Cellulose-Amine Porous Materials: The Effect of Activation Method on Structure, Textural Properties, CO Capture, and Recyclability.

CO capture via physical adsorption on activated porous carbons represents a promising solution towards effective carbon emission mitigation. Additionally, production costs can be further decreased by utilising biomass as the main precursor and applying energy-efficient activation. In this work, we developed novel cellulose-based activated carbons modified with amines (diethylenetriamine (DETA), 1,2-bis(3-aminopropylamino)ethane (BAPE), and melamine (MELA)) with different numbers of nitrogen atoms as in situ -doping precursors. We investigated the effect of hydrothermal and thermal activation on the development of their physicochemical properties, which significantly influence the resulting CO adsorption capacity. This process entailed an initial hydrothermal activation of biomass precursor and amines at 240 °C, resulting in , and materials. Thermal samples (, , and ) were synthesised from hydrothermal materials by subsequent KOH chemical activation and pyrolysis in an inert argon atmosphere. Their chemical and structural properties were characterised using elemental analysis (CHN), infrared spectroscopy (IR), scanning electron microscopy (SEM), and thermogravimetric analysis (TG). The calculated specific surface areas () for thermal products showed higher values (998 m g for , 1076 m g for , and 1348 m g for ) compared to the hydrothermal products (769 m g for , 833 m g for , and 1079 m g for ). Carbon dioxide adsorption as measured by volumetric and gravimetric methods at 0 and 25 °C, respectively, showed the opposite trend, which can be attributed to the reduced content of primary adsorption sites in the form of amine groups in thermal products. N and CO adsorption measurements were carried out on hydrothermal () and pyrolysed cellulose (), which showed a several-fold reduction in adsorption properties compared to amine-modified materials. The recyclability of , which showed the highest CO adsorption capacity (7.34 mmol g), was studied using argon purging and thermal regeneration over five adsorption/desorption cycles.