Elastic layer-structured metal-organic framework (MOF)-11 {ELM-11: [Cu(BF4)2 (4,4′-bipyridine)2]}, which is a crystalline porous material, is a promising adsorbent for high-throughput and high-efficiency separation processes of CO2 because of its peculiar adsorption characteristics originating from the flexibility of the crystal framework. However, the exposure of ELM-11 to water vapor has been reported to reduce its CO2 capacity, which is problematic for processing feed gases that contain a certain concentration of water vapor. In this study, we investigated the stability of ELM-11 against water vapor exposure to reveal the mechanism of CO2 capacity reduction. Our combined measurements of adsorption isotherms and X-ray diffraction patterns indicated that the CO2 capacity reduction was caused by the partial formation of a crystalline subphase upon adsorption of water molecules and the subsequent formation of an amorphous phase to relax the crystalline grain boundaries. Because a higher supply rate of water molecules resulted in a larger amount of subphase formation, we concluded that the structural subphase was a metastable kinetically controlled structure, formed through the rate-dependent adsorption of water molecules. These results suggest that slowing the adsorption rate is an effective approach to suppress the formation of the subphase; therefore, we proposed the covering of ELM-11 surfaces with porous shells. We used ELM-12 {[Cu(CF3SO3)2 (4,4′-bipyridine)2]} as a shell material because of its robust stability against water adsorption and affinity with ELM-11. The ELM-12 shell decreased the adsorption rate of water molecules compared with that of bare ELM-11, resulting in the suppression of subphase formation and preventing CO2 capacity reduction. Although further optimization of the shell thickness and coverage is required to keep the capacity completely unchanged, controlling the adsorption rate of water molecules is successfully demonstrated to be possible with shell formation, which is key for industrial applications of ELM-11.
The existence of surface nanobubbles has already been confirmed by variable detection methods, but the mechanism of their extraordinary stability remains unclear and has aroused widespread research interest in the past 2 decades. Experiments and theoretical analyses have tried to account for these stabilities such as the very long lifetime, very high pressure and very small contact angle. Attractive hydrophobic potential was applied to complement the pinning-oversaturation theory and successfully explain the survival of surface nanobubbles in undersaturation environment by some researchers. However, the survival of nanobubbles on hydrophilic surface still requires sizeable oversaturation. In this paper, we introduce the variable surface tensions, namely Tolman-dependence and state-dependence, and show that they effectively promote the stability of nanobubbles. The decrease in surface tension can lead to larger contact angle and even make the nanobubbles survivable on the highly hydrophilic surface. In Tolman-dependence, the changing rate in the contact angle evolution slows down, which is more obvious when the bubble size is close to the Tolman length. The contact angle is also getting larger in the state-dependence, and the increase of the gas saturation degree is beneficial to the stability of surface nanobubbles. With the gas saturation ratio of 3, the bubbles on the quite hydrophilic surface can also be stable, while grow up on the hydrophobic surface. The variable surface tensions weaken the need of saturation degree for the surface nanobubbles’ stability.