Abstract
In this research, we successfully synthesized nitrogen-enriched microporous carbon through a meticulous process involving two different activation procedures. Initially, polybenzoxazine was carbonized at 800 °C to create a precursor material, which was then activated with two different activating agents (KOH and KMnO4) at the same temperature. This activation significantly enhanced the material’s porosity, increasing its specific surface area from 335 m2/g (KOH activated) to 943 m2/g (KMnO4 activated). XPS analysis confirmed the presence of nitrogen functionalities, including secondary-N, oxide-N, pyridone-N, and pyridine-N, which are critical for CO2 adsorption. Adsorption tests demonstrated a high CO2 uptake of 3.8 mmol/g at 25 °C and 1 bar, driven by a combination of physisorption (physical interaction with the surface area) and chemisorption (chemical interaction with nitrogen sites). This high adsorption capacity can be attributed to the carbon’s substantial surface area, significant micropore volume, and the interconnected network of pores, which together provide structural stability and facilitate the diffusion of CO2 molecules. These findings suggest that this nitrogen-enriched microporous carbon, derived from polybenzoxazine, holds significant promise as a highly efficient material for applications in CO2 capture and storage.
Published Version
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