Thermally induced phase separation PVDF membrane fabricated by using NaCl coagulation bath: relation of membrane surface morphology and permeation performance

Abstract

Efforts have been made in thermally induced phase separation (TIPS) process to modify the morphology of polyvinylidene fluoride (PVDF) membranes in order to improve their permeation performance and mechanical properties. Nevertheless, many methods not only altered the outer surface but also impacted the overall membrane structure, resulting in a trade-off between permeability and mechanical properties. In this study, we utilized a modified TIPS process to refine the outer surface morphology without altering the bulk structure. This was achieved by introducing NaCl in the coagulation bath. The PVDF membranes were fabricated using a dope with water insoluble diluent dimethyl phthalate (DMP) as main solvent and water-soluble additives polyethylene glycol 400 (PEG400)/triethylene glycol (TEG) as pore formers. The inclusion of NaCl in the coagulation bath serves to decrease the solubility of PEG within this medium, owing to the salting-out effect. Consequently, the NaCl concentration in the coagulation bath emerges as a crucial factor in regulating the migration of PEG400 toward the membrane surface. This control mechanism facilitates the precise adjustment of the outer surface morphology in the fabrication of membranes. As the NaCl concentration increases in the coagulation bath, the outer surface of the fabricated membrane transited from a mesh-like structure to a spherulite structure. As 0.5 mol L−1 NaCl was added to the coagulation bath, the membranes displayed a pure water permeability of 1073.9 L m−2 h−1 bar−1 while maintaining a narrow pore size distribution. Compared to the membranes fabricated without NaCl addition, the increment of the PWP contributed to the slight increase in mean pore size from 65 nm to 84 nm. Meanwhile, the water-insoluble diluent DMP was not affected by the addition of NaCl, which means that the bulk structure of the membrane could be maintained. Consequently, the increase in permeability did not compromise the mechanical properties of the membranes. All the membranes fabricated in this study maintained a reasonable tensile strength of approximately 3 MPa. This study introduces a simple and environmental method to increase the permeability effectively and fine-tune the pore size of the TIPS membranes while having little effect on the bulk structure. Furthermore, the study provides valuable insights into how changes in outer surface morphology can impact the pore size and permeability of TIPS PVDF membranes.