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用于基准CH/CO分离的含氟阴离子空间分隔孔金属有机框架

Metal-Organic Framework with Space-Partition Pores by Fluorinated Anions for Benchmark CH/CO Separation.

作者信息

Zhang Yuanbin, Han Yan, Luan Binquan, Wang Lingyao, Yang Wenlei, Jiang Yunjia, Ben Teng, He Yabing, Chen Banglin

机构信息

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Materials Science, Zhejiang Normal University, Jinhua 321004, P.R. China.

IBM Thomas J. Watson Research, Yorktown Heights, New York 10598, United States.

出版信息

J Am Chem Soc. 2024 Jun 26;146(25):17220-17229. doi: 10.1021/jacs.4c03442. Epub 2024 Jun 11.

Abstract

The efficient separation of CH from CH/CO or CH/CO/CH mixtures is crucial for achieving high-purity CH (>99%), essential in producing contemporary commodity chemicals. In this report, we present ZNU-12, a metal-organic framework with space-partitioned pores formed by inorganic fluorinated anions, for highly efficient CH/CO and CH/CO/CH separation. The framework, partitioned by fluorinated SiF anions into three distinct cages, enables both a high CH capacity (176.5 cm/g at 298 K and 1.0 bar) and outstanding CH selectivity over CO (13.4) and CH (233.5) simultaneously. Notably, we achieve a record-high CH productivity (132.7, 105.9, 98.8, and 80.0 L/kg with 99.5% purity) from CH/CO (v/v = 50/50) and CH/CO/CH (v/v = 1/1/1, 1/1/2, or 1/1/8) mixtures through a cycle of adsorption-desorption breakthrough experiments with high recovery rates. Theoretical calculations suggest the presence of potent "2 + 2" collaborative hydrogen bonds between CH and two hexafluorosilicate (SiF) anions in the confined cavities.

摘要

从CH/CO或CH/CO/CH混合物中高效分离CH对于获得高纯度CH(>99%)至关重要,这在生产当代商品化学品中必不可少。在本报告中,我们展示了ZNU-12,一种由无机氟化阴离子形成具有空间分隔孔的金属有机框架,用于高效CH/CO和CH/CO/CH分离。该框架由氟化SiF阴离子分隔成三个不同的笼,能够同时实现高CH容量(298 K和1.0 bar下为176.5 cm/g)以及对CO(13.4)和CH(233.5)的出色CH选择性。值得注意的是,通过具有高回收率的吸附-解吸突破实验循环,我们从CH/CO(v/v = 50/50)和CH/CO/CH(v/v = 1/1/1、1/1/2或1/1/8)混合物中实现了创纪录的高CH生产率(纯度为99.5%时分别为132.7、105.9、98.8和80.0 L/kg)。理论计算表明在受限腔内CH与两个六氟硅酸盐(SiF)阴离子之间存在有效的“2 + 2”协同氢键。

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