RESUMEN
The confinement of small amounts of benzene in InOF-1 (Bz@InOF-1) shows a contradictory behavior in the capture of CO2 and SO2. While the capture of CO2 is increased 1.6 times, compared to the pristine material, the capture of SO2 shows a considerable decrease. To elucidate these behaviors, the interactions of CO2 and SO2 with Bz@InOF-1 were studied by DFT periodical calculations postulating a plausible explanation: (a) in the case of benzene and CO2, these molecules do not compete for the preferential adsorption sites within InOF-1, providing a cooperative CO2 capture enhancement and (b) benzene and SO2 strongly compete for these preferential adsorption sites inside the MOF material, reducing the total SO2 capture.
RESUMEN
The CO2 capture performance of InOF-1 was optimised by confining small amounts of MeOH within its micropores (MeOH@InOF-1). In comparison with fully activated InOF-1, MeOH@InOF-1 shows a 1.30 and 4.88-fold increase in CO2 capture capacity for kinetic and static isothermal CO2 adsorption experiments respectively. Density functional theory calculations coupled with forcefield based-Monte Carlo simulations revealed that such an enhancement is assigned to an increase of the degree of confinement felt by the CO2 molecules resulting from the formation of a lump at the vicinity of the µ2-OH groups since MeOH strongly interacts with these adsorption sites and is thus highly localized in this region.
RESUMEN
Water and ethanol stabilities of the crystal structure of the Cu-based metal-organic framework (MOF) HKUST-1 have been investigated. Vapour (water and ethanol) sorption isotherms and cyclability were measured by a dynamic strategy. The ethanol sorption capacity of HKUST-1 at 303 K remained unchanged contrasting water sorption (which decreased along with the sorption experiment time). Considering the binding energy of each sorbate with the open Cu(ii) sites, obtained by the use of diffusion coefficients, we showed the superior crystal stability of the HKUST-1 framework towards ethanol. Finally, a small quantity of ethanol (pre-adsorbed) slightly enhanced CO2 capture without crystal structure degradation.
RESUMEN
CO2 capture of InOF-1 was enhanced 3.6-fold, at 1 bar and 30 °C, by confining EtOH within its pores. Direct visualisation by single crystal X-ray diffraction revealed that EtOH divides InOF-1 channels in wide sections separated by "bottlenecks" caused by EtOH molecules bonded to the µ2-OH functional groups of InOF-1.
RESUMEN
The water-stable material NOTT-401 was investigated for CO2 capture under humid conditions. Water adsorption properties of NOTT-401 were studied, and their correlation with CO2 sequestration at different relative humidities (RHs) showed that the CO2 capture increased from 1.2 wt % (anhydrous conditions) to 3.9 wt % under 5% RH at 30 °C, representing a 3.2-fold improvement.