Inner-selective polyethersulfone-polydimethylsiloxane (PES-PDMS) thin film composite hollow fiber membrane for CO2/N2 separation at high pressures

聚二甲基硅氧烷 渗透 材料科学 气体分离 化学工程 烟气 聚合物 纤维 体积热力学 复合数 复合材料 纳米技术 化学 有机化学 渗透 生物化学 物理 量子力学 工程类
作者
Baiwang Zhao,Jun Wen Wong,Can Zeng Liang,Ji Wu,Tai‐Shung Chung,Sui Zhang
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:323: 124439-124439 被引量:7
标识
DOI:10.1016/j.seppur.2023.124439
摘要

Carbon dioxide (CO2) is the dominant greenhouse gas (GHG) and thus CO2 capture from flue gas of power plants, the main anthropogenic source of emission, is a key approach to mitigating the climate change. Thin-film composite (TFC) membranes have received extensive research attention recently as a promising post-combustion CO2 capture (CO2/N2) technology owing to its energy-efficiency, design versatility and upscaling potential. However, studies with the most industrially relevant membrane configuration, the hollow fibers, are rather limited for this application. Herein, we developed an inner-selective polyethersulfone-polydimethylsiloxane (PES-PDMS) TFC hollow fiber membrane by inner coating PDMS in the lumen of PES hollow fibers and then pressurizing the hollow fibers for CO2/N2 separation. The optimal PES-PDMS TFC membrane can achieve a CO2 permeance of 2150 GPU and a CO2/N2 selectivity of 20 when the operating pressure was between 20–22 bar, which holds good potential for post-combustion CO2 capture. The high separation performance arises from a combination of the stretched PES and PDMS layers. The micro-deformation of both layers under high pressures at the lumen side could possibly reduce the selective layer thickness. It may also induce polymer chain orientation, increase the fractional free volume, and potentially create free volume with smaller sizes, thus enhancing the CO₂ permeability and CO₂/N₂ selectivity from the PDMS and PES layers.
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