In the CO2 capture process, solid acid catalysts have been widely adopted to decrease energy consumption in the amine regeneration process owing to abundant acid sites. However, acid sites unavoidably degenerate in the basic amine solution. To address the challenge, nonacid carbon materials including carbon molecular sieves, porous carbon, carbon nanotubes, and graphene are first proposed to catalyze amine regeneration. It is found that carbon materials can significantly increase the CO2 desorption amount by 47.1-72.3% and reduce energy consumption by 32-42%. In 20 stability experiments, CO2 loading was stable with the max difference value of 0.01 mol CO2/mol monoethanolamine (MEA), and no obvious increase in the relative heat duty (the maximum difference is 4%) occurred. The stability of carbon materials is superior to excellent solid acid catalysts, and the desorption performance is comparable. According to the results of theoretical calculation and experimental characterization, the electron-transfer mechanism of nonacid carbon materials is proposed, which is not only beneficial for MEA regeneration but also the probable reason for the stable catalytic activity. Owing to the excellent catalytic performance of carbon nanotube (CNT) in the HCO3- decomposition, nonacid carbon materials are quite promising to enhance the desorption performance of novel blend amines, which will further reduce the cost of carbon capture in the industry. This study provides a new strategy to develop stable catalysts used for amine energy-efficient regeneration.
Keywords: CO2 capture; amine regeneration; carbon catalysts; heat duty; simulation.