Highly efficient catalytic direct air capture of CO2 using amphoyeric amino acid sorbent with acid-base bi-functional 3D graphene catalyst

被引:4
作者
Wang, Lei [1 ,2 ]
Gao, Yanyang [3 ]
Luo, Jianmin [4 ]
Wang, Xiaoxing [5 ]
Davis, Richard [1 ]
Yu, Jianjia [6 ,7 ]
Mao, Dongsen [2 ]
Cheng, Fangqin [3 ]
Hu, Yun Hang [8 ]
Toan, Sam [1 ]
Fan, Maohong [9 ,10 ,11 ]
机构
[1] Univ Minnesota Duluth, Dept Chem Engn, Duluth, MN 55812 USA
[2] Shanghai Inst Technol, Sch Chem & Environm Engn, Shanghai 201418, Peoples R China
[3] Shanxi Univ, Coll Environm & Resource Sci, Taiyuan 030006, Shanxi, Peoples R China
[4] Shaoguan Univ, Sch Chem & Civil Engn, Shaoguan 512005, Peoples R China
[5] New Mexico Inst Min & Technol, Petr Recovery Res Ctr, Socorro, NM 87801 USA
[6] New Mexico Inst Min & Technol, Dept Chem Engn, Socorro, NM 87801 USA
[7] New Mexico Petr Recovery Res Ctr, Socorro, NM 87801 USA
[8] Michigan Technol Univ, Dept Mat Sci & Engn, Houghton, MI 49931 USA
[9] Univ Wyoming, Coll Engn & Phys Sci, Laramie, WY 82071 USA
[10] Univ Wyoming, Sch Energy Resources, Laramie, WY 82071 USA
[11] Georgia Inst Technol, Coll Engn, Atlanta, GA 30332 USA
关键词
Direct air capture; CO2; capture; Amino acid; 3D Graphene; AQUEOUS POTASSIUM LYSINATE; CARBON-DIOXIDE CAPTURE; EQUILIBRIUM SOLUBILITY; DIRECT CONVERSION; ABSORPTION; MONOETHANOLAMINE; PERFORMANCE; VISCOSITY; DENSITY; SALTS;
D O I
10.1016/j.cej.2023.147120
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Direct air capture (DAC) of CO2 is vital for combating global climate change, but DAC technologies have a low absorption efficiency due to the low concentration (-400 ppm) of atmospheric CO2. A novel DAC technology was developed to solve this issue using lysine (an amino acid) as a sorbent and N-doped 3D graphene as an absorption/desorption-enhanced bifunctional catalyst. Introducing only 500 ppm N-3DG catalyst increased the working time (>= 90% CO2 absorption efficiency) by 233% and its absorption capacity by 197%. The catalyst also significantly accelerated the CO2 working desorption capacity and rate by-280% and-338% at 70 degrees C, enabling regeneration of the sorbent by utilizing low-temperature waste heats. Furthermore, the excellent stability of the system was confirmed by 50 cyclic tests. The chemical mechanism driving catalytic CO2 capture was postulated and confirmed by density functional theory computations. This study provides a new strategy for developing next-generation DAC technologies.
引用
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页数:11
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