NaNO2-loaded mesoporous MgO for high-efficiency CO2 capture: Synthesis, characterization and novel mechanistic insights
Yulian Wang , Jiayi Liu , Jinze Song , Junze Gu , Binyan Wang , Rui Guan , Keqing Li , Wanzhong Yin , Haoran Sun , Huili Han
Int J Min Sci Technol ›› 2026, Vol. 36 ›› Issue (4) : 887 -902.
The development of efficient CO2 adsorbents is critical for achieving net-zero targets. MgO represents a promising solid adsorbent for CO2 capture, yet its limited specific surface area and insufficient active sites restrict its adsorption capacity under moderate temperature conditions. A rod-like anhydrous MgCO3 precursor was hydrothermally synthesized and calcined at 500 °C for 3 h to obtain porous MgO (184.9 m2 g−1, 0.38 cm3/g), which was then modified with 20% NaNO2 (by mole) via impregnation. This adsorbent achieved an adsorption capacity of 12.6 mmol g−1 after 120 min under a pure CO2 atmosphere at 325 °C. Comprehensive characterization reveals that NaNO2 modification leads to the NaNO3 and Na2CO3 formation on the MgO surface during calcination. The introduced NaNO3 effectively promotes oxygen vacancy formation, while the generated Na2CO3 serves as heterogeneous nucleation sites, collectively reducing the reaction energy barrier and enhancing interfacial mass transfer. This synergistic effect facilitates the MgCO3 formation followed by its conversion to the thermodynamically more stable Na2Mg(CO3)2. Kinetic studies elucidate that adsorption is dominated by surface chemical reactions and diffusion mechanisms at different stages. These fundamental insights into the adsorption mechanisms of nitrite-modified MgO provide valuable guidance for the rational design of advanced MgO-based CO2 adsorbents with enhanced performance.
CO2 capture / MgO-based adsorbents / NaNO2 loading / NaNO3 and Na2CO3 / Synergistic effect
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