成核
材料科学
聚丙烯
有机磷
铝
钠
硬脂酸盐
化学工程
复合材料
高分子化学
高分子科学
化学
有机化学
冶金
工程类
杀虫剂
生物
农学
作者
Li Jiao,Xin Meng,Chenyang Li,Jiang Wang,Jingyu Wang,Pu Du,Yichen Xu
摘要
ABSTRACT Bis [2,2′‐methylene‐bis(4,6‐di‐tert‐butylphenoxy) phosphoric acid] hydroxyl aluminum (OPAl) is a promising α‐nucleating agent for improving the crystallization and mechanical properties of impact polypropylene copolymer (IPC). However, its poor dispersion due to agglomeration limits its effectiveness. To address this, sodium stearate (NaSt) was introduced to form a composite nucleating system (OPAl‐NaSt). In situ variable‐temperature FTIR revealed a red shift and broadening of the carboxylate (COO − ) peak, confirming hydrogen bond formation between OPAl and NaSt. This interaction enhanced OPAl dispersion in the nonpolar IPC matrix. SEM and molecular dynamics simulations further supported the improved dispersion and molecular compatibility. DSC analysis showed a 16.1°C increase in crystallization peak temperature, indicating faster crystallization, while POM revealed refined spherulite structures. The reduced crystallization activation energy confirmed enhanced crystallization kinetics. As a result, the mechanical properties of IPC improved significantly: tensile strength increased by 12.8%, flexural modulus by 37.9%, and impact strength by 16.7%. The OPAl‐NaSt system outperformed the commercial nucleating agent NA‐21. This study offers a cost‐effective strategy to achieve balanced rigidity and toughness in IPC through synergistic nucleation and dispersion control.
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