Efficient purification of ethene by an ethane-trapping metal-organic framework

被引:540
作者
Liao, Pei-Qin [1 ]
Zhang, Wei-Xiong [1 ]
Zhang, Jie-Peng [1 ]
Chen, Xiao-Ming [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
HIGHLY SELECTIVE SEPARATION; OLEFIN/PARAFFIN SEPARATIONS; HYDROCARBON SEPARATIONS; PI-COMPLEXATION; ADSORPTION; ETHYLENE; COORDINATION; SORPTION; OLEFINS; TRICARBOXYLATE;
D O I
10.1038/ncomms9697
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
Separating ethene (C2H4) from ethane (C2H6) is of paramount importance and difficulty. Here we show that C2H4 can be efficiently purified by trapping the inert C2H6 in a judiciously designed metal-organic framework. Under ambient conditions, passing a typical cracked gas mixture (15: 1 C2H4/C2H6) through 1 litre of this C2H6 selective adsorbent directly produces 56 litres of C2H4 with 99.95% + purity (required by the C2H4 polymerization reactor) at the outlet, with a single breakthrough operation, while other C2H6 selective materials can only produce ca. <= 1 litre, and conventional C2H4 selective adsorbents require at least four adsorption-desorption cycles to achieve the same C2H4 purity. Single-crystal X-ray diffraction and computational simulation studies showed that the exceptional C2H6 selectivity arises from the proper positioning of multiple electronegative and electropositive functional groups on the ultramicroporous pore surface, which form multiple C-H center dot center dot center dot N hydrogen bonds with C2H6 instead of the more polar competitor C2H4.
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页数:9
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