Increasing the Permeability of Polyphenylene Sulfone Hollow Fiber Ultrafiltration Membranes by Switching the Polymer End Groups

Abstract

The influence of the molecular weight and chemical structure of polyphenylene sulfone (PPSU) end groups on the formation of the porous structure of ultrafiltration (UF) hollow fiber membranes was investigated. Polymers with a molecular weight ranging from 67 to 81 kg/mol and with a hydroxyl-to-chlorine end group ratio ranging from 0.43 to 17.0 were synthesized. The excess of end groups was achieved during polymer synthesis by adding one of the following monomers: hydroxyl (excess DHBP) or chlorine (excess DCDPS). For the first time, it was found that the stability of PPSU solutions is determined not by the molecular weight of the polymer, but by the chemical structure of its end groups. The stability of polymer solutions increases with the increasing proportion of chlorine groups. The SEM method showed that with the increasing molar fraction of chlorine end groups in the polymer, a more open porous structure forms on the outer surface of the hollow fiber membranes derived from it. The maximum UF permeance of the hollow fiber membranes for water was achieved with the PPSU sample containing the highest chlorine end group content, amounting to 136 L/(m2·h·bar), with a high rejection of the model substance Blue Dextran (at 94.7%). This represents the best result currently reported among unmodified PPSU hollow fiber membranes.