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The present study deals with the characterization of the polymeric materials viz., nylon‐66 and 30% glass fibre reinforced nylon‐66 (GF Nylon‐66) by employing FTIR and thermal measurements. The complete vibrational band assignment made available for nylon‐66 and GF nylon‐66 using FTIR spectra confirm their chemical structure. FTIR spectroscopy provides detailed information on polymer structure through the characteristic vibrational energies of the various groups present in the molecule. The thermal behavior of nylon‐66 and GF nylon‐66 essential for proper processing and fabrication was studied from TGA and DTA thermograms. The thermal stability of the polymers was studied from TGA and the activation energy for the degradation of the polymeric materials was calculated using Murray‐White plot and Coats‐Redfern plot. The polymer with high activation energy is more thermally stable. GF nylon‐66 is found to be more thermally stable than nylon‐66. The major thermal transitions such as crystalline melting temperature (T m ) and degradation temperature (T d ) of the polymers were detected from DTA curves. The melting behaviour of the polymer depends upon the specimen history and in particular upon the temperature of crystallization. The melting behaviour also depends upon the rate at which the specimen is heated. The various factors such as molar mass and degree of chain branching govern the value of T m in different polymers.
Charles et al. (Sun,) studied this question.