among hydrogen molecules inside adsorption layer from the previous experimental data of hydrogen adsorption on A- and X-type zeolites. The results show that the energies of hydrogen-hydrogen interactions inside the adsorption layer are negative values, indicating that the attractions among the adsorbed hydrogen molecules are prominent in the present work. And the influence of hydrogen molecules outside adsorption layer on the adsorbed hydrogen molecule is not important.


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