Challenges to Accurate Evaluation of Bulk Hardness from Nanoindentation Testing at Low Indent Depths

Pengcheng Zhu, Yajie Zhao, Shradha Agarwal, J. Hay, J. Henry, S. Zinkle
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引用次数: 1

Abstract

Estimations of bulk hardness from nanoindentation data are frequently subject to considerable uncertainties, due to indentation size effects, potential pileup effects, and potential influence of surface quality or test methods. In this study, we examined materials science principles of nanoindentation test methods to enable accurate prediction of bulk hardness for a series of high purity Fe and Fe alloys containing 3-25 wt. %Cr. These materials were tested in as-annealed and thermally aged (100-900 hours at 475 oC for 14-25 wt. %Cr) conditions to produce Cr-rich a’ precipitates of varying size and density (bulk Vickers hardness values of ~50 to 350 VHN). Nanoindentation performed with a Berkovich indenter using constant strain rate (0.05 to 0.5 /s) and constant loading rate test methods provided comparable bulk equivalent hardness (H0) extracted by Nix-Gao model, indicating a weak strain rate sensitivity of the investigated materials at room temperature. Results from electropolished and fine mechanically polished samples were found to give comparable measured hardness. Conversely, material pileup adjacent to the indented area produced a 7-20% correction to the indent contact area. The Nix-Gao fitted nanoindentation H0 after pileup corrections agreed quantitatively better with the bulk Vickers hardness than the uncorrected H0 values. The model-predicted (dispersed barrier hardening superposition) and measured strength values agreed for aged Fe18Cr, indicating that Nix-Gao model combined with pileup corrections significantly improved the accuracy of hardness evaluation by nanoindentation. Analytic and experimental analyses demonstrate that inappropriate methods such as hardness ratios or changes at a reference depth (applied in many prior nanoindentation studies) can cause quantitative errors in bulk hardness estimates as large as 60% due to indentation size effects.
低压痕深度纳米压痕测试中准确评估体硬度的挑战
由于压痕尺寸效应、潜在的堆积效应以及表面质量或测试方法的潜在影响,从纳米压痕数据中估计体硬度经常受到相当大的不确定性。在这项研究中,我们研究了纳米压痕测试方法的材料科学原理,以便准确预测一系列含3- 25wt . %Cr的高纯铁和铁合金的体硬度。这些材料在退火和热时效(在475℃,14- 25wt . %Cr, 100-900小时)条件下进行测试,产生不同尺寸和密度的富Cr a '沉淀(体维氏硬度值约50至350 VHN)。采用恒应变速率(0.05 ~ 0.5 /s)和恒加载速率测试方法使用Berkovich压头进行纳米压痕测试,获得的体等效硬度(H0)与采用Nix-Gao模型提取的硬度相当,表明所研究材料在室温下应变速率敏感性较弱。结果发现,电抛光和精细机械抛光样品的测量硬度相当。相反,靠近压痕区域的材料堆积会对压痕接触区域产生7-20%的修正。与未校正的H0值相比,经过堆积校正后的Nix-Gao拟合的纳米压痕H0值与体维氏硬度的定量一致性更好。时效Fe18Cr的模型预测值(分散障碍硬化叠加)与实测值一致,表明结合堆积修正的Nix-Gao模型显著提高了纳米压痕硬度评估的准确性。分析和实验分析表明,不适当的方法,如硬度比或参考深度的变化(在许多先前的纳米压痕研究中应用)可能导致由于压痕尺寸影响而导致体硬度估计的定量误差高达60%。
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