We have experimentally determined the binding energies of Xe, CH4, and Ne on samples of closed-ended single-wall nanotube (SWNT) bundles. We find values for these quantities which are larger by approximately 75% on the SWNT samples than the values found for the same adsorbates on planar graphite. We have also determined the monolayer capacity of a SWNT sample using Xe and Ne adsorption. A comparison of all of our results leads us to conclude that none of the gases studied adsorb on the interstitial channels in the SWNT bundles.
Using volumetric adsorption techniques, we have measured the adsorption of argon on Cu3(BTC)2(H2O)3, (BTC = benzene-1,3,5-tricarboxylate), a microporous metal-organic framework structure, at temperatures between 66 and 143 K. In addition to the experiments, we have used Grand Canonical Monte Carlo simulations to calculate the adsorption isotherm of argon at 87 K. Our experimental and theoretical results are compared to those of previous studies. The experiments were performed using a high density of points, allowing us to obtain, in detail, the isosteric heat's coverage dependence. Our values from the simulations are in reasonable agreement with those obtained in the experiments.
We report on adsorption results obtained on bundles of HiPco nanotubes. We compare the values for the specific surface area of these nanotubes, measured by performing monolayer completion determinations on the same sample with four different adsorbates. We also present adsorption results for neon on the HiPco nanotubes at coverages beyond monolayer completion. The second layer neon data are compared to data obtained for the same adsorbate on lower purity arc discharge nanotubes.
We present adsorption isotherm results for Ne, CH4, and Xe on bundles of close-ended single-wall carbon nanotubes, for coverages above the completion of the first layer. We find a small, sharp, substep present in the second-layer data for Ne and CH4, and a weaker feature, that produces an isothermal compressibility peak, for Xe. The size and location of the feature allows its tentative identification as a new, second-layer, one-dimensional phase, in which the atoms sit atop high binding energy sites in the second layer.
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