Rearranged Copolyurea Networks for Selective Carbon Dioxide Adsorption at Room Temperature

Copolyurea networks (co-UNs) were synthesized via crosslinking polymerization of a mixture of tetrakis(4-aminophenyl)methane (TAPM) and melamine with hexamethylene diisocyanate (HDI) using the organic sol-gel polymerization method. The subsequent thermal treatment of between 200 and 400 & DEG;C induced the sintering of the powdery polyurea networks to form porous frameworks via urea bond rearrangement and the removal of volatile hexamethylene moieties. Incorporating melamine into the networks resulted in a higher nitrogen content and micropore ratio, whereas the overall porosity decreased with the melamine composition. The rearranged network composed of the tetraamine/melamine units in an 80:20 ratio showed the highest carbon dioxide adsorption quantity at room temperature. The results show that optimizing the chemical structure and porosity of polyurea-based networks can lead to carbon dioxide adsorbents working at elevated temperatures.

Automated summary

Copolyurea networks were synthesized by crosslinking polymerization of tetrakis(4-aminophenyl)methane and melamine, resulting in higher nitrogen content and micropore ratio but lower overall porosity when melamine was incorporated. Networks rearranged with a 80:20 ratio of tetraamine/melamine units showed the highest carbon dioxide adsorption quantity at room temperature.