膜
电化学
阻塞效应
质子交换膜燃料电池
氧化物
离子
质子
质子输运
亚苯基
化学工程
化学
材料科学
电极
聚合物
有机化学
工程类
物理化学
物理
量子力学
生物化学
发展心理学
心理学
作者
Seol A Jang,Jung‐Je Woo,Jung-Eun Cha,Young Woo Choi,Jong Hak Kim
出处
期刊:Desalination
[Elsevier]
日期:2024-10-01
卷期号:586: 117888-117888
被引量:1
标识
DOI:10.1016/j.desal.2024.117888
摘要
Anion exchange membranes are crucial in processes involving acids and bases, yet they often suffer from proton leakage, which diminishes system efficiency and membrane durability. To tackle this challenge, a novel polymeric structural approach was assessed to enhance proton-blocking performance. This approach scrutinized the interaction between protons and proton-attracting chemical species in the presence or absence of dimethyl (DM) groups within the poly(phenylene oxide) structure, and compared with the commercially available poly(aryl piperidinium) (PiperION) membrane containing strongly hydrophobic -CF3 groups. The findings revealed proton-blocking efficiencies of 60 % for PiperION, 62 % for PPO, and 72 % for DMPPO, with corresponding proton permeabilities of 36.71 × 10−6 cm2·s−1, 17.30 × 10−6 cm2·s−1, and 7.58 × 10−6 cm2·s−1, respectively. These results suggest enhanced proton-blocking performance with DM groups, while -CF3 groups do not provide a substantial improvement. Moreover, PPO-based membranes, when reinforced as composites, demonstrated superior proton-blocking capabilities compared to non-reinforced counterparts. These findings underscore the significance of designing anion exchange membranes with reduced proton interactions to achieve optimal proton-blocking performance in electrochemical systems.
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