Shaanxi Key Laboratory of Optoelectronic Functional Materials and Devices, School of Materials Science and Chemical Engineering, Xi'an Technological University, Xi'an710021, P. R. China.
Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XHAmsterdam, The Netherlands.
ACS Appl Mater Interfaces. 2023 May 17;15(19):23538-23545. doi: 10.1021/acsami.3c04225. Epub 2023 May 7.
The achievement of direct CH separation from C hydrocarbons is very challenging in the petrochemical industry due to their similar molecular sizes, boiling points, and physicochemical properties. In this work, a nonpolar/inert ultramicroporous metal-organic framework (MOF), [Co(μ-OH)(tipa)(bpy)]·3DMF·6HO (), with stand-alone one-dimensional square tubular channels was successfully constructed, its pore enriched with plenty of aromatic rings causing nonpolar/inert pore surfaces. The MOF shows preferential adsorption of CH compared to CH and CH in the low-pressure region, which is further verified by adsorption heats and selectivities. The CH separation potential in one step for binary CH/CH (50/50 and 10/90) and ternary CH/CH/CH (89/10/1) is also examined by transient breakthrough simulations. Moreover, grand canonical Monte Carlo simulations demonstrate that the unique reversed adsorption mechanism is due to the shortest and most number of C-H···π interactions between CH and the framework.
由于 C 烃类的分子大小、沸点和物理化学性质相似,因此在石化工业中实现直接 CH 分离非常具有挑战性。在这项工作中,成功构建了一种具有独立一维正方形管状通道的非极性/惰性超微孔金属有机骨架(MOF),[Co(μ-OH)(tipa)(bpy)]·3DMF·6H 2 O(),其孔中富含大量芳香环,导致非极性/惰性孔表面。MOF 在低压区优先吸附 CH 而不是 CH 和 CH,这通过吸附热和选择性进一步得到证实。通过瞬态突破模拟还检查了二元 CH/CH(50/50 和 10/90)和三元 CH/CH/CH(89/10/1)一步法的 CH 分离潜力。此外,巨正则蒙特卡罗模拟表明,独特的反向吸附机制是由于 CH 与骨架之间最短和最多的 C-H···π 相互作用。