Enabling alternative ethylene production through its selective adsorption in the metal-organic framework Mn2(m-dobdc)

被引:47
作者
Bachman, Jonathan E. [1 ,2 ]
Reed, Douglas A. [3 ]
Kapelewski, Matthew T. [3 ]
Chachra, Gaurav [4 ]
Jonnavittula, Divya [4 ]
Radaelli, Guido [4 ]
Long, Jeffrey R. [2 ,3 ,5 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[4] Siluria Technol Inc, 409 Illinois St, San Francisco, CA 94158 USA
[5] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
CARBON-DIOXIDE CAPTURE; IRON(II) COORDINATION SITES; HYDROCARBON SEPARATIONS; HIGH-CAPACITY; METHANE; CATALYSTS; CO2; CONVERSION; ZEOLITE; STORAGE;
D O I
10.1039/c8ee01332b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The unique adsorptive properties of metal-organic frameworks open the door to new processes for energy and raw materials production. One such process is the oxidative coupling of methane for the generation of ethylene, which has limited viability due to the high cost of cryogenic distillation. Rather than employing such a traditional separation route, we propose the use of a porous material that is highly selective for ethylene over a wide range of gases in an energy- and cost-effective adsorbent-based separation process. Here, we analyze the metal-organic frameworks M-2(m-dobdc) (M = Mg, Mn, Fe, Co, Ni; m-dobdc(4-) = 4,6-dioxido-1,3-benzenedicarboxylate), featuring a high density of coordinatively-unsaturated M2+ sites, along with the commercial adsorbent zeolite CaX, for their ability to purify ethylene from the effluent of an oxidative coupling of methane process. Our results show that unique metal-adsorbate interactions facilitated by Mn-2(m-dobdc) render this material an outstanding adsorbent for the capture of ethylene from the product mixture, enabling this potentially disruptive alternative process for ethylene production.
引用
收藏
页码:2423 / 2431
页数:9
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