渗透力
丙烯酸
化学工程
细菌纤维素
膜
自愈水凝胶
纤维素
功率密度
能量转换效率
化学
缓压渗透
多孔性
羧甲基纤维素
聚合物
材料科学
高分子化学
正渗透
有机化学
钠
单体
功率(物理)
光电子学
反渗透
工程类
物理
量子力学
生物化学
作者
Zhe Sun,Yudi Kuang,Mehraj Ahmad,Yang Huang,Sha Yin,Farzad Seidi,Sha Wang
标识
DOI:10.1016/j.carbpol.2023.120556
摘要
Hydrogel with 3D networks have shown great potential for ion transportation and energy conversion. However, the micron size pores of hydrogel greatly limit the ion selectivity and energy conversion performance. Here, we report a bacterial cellulose (BC) derived hydrogel membrane with double-network (DN) and tailored ion transport channels by rationally filling acrylic acid (AAc)-co-acrylamide (AAm)-co-methyl methacrylate (MMA) polymers into BC hydrogel micropores. Fabricated AAM/BC DN hydrogel membrane displays a unique hierarchical interconnected porous structure and 3D cation transport channels. From the results, the maximum power density reached up to 7.63 W·m-2 at 50-fold salinity gradient under alkaline conditions (pH 11). Interestingly, the power density of 45.5 W·m-2 was achieved through acid-base neutralization reaction. Furthermore, hydrogel successfully obtained a power density of 28.4 W·m-2 from a mixed system of paper black liquor wastewater/seawater. The results of this investigation suggested the enormous potential of BC-based nanofluidic membrane in sustainable osmotic energy conversion.
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