Impact of ionic strength and surface charge on ceramic membrane fouling by oil-in-water emulsions

Abstract

Large amounts of oily wastewater, which can be defined as produced water, are generated in oilfields. Ultrafiltration (UF) serves as an effective and economical method to purify produced water. Unfortunately, membrane fouling during produced water treatment is severe. In this paper, the effects of the ionic strength (1, 20, and 100 mM) as well as different surfactants on the membrane fouling are investigated. Four surfactants, including SDS (anionic), APG (non-ionic), CTAB (cationic) and DDAPS (zwitterionic), were selected for this study. The Derjaguin-Landau-Verwey-Overbeek (DLVO) and extended DLVO (XDLVO) models were used to quantify interactions between the membrane-oil droplet and deposited oil layer-oil droplet surfaces and to compare these interactions with the fouling experiments. The (X)DLVO interaction energies of the membrane-oil droplet exhibited a strong agreement with the fouling tendencies at 1 mM salinity. The SiC-deposited (B20) membrane showed less reversible and irreversible membrane fouling than the Al₂O₃ (B0) membrane when filtering negatively charged O/W emulsions stabilized with SDS, APG, or DDAPS. The DLVO model predicted a higher fouling tendency at higher salinity levels during the filtration of SDS, APG, or DDAPS-stabilized O/W emulsions and a decreased fouling tendency for CTAB-stabilized emulsion with the B20 membrane. However, at higher salinity levels, the XDLVO energy barrier was affected by both the repulsive electrostatic double layer (EL) interaction and attractive Lewis acid-base (AB) interaction. By comparing both experiments and (X)DLVO modeling, this study improves the fundamental understanding of the effect of ionic strength and surfactant types on reversible and irreversible fouling of the Al₂O₃ and SiC-coated membranes fouling by O/W emulsions.