Introduction of cross-linking agents to enhance the performance and chemical stability of polyethyleneimine-impregnated CO2 adsorbents: Effect of different alkyl chain lengths
- Authors
- Jeon, Sunbin; Min, Jinseo; Kim, Sung Hyun; Lee, Ki Bong
- Issue Date
- 15-10월-2020
- Publisher
- ELSEVIER SCIENCE SA
- Keywords
- CO2 capture; Cross-linked PEI; Alkyl chain length; Chemical stability
- Citation
- CHEMICAL ENGINEERING JOURNAL, v.398
- Indexed
- SCIE
SCOPUS
- Journal Title
- CHEMICAL ENGINEERING JOURNAL
- Volume
- 398
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/52445
- DOI
- 10.1016/j.cej.2020.125531
- ISSN
- 1385-8947
- 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 degrees C with 15% CO2 balanced by N-2 for 10 min and regeneration at 130 degrees 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.
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