Non-isothermal crystallization and thermal degradation studies on nylons 7,10 and 10,7 as isomeric odd-even and even-odd polyamides

• Published in: Thermochimica acta Vol. 735; p. 179721
• Main Authors: Arioli, Matteo, Franco, Lourdes, Puiggalí, Jordi
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.05.2024
• Subjects: Activation energy; Crystallization kinetics; Isoconversional methods; Non-isothermal processes; Nylons; Polyamides; Thermal degradation mechanism; Thermal degradation mechanism; Crystallization kinetics; Polyamides; Nylons; Isoconversional methods; Activation energy; Non-isothermal processes
• ISSN: 0040-6031; 1872-762X
• DOI: 10.1016/j.tca.2024.179721

•Crystallization of nylons 7,10 and 10,7 was simulated by isoconversional methods.•Crystallization rates of isomeric nylons depended on the disposition of amide groups.•Thermal degradation of nylons 7,10 and 10,7 followed an Avrami mechanism.•Simple and complex degradation mechanisms were found for nylons 7,10 and 10,7. Aliphatic polyamides (nylons) show a remarkable variability in terms of crystallographic structures, polymorphic transitions and crystal morphology despite all polymers of this family have a simple constitution that is based on amide groups and polymethylene segments. Nylons derived from diamines and dicarboxylic acids having different parity (e.g., even or odd) have peculiar characteristics due to the difficulty of establishing an optimal hydrogen-bonding geometry when molecular chains adopt a typical all trans conformation. In this work, two isomeric odd-even (nylon 7,10) and even-odd (nylon 10,7) polyamides with the same methylene/amide ratio have been studied. Specifically, crystallization kinetics have been evaluated from calorimetric data, while thermal degradation mechanisms from thermogravimetric analysis. Classical methods (e.g., Avrami) together with isoconversional analyses have been considered for crystallization studies, being found significant differences between both nylons in terms of nucleation and activation energies. The isoconversional analyses of the non-isothermal crystallization allowed to determine the temperature dependence of both the crystal growth and the overall crystallization rate that points out the slower crystallization process of nylon 10,7. Isoconversional methods (integral and differential) were applied to evaluate thermal degradation. The mechanism was similar for both nylons (e.g., A3/2 and A1.8 for nylons 7,10 and 10,7, respectively), although a remarkable difference was determined for the corresponding activation energies (175 and 210 kJ/mol for nylons 7,10 and 10,7, respectively).