## Abstract Our previous work showed that drawing polyamide 66 (PA 66) fibers at room temperature does not change the degree of crystallinity, but only increases the molecular orientation. We therefore have used a series PA 66 fibers with different draw ratios to establish a direct correlation betw
Effect of the microstructure on the dye diffusion and mechanical properties of polyamide-6 fibers
β Scribed by N. Vasanthan
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 158 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0887-6266
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β¦ Synopsis
Abstract
The morphology, mechanical properties, and dye diffusion of drawn and heatβset polyamideβ6 (PA6) yarns were examined. Correlations between the microstructure of PA6 yarns and the dye diffusion coefficients and mechanical properties were established. The crystallinity of PA6 yarns was estimated with density and Fourier transform infrared spectroscopy measurements. A decrease in the Ξ³ crystallinity and an increase in the Ξ³βcrystallite size with the draw ratio were observed and attributed to the disappearance of small crystallites and an increase in the average Ξ³βcrystallite size population during the deformation process. The scouring treatment increased the total crystallinity, almost entirely as a result of an increase in the Ξ± fraction. Thermally induced crystallization involved increases in both crystalline phases (Ξ± and Ξ³) and did not involve crystalβtoβcrystal transformation, whereas drawing PA6 yarns involved both crystallization of the amorphous phase in the Ξ± form and Ξ³βΞ± transformation. A sharp decrease in the diffusion coefficient with an increasing draw ratio of PA6 yarns was correlated with an increasing amorphous orientation. The influence of thermally induced crystallinity on the diffusion coefficient seemed exceptionally strong. The mechanical properties of PA6 yarns were examined and correlated with structural changes. It was demonstrated that the crystallinity had a direct correlation with the terminal modulus and extension at break, whereas there was no correlation with the initial modulus. Β© 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 349β357, 2007
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