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Direct Visualization of the Hydration Layer on Alumina Nanoparticles with the Fluid Cell STEM in situ

机译:通过液位STEM直接观察氧化铝纳米颗粒上的水化层

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摘要

Rheological behavior of aqueous suspensions containing nanometer-sized powders is of relevance to many branches of industry. Unusually high viscosities observed for suspensions of nanoparticles compared to those of micron size powders cannot be explained by current viscosity models. Formation of so-called hydration layer on alumina nanoparticles in water was hypothesized, but never observed experimentally. We report here on the direct visualization of aqueous suspensions of alumina with the fluid cell in situ. We observe the hydration layer formed over the particle aggregates and show that such hydrated aggregates constitute new particle assemblies and affect the flow behavior of the suspensions. We discuss how these hydrated nanoclusters alter the effective solid content and the viscosity of nanostructured suspensions. Our findings elucidate the source of high viscosity observed for nanoparticle suspensions and are of direct relevance to many industrial sectors including materials, food, cosmetics, pharmaceutical among others employing colloidal slurries with nanometer-scale particles.
机译:含有纳米级粉末的水悬浮液的流变行为与许多工业部门有关。当前的粘度模型无法解释纳米颗粒悬浮液与微米级粉末相比异常高的粘度。假设在水中的氧化铝纳米颗粒上形成了所谓的水合层,但从未在实验中观察到。我们在这里报道了氧化铝与水细胞原位悬浮的水悬浮液的直接可视化。我们观察到在颗粒聚集体上形成的水合层,并表明这种水合聚集体构成了新的颗粒组装体并影响了悬浮液的流动行为。我们讨论了这些水合纳米团簇如何改变有效固体含量和纳米结构悬浮液的粘度。我们的发现阐明了纳米颗粒悬浮液所观察到的高粘度来源,并且与许多工业部门直接相关,包括材料,食品,化妆品,制药等,其中采用了具有纳米级颗粒的胶体浆料。

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