Guo Shuang, Fang Chuanjie, Li Jiaqi, Wang Xiaohe, Feng Weilin, Guo Hukang, Xie Ming, Zhuang Yongbing, Lee Young Moo, Zhu Liping
MOE Key Laboratory of Macromolecular Synthesis and Functionalization, MOE Engineering Research Center of Membrane and Water Treatment Technology, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
Department of Polymer Science and Engineering, Department of Chemical Engineering, University of Bath, Bath, BA2 7AY, UK.
Adv Sci (Weinh). 2025 Aug;12(30):e16748. doi: 10.1002/advs.202416748. Epub 2025 May 29.
Microporous polymer membranes with high solvent permeability are pivotal for upgrading molecular separations in organic solvents, but this remains challenging due to numerous sub-0.4 nm ultra-micropores resulting from local tight packing, which limit solvent-accessibility. Herein, a microporous polyimide with high intrinsic free volume [PI-TB-NDI, naphthalenediimide (NDI) and Tröger's base (TB)] is synthesized for organic solvent nanofiltration. The resulting polymer showed high free volume because of fused aromatic rings and a twisted structure. Aromatic rings enhanced solvent resistance due to strong molecular interaction, but increased detrimental local tight packing as well. To suppress local tight packing without compromising the molecular interactions vital for stability, an ortho-methyl group is deliberately introduced onto the TB unit to increase both intra- and inter-molecular steric hindrance, imparting an H-shaped TB-NDI-TB molecular stent. On the introduction of ortho-methyl groups, the sub-0.4 nm ultra-micropores are enlarged to ultra-micropores (0.6-0.7 nm) to give the membrane with rich solvent-accessible sub-nanochannels. This resulted in an unprecedented enhancement of solvent permeability, with ethanol permeability 2-8 times greater than that of state-of-the-art polymer membranes with similar selectivity. These findings advance the design strategy of microporous membranes with well-tailored free volume without post-treatments, enabling upscaling and efficient separation of precious species in organic solvents.
具有高溶剂渗透性的微孔聚合物膜对于提升有机溶剂中的分子分离至关重要,但由于局部紧密堆积产生大量亚0.4纳米的超微孔,这限制了溶剂可及性,使得实现这一点仍具有挑战性。在此,合成了一种具有高固有自由体积的微孔聚酰亚胺[PI-TB-NDI,萘二亚胺(NDI)和特罗格碱(TB)]用于有机溶剂纳滤。由于稠合芳环和扭曲结构,所得聚合物显示出高自由体积。芳环由于强烈的分子相互作用增强了耐溶剂性,但也增加了有害的局部紧密堆积。为了在不损害对稳定性至关重要的分子相互作用的情况下抑制局部紧密堆积,特意在TB单元上引入邻甲基以增加分子内和分子间的空间位阻,赋予其H形的TB-NDI-TB分子支架。引入邻甲基后,亚0.4纳米的超微孔扩大为超微孔(0.6 - 0.7纳米),使膜具有丰富的溶剂可及亚纳米通道。这导致溶剂渗透性得到前所未有的提高,乙醇渗透率比具有相似选择性的现有聚合物膜高2 - 8倍。这些发现推进了无需后处理即可精确调控自由体积的微孔膜的设计策略,实现了有机溶剂中珍贵物质的放大和高效分离。