Introduction

The development of sustainable production methods is prompting resource-saving ways to produce load-bearing lightweight components. In this context, the use of secondary aluminum offers attractive opportunities, as up to 95% of the energy required for primary production can be saved.1 Secondary alloys fulfill the requirements in die casting and enable a cost-efficient production of complex components. Furthermore, AlZnMg(Cu) wrought alloys reach tensile strengths above 700 MPa; hence, these alloys satisfy the mechanical requirements in structural components.2 The alloying elements zinc, magnesium, and copper with a proportion of 0.5–2 wt.% form complex intermetallic phases that control the material properties and enable high hardenability and high strengths.3,4 First, the η-(MgZn2) phase must be mentioned, which is a hexagonal Laves phase in which extremely dense packings are formed due to favorable atomic radii.5 In dependence of the geometrical and chemical conditions, many possible stoichiometric compositions from MgZn2 to Mg(ZnAlCu)2 are possible, but the phase is usually specified with MgZn2.6 In this phase, zinc can be substituted by aluminum and copper, but high copper content has a destabilizing effect.6,7 In addition, the cubic T-(Al2Mg3Zn3), orthorhombic S-(Al2CuMg), and, at high zinc levels, cubic Z-(Mg2Zn11) phase can occur. Both η- and T-phases form a quasi-binary eutectic with aluminum. In general, the occurrence of these phases depends on the concentration ratio of Zn/Mg. At a ratio Zn/Mg > 2, the formation of η-(MgZn2) predominantly occurs; at Zn/Mg ≤ 2, T-(Al2Mg3Zn3) dominates.8 For a long time, only MgZn2 was investigated for precipitation strengthening. However, in most commercially used AlZnMg(Cu) alloys, both η- and T-phases occur. The Zn/Mg ratio and combined Zn + Mg content are crucial for the final properties of AlZnMg(Cu) alloys. With a Zn + Mg content of 2–5 wt.%, little or no hardening effect is present, whereas good castability is given only up to a Zn + Mg content of approximately 6 wt.%. Although high Zn + Mg contents lead to high strengths, they also increase the susceptibility to stress corrosion cracking.10

Copper affects the precipitation kinetics of the alloys and significantly increases the strength. At a ratio of Cu/Mg < 1 or a copper content < 2.5 wt.%, the element is predominantly dissolved in η- and T-phases.9 In the Al + η-(MgZn2) eutectic, 16–18 wt.% copper is soluble, which results from the high copper solubility of MgZn2. It promotes the formation of η-(Mg(Zn,Al,Cu)2), since more copper can be dissolved here than in T-(Al2Mg3Zn3) (27–28 wt.% Cu) 10. However, high copper contents cause the formation of S-(Al2CuMg), θ-(Al2Cu), and in combination with iron, of Al7Cu2Fe. Particularly for corrosive reasons, the formation of such phases is undesirable. Therefore, the complete solution of copper in η-(MgZn2) and T-(Al2Mg3Zn3) particles is preferred.

In the heat treatment, η-phases rapidly dissolve in the aluminum matrix. T- and S-phases show a more difficult solution behavior, which results from their higher formation temperatures.11 In general, the precipitation sequence of AlZnMg(Cu) alloys can be subdivided into:2,12

$$ \begin{aligned} & {\text{Supersaturated}}\;\alpha_{{{\text{Al}}}} \to {\text{clusters}} \to {\text{coherent}}\;{\text{GP(I),}}\;{\text{GP(II)}}\;{\text{zones}} \\ & \quad \to {\text{semicoherent}}\;\eta^{{\prime }} \to {\text{incoherent}}\;\eta {\text{ - (MgZn}}_{{2}} {)}\;{\text{or}}\;{\text{T } - \text{ }}\left( {{\text{Al}}_{{2}} {\text{Mg}}_{3} {\text{Zn}}_{3} } \right) \\ \end{aligned} $$

The casting of AlZnMg(Cu) alloys is known to be difficult. The large solidification interval and complex solidification morphology favor the formation of hot cracks. High cooling rates, as in gravity die casting or high-pressure die casting, can further increase the risk of hot cracking compared to sand casting.13,14

In this work, secondary AlZnMg(Cu) die-cast alloys are developed using thermodynamic simulations and casted into experimental tests. Then, the mechanical properties and microstructures of the materials are analyzed.

Experimental Methods

The selected alloys must simultaneously achieve casting, mechanical, and corrosion properties; therefore, the material development was supported by thermodynamic simulations. In those calculations, solidification processes and phase compositions of the materials were simulated (Table 1). With the selected Zn/Mg ratios, the formation of T-(Al2Mg3Zn3) was forced; therefore, the copper contents had to be adjusted to the lower copper solubility of the T-(Al2Mg3Zn3) phase (Table 2). As secondary alloys, these materials also contain iron, silicon, chromium, and manganese. The content of these accompanying elements in AlZn4Mg3Cu(Fe) is twice as high as in AlZn5Mg4Cu. This variation should give information about the influence of these elements on the phase formation. For grain refinement, titanium was used in AlZn4Mg3Cu(Fe), and TiB2 was used in AlZn5Mg4Cu to highlight the effectiveness of different grain refining elements.

