Abstract
Using realistic models of single-walled carbon nanohorns and their single-walled carbon nanotube counterparts, we study the equilibrium separation of CO2-CH4 mixtures near ambient operating conditions by using molecular simulations. We show that regardless of the studied operating conditions (i.e., total CO2-CH4 mixture pressures and mole fractions of mixture components in the bulk phase), single-walled carbon nanohorns maximize the CO2-CH4 equilibrium separation factor. Optimized samples of single-walled carbon nanohorns consisting of narrow tubular parts capped with horn-shaped tips show highly selective adsorption of CO2 over the CH4 mixture component, with the CO2-CH4 equilibrium separation factor of similar to 8-12. A large surface-to-volume ratio (i.e., enhanced surface forces) and unique defective morphology (i.e., packing of adsorbed molecules in quasi-one/quasi-zero dimensional nano-spaces) of single-walled carbon nanohorns are their key structural properties responsible for the excellent separation performance. Our theoretical simulation results are in quantitative agreement with a recent experimental/theoretical study of the CO2-CH4 adsorption and separation on oxidized single-walled carbon nanohorns [Ohba et Chem. Lett., 40, 2011, 1089]. Both experiment and theory showed that the CO2-CH4 equilibrium separation factor of oxidized samples of single-walled nanohorns measured near ambient operating conditions is similar to 2-5. This reduction in the separation efficiency as compared to optimized samples of single-walled carbon nanohorns is theoretically justified by their lower surface-to-volume ratio (i.e., larger diameters of tubular parts and horn-shaped tips).