Title : Optimization of functional groups in CAU-10(Al) for enhanced acetylene (C₂H₂) storage and effective C₂H₂/CO₂ separation
Abstract:
The adsorptive separation of acetylene (C2H2) from C2H2/CO2 mixtures has emerged as a promising alternative to cryogenic distillation, enabling the production of high-purity C2H2 via safer and more energy-efficient processes. Aluminum-based metal-organic frameworks (MOFs), including MIL-160 and CAU-10-NH2, have demonstrated exceptional acetylene adsorption capacities, exhibiting high selectivity and acetylene packing densities. Recent studies indicate that incorporating heteroatoms into the pore walls of MOFs can significantly enhance C2H2 capture performance. However, a systematic and comparative investigation regarding the influence of various functional groups within an identical MOF structure on their C2H2 sorption behavior remains lacking. In the present work, a series of CAU-10 derivatives were synthesized utilizing Al(III) metal centers and a range of functionalized organic linkers, including unmodified terephthalate (-H) and its substituted analogues (-OH, -F, -NO2, -NH2, and -CH3), to probe their C2H2 and CO2 adsorption characteristics systematically. The C2H2/CO2 separation efficacy was evaluated through single-component adsorption isotherms, ideal adsorbed solution theory (IAST) calculations, and dynamic breakthrough experiments under both dry and humid conditions. Remarkably, CAU-10-CH3 exhibited a record acetylene packing density of 543 g L?¹ at 25?°C, which is 2.8-fold higher than the corresponding CO2 uptake at 1 bar. Comparative dynamic breakthrough experiments involving CAU-10-CH3 and CAU-10-NH2 further validated CAU-10-CH3 as a leading candidate for selective acetylene adsorption under variable humidity conditions1.