Microporous metal-organic framework with potential for carbon dioxide capture at ambient conditions

被引:768
作者
Xiang, Shengchang [1 ,2 ]
He, Yabing [1 ]
Zhang, Zhangjing [1 ,2 ]
Wu, Hui [3 ,4 ]
Zhou, Wei [3 ,4 ]
Krishna, Rajamani [5 ]
Chen, Banglin [1 ]
机构
[1] Univ Texas San Antonio, Dept Chem, San Antonio, TX 78249 USA
[2] Fujian Normal Univ, Coll Mat Sci & Engn, Fujian Prov Key Lab Polymer Mat, Fuzhou 350007, Fujian, Peoples R China
[3] NIST Ctr Neutron Res, Gaithersburg, MD 20899 USA
[4] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[5] Univ Amsterdam, Vant Hoff Inst Mol Sci, NL-1098 XH Amsterdam, Netherlands
关键词
ZEOLITIC IMIDAZOLATE FRAMEWORKS; ADSORPTION EQUILIBRIUM; CO2; ADSORPTION; HIGH-CAPACITY; CU-BTC; SEPARATION; SITES; STORAGE; FUNCTIONALITY; BREAKTHROUGH;
D O I
10.1038/ncomms1956
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Carbon dioxide capture and separation are important industrial processes that allow the use of carbon dioxide for the production of a range of chemical products and materials, and to minimize the effects of carbon dioxide emission. Porous metal-organic frameworks are promising materials to achieve such separations and to replace current technologies, which use aqueous solvents to chemically absorb carbon dioxide. Here we show that a metal-organic frameworks (UTSA-16) displays high uptake (160 cm(3) cm(-3)) of CO2 at ambient conditions, making it a potentially useful adsorbent material for post-combustion carbon dioxide capture and biogas stream purification. This has been further confirmed by simulated breakthrough experiments. The high storage capacities and selectivities of UTSA-16 for carbon dioxide capture are attributed to the optimal pore cages and the strong binding sites to carbon dioxide, which have been demonstrated by neutron diffraction studies.
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页数:9
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