A series of mesoporous MgO samples with different morphologies were synthesized through a simple hydrothermal treatment and NaNO 3 /NaNO 2 were used as promoters to enhance CO 2 capture capacity at an intermediate temperature range (200-400 °C). The effects of hydrothermal solution pH and content of promoters were examined to determine the optimal synthesis conditions. The influence of operational temperatures, CO 2 partial pressure, and performance over repeated cycles was investigated and the reaction mechanism was discussed. The mesoporous MgO promoted by NaNO 3 /NaNO 2 exhibited a CO 2 capture capacity as high as 19.8 mmol•g-1 at 350 °C in the presence of 0.85 bar of CO 2 within only 50 min. A "three-stage" reaction process was proposed based on a detailed sorption kinetics study, namely Stage I: initiating interactions between CO 2 and exposed MgO; Stage II: generation and accumulation of Mg 2+ and CO 3 2-; and Stage III: fast carbonation. Gradual deterioration of sorbents was found over the first 5 cycles followed by stable regenerability in the 5-15 th cycles. A kinetic study of the 15 th cycle suggests that the deactivation of sorbents inhibited the accumulation of Mg 2+ and CO 3 2in Stage II and suppressed the carbonation in Stage III. A range of characterizations were undertaken revealing the morphology and structure of both fresh and regenerated sorbents. The results confirmed that, other than the sintering effect due to phase transition, the transformation of MgO skeleton is also an important contributor to the gradual deactivation of the sorbents over the first 5 cycles. More severe sintering effect under harsh decarbonation conditions suppressed the stability of the sorbents over cycles.