膜
复合数
纤维
材料科学
气体分离
化学工程
薄膜复合膜
分离(统计)
复合材料
色谱法
化学
计算机科学
工程类
生物化学
机器学习
反渗透
作者
Sergio V. Gutiérrez-Hernández,Fernando Pardo,Andrew B. Foster,Peter M. Budd,Gabriel Zarca,Ane Urtiaga
标识
DOI:10.1016/j.seppur.2025.132254
摘要
In this work, we explored for the first time the gas separation performance of a branched PIM-1 polymer (11 % substituted) in a hollow fiber-thin film composite membrane (HF–TFCM) configuration. HF-TFCMs were successfully obtained by the dip-coating methodology with a 1–2 µm thin selective layer of the branched PIM-1 (B-PIM-1). The permeability of these membranes to pure carbon dioxide, methane, nitrogen, carbon monoxide and hydrogen was tested in a tubular membrane module. The herein prepared HF-TFCMs offered a remarkable initial CO 2 permeance of 650 GPU, along with ideal gas selectivity of 20.8 and 14.8 for CO 2 /N 2 and CO 2 /CO separations, respectively. In addition, the aging of the B-PIM-1 HF-TFCM was weekly monitored over 307 days, showing a 54 % permeance drop for CO 2 with a 24 % drop in CO 2 /N 2 selectivity, highlighting a moderate aging resistance of the B-PIM-1 structure. The membrane performance for mixed gas separation was further explored with CO 2 /N 2 mixtures in the range 10–70 CO 2 vol%, and, for the first time, with a CO 2 /CO mixture (50/50 vol%), showing similar performance to that observed with pure gases for CO 2 /N 2 separation and only a slightly lower CO 2 permeance in CO 2 /CO separation. These results emphasize the potential of B-PIM-1 hollow fibers for the recovery of CO 2 from CO 2 /N 2 and CO 2 /CO mixtures. In addition, gas sorption isotherms of all gases at 30 °C were obtained and modelled. The solubility results showed that the branched structure did not affect gas solubility compared to the conventional predominantly di-substituted PIM-1.
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