“…Consequently, the nascent structure formed after the onset of phase separation should not be regarded as static, since structure‐forming effects can result from a steady mass transfer until solidification is reached . If a critical viscosity is reached, the polymer solution turns into a gel state and solidifies, as coalescence and other coarsening mechanisms are no longer possible …”
This work presents a comparative study on the formation of polyethersulfone ultrafiltration membranes via nonsolventinduced phase separation (NIPS) in two different solvent systems. N-methyl-2-pyrrolidone was chosen as conventional solvent and 2-pyrrolidone as a greener alternative. The overall objective was to obtain a mechanistic clarification of the membrane formation process in dependence of the most important controlling parameters. By performing different series of experiments, it was possible to determine the differences between the two solvents regarding the effects of variations in nonsolvent additives, polymer concentration, and precipitation conditions. It was found that a raising concentration of several nonsolvents, the increase of the polymer concentration and changes in the precipitation conditions can suppress the formation of macrovoids, regardless of the applied solvent. In contrast, differences were observed with regard to the performance of the membrane prototypes. This study improves the understanding of membrane formation via NIPS and identifies the effects of different variables. It shows that the choice of the solvent is essential for the dominating formation mechanisms and therefore for the resulting membrane features. It also proves that green solvents can substitute hazardous solvents if the influencing variables are well-understood in order to control them for obtaining desired membrane properties.
“…Consequently, the nascent structure formed after the onset of phase separation should not be regarded as static, since structure‐forming effects can result from a steady mass transfer until solidification is reached . If a critical viscosity is reached, the polymer solution turns into a gel state and solidifies, as coalescence and other coarsening mechanisms are no longer possible …”
This work presents a comparative study on the formation of polyethersulfone ultrafiltration membranes via nonsolventinduced phase separation (NIPS) in two different solvent systems. N-methyl-2-pyrrolidone was chosen as conventional solvent and 2-pyrrolidone as a greener alternative. The overall objective was to obtain a mechanistic clarification of the membrane formation process in dependence of the most important controlling parameters. By performing different series of experiments, it was possible to determine the differences between the two solvents regarding the effects of variations in nonsolvent additives, polymer concentration, and precipitation conditions. It was found that a raising concentration of several nonsolvents, the increase of the polymer concentration and changes in the precipitation conditions can suppress the formation of macrovoids, regardless of the applied solvent. In contrast, differences were observed with regard to the performance of the membrane prototypes. This study improves the understanding of membrane formation via NIPS and identifies the effects of different variables. It shows that the choice of the solvent is essential for the dominating formation mechanisms and therefore for the resulting membrane features. It also proves that green solvents can substitute hazardous solvents if the influencing variables are well-understood in order to control them for obtaining desired membrane properties.
“…As the polymer solution film immersed into a coagulation bath through this process, it undergoes phase separation into a polymer rich phase and a polymer lean phase. The phase separation would be continued until the polymer‐rich phase is solidified and the membrane structure is formed . It has been proposed by different researchers that the gelation is the main mechanism leading to skin formation through this technique by suppressing L‐L demixing due to kinetic hindering caused by the high viscosity of a gelled polymer solution in the skin of the membrane .…”
Section: Gelation Mechanismmentioning
confidence: 99%
“…To achieve a better control on the structures of the preferable membrane, well knowledge of the gelation and vitrification mechanisms of a particular system is essential. Thermodynamic investigations regarding study of polymer dissolution and gelation behavior in membrane formation systems has been of interests for different authors throughout the years . However, as different mechanisms affect thermoreversible gelation behavior of casting solutions more comprehensive studies should be done for well thermodynamic description of a ternary membrane fabrication system and how it affects membrane structure with emphasis on demixing and gelation behavior.…”
Section: Introductionmentioning
confidence: 99%
“…Li et al investigated the gelation and demixing behavior of PSF and poly(ether sulfone) (PES) amorphous polymers in a mixture of different solvents and water as nonsolvent. Kim et al studied the vitrification phenomena in the ternary system of PSF/N‐methyl‐2‐pyrrolidinone (NMP)/water using differential scanning calorimeter (DSC) measurements at different compositions. The related vitrification line was determined and related mechanisms were discussed.…”
“…In addition, as shown in Tables 1 and 2 Increasing of the solvent into the coagulation bath is more complex for CH 4 and N 2 gases. In the first case, the solvent tends to increase surface defects that causes the increase in the permeation of CH 4 [20,21]. Additionally, solvent causes delayed demixing which decreases highly the number of finger-like voids and eventually tends to decrease the permeances of gas molecules.…”
Section: Effect Of the Solvent Content Of The Coagulation Bathmentioning
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