Efficient adsorption separation of methane from C2–C3 hydrocarbons in a Co(II)-nodes metal–organic framework

Abstract

Methane (CH4) as a substitute for other mineral fuels plays a crucial role in reducing energy consumption and preventing environmental pollution. The present study employs a solvothermal method to fabricate a porous framework Co-metal–organic framework (Co-MOF) containing two distinct secondary building units (SBUs): an anionic [Co2(μ2-OH)(COO)4(H2O)] and a neutral [CoN2(COO)2]. Notably, within the anionic SBUs, the coordinated water molecules induce the generation of divergent unsaturated Co(II) centers in the unidirectional porous channels, thereby creating open metal sites. The adsorption performance of Co-MOF towards pure component gases was systematically investigated. The results demonstrated that Co-MOF exhibits superior adsorption capacity for C2–C3 hydrocarbons compared to CH4, which offering the potential for efficient adsorption and separation of CH4 from C2–C3 hydrocarbons. The gas selectivity separation ratios of Co-MOF for C2H6/CH4 and C3H8/CH4 were calculated using the ideal adsorbed solution theory method at 273/298 K and 0.1 MPa. The results revealed that Co-MOF achieved remarkable equilibrium separation selectivity for CH4 and C2–C3 hydrocarbon gases among non-modified MOFs, signifying the potential of the synthesized Co-MOF for efficient recovery and purification of CH4 from C2–C3 hydrocarbons. Breakthrough experiments further demonstrate the ability of Co-MOF to purify methane from C2–C3 hydrocarbons in practical gas separation scenarios. Additionally, molecular simulation calculations further substantiate the propensity of anionic SBUs to interact with C2–C3 hydrocarbon compounds. This study provides a novel paradigm for the development of porous MOF materials in the application of gas mixture separation.