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用于加速丙烯/丙烷筛分的温度响应性多孔晶体中的精致柔软性

Delicate Softness in a Temperature-Responsive Porous Crystal for Accelerated Sieving of Propylene/Propane.

作者信息

Huang Yuhang, Wan Jingmeng, Pan Ting, Ge Kai, Guo Yanan, Duan Jingui, Bai Junfeng, Jin Wanqin, Kitagawa Susumu

机构信息

State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing 211816, China.

School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, China.

出版信息

J Am Chem Soc. 2023 Nov 8;145(44):24425-24432. doi: 10.1021/jacs.3c10277. Epub 2023 Oct 25.

Abstract

Soft nanoporous crystals with structural dynamics are among the most exciting recently discovered materials. However, designing or controlling a porous system with delicate softness that can recognize similar gas pairs, particularly for the promoted ability at increased temperature, remains a challenge. Here, we report a soft crystal () with a one-dimensional (1D) channel that expands and contracts delicately around 4 Å at elevated temperature. The completely different adsorption processes of propane (CH: kinetic dominance) and propylene (CH: thermodynamic preference) allow the crystal to show a sieving separation of this mixtures (9.9 min·g) at 273 K, and the performance increases more than 2-fold (20.4 min·g) at 298 K. This phenomenon is contrary to the general observation for adsorption separation: the higher the temperature, the lower the efficiency. Gas-loaded in situ powder X-ray analysis and modeling calculations reveal that slight pore expansion caused by the increased temperature provides plausible nanochannel for adsorption of the relatively smaller CH while maintaining constriction on the larger CH. In addition, the separation process remains unaffected by the general impurities, demonstrating its true potential as an alternative sorbent for practical applications. Moving forward, the delicate crystal dynamics and promoted capability for molecular recognition provide a new route for the design of next-generation sieve materials.

摘要

具有结构动力学的软纳米多孔晶体是近年来发现的最令人兴奋的材料之一。然而,设计或控制一个具有精细柔软度的多孔系统,使其能够识别相似的气体对,特别是在升高温度时具有增强的能力,仍然是一个挑战。在此,我们报道了一种具有一维(1D)通道的软晶体(),该通道在升高温度时会在约4 Å左右微妙地扩张和收缩。丙烷(CH:动力学主导)和丙烯(CH:热力学偏好)完全不同的吸附过程使得该晶体在273 K时能够对这种混合物进行筛分分离(9.9分钟·克),并且在298 K时性能提高了两倍多(20.4分钟·克)。这种现象与吸附分离的一般观察结果相反:温度越高,效率越低。气体原位加载粉末X射线分析和模型计算表明,温度升高引起的轻微孔隙扩张为相对较小的CH的吸附提供了合理的纳米通道,同时对较大的CH保持收缩。此外,分离过程不受一般杂质的影响,证明了其作为实际应用中替代吸附剂的真正潜力。展望未来,精细的晶体动力学和增强的分子识别能力为下一代筛分材料的设计提供了一条新途径。

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