结晶度
成核
结晶
乙二醇
材料科学
化学工程
石墨烯
氧化物
聚合物
环氧乙烷
纳米复合材料
晶体生长
Crystal(编程语言)
PEG比率
动力学
高分子化学
化学
纳米技术
结晶学
有机化学
复合材料
共聚物
物理
量子力学
工程类
程序设计语言
财务
计算机科学
经济
冶金
作者
Jia‐Zhuang Xu,Zijing Zhang,Huan Xu,Jing-Bin Chen,Rong Ran,Zhong‐Ming Li
出处
期刊:Macromolecules
[American Chemical Society]
日期:2015-07-14
卷期号:48 (14): 4891-4900
被引量:100
标识
DOI:10.1021/acs.macromol.5b00462
摘要
Nanofillers can act as effective heterogeneous nucleation agents for semicrystalline polymers; however, it never facilitates the crystal growth. In the current work, we proposed a facile strategy to enhance the crystallization kinetics of poly(l-lactic acid) (PLLA) by simultaneously accelerating the crystal nucleation and growth. Herein, we synthesized poly(ethylene glycol) (PEG) grafted graphene oxide (GO) (PEGgGO). Pronounced effects of PEGgGO on the crystalline morphology and crystallization rate of PLLA were explicitly clarified by direct morphological observation and quantitative crystallization kinetics analysis. The results manifested that, in contrast to the unmodified GO, PEGgGO desirably dispersed in PLLA and also preserved the high nucleation ability. More importantly, the flexible PEG chains on GO served as a chain mobility promoter and boosted the crystal growth rate of PLLA. Compared to the PLLA/GO nanocomposite containing 0.5 wt % GO, the nucleation density and crystal growth rate of the PLLA/PEGgGO one were increased by 110% and 14.3% at the crystallization temperature of 130 °C, respectively, leading to 52.2% relative augment in the final crystallinity. Our proposed methodology offers the flexibility of fabricating the polymer nanocomposits with well-dispersed nanofillers and also high crystallinity, by which the step toward the high-performance nanocomposites will be further.
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