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Investigation of phase composition and nanoscale microstructure of high-energy ball-milled MgCu sample

机译:高能球磨MgCu样品的相组成和纳米级微观结构研究

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The ball milling technique has been successfully applied to the synthesis of various materials such as equilibrium intermetallic phases, amorphous compounds, nanocrystalline materials, or metastable crystalline phases. However, how the phase composition and nanoscale microstructure evolute during ball milling in various materials is still controversial due to the complex mechanism of ball milling, especially in the field of solid-state amorphization caused by ball milling. In the present work, the phase evolution during the high-energy ball milling process of the Mg and Cu (atomic ratio is 1:1) mixed powder was investigated. It was found that Mg firstly reacts with Cu, forming the Mg~(2)Cu alloy in the primary stage of ball milling. As the milling time increases, the diffracted peaks of Mg~(2)Cu and Cu gradually disappear, and only a broad halo peak can be observed in the X-ray diffraction pattern of the final 18-h milled sample. As for this halo peak, lots of previous studies suggested that it originated from the amorphous phase formed during the ball milling. Here, a different opinion that this halo peak results from the very small size of crystals is proposed: As the ball milling time increases, the sizes of Mg~(2)Cu and Cu crystals become smaller and smaller, so the diffracted peaks of Mg~(2)Cu and Cu become broader and broader and result in their overlap between 39° and 45°, at last forming the amorphous-like halo peak. In order to determine the origin of this halo peak, microstructure observation and annealing experiment on the milled sample were carried out. In the transmission electron microscopy dark-field image of the milled sample, lots of very small nanocrystals (below 20?nm) identified as Mg~(2)Cu and Cu were found. Moreover, in the differential scanning calorimetry curve of the milled sample during the annealing process, no obvious exothermic peak corresponding to the crystallization of amorphous phase is observed. All the above results confirm that the broad halo diffracted peak in the milled MgCu sample is attributed to the overlap of the broadened peaks of the very small Mg~(2)Cu and Cu nanocrystalline phase, not the MgCu amorphous phase. The whole milling process of MgCu can be described as follows: Mg + Cu → Mg 2 Cu + Cu → Mg 2 Cu nanocrystal + Cu nanocrystal .
机译:球磨技术已经成功地应用于各种材料的合成,例如平衡金属间相,非晶态化合物,纳米晶体材料或亚稳晶相。然而,由于球磨的复杂机理,尤其是在由球磨引起的固态非晶化领域,在各种材料的球磨过程中相组成和纳米级微观结构如何演变仍存在争议。在本工作中,研究了Mg和Cu(原子比为1:1)混合粉末在高能球磨过程中的相变。研究发现,Mg首先与Cu发生反应,在球磨的初期形成Mg〜(2)Cu合金。随着研磨时间的增加,Mg〜(2)Cu和Cu的衍射峰逐渐消失,最终的18h研磨样品的X射线衍射图中只能观察到宽的光晕峰。至于这个晕峰,许多先前的研究表明,它是由球磨过程中形成的非晶相引起的。在这里,提出了一个不同的观点,认为该晕峰是由非常小的晶体尺寸引起的:随着球磨时间的增加,Mg〜(2)Cu和Cu晶体的尺寸越来越小,因此Mg的衍射峰〜(2)Cu和Cu变得越来越宽,导致它们在39°和45°之间重叠,最后形成了无定形的晕峰。为了确定该晕峰的起源,对研磨后的样品进行了显微组织观察和退火实验。在研磨后的样品的透射电子显微镜暗场图像中,发现了许多非常小的纳米晶体(20?nm以下),被识别为Mg〜(2)Cu和Cu。此外,在退火过程中的研磨样品的差示扫描量热曲线中,未观察到明显的放热峰,该放热峰对应于非晶相的结晶。所有以上结果证实,研磨后的MgCu样品中宽的光晕衍射峰归因于极小的Mg〜(2)Cu和Cu纳米晶相而不是MgCu非晶相的宽峰的重叠。 MgCu的整个研磨过程可以描述为:Mg + Cu→Mg 2 Cu + Cu→Mg 2 Cu纳米晶+ Cu纳米晶。

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