小角X射线散射
成核
散射
相(物质)
化学
结晶学
水溶液
化学物理
摩尔质量
光散射
静态光散射
动能
同系序列
分子
分析化学(期刊)
材料科学
物理化学
光学
色谱法
有机化学
物理
聚合物
量子力学
作者
Rolf Michels,G. Goerigk,Ulla Vainio,Jérémie Gummel,Klaus Huber
摘要
The formation of azo dyestuff aggregates in dilute aqueous solution induced by the addition of Mg 2+, Ca 2+, Sr 2+, or Ba 2+ ions is followed by time-resolved static light scattering (SLS) and time-resolved small-angle X-ray scattering (SAXS). Time-dependent molar mass data of the growing aggregates is interpreted by means of a kinetic model introduced by Lomakin et al. ( Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 1125) for the description of β-amyloid aggregation. This interpretation reveals significant trends within the homologous series of alkaline earth cations. The trends refer to the nucleation and the growth rate of the dyestuff fibers. Time-resolved SAXS experiments indicate that these first two stages are followed by a third one during which a network forms by partial lateral alignment of fibers. At high enough dyestuff concentrations, this network formation even leads to a gel-like phase. Anomalous SAXS (ASAXS) on such a gel phase formed upon the addition of Sr 2+ revealed the extent of neutralization of the dyestuff molecules within the gel by the specifically interacting alkaline earth cations.
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