journal article·2023-04-26

Wood-Inspired Ultrafast High-Performance Adsorbents for CO2 Capture

Bozhen Wu, Xuejiao Song, Dongchen Zheng, Qianyun Tan, Yong Yao, Fa-Qian Liu

ACS Applied Materials & Interfaces· Volume 15· Issue 16
Publisher page

Abstract

Under favorable regeneration conditions (120 °C, 100% CO 2 ), ultrafast adsorption kinetics and excellent long-term cycle stability are still the biggest obstacles for amine-based solid CO 2 adsorbents. Inspired by natural wood, a biochar with a highly ordered pore structure and excellent thermal conductivity was prepared and used as a carrier of organic amines to prepare ideal CO 2 adsorbents. The results showed that the prepared adsorbent has a very high adsorption working capacity (4.23 mmol CO 2 ·g –1 ), and its performance remains stable even after 30 adsorption–desorption cycles in the harsh desorption environment (120 °C, 100% CO 2 ). Due to the existence of the hierarchical structure, the adsorbent exhibited ultra-fast adsorption kinetics, and the reaction rate constant is 37 times higher than that of traditional silica. This adsorbent also showed a very low regeneration heat of 1.64 MJ·kg –1 (CO 2 ), which is especially important for the practical application. Therefore, these biochar-based adsorbents derived from natural wood make the CO 2 capture process promising.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Carbon Dioxide Capture Technologies · Membrane Separation and Gas Transport · Covalent Organic Framework Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Materials Science and Engineering, Zhejiang University of Technology, Hangzhou 310014, PR China

School of Chemical Engineering and Technology, Sun Yat-sen University, Zhuhai 519082, China

Guangdong Energy Group Science and Technology Research Institute CO., Ltd., Guangzhou 510630, China

Funding

National Natural Science Foundation of China · Guangdong Basic and Applied Basic Research Foundation

References (40)

Show source-provided references
1. 10.1016/j.pecs.2022.10105510.1016/j.pecs.2022.101055 ↗
2. 10.1007/s00376-022-1467-x10.1007/s00376-022-1467-x ↗
3. 10.1039/d1ta07856a10.1039/d1ta07856a ↗
4. 10.1021/acsami.7b1149210.1021/acsami.7b11492 ↗
5. 10.1021/acs.est.6b0062710.1021/acs.est.6b00627 ↗
6. 10.1021/acs.iecr.6b0427010.1021/acs.iecr.6b04270 ↗
7. 10.1021/am507465f10.1021/am507465f ↗
8. 10.1021/acsami.6b1108710.1021/acsami.6b11087 ↗
9. 10.1039/c9cs00827f10.1039/c9cs00827f ↗
10. 10.1002/adma.20150500410.1002/adma.201505004 ↗
11. 10.1016/j.jenvman.2022.11643810.1016/j.jenvman.2022.116438 ↗
12. 10.1021/acssuschemeng.9b0270010.1021/acssuschemeng.9b02700 ↗
13. 10.1021/acsami.5b0754510.1021/acsami.5b07545 ↗
14. 10.1002/cssc.20160154510.1002/cssc.201601545 ↗
15. 10.1002/cssc.20130123110.1002/cssc.201301231 ↗
16. 10.1016/j.micromeso.2011.10.03110.1016/j.micromeso.2011.10.031 ↗
17. 10.1021/cm303931q10.1021/cm303931q ↗
18. 10.1021/am500089g10.1021/am500089g ↗
19. 10.1016/j.compscitech.2021.10878110.1016/j.compscitech.2021.108781 ↗
20. 10.1039/d1ta01403j10.1039/d1ta01403j ↗
21. 10.1039/c5ta01536g10.1039/c5ta01536g ↗
22. 10.1002/adma.20120442710.1002/adma.201204427 ↗
23. 10.1021/am100786z10.1021/am100786z ↗
24. 10.1021/jp208766u10.1021/jp208766u ↗
25. 10.1021/jp107754g10.1021/jp107754g ↗
26. 10.1016/j.biortech.2022.12845610.1016/j.biortech.2022.128456 ↗
27. 10.1002/adma.20170345310.1002/adma.201703453 ↗
28. 10.7503/cjcu2019041810.7503/cjcu20190418 ↗
29. 10.1007/s11696-022-02397-510.1007/s11696-022-02397-5 ↗
30. 10.1016/j.chemosphere.2022.13755310.1016/j.chemosphere.2022.137553 ↗
31. 10.1016/j.carbon.2012.09.00610.1016/j.carbon.2012.09.006 ↗
32. 10.1021/nn700271310.1021/nn7002713 ↗
33. 10.1039/c4ra13710h10.1039/c4ra13710h ↗
34. 10.1038/ncomms1264010.1038/ncomms12640 ↗
35. 10.1039/c6ee00601a10.1039/c6ee00601a ↗
36. 10.1016/j.ces.2011.06.07010.1016/j.ces.2011.06.070 ↗
37. 10.1021/am500089g10.1021/am500089g ↗
38. 10.1016/j.compchemeng.2017.08.00610.1016/j.compchemeng.2017.08.006 ↗
39. 10.1134/s106378340611003510.1134/s1063783406110035 ↗
40. 10.1002/ghg.142710.1002/ghg.1427 ↗