Abstract
Polyethyleneimine (PEI)-functionalized silica-based CO2 adsorbents are well known to irreversibly form urea during the regeneration process at high temperatures and under CO2-rich atmospheric conditions. The formation of urea is a critical drawback that substantially reduces the cyclic performance of PEI-functionalized adsorbents. In this study, epoxy cross-linkers were introduced to PEI to suppress the formation of urea. Pristine PEI and epoxy cross-linked PEI were impregnated into mesostructured cellular foam silica using a dry impregnation method. In particular, epoxy cross-linkers with different alkyl chain lengths were used, and the effect of the alkyl chain length of the cross-linkers on the chemical stability and CO2 adsorption performance of adsorbents was scrutinized. The suppression of urea formation improved as the alkyl chain length of the cross-linkers increased. The adsorbent functionalized with epoxy cross-linked PEI exhibited an approximately three times higher working capacity (0.71 mmol g−1) than the adsorbent functionalized with pristine PEI (0.23 mmol g−1) after 40 rapid cycles comprising adsorption at 100 °C with 15% CO2 balanced by N2 for 10 min and regeneration at 130 °C with 100% CO2 for 5 min. It is believed that the alkyl chain of the cross-linkers acted as a spacer that could hinder the urea formation, enhancing the chemical stability and CO2 adsorption performance of PEI-functionalized adsorbents.
Original language | English |
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Article number | 125531 |
Journal | Chemical Engineering Journal |
Volume | 398 |
DOIs | |
Publication status | Published - 2020 Oct 15 |
Keywords
- Alkyl chain length
- CO capture
- Chemical stability
- Cross-linked PEI
ASJC Scopus subject areas
- Chemistry(all)
- Environmental Chemistry
- Chemical Engineering(all)
- Industrial and Manufacturing Engineering