Liu Qi, Gao Huanhuan, Zha Liyun, Hu Zuming, Ma Yu, Yu Muhuo, Chen Lei, Hu Wenbing
Key Laboratory of High Performance Polymer Materials and Technology, State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Phys Chem Chem Phys. 2014 Aug 7;16(29):15152-7. doi: 10.1039/c4cp00792a.
The properties of polymer fibers are determined by their inner structures. We performed dynamic Monte Carlo simulations of early-stage solidification in the fluid filaments of stretched polymer solutions after extrusion into a coagulation bath upon fiber spinning. We observed that the radial temperature gradient dominates polymer crystallization to form an oriented crystalline skin (from single to multiple layers), while the radial non-solvent influx dominates phase separation to form a concentrated but less oriented core. The skin-core structure offers fibers a balanced performance between strength and toughness similar to plant stems, which can be tuned by the interplay of phase transitions. Our molecular-level observations facilitate a systematic understanding of the microscopic mechanism of fiber-spinning, which will pave a way towards making excellent polymer fibers.
聚合物纤维的性能由其内部结构决定。我们对拉伸聚合物溶液的流体细丝在纺丝过程中挤出到凝固浴后早期凝固过程进行了动态蒙特卡罗模拟。我们观察到,径向温度梯度主导聚合物结晶,形成取向结晶皮层(从单层到多层),而径向非溶剂流入主导相分离,形成浓缩但取向较差的芯部。皮层-芯部结构赋予纤维在强度和韧性之间的平衡性能,类似于植物茎干,这种性能可通过相变的相互作用进行调节。我们在分子水平上的观察有助于系统理解纺丝的微观机制,这将为制造优异的聚合物纤维铺平道路。