A Scalable Pore‐space‐partitioned Metal‐organic Framework Powered by Polycatenation Strategy for Efficient Acetylene Purification

Abstract Efficient separation of acetylene (C 2 H 2 ) from carbon dioxide (CO 2 ) and ethylene (C 2 H 4 ) is a significant challenge in the petrochemical industry due to their similar physicochemical properties. Pore space partition (PSP) has shown promise in enhancing gas adsorption capacity and selectivity by reducing pore size and increasing the density of guest binding sites. Herein, we firstly employ the 2D→3D polycatenation strategy to construct a PSP metal‐organic framework (MOF) Ni‐dcpp‐bpy , incorporating functional N/O sites to enhance C 2 H 2 purification. The polycatenated framework with optimized pore size and regularity, exhibiting significant improvements over traditional PSP MOFs by resolving the critical contradiction of balancing C 2 H 2 uptake (98.5 cm 3 g −1 at 298 K, 100 kPa) and selectivity of C 2 H 2 /CO 2 (3.4), C 2 H 2 /C 2 H 4 (5.9), and C 2 H 2 /CH 4 (96.4) in a MOF. Breakthrough experiments confirm high‐purity C 2 H 4 (>99.9 %) and high C 2 H 2 productivity from binary and ternary mixtures. Notably, Ni‐dcpp‐bpy exhibits excellent water stability, scalability, and regenerability after 20 cycles for separating C 2 H 2 /CO 2 . Theoretical calculations verify that the strong binding of C 2 H 2 is mainly attributed to the C−H⋅⋅⋅O/N interactions between host Ni‐dcpp‐bpy and guest C 2 H 2 molecules. The polycatenation strategy not only improved industrial C 2 H 2 purification efficiency but also enriched the design diversity of customized MOFs for other gas separation applications.