Wang Jianing, Zhang Jing, Zhu Yanlong, Yang Shuo, Dong Zhenfeng, Zhang Xiuqin, Wang Rui
School of Materials Design & Engineering, Beijing Institute of Fashion Technology, Beijing 100029, China.
Beijing Key Laboratory of Clothing Materials R & D and Assessment, Beijing Engineering Research Center of Textile Nanofiber, Beijing Institute of Fashion Technology, Beijing 100029, China.
ACS Omega. 2025 May 8;10(19):19444-19452. doi: 10.1021/acsomega.4c11028. eCollection 2025 May 20.
Strong hydrogen bonding and the fast crystallization rate of polyamide 66 (PA66) bring difficulties in the fabrication of high-performance PA66 fibers. In this work, calcium chloride (CaCl) was used as a modifier to regulate the crystallization rate and drawing performance of PA66. With the increased presence of CaCl, the viscosity of PA66/CaCl increased, and the crystallization rate was significantly suppressed. At 5 wt % CaCl, the crystallinity decreased from 31.36 to 19.52%, indicating a notable inhibition effect. The isothermal FTIR mechanism studies elucidated that a blueshift of the N-H stretching vibration can be observed, which resulted from the complexation between Ca and the oxygen atoms on the amide groups disrupting the original hydrogen bond. The inhibition of hydrogen bonds promotes the fabrication of PA66 fiber with a draw ratio at 3.5 and a breaking strength at 5.16 cN/dtex. This work provides an effective way to enhance the spinnability and drawability of PA66 fibers.
聚酰胺66(PA66)强大的氢键作用和快速的结晶速率给高性能PA66纤维的制造带来了困难。在这项工作中,氯化钙(CaCl)被用作改性剂来调节PA66的结晶速率和拉伸性能。随着CaCl含量的增加,PA66/CaCl的粘度增大,结晶速率显著受到抑制。在CaCl含量为5 wt%时,结晶度从31.36%降至19.52%,表明有显著的抑制作用。等温傅里叶变换红外光谱(FTIR)机理研究表明,可以观察到N-H伸缩振动的蓝移,这是由于Ca与酰胺基团上的氧原子络合,破坏了原来的氢键。氢键的抑制促进了PA66纤维的制造,其拉伸比为3.5,断裂强度为5.16 cN/dtex。这项工作为提高PA66纤维的可纺性和拉伸性提供了一种有效方法。