Wood-Inspired Ultrafast High-Performance Adsorbents for CO2 Capture

被引:10
|
作者
Wu, Bozhen [1 ]
Song, Xuejiao [1 ]
Zheng, Dongchen [2 ]
Tan, Qianyun [2 ]
Yao, Yong [3 ]
Liu, Fa-Qian [2 ]
机构
[1] Zhejiang Univ Technol, Coll Mat Sci & Engn, Hangzhou 310014, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem Engn & Technol, Zhuhai 519082, Peoples R China
[3] Guangdong Energy Grp Sci Technol Res Inst CO Ltd, Guangzhou 510630, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; capture; solid adsorbents; wood; ultrafast kinetics; biochar; COVALENT ORGANIC FRAMEWORKS; HEAT-CAPACITY; POLYETHYLENEIMINE; SILICA; ADSORPTION; GRAPHENE; PEI;
D O I
10.1021/acsami.3c02597
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Under favorable regeneration conditions (120 degrees C, 100% CO2), ultrafast adsorption kinetics and excellent long-term cycle stability are still the biggest obstacles for amine-based solid CO2 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 CO2 adsorbents. The results showed that the prepared adsorbent has a very high adsorption working capacity (4.23 mmol CO2 center dot g-1), and its performance remains stable even after 30 adsorption-desorption cycles in the harsh desorption environment (120 degrees C, 100% CO2). 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 center dot kg-1 (CO2), which is especially important for the practical application. Therefore, these biochar-based adsorbents derived from natural wood make the CO2 capture process promising.
引用
收藏
页码:20325 / 20333
页数:9
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