“…3(d)), which are convenient for fast carbonation. 42 Subsequently, the maximum rate of carbonation decreased to 3.84 s À1 along with the CO 2 uptake in the 30 th cycle due to (i) slight sintering leading to the decrease of pore volume (Table 1) and (ii) continuous formation of gehlenite (Fig. S9 †), which is inert with regard to CO 2 capture.…”
“…3(d)), which are convenient for fast carbonation. 42 Subsequently, the maximum rate of carbonation decreased to 3.84 s À1 along with the CO 2 uptake in the 30 th cycle due to (i) slight sintering leading to the decrease of pore volume (Table 1) and (ii) continuous formation of gehlenite (Fig. S9 †), which is inert with regard to CO 2 capture.…”
“…Its CO 2 capture capacity decreased from 0.59 at the rst cycle to 0.51 at the 28 th cycle and correspondingly, the carbonation conversion reduced from 0.94 to 0.81, demonstrating high reactivity and stability of this sorbent over long-term cyclic operation. 416 Recently, Amos et al 417 reported that the stability of CaO supported on mesoporous Ca x Al y O z is superior to that supported on macro/mesoporous hierarchical Ca x Al y O z , and it was believed that the formed CaO layer might be too thick on the surface of macro/mesoporous structure. MgO is another well studied supporting material for enhancing the sintering-resistant properties of CaO.…”
Carbon dioxide (CO2) capture using solid sorbents has been recognized as a very promising technology that has attracted intense attention from both academic and industrial fields in the last decade.
“…50,51 As an alternatively, nanostructured CaO can be inversely grafted onto refractory macro/mesoporous supports. [52][53][54] However, these procedures lack the ability to tailor the textural properties or requires a relatively large account of inert stabilizer. Recently, template-assisted synthesis has emerged as a method to design porous core-shell nanostructured CaO-based sorbents, composed of a refractory thin shell and active nanosized CaO-riched core.…”
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