Enhanced desalination performance of forward osmosis membranes based on reduced graphene oxide laminates coated with hydrophilic polydopamine
Forward osmosis (FO) processes have been recognized as a low energy required next-generation desalination technology, but the low performance of polymeric membranes remains a bottleneck in the practical application of FO. Graphene oxide (GO) membranes possess a huge potential as an alternative to po...
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Published in | Carbon (New York) Vol. 117; pp. 293 - 300 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Elsevier Ltd
01.06.2017
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | Forward osmosis (FO) processes have been recognized as a low energy required next-generation desalination technology, but the low performance of polymeric membranes remains a bottleneck in the practical application of FO. Graphene oxide (GO) membranes possess a huge potential as an alternative to polymeric membranes because of their facile fabrication procedure, ultra-thin thickness, controllable pore size, and outperformance of competing materials in terms of water transport rate; the low stability of GO laminates under water and their hydrophobic property (if GO laminates are reduced) remain as problems requiring solution prior to their practical implementation. To solve these problems, herein, the chemical reduction of GO laminates and a hydrophilic adhesive polydopamine (pDA) layer were applied. Reduced GO (rGO) laminates sustainably retained their compacted nanochannels (3.45 Å) compared to pristine GO laminates, which increased the selectivity of hydrated ions. In addition, adding a pDA coating onto the rGO laminates improved the hydrophilicity of the rGO laminate surface, which accelerated the water absorption speed. As a result of these synergistic effects, pDA-coated rGO (pDA-rGO) membranes achieved an outstanding water flux of 36.6 L/m2·h, with a reverse solute flux of 0.042 mol/m2·h and a high salt rejection rate of 92.0% in FO.
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ISSN: | 0008-6223 1873-3891 |
DOI: | 10.1016/j.carbon.2017.03.005 |