We report on a novel approach for the measurement of gas adsorption in microporous solids using X-ray computed tomography (CT) that we refer to as digital adsorption . Similar to conventional macroscopic methods, the proposed protocol combines observations with an inert and an adsorbing gas to produce equilibrium isotherms in terms of the truly measurable quantity in an adsorption experiment, namely, the surface excess. Most significantly, X-ray CT allows one to probe the adsorption process in three dimensions, so as to build spatially resolved adsorption isotherms with a resolution of approximately 10 mm 3 within a fixed-bed column. Experiments have been carried out at 25 °C and in the pressure range 1–30 bar using CO 2 on activated carbon, zeolite 13X, and glass beads (as control material), and the results are validated against literature data. A scaling approach was applied to analyze the whole population of measured adsorption isotherms (∼7600), leading to single universal adsorption isotherm curves that are descriptive of all voxels for a given adsorbate/adsorbent system. By analyzing the adsorption isotherms at multiple length scales (from 1 mm 3 to 1 cm 3 ), packing heterogeneity was identified as the main contributor for the larger spatial variability in the adsorbed amount observed for the activated carbon rods as compared to zeolite pellets. We also show that this technique is readily applicable to a large spectrum of commercial porous solids and that it can be further extended to weakly adsorbing materials with appropriate protocols that reduce measurement uncertainties. As such, the obtained results prove the feasibility of digital adsorption and highlight substantial opportunities for its wider use in the field of adsorptive characterization of porous solids.
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Joss et al. (2017) studied this question.
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