Antiscaling efficacy of CaCO3 and CaSO4 on polyethylene glycol (PEG)-modified reverse osmosis membranes in the presence of humic acid: interplay of membrane surface properties and water chemistry. Issue 7 (7th February 2017)

• Record Type: Journal Article
• Authors: Ray, Jessica R.; Wong, Whitney; Jun, Young-Shin
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 7(2017)
• Page Start: 5647
• Page End: 5657
• Publication Date: 2017-02-07
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp08569e
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : A specific polyethylene glycol (PEG)–humic acid–SO4 2− interaction results in promoted CaSO4 colloidal formation on PEG reverse osmosis membrane surfaces. Abstract : Mineral scaling persists in many water treatment processes. More specifically, it can significantly reduce the efficacy of aromatic polyamide (PA) membranes during reverse osmosis (RO) water treatment. Previous studies have integrated hydrophilic materials, such as polyethylene glycol (PEG), onto RO membranes to combat scaling from generally hydrophobic feed water constituents; however, there are still outstanding knowledge gaps regarding the interplay of the modified membrane surface chemistry and the water chemistry in complex RO feed waters. In this work, we have investigated the mechanisms of hydrophilic PEG-grafted PA membranes in reducing mineral scaling from calcium carbonate (CaCO3 ) and calcium sulfate (CaSO4 ) in the presence of humic acid (HA). Based on surface and solution analyses, we found that colloidal formation was significantly reduced on PA–PEG surfaces in systems without HA. When HA was introduced, CaCO3 scaling was reduced on both virgin and PA–PEG membrane surfaces; while, interestingly, synergistic PEG–HA–CaSO4 interactions increased CaSO4 colloidal formation on PA–PEG membranes. Promoted CaSO4 formation results from a high negative surface charge near the PEG-modified membrane surface when HA and SO4 2− are present, attracting more Ca 2+ to form CaSO4 . The results of this work provide new information about colloidal formation at water–membrane interfaces for designing better PEG and PEG-based scale-resistant desalination membranes.