共聚物
材料科学
聚结(物理)
粒径
动态光散射
聚苯乙烯
化学工程
高分子化学
剪切速率
退火(玻璃)
胶束
增容
聚合物混合物
聚合物
纳米颗粒
复合材料
化学
纳米技术
流变学
物理化学
水溶液
工程类
天体生物学
物理
作者
C. W. Macosko,Philippe Guégan,Ashish K. Khandpur,Akinari Nakayama,Philippe Maréchal,Takashi Inoue
出处
期刊:Macromolecules
[American Chemical Society]
日期:1996-01-01
卷期号:29 (17): 5590-5598
被引量:431
摘要
Poly(methyl methacrylate) (PMMA) was melt mixed 30:70 into polystyrene (PS) with and without symmetric P(S-b-MMA) diblock copolymers. The molecular weight of the components was varied. After 5 min of shear mixing, the PMMA was dispersed into roughly spherical, submicron particles. Particle size was measured by light scattering and transmission electron microscopy. As little as 1% copolymer led to a significant reduction in PMMA particle size, although larger amounts were needed to make the particles stable to annealing (180 °C for 15 min). The principle role of block copolymers in controlling morphology appears to be in preventing coalescence. Preventing dynamic coalescence leads to size reduction, while preventing static coalescence results in stability or compatibilization. We estimate that less than 5% of the interface needs to be covered to prevent dynamic coalescence while ∼20% is necessary to impart static stability. Mobility, critical micelle concentration, and molecular weight of the block copolymer also appear to be important. Lowering the molecular weight of the PMMA phase from 43 000 to 11 000 resulted in dramatically lower particle size (700 vs 60 nm). These variables are discussed in terms of a qualitative balance between rate of diffusion and rate of area generation during blending.
科研通智能强力驱动
Strongly Powered by AbleSci AI