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Effect of pelletization pressure on the physical and mechanical properties of (Bi, Pb)-2223 superconductors

机译:颗粒化压力对(Bi,Pb)-2223超导体物理和力学性能的影响

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Conventional solid-state reaction technique was used to prepare bulk samples with nominal composition of (Bi, Pb)(2)Sr2Ca2Cu3O10+delta superconductors. The prepared powder was pelletized at different pressure (P = 0.3, 0.7, 1.0, 1.4 and 1.9 GPa) before the calcination process. Structural parameters and phase purity were evaluated using x-ray diffraction (XRD). The formation of the tetragonal major phase is improved with increasing the pelletization pressure up to 1.4 GPa. The morphology and elemental compositions were performed by using scanning electron microscope (SEM) and energy dispersive x-ray spectroscopy (EDX), respectively. The results showed the enhancement of the grain alignment at an optimum pelletization pressure of 1.4 GPa with a decrease in the porosity percentages. Superconducting transition temperature (T-c) and the critical current density (J(c)) were obtained by means of DC electrical resistivity and the voltage-current characteristic, respectively. Both T-c and J(c) are improved with increase the pelletization pressure up to 1.4 GPa. Room temperature Vickers microhardness H-v measurement was performed at different applied loads (0.245-9.8 N) and times (10-60 s). As a result of the H-v measurements, all the prepared samples have a normal indentation size effect behaviour. It was found that P = 1.4 GPa was the optimal pressure to improve the microhardness in the (Bi, Pb)-2223 phase. The measured H-v data were theoretically analysed using Meyer's law, the Hays-Kendall approach, the elastic plastic deformation model and the proportional sample resistance. The last model was recognized to be the best theoretical one describing the true H-v values for the considered phase. Room temperature indentation creep analysis was also performed using time-dependent microhardness to identify the operative creep mechanisms in the measured samples.
机译:使用常规的固态反应技术用(Bi,Pb)(2)Sr2Ca2Cu3O10 + Delta超导体的标称组成制备批量样品。在煅烧过程之前,将制备的粉末在不同的压力下造粒(P = 0.3,0.7,1.0,1.4和1.9GPa)。使用X射线衍射(XRD)评估结构参数和相纯度。随着高达1.4GPa的颗粒化压力增加,改善了四边形主相的形成。通过使用扫描电子显微镜(SEM)和能量分散X射线光谱(EDX)来进行形态和元素组合物。结果表明,在孔隙率百分比下降的最佳颗粒化压力下,在最佳颗粒化压力下提高晶粒对准。通过DC电阻率和电压电流特性获得超导转变温度(T-C)和临界电流密度(J(C))。 T-C和J(c)都提高了高达1.4GPa的造粒压力。室温Vickers微硬度H-V测量在不同施加的载荷(0.245-9.8n)和时间(10-60s)下进行。由于H-V测量,所有制备的样品都具有正常的凹口尺寸效应行为。发现P = 1.4 GPA是改善(Bi,Pb)-2223相中的微硬度的最佳压力。使用Meyer的定律,Hays-Kendall方法,弹性塑性变形模型和比例样品电阻理论上分析了测量的H-V数据。最后一个模型被认为是描述所考虑的阶段真正的H-V值的最佳理论上。室温缩进蠕变分析也使用时间依赖性微硬度进行,以鉴定测量样品中的操作蠕变机制。

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