Effects of inorganic ions with different concentrations on the nanofiltration separation performance of perfluorobutane sulfonic acid (PFBS).

Perfluorobutane sulfonic acid (PFBS) is a kind of anthropogenic recalcitrant contaminant that has posed a threat to drinking water safety and brought widespread public health concerns. Nanofiltration (NF) is an effective way to remove PFBS from drinking water, while the removal is influenced by coexisting ions. To investigate the effects and intrinsic mechanisms of coexisting ions on the rejection of PFBS, poly(piperazineamide) NF membrane was utilized in this work. Results showed that most cations and anions in the feedwater could effectively improve PFBS rejection and simultaneously reduce NF membrane permeability. In most cases, the decrease in NF membrane permeability corresponded to an increase in the valence of cations or anions. When cations (Na, K, Ca, and Mg) were present, the rejection of PFBS was effectively improved from 79% to more than 91.07%. Under these conditions, electrostatic exclusion was the dominant NF rejection mechanism. This was also the leading mechanism for 0.1 mmol/L Fe coexisted condition. As the concentration of Fe increased to 0.5-1 mmol/L, intensified hydrolyzation would accelerate the formation of the cake layers. The differences in the cake layer characteristics led to the different rejection trends of PFBS. For anions (SO and PO), both sieving effects and electrostatic exclusion were enhanced. As anionic concentration raised, the NF rejection of PFBS increased to above 90.15%. By contrast, the effect of Cl on PFBS rejection was also affected by coexisting cations in the solution. The dominant NF rejection mechanism was electrostatic exclusion. Accordingly, it is suggested that the usage of negatively charged NF membranes could facilitate the efficient separation of PFBS under ionic coexisting conditions, thereby ensuring the safety of drinking water.