Periyasamy Thirukumaran, Asrafali Shakila Parveen, Lee Jaewoong
Department of Fiber System Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Polymers (Basel). 2025 Jan 26;17(3):343. doi: 10.3390/polym17030343.
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 KMnO) at the same temperature. This activation significantly enhanced the material's porosity, increasing its specific surface area from 335 m/g (KOH activated) to 943 m/g (KMnO activated). XPS analysis confirmed the presence of nitrogen functionalities, including secondary-N, oxide-N, pyridone-N, and pyridine-N, which are critical for CO adsorption. Adsorption tests demonstrated a high CO 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 CO molecules. These findings suggest that this nitrogen-enriched microporous carbon, derived from polybenzoxazine, holds significant promise as a highly efficient material for applications in CO capture and storage.
在本研究中,我们通过一个涉及两种不同活化程序的精细过程成功合成了富氮微孔碳。首先,将聚苯并恶嗪在800℃碳化以制备前驱体材料,然后在相同温度下用两种不同的活化剂(KOH和KMnO)对其进行活化。这种活化显著提高了材料的孔隙率,使其比表面积从335 m²/g(KOH活化)增加到943 m²/g(KMnO活化)。XPS分析证实了氮官能团的存在,包括仲氮、氧化氮、吡啶酮氮和吡啶氮,这些对于CO吸附至关重要。吸附测试表明,在25℃和1 bar下,由于物理吸附(与表面积的物理相互作用)和化学吸附(与氮位点的化学相互作用)的共同作用,CO的高吸附量为3.8 mmol/g。这种高吸附容量可归因于碳的大量表面积、显著的微孔体积以及相互连接的孔网络,它们共同提供了结构稳定性并促进了CO分子的扩散。这些发现表明,这种源自聚苯并恶嗪的富氮微孔碳作为一种用于CO捕获和存储的高效材料具有巨大的潜力。