小角X射线散射
聚合物
成核
材料科学
微流控
毫秒
动力学
化学工程
扩散
乙二醇
化学物理
高分子化学
散射
纳米技术
化学
有机化学
热力学
光学
复合材料
工程类
物理
天文
量子力学
作者
Joseph Kalkowski,Chang Liu,Paola León-Plata,Magdalena Szymusiak,Pin Zhang,Thomas C. Irving,Weifeng Shang,Osman Bilsel,Ying Liu
出处
期刊:Macromolecules
[American Chemical Society]
日期:2019-04-15
卷期号:52 (9): 3151-3157
被引量:23
标识
DOI:10.1021/acs.macromol.8b02257
摘要
Utilizing synchrotron small-angle X-ray scattering (SAXS) integrated with a microfluidic device, micellization kinetics of a diblock co-polymer, poly(ethylene glycol)- b -poly(caprolactone), was measured in situ with millisecond temporal and micrometer spatial resolution. The evolutionary regimes of polymer micellization, nucleation, fusion, and insertion were directly observed. The five-inlet microfluidic device provided steady continuous mixing of the polymer solution and the antisolvent. The solvent replacement was mainly dominated by lateral diffusion across the hydrodynamically focused central layer, whose thickness could be precisely designed and manipulated from the mass balance of the partitioning streams. Knowing the micellization kinetics of the polymers is essential for the design and optimization of self-assembled polymeric nanostructures. The technique of integrating SAXS with microfluidic devices can be translatable to other systems for a breadth of applications.
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