Display Settings:

Format

Send to:

Choose Destination
Water Res. 2012 May 15;46(8):2683-92. doi: 10.1016/j.watres.2012.02.023. Epub 2012 Feb 21.

Comparison of the removal of hydrophobic trace organic contaminants by forward osmosis and reverse osmosis.

Author information

  • 1Strategic Water Infrastructure Laboratory, School of Civil Mining and Environmental Engineering, University of Wollongong, Wollongong, NSW 2522, Australia.

Abstract

We compared the rejection behaviours of three hydrophobic trace organic contaminants, bisphenol A, triclosan and diclofenac, in forward osmosis (FO) and reverse osmosis (RO). Using erythritol, xylose and glucose as inert reference organic solutes and the membrane pore transport model, the mean effective pore size of a commercial cellulose-based FO membrane was estimated to be 0.74 nm. When NaCl was used as the draw solute, at the same water permeate flux of 5.4 L/m(2) h (or 1.5 μm/s), the adsorption of all three compounds to the membrane in the FO mode was consistently lower than that in the RO mode. Rejection of bisphenol A and diclofenac were higher in the FO mode compared to that in the RO mode. Because the molecular width of triclosan was larger than the estimated mean effective membrane pore size, triclosan was completely rejected by the membrane and negligent difference between the FO and RO modes could be observed. The difference in the separation behaviour of these hydrophobic trace organics in the FO (using NaCl the draw solute) and RO modes could be explained by the phenomenon of retarded forward diffusion of solutes. The reverse salt flux of NaCl hinders the pore diffusion and subsequent adsorption of the trace organic compounds within the membrane. The retarded forward diffusion effect was not observed when MgSO(4) and glucose were used as the draw solutes. The reverse flux of both MgSO(4) and glucose was negligible and thus both adsorption and rejection of BPA in the FO mode were identical to those in the RO mode.

Crown Copyright © 2012. Published by Elsevier Ltd. All rights reserved.

PMID:
22402269
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Icon for Elsevier Science
    Loading ...
    Write to the Help Desk