Performance improvement of Na4SiO4 doped with Li2CO3-K2CO3 for high-temperature CO2 capture and thermochemical energy storage

被引:7
作者
Ling, Changjian [1 ,2 ]
Wang, Zirui [1 ]
Tang, Zhongfeng [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] POB 800-204, Shanghai 201800, Peoples R China
基金
中国国家自然科学基金;
关键词
Na4SiO4; Doping; Density functional theory; Thermochemical energy storage; LITHIUM ORTHOSILICATE; SORBENTS; ADSORPTION; RAMAN; XRD;
D O I
10.1016/j.cej.2023.146921
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Na4SiO4 is regarded as a new candidate of high-temperature CO2 sorbent. However, the sorption/desorption temperature of Na4SiO4 is high, and cyclic sorption capacity is low. In this study, Na4SiO4 sorbents doped with Li2CO3-K2CO3 (LiKCO3) were synthesized, and the dynamic, isothermal, and cyclic CO2 capture performances were investigated to improve the performance. The maximum CO2 sorption capacity of Na4SiO4-20LiKCO3 reached 20.64 wt% at 725 degrees C, and the cyclic sorption capacity was about 50 % higher than that of pure Na4SiO4. The results indicated that LiKCO3 doping could efficiently decrease the optimal sorption/desorption temperature of Na4SiO4. Furthermore, the maximum conversion efficiency and energy storage density of Na4SiO4-20LiKCO3 reached high levels of 95.7 % and 788 kJ/kg, respectively. Finally, the CO2 chemisorption mechanisms on the Na4SiO4 and Na4SiO4-LiKCO3 co-adsorption surfaces were studied via density functional theory calculations. LiKCO3 doping could enhance CO2 adsorption energy and C-OS covalent interaction on the sorbent surface and the energy levels of the CO2/Na4SiO4-LiKCO3 system were reduced. These changes were beneficial to CO2 chemisorption and agreed well with the experimental values. Thus, Na4SiO4 doped with LiKCO3 had high potential for high-temperature CO2 capture and thermochemical energy storage.
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页数:10
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