Fine Tuning the Pore Surface in Zirconium Metal−Organic Frameworks for Selective Ethane/Ethylene Separation

Authors

Yuchen Hu, University of Nebraska-Lincoln
Yanshu Shi, University of Texas at San Antonio
Yi Xie, University of Texas at San Antonio
Rebecca Shu Hui Khoo, Lawrence Berkeley National Laboratory
Christian Fiankor, University of Nebraska-Lincoln
Xu Zhang,, Huaiyin Normal University
Banglin Chen, University of Texas at San Antonio
Jian Zhang, University of Nebraska-LincolnFollow

Date of this Version

10-14-2022

Citation

ACS Appl. Eng. Mater. 2023, 1, 334−340. https://doi.org/10.1021/acsaenm.2c00079

Comments

Used by permission.

Abstract

Ethylene is an important chemical feedstock for production of polymers and high-value organic chemicals, and yet its conventional purification process is plagued with high consumption of energy. Metal−organic frameworks (MOFs) provide a suitable adsorption platform for selective ethane/ ethylene separation thanks to their structural diversity, tunable pore characteristics, designable pore sizes, and high pore volumes. Although there are empirical design rules like avoiding open metal sites and creating nonpolar pore surfaces for development of adsorptive MOFs, it is still challenging to design robust MOFs that can realize direct ethane-selective separation. Herein, we systematically designed and synthesized three Zr-MOFs based on the assembly of angular ligands and 12-connected Zr₆ clusters that feature the pcu network structure. By changing the size and flexibility of the substituent on the angular ligand, we were able to prevent interpenetration and identified NPF-802, which exhibits good C₂H₆/C₂H₄ separation performance that is attributed to the bulky and inert tert-butyl groups of its carbazole ligand. This work provides insights for design of ligands of MOFs with suitable pore environments to address important and challenging gas separations.