2025 AIChE Annual Meeting

(418g) CO?-Activated Cellulose Biochar for CO? Capture

Authors

Hema Ramsurn, The University of Tulsa
Mike Volk, University of Tulsa
Biomass-based carbon capture offers a promising pathway for reducing carbon emissions and sequestering atmospheric CO2. Currently, it is estimated that nearly 10% of global emissions could be reduced if biomass is used for carbon capture. Improving the porous structure of biochar through activation processes plays a key role in CO2 adsorption. The use of CO₂ as an activation agent for biochar has been recently explored and offers a cleaner and more environmentally friendly approach compared to KOH activation, which requires strong chemical agents. This research wants to investigate CO2 as an activation gas to enhance the adsorption sites of biochar so that CO2 can be subsequently captured in this material. We are looking at synthesizing cellulose-derived biochar using hydrothermal carbonization at 300 °C and activating it using CO2 (at different temperatures (700–1000 °C) in an inert nitrogen atmosphere). CO₂ activation will be performed at different flow rates (25–75 mL/min) to assess its impact on micropore formation, surface area and adsorption capacity. CO2 activation is expected to open inaccessible micropores or form new ones and increase the pore network of the activated biochar. Small-angle x-ray scattering (SAXS) will be used to analyze the micropore formation and surface area of the activated biochar, and thermogravimetric analysis (TGA) to investigate the adsorption capacity. The CO2-activated samples will then be compared to two conventional activation methods: thermal (700–1000 °C) and/or KOH activation.

Preliminary results indicate that increasing the activation temperature from 800°C to 900 °C enhances micropore formation, significantly improving adsorption capacity. However, temperatures above 900 °C may induce partial micropore collapse, reducing the biochar’s overall effectiveness for CO₂ capture. We found that as the activation temperature increases beyond 800°C, CO₂ adsorption decreases which is consistent with observed micropore collapse at 1000 °C. Overall, at the same activation temperature, CO₂ performed better than just thermal activation. We further found that increasing the CO₂ flow rate during activation did not enhance pore development and adsorption capacity. These findings provide valuable insights into optimizing biochar activation for enhanced CO₂ sequestration.