Flame-retardant AEMs based on organic-inorganic composite polybenzimidazole membranes with enhanced hydroxide conductivity

被引:21
|
作者
Li, Jinsheng [1 ,2 ,3 ]
Wang, Shuang [1 ,3 ]
Liu, Fengxiang [1 ]
Chen, Hao [1 ]
Wang, Xu [1 ]
Mao, Tiejun [1 ]
Wang, Di [1 ]
Liu, Geng [1 ]
Wang, Zhe [1 ,3 ]
机构
[1] Changchun Univ Technol, Coll Chem Engn, Changchun 130012, Jilin, Peoples R China
[2] Changchun Univ Technol, Sch Mat Sci & Engn, Changchun 130012, Jilin, Peoples R China
[3] Changchun Univ Technol, Adv Inst Mat Sci, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Polybenzimidazole; 1-butyl-3-methyl imidazolium phosphotungstate; Flame-retardant; Solid electrolyte; ANION-EXCHANGE MEMBRANES; IONIC LIQUID; MULTIBLOCK COPOLYMERS; ACID; SOLVATION; STABILITY; TRANSPORT; EVOLUTION; SULFONE;
D O I
10.1016/j.memsci.2019.117306
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Efficient anionic conductivity accompanied with flam-resistance is of great importance for solid electrolyte. Herein, anion exchange membranes (AEMs) based on polybenzimidazole (PBI) and 1-butyl-3-methyl imidazolium phosphotungstate (PWA-IL) have been prepared. The obtained PWA-IL can be dispersed in PBI matrix uniformly aiming to enhance the anion conductivity. Especially, it is found that PWA-IL endows the composite membranes with flame-resistance features. Such a phenomenon may be rooted from the nature of non-flammable of 1- butyl-3-methylimidazolium bis (trifluoromethylsulfony)imide (IL) and phosphotungstic acid (PWA), which constitute the organic-inorganic filler PWA-IL. Simultaneously, the anionic conductivity of the obtained composite membranes improved from 48.9 mS cm(-1) to 75.8 mS cm(-1) under fully hydrated conditions at 80 degrees C. Enlarged elongation and small decline in tensile strength was observed due to the plasticization from 1-butyl-3-methyl imidazolium phosphotungstate. Polybenzimidazole backbones provide tough mechanical properties (strength more than 60 MPa and elongation more than 6%) and good thermal stability, which meet the need of wide applications.
引用
收藏
页数:7
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