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Modelling and Measurements of Densities at Solidification of Magnesium Casting Alloys

机译:镁铸造合金凝固时密度的建模与测量

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The purpose of this study is to provide experimental measurements of volume changes in commercial magnesium pressure die casting alloys, and to present a general methodology by which it is possible to make accurate calculations of the volume changes in the solidification interval of multi-component magnesium alloys. The density and volume changes are important in simulation of porosity formation in magnesium castings. Density measurements were made in a specialised push-rod dilatometer for both solid and liquid state. The solid density depends on the alloy composition. A most significant effect is due to aluminium which increases the density of the magnesium alloy. As an example, AZ91 (~9% Al) has 2.8% higher density than AM20 (~2% Al) at room temperature. At the liquidus temperature, AZ91 has 3.8% higher density than AM20. Above the melting temperature, an average of the densities at heating and cooling respectively, have been evaluated. The liquid expansion/contraction is in the region of 0.24 ― 0.27 kg/m~3·C or 1.54 ― 1.71 vol.% per 100℃ temperature change. The not direct accessible densities are appearing in the two-phase temperature region. The shrinkage at solidification can be measured until a dendrite network has formed. The fraction solid at this point, the coherency point, is normally around 0.25―0.4, depending on the solidification rate and mode. For the alloys investigated this shrinkage varies from about 0.92 to 3.45%. The following shrinkage has been modelled due to non measurable quantities of the densities in the melt and in solid. The measurements were used to validate models for the molar volumes. The difference between measured and modelled densities is in the range of 0.5%, which is smaller than the accuracy of the experiments. The density calculations have been fully coupled to a deterministic simulation of the solidification sequence including segregation of the elements.
机译:这项研究的目的是提供商品化镁压铸合金中体积变化的实验测量,并提供一种通用方法,通过该方法可以准确计算多组分镁合金凝固间隔中的体积变化。 。密度和体积变化对于模拟镁铸件中的孔隙形成非常重要。密度测量是在专用推杆膨胀仪中进行的,用于固态和液态。固体密度取决于合金成分。最显着的效果是由于铝增加了镁合金的密度。例如,在室温下,AZ91(〜9%Al)的密度比AM20(〜2%Al)高2.8%。在液相线温度下,AZ91的密度比AM20高3.8%。在熔化温度以上,分别评估了加热和冷却时的平均密度。每100℃温度变化,液体的膨胀/收缩在0.24〜0.27kg / m〜3·C或1.54〜1.71vol。%的范围内。不可直接访问的密度出现在两相温度区域中。可以测量凝固时的收缩率,直到形成树枝状网络。在这一点上的固体分数(凝聚点)通常约为0.25-0.4,这取决于凝固速率和模式。对于所研究的合金,收缩率在约0.92至3.45%之间变化。由于无法测量熔体和固体中的密度,因此对以下收缩率进行了建模。该测量用于验证摩尔体积的模型。测得的密度与模型密度之间的差异在0.5%的范围内,小于实验的准确性。密度计算已完全与凝固顺序的确定性模拟(包括元素隔离)耦合在一起。

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