Transition metal cation-exchanged SSZ-13 zeolites for CO2 capture and separation from N2

被引:82
作者
Sun, Mingzhe [1 ,2 ]
Gu, Qinfen [3 ]
Hanif, Aamir [1 ,2 ]
Wang, Tianqi [2 ]
Shang, Jin [1 ,2 ]
机构
[1] City Univ Hong Kong, Shenzhen Res Inst, 8 Yuexing 1st Rd,Shenzhen Hitech Ind Pk, Shenzhen, Peoples R China
[2] City Univ Hong Kong, Sch Energy & Environm, Kowloon, Tat Chee Ave, Hong Kong, Peoples R China
[3] Australian Synchrotron ANSTO, 800 Blackburn Rd, Clayton, Vic 3168, Australia
基金
中国国家自然科学基金;
关键词
CO2; capture; Adsorption; Zeolites; SOLVENT VAPOR RECOVERY; CARBON-DIOXIDE; ADSORPTION; TEMPERATURE; EQUILIBRIUM; AMMONIA; METHANE; GASES; HEAT;
D O I
10.1016/j.cej.2019.03.234
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
CO2 capture from post-combustion flue gas mixture (CO2 /N-2:15/85) is challenging and requires adsorbents with high capacity and high selectivity toward CO2. Our work validated the potential of transition metal cationexchanged SSZ-13 zeolites for efficient CO2 capture, as evaluated by unary static isothermal adsorption and binary dynamic column breakthrough experiments as well as predicted performance in pressure/vacuum swing adsorption (P/VSA) process. Among the investigated transition metals (Co(II), Ni(II), Zn(II), Fe(III), Cu(II), Ag(I), La(III), and Ce(III)) exchanged SSZ-13, Co(II)/SSZ-13 and Ni(II)/SSZ-13 showed the highest CO(2 )uptake (4.49 and 4.45 mmol/g, respectively) and superior selectivity of CO2 over N-2 (52.55 and 42.61, respectively) at 273 K and 1 atm. We attribute such outstanding separation performance to the Pi backdonation exclusively formed between CO2 and transition metal cation sites. This demonstrates a new approach of developing adsorbents for CO2 capture in the real-world industrial processes.
引用
收藏
页码:1450 / 1458
页数:9
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