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Real-time observation of cation exchange kinetics and dynamics at the muscovite-water interface

机译:实时观察白云母-水界面的阳离子交换动力学

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摘要

Ion exchange at charged solid–liquid interfaces is central to a broad range of chemical and transport phenomena. Real-time observations of adsorption/desorption at the molecular-scale elucidate exchange reaction pathways. Here we report temporal variation in the distribution of Rb+ species at the muscovite (001)–water interface during exchange with Na+. Time-resolved resonant anomalous X-ray reflectivity measurements at 25 °C reveal that Rb+ desorption occurs over several tens of seconds during which thermodynamically stable inner-sphere Rb+ slowly transforms to a less stable outer-sphere Rb+. In contrast, Rb+ adsorption is about twice as fast, proceeding from Rb+ in the bulk solution to the stable inner-sphere species. The Arrhenius plot of the adsorption/desorption rate constants measured from 9 to 55 °C shows that the pre-exponential factor for desorption is significantly smaller than that for adsorption, indicating that this reduced attempt frequency of cation detachment largely explains the slow cation exchange processes at the interface.
机译:带电固液界面的离子交换是广泛的化学和传输现象的中心。在分子尺度上的吸附/解吸的实时观察阐明了交换反应途径。在这里,我们报告了与Na + 交换期间白云母(001)-水界面处Rb + 物种分布的时间变化。在25°C下的时间分辨共振X射线反常反射率测量结果表明,Rb + 的解吸发生在数十秒内,在此期间热力学稳定的内球体Rb + 缓慢转变到不稳定的外球面Rb + 。相比之下,从本体溶液中的Rb + 到稳定的内球物质,Rb + 的吸附速度大约是原来的两倍。从9到55 C测得的吸附/解吸速率常数的Arrhenius图表明,解吸的前指数因子显着小于吸附的前指数因子,表明这种降低的阳离子分离尝试频率很大程度上解释了缓慢的阳离子交换过程在界面上。

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