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Tuning the selectivity of light hydrocarbons in natural gas in a family of isoreticular MOFs

机译:在一系列等网状MOF中调节天然气中轻烃的选择性

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摘要

Purification of methane from other light hydrocarbons in natural gas is a topic of intense research due to its fundamental importance in the utilization of natural gas fields. Porous materials have emerged as excellent alternative platforms to conventional cryogenic methodologies to perform this task in a cost- and energy-efficient manner. Here we report a new family of isoreticular chiral MOFs, prepared from oxamidato ligands derived from natural amino acids L-alanine, L-valine and L-leucine, where, by increasing the length of the alkyl residue of the amino acid, the charge density of the MOF's channels can be tuned (1 > 2 > 3), decreasing the adsorption preference towards methane over light hydrocarbons thus improving this purification process. The validity of our rational design strategy has been proved by a combination of single-component adsorption isotherms, adsorption kinetics of CH4, C2H6, C3H8 and n-C4H10, and breakthrough experiments of binary CH4/C2H6 and CH4/C3H8 mixtures.
机译:从天然气中的其他轻质烃中提纯甲烷是一项紧迫的研究课题,因为它在利用天然气领域中具有根本的重要性。多孔材料已经成为常规低温方法的优良替代平台,可以以节省成本和节省能源的方式执行此任务。在这里,我们报道了一个新的同网状手性MOF家族,它是由天然氨基酸L-丙氨酸,L-缬氨酸和L-亮氨酸衍生的草酰胺配体制备的,其中,通过增加氨基酸的烷基残基的长度,电荷密度可以调整MOF通道的通道数(1> 2> 3),从而降低了甲烷对轻质烃的甲烷吸附偏好,从而改善了该纯化过程。单组分吸附等温线,CH4,C2H6,C3H8和n-C4H10的吸附动力学以及二元CH4 / C2H6和CH4 / C3H8混合物的突破实验相结合,证明了我们合理设计策略的有效性。

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