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首页> 外文期刊>Journal of Materials Engineering and Performance >Comparison of Optical and SEM-BEI Inclusion Analyses of VIM-VAR Nickel-Titanium Alloy
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Comparison of Optical and SEM-BEI Inclusion Analyses of VIM-VAR Nickel-Titanium Alloy

机译:VIM-VAR镍钛合金的光学和SEM-BEI夹杂物分析的比较

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The ASTM Standard for NiTi alloys does not specify the method to be used for the analysis of inclusions. Quantitative analysis is generally done by optical metallography with a computer program to measure size and area fraction. This study gives a comparison of quantitative analyses of inclusions by scanning electron microscopy using backscattered electron imaging (SEM-BEI) and quantitative analyses by optical metal-lography. Seven samples of 6.3-mm hot-rolled NiTi were evaluated. The coil samples were selected to exhibit a wide range of inclusion content. Each sample had a different Ni to Ti ratio corresponding to a different transformation temperature range (TTR) from A_s = -25℃ (Ni = 50.79 a/o) to A_s = +95℃ (Ni = 49.63 a/o). Quantitative analyses by optical and by SEM-BEI are in reasonable good agreement for maximum particle size and maximum area fraction. Both methods of analysis show that carbide and intermetallic oxide inclusion populations in VIM-VAR hot-rolled coil vary significantly in the amount and size of inclusions with the alloy transformation temperature. Therefore, an analysis of a larger number of samples at each TTR is needed to develop statistically precise data. All carbide inclusions were less than 12.5 μm and less than 1.0% area fraction in all the samples. Maximum size and area fraction of carbides decreased as TTR increased. Intermetallic oxide size and area fraction increased with increasing TTR Intermetallic oxides are fractured and separated from the matrix during hot working. However, stringering is very limited. The fracturing appears to happen in high TTR alloys but not in low TTR alloys. This dependence on TTR suggests that chemistry in or around the oxides affects their fracture behavior.
机译:NiTi合金的ASTM标准未指定用于分析夹杂物的方法。定量分析通常通过光学金相学和计算机程序来完成,以测量尺寸和面积分数。本研究比较了使用背向散射电子成像(SEM-BEI)的扫描电子显微镜对夹杂物的定量分析和光学金相分析的定量分析的比较。评估了七个6.3毫米热轧NiTi样品。选择线圈样品以表现出广泛的夹杂物含量。每个样品具有不同的镍钛比,对应于从A_s = -25℃(Ni = 50.79 a / o)到A_s = + 95℃(Ni = 49.63 a / o)的不同转变温度范围(TTR)。通过光学和SEM-BEI进行的定量分析在最大粒径和最大面积分数方面具有合理的良好一致性。两种分析方法均表明,VIM-VAR热轧卷材中碳化物和金属间氧化物的夹杂物数量随合金转变温度的变化而显着变化。因此,需要对每个TTR处的大量样本进行分析,以开发统计上精确的数据。在所有样品中,所有碳化物夹杂物均小于12.5μm,且面积分数小于1.0%。随着TTR的增加,碳化物的最大尺寸和面积分数减小。金属间氧化物的尺寸和面积分数随TTR的增加而增加。金属间氧化物在热加工过程中会破裂并与基体分离。但是,穿线非常有限。断裂似乎发生在高TTR合金中,而不发生在低TTR合金中。这种对TTR的依赖性表明,氧化物内部或周围的化学性质会影响其断裂行为。

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