Abstract

Electrodialysis (ED) is a promising emerging electrochemical membrane technology for nutrient concentration and recovery from wastewater. However associated environmental safety aspects have to be assessed before utilizing concentrated nutrient produced by ED, for instance as fertilizer. Municipal wastewaters contain various micropollutants that have the potential of being concentrated during the ED treatment processes. This study quantified the transport of pharmaceuticals during ED nutrient recovery from synthetic centrate wastewater. Specifically, it is evaluated whether pharmaceutical micropollutants are mobile, and therefore able to transport across the cation exchange membranes and concentrate into the ED concentrate product. Results demonstrate that NH4+-N, PO43--P and K+ could be concentrated up to 5 times in the concentrated ED product (3700–4000 mg/L NH4+-N, 21–25 mg/L PO43--P, 990–1040 mg/L K+). Target micropollutants, such as diclofenac, carbamazepine and furosemide were largely retained in the diluent, with less than 8% being transported across to the concentrate product (feed micropollutant concentration 10 or 100 μg/L) based on the final target pharmaceutical amounts in the ED concentrate product (μg). Some transport of micropollutants such as atenolol, metoprolol and hydrochlorothiazide was observed to the concentrate product. For instance a final concentration of 10.3, 9.4 and 8.6 μg/L on average was measured for these pollutants in the final ED concentrate product (final volume ∼1 L) in experiments with a feed water (initial volume 20 L) containing only 10 μg/L of target pharmaceuticals. Transport of pharmaceuticals across the ED membranes was concluded to be dominated mainly by the molecule hydrophobicity/hydrophilicity as well as electrostatic interactions between pharmaceutical molecules and ED membranes. Particularly excluded were those having a negative charge and high hydrophobicity such as diclofenac and ibuprofen.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.