Mixed Alkanolamine-Polyethylenimine Functionalized Silica for CO₂ Capture
Abstract
High amine efficiency amine-modified silica adsorbents with fast adsorption rates have been developed by adding amine species including hydroxyl groups into polyethyleneimine (PEI)-loaded mesoporous silica for CO2 capture. Two amine species of diethanolamine (DEA) and 3-amino-1,2-propanediol (AP) including hydroxyl groups were introduced into PEI to reduce the CO2 diffusion resistance and increase the active CO2 adsorption sites. The DEA promoted adsorbents were found to exhibit much higher adsorption capacity than AP promoted adsorbents. Through tuning the ratio of PEI to DEA in amine mixture during adsorbent impregnation step, a threshold value of PEI/DEA weight ratio (~50 : 50) was found, where the maximum CO2 capacity of 2.93 mmol/g was achieved under dry CO2 at 35 °C.The adsorption capacity for this newly synthesized adsorbent increased by 50 % in comparison to PEI-silica materials. Their amine efficiency was 0.40 mol CO2/mol N, which was more than twice than that of PEI-silica (0.17 mol CO2/mol N). Under simulated humid flue gas conditions, the DEA promoted adsorbents had a CO2 breakthrough capacity qb of 1.57 mmol/g and a CO2 capacity q50 of 2.49 mmol/g. Such adsorbents possess good reversibility and the adsorption capacity is nearly stable after two adsorption-desorption cycles. The synthesis methodology reported in this investigation proves to be an efficient strategy to develop highly efficient amine-impregnated adsorbents.
Recommended Citation
Y. Fan et al., "Mixed Alkanolamine-Polyethylenimine Functionalized Silica for CO₂ Capture," Energy Technology, vol. 7, no. 2, pp. 253 - 262, Wiley-VCH Verlag, Feb 2019.
The definitive version is available at https://doi.org/10.1002/ente.201800481
Department(s)
Chemical and Biochemical Engineering
Keywords and Phrases
3-amino-1,2-propanediol; amine efficiency; amine-impregnated silica; CO2 capture; diethanolamine; polyethyleneimine
International Standard Serial Number (ISSN)
2194-4288
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2019 Wiley-VCH Verlag, All rights reserved.
Publication Date
01 Feb 2019
Comments
The authors gratefully acknowledge the financial support of Science Foundation of China University of Petroleum, Bejing (Grant. No. 2462015YJRC017) and the National Natural Science Foundation of China (Grant No. 21506252).