Optimized Nanospace Of Coordination Isomers With Selenium Sites For Acetylene Separation

INORGANIC CHEMISTRY FRONTIERS(2020)

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摘要
The safe storage and separation of acetylene (C2H2) is difficult and essential, due to its explosive properties and wide usage for various industrial products. With a generally low energy cost, highly efficient adsorption separation has been considered as a promising solution. Taking advantage of the inbuilt nature of a tunable pore space, a porous coordination polymer (NTU-56) was prepared from a selenium-containing carboxylate ligand and Cu(2+)ions. Triggered by water at different temperatures,NTU-56transformed into two other porous frameworks (NTU-57andNTU-58) with different topologies and pore environments. Single-component gas adsorption experiments showed that this new group of porous isomers featured systematically varied adsorption selectivity for C2H2/CO2, two gases that have extremely similar molecular sizes and boiling points. More interestingly, among the isomers,NTU-58, a rare 2D, flexible, and water-stable framework, has the highest C(2)H(2)uptake (60 cm(3)g(-1)) and C2H2/CO(2)selectivity (13.9, 1/1, v/v, 1 bar) at 273 K, derived from the synergetic effect of the unique pore sizes (4.5 and 5.5 angstrom) and pore surface polarity, where the Cu(2+)and selenium sites are exposed for preferred C(2)H(2)interactions. Efficient and recyclable C2H2/CO(2)separation was also confirmedviabreakthrough experiments, even with wet feed-gas.
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