Nitrogen Rejection from Methane via a “Trapdoor” K-ZSM-25 Zeolite

化学 甲烷 沸石 ZSM-5型 无机化学 氮气 催化作用 有机化学
作者
Jianhua Zhao,Seyed Hesam Mousavi,Gongkui Xiao,Abdol Hadi Mokarizadeh,Thomas Moore,Kaifei Chen,Qinfen Gu,Ranjeet Singh,Ali Zavabeti,Jefferson Zhe Liu,Paul A. Webley,Gang Kevin Li
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:143 (37): 15195-15204 被引量:22
标识
DOI:10.1021/jacs.1c06230
摘要

Nitrogen (N2) rejection from methane (CH4) is the most challenging step in natural gas processing because of the close similarity of their physical-chemical properties. For decades, efforts to find a functioning material that can selectively discriminate N2 had little outcome. Here, we report a molecular trapdoor zeolite K-ZSM-25 that has the largest unit cell among all zeolites, with the ability to capture N2 in favor of CH4 with a selectivity as high as 34. This zeolite was found to show a temperature-regulated gas adsorption wherein gas molecules' accessibility to the internal pores of the crystal is determined by the effect of the gas–cation interaction on the thermal oscillation of the "door-keeping" cation. N2 and CH4 molecules were differentiated by different admission-trigger temperatures. A mild working temperature range of 240–300 K was determined wherein N2 gas molecules were able to access the internal pores of K-ZSM-25 while CH4 was rejected. As confirmed by experimental, molecular dynamic, and ab initio density functional theory studies, the outstanding N2/CH4 selectivity is achieved within a specific temperature range where the thermal oscillation of door-blocking K+ provides enough space only for the relatively smaller molecule (N2) to diffuse into and through the zeolite supercages. Such temperature-regulated adsorption of the K-ZSM-25 trapdoor zeolite opens up a new approach for rejecting N2 from CH4 in the gas industry without deploying energy-intensive cryogenic distillation around 100 K.

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