Synthesis of graphene oxide membranes and their behavior in water and isopropanol

被引:54
作者
Aher, Ashish [1 ]
Cai, Yuguang [1 ]
Majumder, Mainak [2 ]
Bhattacharyya, Dibakar [1 ]
机构
[1] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
[2] Monash Univ, Dept Mech Engn & Aerosp Engn, Nanoscale Sci & Engn Lab, Clayton, Vic 3800, Australia
基金
美国国家科学基金会; 澳大利亚研究理事会;
关键词
ATOMIC-STRUCTURE; GRAPHITE OXIDE; SEPARATION; STABILITY; TRANSPORT; ULTRATHIN;
D O I
10.1016/j.carbon.2017.01.086
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Graphene oxide (GO) membrane has been synthesized on commercial polysulfone ultrafiltration membranes (Pore size: 17 nm) using the drop casting method followed by baking at 90 degrees C for 24 h. Baking resulted in the reduction of GO and removal of bulk water intercalated in the GO sheets. Deposited GO film showed high stability under shear stress variation. This work shows that water adsorption on the GO membrane determines its permeation performance. Despite the higher viscosity of isopropyl alcohol (IPA), its permeability was 7 times higher than water through the baked ("dry") GO membranes, which were never contacted with water. However, IPA permeability of GO membranes dropped to 44% (of deionized water) when contacted with water ("hydrated" or "wet" GO membranes). Extensive size exclusion (rejection) studies with various dye and dendrimer molecules showed pore size reduced from 3.3 nm in the "dry" state to 1.3 nm in the "wet" state of GO membranes. FT-IR characterization of GO membrane suggested adsorption of water on the nanochannels of the active layer. Also, significant decay in flux was observed for water (82% of its initial flux) as compared to IPA (38% of its initial flux) for initially dry GO membranes. (C) 2017 Published by Elsevier Ltd.
引用
收藏
页码:145 / 153
页数:9
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