Hydroxyl‐Functionalized Polymers of Intrinsic Microporosity and Dual‐Functionalized Blends for High‐Performance Membrane‐Based Gas Separations
Yingge Wang, Nasser Alaslai, Bader S. Ghanem, Xiaohua Ma, Xiaofan Hu, Marcel Balçık, Qing Liu, Mahmoud A. Abdulhamid, Yu Han, Mohamed Eddaoudi, Ingo Pinnau
Abstract
Abstract Membrane technology has shown significant growth during the past two decades in the gas separation industry due to its energy‐savings, compact and modular design, continuous operation, and environmentally benign nature. Robust materials with higher permeability and selectivity are key to reduce capital and operational cost, pushing it forward to replace or debottleneck conventional energy‐intensive unit operations such as distillation. Recently designed ladder polymers of intrinsic microporosity (PIM) and polyimides of intrinsic microporosity (PIM‐PI) with pores <20 Å have demonstrated excellent gas permeation performance. Here, a series of plasticization‐resistant PIM‐based membrane materials is reported, including the first example of a hydroxyl‐functionalized triptycene‐ and Tröger's base‐derived ladder PIM and two PIM‐PI homopolymers and a series of dual‐functionalized polyimide blends containing hydroxyl‐ and carboxyl‐functionalized groups. Specifically, 4,4′‐(hexafluoroisopropylidene)diphthalic anhydride (6FDA)‐based PIM‐PI blends demonstrated extremely high selectivity for a variety of industrially important applications. An optimized polyimide blend containing ─OH and ─COOH groups showed permselectivity values of 136 for CO 2 /CH 4 , 11.4 for O 2 /N 2 and 636 for H 2 /CH 4 . Such extreme size‐sieving capabilities are attributed to physical crosslinking induced by strong hydrogen bonding forming tightly structured polymer networks. The study provides a new general strategy for developing plasticization resistant, robust, and highly‐selective PIM‐based membrane materials.