(64b) Synthesis of Metal-Organic Framework/Activated Biochar Composites for Carbon Capture | AIChE

(64b) Synthesis of Metal-Organic Framework/Activated Biochar Composites for Carbon Capture

Authors 

Labbé, N., University of Tennessee
Abdoulmoumine, N., University of Tennessee
With atmospheric carbon dioxide (CO2) concentration continuing to rise, novel materials need to be developed for capturing carbon. Metal-organic frameworks (MOFs) are metal-based adsorbents that have high surface areas for adsorbing CO2 but are structurally susceptible to water vapor. Meanwhile, activated biochars are hydrophobic carbon-based adsorbents that have high surface areas for adsorbing CO2 but low CO2 selectivity. Such materials can be combined through composite synthesis to minimize their detrimental properties. In this work, magnesium-metal-organic framework-74 (Mg-MOF-74) crystallites were grown on activated biochar with different dimethylformamide (DMF):ethanol:deionized (DI) water concentration ratios (10:1:1, 15:1:1, 20:1:1) through a solvothermal approach to optimize CO2 adsorption. X-ray diffraction (XRD) highlighted that the MOF-74 crystal structure was maintained during composite synthesis however the crystallite size decreased with the addition of activated biochar and increasing DMF concentration from 362 to 308-352 Å. Fourier-transform infrared (FTIR) spectroscopy revealed that MOF-74 functionalities were retained through composite synthesis but that significant differences in ligand functionality existed between Mg-MOF-74 and the composites and by DMF concentration. However, through nitrogen (N2) physisorption, specific surface area decreased during composite synthesis from 1080 to 191-204 m2/g due to blockage of the activated biochar pores by the MOF crystallites. Despite this loss of surface area, CO2 adsorption capacity increased from 0.76 to 1.04-2.00 mmol/g through composite synthesis with the 15:1:1 composite adsorbing the most CO2. This finding indicated that open metal sites in Mg-MOF-74 crystallites improved carbon capture onto AB.