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Adsorption: Journal of the International Adsorption Society (v.5, #2)
The Potentials of Pulsed Field Gradient NMR for Investigation of Porous Media by Frank Stallmach; Jörg Kärger (pp. 117-133).
PFG NMR self-diffusion studies provide information on the translational mobility of fluid molecules. Since in porous media the diffusion path of fluid molecules in the pore space is affected by interaction with the pore wall, PFG NMR measurements are sensitive to structural peculiarities of the confining porous medium. The pore space properties which can be investigated depend on length scales set by the PFG NMR experiment in respect to the typical size of the structural feature studied. Based upon these length scales, an interpretation pattern for PFG NMR self-diffusion studies in porous media is given. PFG NMR self-diffusion studies in macro- and microporous systems such as sedimentary rocks and zeolite crystallites, respectively, are reviewed.
Keywords: nuclear magnetic resonance; self-diffusion; pore structure; zeolite; sedimentary rock
A Temperature Frequency Response Method for Adsorption Kinetics Measurements by Ph. Grenier; A. Malka-Edery; V. Bourdin (pp. 135-143).
A Frequency Response Method based on the infrared measurement of the sample temperature has been developed for adsorption kinetics measurements. It consists in modulating the experimental chamber volume at constant frequency. The complex ratio of the temperature response over the pressure response is independent of time but is a function of the frequency depending on all the kinetics parameters of the system. This method is accurate and allows to measure very fast kinetics. Its major drawback is that a spurious signal is observed at high pressure in absence of adsorption. The results obtained with silicalite-propane and NaX-carbon dioxide are compared with results obtained from other techniques (NMR, permeation, etc.).
Keywords: diffusion; kinetics measurements; frequency response; NaX zeolite; silicalite
Pure and Binary Gas Adsorption Equilibria and Kinetics of Methane and Nitrogen on 4A Zeolite by Isotope Exchange Technique by R.J. Mohr; D. Vorkapic; M.B. Rao; S. Sircar (pp. 145-158).
The Isotope Exchange Technique (IET) was used to simultaneously measure pure and binary gas adsorption equilibria and kinetics (self-diffusivities) of CH4 and N2 on pelletized 4A zeolite. The experiment was carried out isothermally without disturbing the adsorbed phase. CH4 was selectively adsorbed over N2 by the zeolite because of its higher polarizability. The multi-site Langmuir model described the pure gas and binary adsorption equilibria fairly well at three different temperatures. The selectivity of adsorption of CH4 over N2 increased with increasing pressure at constant gas phase composition and temperature. This curious behavior was caused by the differences in the sizes of the adsorbates. The diffusion of CH4 and N2 into the zeolite was an activated process and the Fickian diffusion model described the uptake of both pure gases and their mixtures. The self-diffusivity of N2 was an order of magnitude larger than that for CH4. The pure gas self-diffusivities for both components were constants over a large range of surface coverages (0 < θ < 0.5). The self-diffusivities of CH4 and N2 from their binary mixtures were not affected by the presence of each other, compared to their pure gas self-diffusivities at identical surface coverages.
Keywords: kinetics; isotope-exchange; nitrogen; adsorption; methane; zeolite; equilibria
Impedance Spectroscopic Measurements of Pure Gas Adsorption Equilibria on Zeolites by R. Staudt; H. Rave; J.U. Keller (pp. 159-167).
Physisorption equilibria of gases on inert porous solids like activated carbon or molecular sieves can be characterized by measuring the (frequency dependent) capacitance of a capacitor filled with a sample adsorbent. This quantity strongly depends not only on the physico-chemical structure of the empty adsorbent in vacuum, but also on the permanent or induced dipole moments of the molecules adsorbed and of the fluid phase. Consequently, it should be possible to determine the excess mass being adsorbed on the internal surface of a highly porous solid by measurements of the dielectric constant. The aim of this work is to show for various pure gases and adsorbents that the change of the capacitance of an adsorption system depends on the adsorbed mass. Therefore, this effect can be used to characterize porous solids and their adsorbates and, for example, to check the state or the quality of industrial adsorbents during a process on site if calibration measurements have been taken (Staudt et al., 1994, 1998).
Keywords: impedance spectroscopy; uptake curve; adsorption; polarization of adsorbate; dielectric properties of adsorbed phases
Measurement of Excess Functions of Binary Gas Mixtures Adsorbed in Zeolites by Adsorption Calorimetry by Flor Siperstein; Raymond J. Gorte; Alan L. Myers (pp. 169-176).
Adsorption equilibria and heats of adsorption were measured for mixtures of ethylene and ethane on NaX at 298 K. The pure-component isosteric heat of adsorption of ethane increases with loading due to gas-gas interactions; the heat of adsorption of ethylene is approximately constant with loading because of a balance between cooperative interactions and gas-solid energetic heterogeneity. This mixture, which is nearly ideal on carbon, exhibits moderate negative deviations from ideality on NaX. The nonideality is explained by a difference in the polarities of the molecules: ethylene has a quadrupole moment but ethane is nonpolar. The infinite-dilution activity coefficients are unity in the Henry's law region and decrease exponentially to a value of 0.56 at high loading. Regular-solution theory fails to agree with experiment. All three excess functions (free energy, enthalpy, and entropy) are negative; thus, activity coefficients are less than unity and the enthalpy of mixing in the adsorbed phase is exothermic. These results are consistent with an adsorbed solution in which the molecules are segregated into regions of different composition.
Keywords: activity coefficients; selectivity; adsorption equilibrium; excess functions; calorimetry; gas mixtures