Ultrahigh Carbon Dioxide-Selective Composite Membrane Containing a γ-CD-MOF Layer.

Mixed matrix membranes (MMMs) for CO2 separation have overcome the trade-off between gas permeability and gas selectivity to some extent. However, most MMMs still are prepared in lab- and pilot-scales since the permeability and selectivity of CO2 are not good enough to reach the economically available requirements. Moreover, the fabrication of few MMMs with good separation performance is time-consuming or need harsh conditions. In this study, a novel MOF-based composite membrane (PAN-γ-CD-MOF-PU membrane) was successfully fabricated by a facile and fast spin-coating method. In the two-step coating process, we applied a uniform selective layer of γ-cyclodextrin-MOF (γ-CD-MOF) on porous polyacrylonitrile and then coated a layer of polyurethane on the γ-CD-MOF layer. The entire membrane formation process was about 30 s. The formation of a unique γ-CD-MOF layer greatly improved the separation ability of CO2 (the CO2 permeability is 70.97 barrers; the selectivity to CO2/N2 and CO2/O2 are 253.46 and 154.28, respectively). The gas separation performance can exceed the Robeson upper limit obviously and the selectivity is better than other MOF-based composite membranes. In addition, the PAN-γ-CD-MOF-PU membrane is strong and flexible. Therefore, the PAN-γ-CD-MOF-PU membrane developed in this study has great potential in large-scale industrial separation of CO2.

Facile Fabrication of an AIE-Active Metal-Organic Framework for Sensitive Detection of Explosives in Liquid and Solid Phases.

Nowadays, the practical applications of metal-organic framework (MOF)-based fluorescence detectors are severely hindered because of the complex synthesis process of linkers or heavy metal contamination. The development of a simple, inexpensive, and environmentally friendly fluorescence sensing system remains a huge challenge. In this study, we designed and synthesized a TPE@γ-CD-MOF-K complex using the facile in situ encapsulation method. The unique pore structure of γ-CD-MOF allowed it to effectively include TPE and explosives as guests simultaneously. The TPE@γ-CD-MOF-K showed stronger fluorescence emission than TPE and sensitive fluorescence quenching activities in response to nitro-aromatic compounds in the liquid phase with detection limits as low as 3 ppm. Furthermore, TPE@γ-CD-MOF-K can also effectively detect nitro-aromatic compounds in the solid state, which is very convenient for practical detection of explosives. The unique pore structure of γ-CD-MOF-K and the interaction between K+ and nitro compounds play important roles in solid-state quenching.