Dawelbeit Ahmed, Yu Muhuo
State Key Laboratory for Modification of Chemical Fibres and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China.
Materials (Basel). 2021 May 29;14(11):2938. doi: 10.3390/ma14112938.
A temporary confinement of the quaternary tetramethylammonium tetrafluoroborate (TMA BF) salt among polyamide molecules has been used for the preparation of aliphatic polyamide nylon 6,6 fibres with high-modulus and high-strength properties. In this method, the suppression or the weakening of the hydrogen bonds between the nylon 6,6 segments has been applied during the conventional low-speed melt spinning process. Thereafter, after the complete hot-drawing stage, the quaternary ammonium salt is fully extracted from the drawn 3 wt.% salt-confined fibres and the nascent fibres are, subsequently, thermally stabilized. The structural developments that are acquired in the confined-nylon 6,6 fibres are ascribed to the developments of the overall fibres' properties due to the confinement process. Surprisingly, unlike the neat nylon 6,6 fibres, the X-ray diffraction (XRD) patterns of the as-spun salt-confined fibres have shown diminishing of the (110)/(010) diffraction plane that obtained pseudohexagonal-like β' structural phase. Moreover, the β' pseudohexagonal-like to α triclinic phase transitions took-place due to the hot-drawing stage (draw-induced phase transitions). Interestingly, the hot-drawing of the as-spun salt-confined nylon 6,6 fibres achieved the same maximum draw ratio of 5.5 at all of the drawing temperatures of 120, 140 and 160 °C. The developments that happened produced the improved values of 43.32 cN/dtex for the tensile-modulus and 6.99 cN/dtex for the tensile-strength of the reverted fibres. The influences of the TMA BF salt on the structural developments of the crystal orientations, on the morphological structures and on the improvements of the tensile properties of the nylon 6,6 fibres have been intensively studied.
将四甲基四氟硼酸铵(TMA BF)盐暂时限制在聚酰胺分子之间,已用于制备具有高模量和高强度性能的脂肪族聚酰胺尼龙6,6纤维。在该方法中,在传统的低速熔体纺丝过程中,尼龙6,6链段之间的氢键被抑制或减弱。此后,在完全热拉伸阶段之后,从拉伸的3 wt.%盐限制纤维中完全提取季铵盐,随后将初生纤维进行热稳定处理。受限尼龙6,6纤维中获得的结构发展归因于受限过程导致的整体纤维性能的发展。令人惊讶的是,与纯尼龙6,6纤维不同,初纺盐限制纤维的X射线衍射(XRD)图谱显示获得假六方状β'结构相的(110)/(010)衍射面减弱。此外,由于热拉伸阶段(拉伸诱导相变),发生了从β'假六方相向α三斜相的转变。有趣的是,在120、140和160 °C的所有拉伸温度下,初纺盐限制尼龙6,6纤维的热拉伸均实现了相同的最大拉伸比5.5。所发生的发展使回复纤维的拉伸模量提高到43.32 cN/dtex,拉伸强度提高到6.99 cN/dtex。深入研究了TMA BF盐对尼龙6,6纤维晶体取向的结构发展、形态结构以及拉伸性能改善的影响。