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Investigating the membrane morphology of water/solvent/nylon 6 systems
Author(s) -
Sobhanipour Payman,
Karimi Mohammad
Publication year - 2012
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.38328
Subject(s) - membrane , crystallization , differential scanning calorimetry , chemical engineering , morphology (biology) , solvent , polymer chemistry , materials science , scanning electron microscope , phase (matter) , formic acid , chemistry , chromatography , organic chemistry , composite material , genetics , biology , engineering , biochemistry , physics , thermodynamics
In this study, nylon 6 membranes were prepared in a water coagulation bath with two types of solvents, CaCl 2 –methanol (CaClMe) and formic acid (FA). The morphology of the membranes, which was controlled by the phase behavior of their solutions, were connected to the mechanism of demixing, including liquid–liquid and liquid‐crystallization. Ternary phase diagrams showed that the CaClMe system coagulated significantly faster than the FA system. As observed by scanning electron microscopy, the CaClMe membrane had a porous, interconnected pore structure with macrovoids, whereas the FA membrane had a dense, spherulitic surface with a closed cell morphology. The high reaction surface of the CaClMe membrane with dye molecules provided outstanding dye rejection. Also, thermal analysis by differential scanning calorimetry showed that the slow coagulation of the FA system facilitated the formation of stable α‐form crystals rather than a metastable γ‐form structure. The results show that the phase‐separation mechanism was switched from liquid–liquid to liquid‐crystallization through a change in the solvent type from CaClMe to FA. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013