材料科学
原位
铜
相(物质)
化学工程
复合材料
冶金
有机化学
化学
工程类
作者
Ravi Sharma,Shiara Uyttersprot,Gino V. Baron,Joeri Denayer
标识
DOI:10.1021/acsami.5c04227
摘要
The use of structured adsorbents is emerging as a promising approach for adsorptive separation processes, and several ex situ structuring routes like extrusion, three-dimensional (3D) printing, and coating over substrates have been extensively investigated. However, in situ growth of adsorbents such as metal-organic frameworks (MOFs) on metal laminates remains underexplored. This study introduces a novel laminate system, where aluminum pieces, inspired by the "LEGO" concept, were designed through CNC milling and used to fabricate embossed/dented copper laminates. These laminates were then coated with ZIF-8 crystals (ZIF-8@Cu) via a direct in situ coating method at room temperature, resulting in a 100 μm coating. The system was assembled, packed in a custom-designed column, and evaluated for alcohol recovery from methanol/water and n-butanol/water mixtures. The ZIF-8@Cu laminates exhibited high adsorption capacities: 0.19 gMeOH/gZIF-8, 0.26 gn-BuOH/gZIF-8, and excellent selectivity toward alcohols (αMeOH/H2O = 8.5; αn-BuOH/H2O = 68). Vapor-phase experiments showed dispersive effects in the elution curve, attributed to the intrinsic properties of ZIF-8 (S-shaped equilibrium isotherm) and mass transfer limitation caused by channel nonuniformities and inlet flow maldistribution. For both separation mixtures, the laminate system was regenerated within 2 h via thermal swing adsorption (TSA), thereby exhibiting the combined benefits of microporosity, low-pressure drop, mechanical stability, and efficient heat transfer. The adsorptive properties were further highlighted in liquid-phase separation, where the laminates selectively captured n-butanol from 2.0 wt % aqueous solution and were successfully regenerated via TSA. This study provides proof of concept for the application of MOF-coated metal laminates in multiple adsorption-desorption cycles, thus highlighting their potential for process intensification.
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