Gao Ling, Liu Haonan, Liang Xiaobin, Ito Makiko, Nakajima Ken
College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang, Hubei, China.
Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology, Tokyo, Japan.
Sci Technol Adv Mater. 2024 Sep 18;25(1):2402685. doi: 10.1080/14686996.2024.2402685. eCollection 2024.
Styrene-based ABA-type triblock copolymers and their blends are widely investigated thermoplastic elastomers (TPEs). The design of tough TPE materials with high strength and resilience requires further clarification of the relationship between microstructure and macroscopic properties of stretched samples. Here, we applied atomic force microscopy (AFM)-based quantitative nanomechanical mapping to study the deformation behavior of poly(styrene--isoprene--styrene) blends under tension. The results indicated that the glassy polystyrene (PS) domains deformed and inhomogeneous stress distributions developed in the initial stretching stage. At 200% strain, the glassy PS domains started to crack. The change in the peak value in the JKR Young's modulus diagram during stretching was consistent with the stress - strain curve. Analysis of the particles before and after stretching suggested that the glassy domains separated and reorganized during stretching.
苯乙烯基ABA型三嵌段共聚物及其共混物是广泛研究的热塑性弹性体(TPE)。设计具有高强度和回弹性的坚韧TPE材料需要进一步阐明拉伸样品的微观结构与宏观性能之间的关系。在此,我们应用基于原子力显微镜(AFM)的定量纳米力学映射来研究聚(苯乙烯-异戊二烯-苯乙烯)共混物在拉伸下的变形行为。结果表明,在初始拉伸阶段,玻璃态聚苯乙烯(PS)域发生变形并出现应力分布不均匀的情况。在200%应变时,玻璃态PS域开始出现裂纹。拉伸过程中JKR杨氏模量图中峰值的变化与应力-应变曲线一致。对拉伸前后颗粒的分析表明,玻璃态域在拉伸过程中发生分离和重组。