We investigated direct calcination of four precursors: calcium oxalate (CaC2O4; denoted as CaO-1), calcium carbonate (CaCO3; CaO-2), calcium d-gluconate monohydrate (C12H22CaO14·H2O; CaO-3), and a commercial calcium carbonate (CaO-4). The effects of precursor selection on CO2 adsorption performance were systematically compared. CaO-1 exhibited superior initial CO2 adsorption capacity (0.63 g/g) due to hierarchical porosity, but suffered a 38% capacity loss after 10 cycles from sintering. Al2O3 doping (CaO-Al2O3, 95/5) enhanced capacity and kinetics (0.65 g/g and 0.23 g/g·min-1, respectively), showing 3% and 43.75% improvements over CaO-1, respectively, though a degradation of 33.8% occurred after 20 cycles. MgO doping (CaO-MgO, 85/15) achieved exceptional cyclic stability, retaining 93% capacity over 10 cycles (55% improvement vs. CaO-1) via inherent sintering resistance. Characterization experiments confirmed their structural evolution: Al2O3 stabilized pore networks, while MgO preserved framework integrity. The results demonstrate that precursor engineering and dopant selection critically influence adsorption kinetics versus cyclic stability trade-offs. Optimal CaO-Al2O3 (95/5) and CaO-MgO (85/15) compositions propose a kinetics-stability decoupling strategy. This dual-dopant approach addresses calcium looping challenges by balancing rapid CO2 capture with structural durability, providing insights for cost-effective adsorbent optimization.
Zhang et al. (Tue,) studied this question.
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