Korea Advanced Institute of Science and Technology · 化学工学
Professor Jong-In Han's research lab specializes in sustainable carbon management and environmental remediation, focusing on innovative technologies for CO2 capture, utilization, and mineralization. The lab develops advanced materials such as magnesium phyllosilicate catalysts and bicarbonate-based microalgae systems to enhance carbon utilization efficiency and enable stable, long-term CO2 sequestration. A key research direction involves integrating CO2 mineralization with desalination processes to simultaneously produce valuable minerals and fresh water from seawater. Additionally, the lab addresses flue gas purification challenges through electrochemical regeneration of NOX absorbents, enabling efficient and reusable nitrogen oxide removal systems.
Figures are computed from collected data and may differ slightly.
A new bicarbonate-based microalgae cultivation system coupled with an electrochemical CO<sub>2</sub>absorption process to improve carbon utilization efficiency.
Magnesium phyllosilicate (Mg–APTES) was developed and explored for its applicability as a potent carbonation catalyst that converts CO2 into carbonate ions. Careful investigation of its surface properties revealed a lamellar structure and the existence of an amine group, which is the expected CO2 capture site. The prepared magnesium phyllosilicate was found to successfully convert gaseous CO2 into HCO3− (bicarbonate ion), actively forming CaCO3 (calcium carbonate) when Ca2+ (calcium ion) was sup
CO2 mineralization sequestrates CO2 in a form of mineral carbonate through chemical reactions of CO2 with metal oxide or alkaline solution. This process is attractive because it has no risk for a leakage of hazardous materials and requires a relatively small area for sequestrating CO2 compared to geological storage. In addition, generated mineral carbonate can be used as useful chemicals if its purity is high enough. One of the recent ideas in CO2 mineralization is integrating it with desalinati
The ever-increasing air pollution has brought the treatment of nitrogen oxides (NOX) to the forefront of flue gas purification. Wet absorption achieves outstanding NOX removal efficiency, but it suffers from an oxidative deactivation of the NOX absorbent, iron(II) thiochelate, by the residual O2 in flue gases. To address this critical issue, we demonstrate a regeneration process to electrochemically reduce the oxidized iron thiochelate into the original form to effectively bind nitric oxide (NO)
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