Surface-Charge Characterization of Nanocomposite Cellulose Acetate/Silver Membranes and BSA Permeation Performance.

Abstract

Membrane processes are a reality in a wide range of industrial applications, and efforts to continuously enhance their performance are being pursued. The major drawbacks encountered are related to the minimization of polarization concentration, fouling, and biofouling formation. In this study, silver nanoparticles were added to the casting solutions of cellulose acetate membranes in order to obtain new hybrid membranes that present characteristics inherent to the silver nanoparticles, namely antibacterial behavior that leads to biofouling reduction. A systematic study was developed to assess the effect of ionic strength, membrane polymeric structure, and silver nanoparticle incorporation on the cellulose acetate (CA) membrane surface charge. Surface charge was quantified by streaming potential measurements and it was correlated with BSA permeation performance. CA membranes were prepared by the phase-inversion method using three casting-solution compositions, to obtain membranes with different polymeric structures (CA400-22, CA400-30, CA400-34). The nanocomposite CA/silver membranes (CA/Ag) were prepared through the incorporation of silver nanoparticles (0.1 and 0.4 wt% Ag) in the casting solutions of the membranes. To evaluate the electrolyte concentration effect on the membranes zeta potential and surface charge, two potassium chloride solutions of 1 mM and 5 mM were used, in the pH range between 4 and 9. The results show that the zeta-potential values of CA/Ag membranes were less negative when compared to the silver-free membranes, and almost independent of the silver content and the pH of the solution. The influence of the protein solution pH and the protein charge in the BSA solutions permeation was studied. The pH conditions that led to the lower permeate fluxes were observed at the isoelectric point of BSA, pH = 4.8.