Design of Ultra-Stable Solid Amine Adsorbents and Mechanisms of Hydroxyl Group-Dependent Deactivation for Reversible CO2 Capture from Flue Gas

Although supported solid amine adsorbents have attracted great attention for CO₂ capture, critical chemical deactivation problems including oxidative degradation and urea formation have severely restricted their practical applications for flue gas CO₂ capture. In this work, we reveal that the nature of surface hydroxyl groups (metal hydroxyl Al-OH and nonmetal hydroxyl Si-OH) plays a key role in the deactivation mechanisms. The polyethyleneimine (PEI) supported on Al-OH-containing substrates suffers from severe oxidative degradation during the CO₂ capture step due to the breakage of amine-support hydrogen bonding networks, but exhibits an excellent anti-urea formation feature by preventing dehydration of carbamate products under a pure CO₂ regeneration atmosphere. In contrast, PEI supported on Si-OH-containing substrates exhibits excellent anti-oxidative stability under simulated flue gas conditions by forming a robust hydrogen bonding protective network with Si-OH, but suffers from obvious urea formation during the pure CO₂ regeneration step. We also reveal that the urea formation problem for PEI-SBA-15 can be avoided by the incorporation of an OH-containing PEG additive. Based on the intrinsic understanding of degradation mechanisms, we successfully synthesized an adsorbent 40PEI-20PEG-SBA-15 that demonstrates outstanding stability and retention of a high CO₂ capacity of 2.45 mmol g^-1 over 1000 adsorption-desorption cycles, together with negligible capacity loss during aging in simulated flue gas (10% CO₂ + 5% O₂ + 3% H₂O) for one month at 60-70 °C. We believe this work makes great contribution to the advancement in the field of ultra-stable solid amine-based CO₂ capture materials.