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Ultrathin and Stable Ionic Liquid Membranes with Bio-Inspired Interlocking Architecture for CO Separation.

作者信息

Xue Yu-Ren, Xu Guang-Chang, Li Kai, Guo Xin-Yu, Wu Jian, Liang Hong-Qing, Yang Hao-Cheng, Zhang Chao, Xu Zhi-Kang

机构信息

MOE Key Lab of Macromolecular Synthesis and Functionalization, and Key Lab of Adsorption and Separation Materials & Technologies of Zhejiang Province, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310058, China.

The "Belt and Road" Sino-Portugal Joint Lab on Advanced Materials, International Research Center for X Polymers, Zhejiang University, Hangzhou, 310058, China.

出版信息

Small. 2025 Jul;21(26):e2503418. doi: 10.1002/smll.202503418. Epub 2025 May 6.

Abstract

The growing demand for energy-efficient carbon capture has spurred significant advancements in supported ionic liquid membranes (SILMs), which utilize ionic liquid (IL) with high CO solubility for continuous gas purification processes. However, conventional SILMs are hindered by a persistent limitation: thick IL layers (> 50 µm) significantly reduce CO permeance to below 1 GPU, while also causing mechanical failure under prolonged operational pressure. Inspired by the interlocking elytra of Tenebrionidae beetles, which use microscale "teeth" to withstand mechanical stress, locked ionic liquid membranes (LILMs) are engineered by composeing two interpenetrating polyamide nanofilms with biomimetic protrusions. These nanofilms confine ILs within cavities formed by protrusions, thinning IL layers to sub-0.5 µm while resisting shear stresses. The LILMs demonstrate a CO/N selectivity of 55 and an enhanced CO permeance of 8.2 GPU, surpassing the performance of conventional SILMs by ≈20-fold while maintaining stability over 168 h of continuous mixed gas separation. By dual-purposing ILs as both solvents for interfacial polymerization and CO transporters, this bio-inspired architecture overcomes the thickness-stability limitations, enabling energy-efficient carbon capture.

摘要

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