Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep19593
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dc.titleHydrophilic Mineral Coating of Membrane Substrate for Reducing Internal Concentration Polarization (ICP) in Forward Osmosis
dc.contributor.authorLiu, Q
dc.contributor.authorLi, J
dc.contributor.authorZhou, Z
dc.contributor.authorXie, J
dc.contributor.authorLee, J.Y
dc.date.accessioned2020-09-10T01:40:37Z
dc.date.available2020-09-10T01:40:37Z
dc.date.issued2016
dc.identifier.citationLiu, Q, Li, J, Zhou, Z, Xie, J, Lee, J.Y (2016). Hydrophilic Mineral Coating of Membrane Substrate for Reducing Internal Concentration Polarization (ICP) in Forward Osmosis. Scientific Reports 6 : 19593. ScholarBank@NUS Repository. https://doi.org/10.1038/srep19593
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175437
dc.description.abstractInternal concentration polarization (ICP) is a major issue in forward osmosis (FO) as it can significantly reduce the water flux in FO operations. It is known that a hydrophilic substrate and a smaller membrane structure parameter (S) are effective against ICP. This paper reports the development of a thin film composite (TFC) FO membrane with a hydrophilic mineral (CaCO3)-coated polyethersulfone (PES)-based substrate. The CaCO3 coating was applied continuously and uniformly on the membrane pore surfaces throughout the TFC substrate. Due to the intrinsic hydrophilicity of the CaCO3 coating, the substrate hydrophilicity was significantly increased and the membrane S parameter was reduced to as low as the current best of cellulose-based membranes but without the mechanical fragility of the latter. As a result, the ICP of the TFC-FO membrane could be significantly reduced to yield a remarkable increase in water flux without the loss of membrane selectivity.
dc.publisherNature Publishing Group
dc.sourceUnpaywall 20200831
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1038/srep19593
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page19593
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