渗透汽化
石墨烯
微观结构
氧化物
聚丙烯腈
渗透
丁醇
材料科学
蒸发
图层(电子)
化学工程
复合数
纳米技术
润湿
膜
复合材料
化学
有机化学
乙醇
冶金
聚合物
工程类
物理
热力学
生物化学
作者
Chi‐Hui Tsou,Quan‐Fu An,Shen–Chuan Lo,Manuel Reyes De Guzman,Wei‐Song Hung,Chien‐Chieh Hu,Kueir‐Rarn Lee,Juin‐Yih Lai
标识
DOI:10.1016/j.memsci.2014.12.039
摘要
We utilized pressure-, vacuum-, and evaporation-assisted self-assembly techniques through which graphene oxide (GO) was deposited on modified polyacrylonitrile (mPAN). The fabricated composite GO/mPAN membranes were applied to dehydrate 1-butanol mixtures by pervaporation. Varying driving forces in the self-assembly techniques induced different GO assembly layer microstructures. XRD results indicated that the GO layer d-spacing varied from 8.3 Å to 11.5 Å. The self-assembly technique with evaporation resulted in a heterogeneous GO layer with loop structures; this layer was shown to be hydrophobic, in contrast to the hydrophilic layer formed from the other two techniques. From the pressure-assisted technique, the composite membrane exhibited exceptional pervaporation performance at 30 °C: concentration of water at the permeate side=99.6 wt% and permeation flux=2.54 kg m−2 h−1. Moreover, the membrane sustained its operating stability at a high temperature of 70 °C: a high water concentration of 99.5 wt% was maintained, and a permeation flux as high as 4.34 kg m−2 h−1 was attained. This excellent separation performance stemmed from the dense, highly ordered laminate structure of GO.
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