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The Isothermal and Nonisothermal Crystallization Kinetics and Morphology of Solvent-Precipitated Nylon 66

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Solvent-precipitated nylon 66 (SP PA66) is a key material used to fabricate microfiltration membranes. The crystallization kinetics and behavior of SP PA66 were investigated through differential scanning calorimetry (DSC), polarized… Click to show full abstract

Solvent-precipitated nylon 66 (SP PA66) is a key material used to fabricate microfiltration membranes. The crystallization kinetics and behavior of SP PA66 were investigated through differential scanning calorimetry (DSC), polarized optical microscopy (POM) and X-ray diffraction (XRD). The Avrami equation was used to describe the isothermal crystallization of SP PA66. Nonisothermal crystallization behaviors were analyzed using Avrami equations modified by Jeziorny, Ozawa and Mo. The Avrami analysis demonstrated that the k values of SP PA66 were higher than those of neat PA66. The n was between 2 and 3 indicating the presence of two- and three-dimensional mode with thermal nucleation. With an increasing cooling rate, the Jeziorny crystallization rate constant increased for SP PA66; however, the Ozawa model was not satisfactory for all SP PA66 samples. The Mo method suggested that SP PA66 had a faster crystallization rate than neat PA66 during the nonisothermal crystallization process. The solvents dissolved nylon 66, rearranged it and formed a regular hydrogen-bonded region. These regions served as nucleation sites and increased the crystallization rate constant in the subsequent melting process. The crystal morphology of the SP PA66 under the POM investigation exhibited Maltese cross spherulites. The sizes of the spherulites of SP PA66 were significantly smaller than those of neat PA66. Wide-angle XRD revealed that SP PA66 had the same crystal structure and a higher crystal perfection than neat PA66.

Keywords: pa66; crystallization; nonisothermal crystallization; precipitated nylon; crystallization kinetics; solvent precipitated

Journal Title: Polymers
Year Published: 2022

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