材料科学
扩展器
己二酸
玻璃化转变
复合材料
炭黑
成核
弹性体
流变学
聚合物
化学工程
聚氨酯
有机化学
天然橡胶
化学
工程类
作者
Yi Li,Xiu‐Li Wang,Hongda Chen,Changyu Han,Dongdong Li
摘要
Abstract Different carbon black (CB) contents in poly(butylene adipate‐ co ‐terephthalate) (PBAT)/poly(3‐hydroxybutyrate‐ co ‐4‐hydroxybutyrate) (P34HB) blends were prepared by melt blending using chain extender multifunctional styrene‐acrylic‐ epoxy random oligomer (ADR), as a compatibilizer. PBAT and P34HB were immiscible, and ADR could react with PBAT and P34HB to improve interfacial adhesion force and molecular entanglement. CB fillers were uniformly and selectively located in the PBAT matrix and could act as a nucleating agent to promote the nucleation of PBAT crystallization. At a CB content of 5 wt%, a percolation network structure of CB was formed. The most interesting result in the work was the achievement of composites with improved rheological and mechanical properties under the synergistic effect of chain extender and CB fillers. The viscoelasticity of the system was markedly improved and a transition from liquid‐like to solid‐like behavior was observed. Young's modulus and yield strength of chain extender modified PBAT/P34HB/CB composite with 10 wt% CB increased by 502% and 69% compared to neat PBAT, and by 89% and 43% compared to PBAT/P34HB binary blend. The combination of improved melt viscoelasticity and mechanical properties will further broaden the practical application of biodegradable polymers. © 2024 Society of Industrial Chemistry.
科研通智能强力驱动
Strongly Powered by AbleSci AI