用户名: 密码: 验证码:
Enabling Graphene Oxide Nanosheets as Water Separation Membranes
详细信息    查看全文
  • 作者:Meng Hu ; Baoxia Mi
  • 刊名:Environmental Science & Technology (ES&T)
  • 出版年:2013
  • 出版时间:April 16, 2013
  • 年:2013
  • 卷:47
  • 期:8
  • 页码:3715-3723
  • 全文大小:436K
  • 年卷期:v.47,no.8(April 16, 2013)
  • ISSN:1520-5851
文摘
We report a novel procedure to synthesize a new type of water separation membrane using graphene oxide (GO) nanosheets such that water can flow through the nanochannels between GO layers while unwanted solutes are rejected by size exclusion and charge effects. The GO membrane was made via layer-by-layer deposition of GO nanosheets, which were cross-linked by 1,3,5-benzenetricarbonyl trichloride, on a polydopamine-coated polysulfone support. The cross-linking not only provided the stacked GO nanosheets with the necessary stability to overcome their inherent dispensability in water environment but also fine-tuned the charges, functionality, and spacing of the GO nanosheets. We then tested the membranes synthesized with different numbers of GO layers to demonstrate their interesting water separation performance. It was found that the GO membrane flux ranged between 80 and 276 LMH/MPa, roughly 4鈥?0 times higher than that of most commercial nanofiltration membranes. Although the GO membrane in the present development stage had a relatively low rejection (6鈥?6%) of monovalent and divalent salts, it exhibited a moderate rejection (46鈥?6%) of Methylene blue and a high rejection (93鈥?5%) of Rhodamine-WT. We conclude the paper by emphasizing that the facile synthesis of a GO membrane exploiting the ideal properties of inexpensive GO materials offers a myriad of opportunities to modify its physicochemical properties, potentially making the GO membrane a next-generation, cost-effective, and sustainable alternative to the long-existing thin-film composite polyamide membranes for water separation applications.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700