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Size-dependent solubility and phase transformation behavior of Sn-Cd nanoparticles in an Al matrix

机译:SN-CD纳米粒子在Al基质中的尺寸依赖性溶解度和相变行为

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Nanoscaled Sn-Cd alloy particles with a nominally equiatomic composition and size in the range of 5-120 nm, embedded in an Al matrix, have been synthesized by rapid solidification processing. The orientation relationship between tin, cadmium and aluminum is given by . Particles in the size range 5-25 nm display a single-phase hcp structure, while particles with size range of 25-120 nm size are found to be phase-separated into a tin-rich phase with bct structure and a cadmium-rich phase with hcp structure. In situ heating studies in the transmission electron microscope indicate that particles having a size range of 5-18 nm always display a single-phase microstructure right up to the melting point and subsequent cooling. The in situ heating experiments revealed complex pathways for transformation for particles having size between 18 and 30 nm. The as-solidified microstructures of over 75% of the particles analyzed, exhibit a two-phase structure in the melt-spun samples. While more than 75% of the particles analyzed by in situ heating and cooling experiments reveal formation of a single-phase structure during resolidification, some of the particles on cooling from molten state solidify into a two-phase microstructure of cadmium and tin solid solution. These particles, on cooling in the microscope, transform to single-phase particles of cadmium-rich solid solution around 110 A degrees C suggesting a kinetically dominated microstructure evolution. In contrast, the particles in the size range 30-120 nm exhibit a two-phase microstructure both during heating and cooling. Size-dependent alloying behavior of the particles could be explained based on models that consider capillary pressure and interfacial energies.
机译:通过快速凝固处理合成了具有名义上赤脂组成和5-120nm的尺寸的纳米级SN-CD合金颗粒,并通过快速凝固处理合成。锡,镉和铝之间的取向关系是给出的。尺寸范围内的颗粒5-25nm显示单相HCP结构,而具有25-120nm尺寸的尺寸范围的颗粒被发现与BCT结构和富镉相中相分离成富含锡的相使用HCP结构。在透射电子显微镜中的原位加热研究表明,尺寸范围为5-18nm的颗粒总是显示单相微观结构直到熔点和随后的冷却。原位加热实验揭示了用于转化的复杂途径,用于尺寸为18至30nm的粒子。在熔融纺样品中,分析的75%颗粒的颗粒的凝固微观结构具有两相结构。虽然通过原位加热和冷却实验分析的超过75%的颗粒,但在调节过程中揭示了形成单相结构的形成,其中一些颗粒在熔融状态冷却至镉和锡固溶溶液的两相微观结构中。这些颗粒在显微镜中冷却,转化为富含镉的固体溶液的单相颗粒,约110℃,表明动力学上占主导地层的微观结构进化。相反,尺寸范围内的颗粒30-120nm在加热和冷却期间表现出两相微观结构。可以基于考虑毛细管压力和界面能量的模型来解释颗粒的大小依赖合金化行为。

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