渗透汽化
膜
渗透
海水淡化
化学工程
材料科学
石墨烯
氧化物
高分子化学
化学
纳米技术
生物化学
工程类
冶金
作者
Xia Zhan,Zhongyong Gao,Rui Ge,Juan Lu,Jiding Li,Wan Xian
出处
期刊:Desalination
[Elsevier]
日期:2022-12-01
卷期号:543: 116106-116106
被引量:22
标识
DOI:10.1016/j.desal.2022.116106
摘要
Graphene oxide (GO) membranes exhibit fascinating properties in pervaporation desalination due to the unimpeded water permeation in two-dimensional (2D) interlaminar channels. The precise construction of interlayer mass transfer nanochannels and regulation of their microenvironment are crucial to break through the trade-off effect of pervaporation desalination performance and achieve high stability of GO membranes. Herein, aminopropylisobutyl polyhedral oligomeric silsesquioxane (NH2-POSS) was intercalated into GO interlayers with glutaraldehyde as crosslinking reagent to fabricate [email protected] hybrid membranes. The intercalation of POSS into GO interlayers provided enlarged interlayer spacing for water permeation and appropriate steric hindrance for ion rejection as well as better swelling resistance, which promoted both of water permeation flux and salt rejection of GO membranes. The optimized [email protected] hybrid membrane displayed an outstanding water flux of 112.7 kg/(m2·h) and 99.98 % salt rejection in desalinating 3.5 wt% NaCl solution at 80 °C. Benefiting from the formation of hydrophilic/hydrophobic heterostructure and crosslinking with glutaraldehyde, [email protected] hybrid membranes could toughly resist membrane swelling and exhibited stable and reliable desalination performance. Desirable stability of pervaporation desalination performance was acquired in the 24 h long-term separation experiment at 80 °C. The study might provide some new insight in designing high-efficiency 2D laminar membranes for pervaporation desalination by elaborate regulation of transport channel size without sacrificing interlayer spacing based on the construction of appropriate hydrophilic/hydrophobic heterostructure.
科研通智能强力驱动
Strongly Powered by AbleSci AI