Cobalt-based metal-organic frameworks promoting magnesium sulfite oxidation with ultrahigh catalytic activity and
1Hebei Key Lab of Power Plant Flue Gas Multi-Pollutants Control, Department of Environmental Science and Engineering, North China Electric Power University, Baoding 071003, PR China; MOE Key Laboratory of Resources and Environmental Systems Optimization, College of Environmental Science and Engineering, North China Electric Power University, Beijing 102206, PR China.
Abstract:
In wet magnesia desulfurization, the ultrahigh stable catalysis of sulfite oxidation is a crucial step in byproduct reclaimation. In this study, a robust and efficient catalyst, Co-MOF-74(4), was synthesized through a facile solvothermal method with an optimal Co/ligand ratio of 4:1. The oxidation rate of magnesium sulfite catalyzed by Co-MOF-74(4) was >2.6 times higher than that of previously reported cobalt-based heterogeneous catalysts. Crucially, almost no attenuation of the catalytic activity was observed even after three reuse cycles. The properties of Co-MOF-74(4) before and after the reaction were characterized. Density functional theory calculations demonstrate that the unsaturated cobalt site on the open framework of Co-MOF-74(4) provides greater opportunity for active Co to be attacked by sulfite ions, resulting in the ultra-high catalytic activity of Co-MOF-74(4). In contrast to the conventional impregnated catalysts, the robust combination of active cobalt with ligands prohibits its stripping from the surface of Co-MOF-74(4) particles. The bond length, angle and lattice parameters have only slight changes after sulfite adsorption, which supports the stability of the catalyst in the reaction process.
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