Table 1 Nominal Compositions of the Experimental Alloys in wt.%
Table 2 Evaluation and Grain Refining Elements of the Experimental Alloys in wt.%

The alloys were prepared in a crucible furnace, and the chemical compositions were checked by a spectrometer analysis (Table 3). Then, the melts were degassed with argon for 45 min. The effectiveness of this treatment was verified by the vacuum density test. For this purpose, the samples were solidified under atmospheric (atm) and vacuum (80 mbar) pressure, from which the apparent densities and density index could be determined. In each case, a value of approximately 2.0 was achieved. The die casting tests were performed with a cold-chamber die casting machine (Table 4). The process was supported by a linear dosing system. An oil emulsion was used as the mold release agent and applied by a spraying equipment. A plate with different wall thicknesses of 3–14 mm served as a mold, but the material characterization was based on the 4 mm sections, as shown in Figure 1. To prevent hot cracks, the mold was tempered at a temperature of 300 °C by oil heating units. The die casting tests were performed without vacuum support.

Table 3 Actual Compositions of the Experimental Alloys in wt.%
Table 4 Casting Parameters
Figure 1
figure 1

Test specimen from the die castings.

Then, the castings were subjected to T6 and T73 heat treatment. AlZnMg(Cu) alloys are usually solutionized at temperatures between 460 and 480 °C for about 10 h. However, for die-cast products, the risk of blistering must be considered, and therefore, a lower temperature is preferred. To determine the optimum solutionizing temperature, preliminary tests were performed. Since blistering was observed at higher temperatures, it was finally set at 390 °C. After a short solutionizing of 2 h, the samples were immediately quenched in water at room temperature. Since long annealing and aging times are energy-consuming and uneconomical, T6 artificial aging was performed at high temperature with short aging time (Table 5), which resulted in an industrially attractive heat treatment (T6*). The T73 artificial aging process was based on literature references.2 After the artificial aging treatment, 6 tensile specimens per alloy and condition were prepared according to DIN 50125:2016-12-E3 × 8 × 30. The tests were performed in accordance with DIN EN ISO 6892-1:2017-02. For the metallographic analysis, the samples were taken from the centers transverse to the melt flow direction, ground with SiC paper, diamond polished, and finally polished with OP-S. Then, the microstructures could be examined with an optical microscope (OM). In addition, 5 hardness measurements were performed using DIN EN ISO 6507-1:2018-07. A more detailed microstructural analysis was executed with the scanning electron microscope (SEM), which was equipped with an energy-dispersive spectroscopy (EDS) detector. For this analysis, an accelerating voltage of 20 kV and the contrast of backscattered electrons were used. Finally, after electrolytic Barker etching, the grain sizes were evaluated in polarized light using the optical microscope. The electrolyte for etching consisted of 50% HBF4 acid with distilled water in a ratio of 1:20 using a voltage of 40 V, a flow rate of 12 l/min, and an etching time of 50 s.

Table 5 Heat Treatment Parameters

Results and Discussion

Since solidification conditions in high-pressure die casting allow extremely limited diffusion, the simulations could be calculated using the Scheil–Gulliver model. Therefore, no diffusion is assumed in the solid phase, but infinitely fast diffusion in the liquid phase and an equilibrium at the solid–liquid interface.15,16 The calculations show a delay of complete solidification due to the formation of segregations, which increases the risk of hot cracking. According to Scheil–Gulliver, solidification ends at approximately 475 °C with the formation of a complex eutectic of Al3Fe, Mg2Si, T-(AlCuMgZn), and aluminum. The alloy AlZn4Mg3Cu(Fe), as shown in Figure 2a, clearly shows a lower proportion of this eutectic than AlZn5Mg4Cu, as shown in Figure 2b, which is due to higher zinc and magnesium levels in the second variant. According to these simulations, the η-(MgZn2) phase does not occur in either variants. Furthermore, the solidification interval of AlZn4Mg3Cu(Fe) is approximately 65 °C higher than of AlZn5Mg4Cu. The higher proportion of the eutectic phase and lower solidification interval could benefit the castability of the alloy AlZn5Mg4Cu.

Figure 2
figure 2

Exemplary calculations of non-equilibrium phases according to Scheil–Gulliver, (a) AlZn4Mg3Cu(Fe) and (b) AlZn5Mg4Cu.

As mentioned, the copper distribution has a significant effect on the material properties of AlZnMg(Cu) alloys. Therefore, the dissolution behavior of the element was tested by an equilibrium simulation at 300 °C (Table 6). In the AlZn5Mg4Cu variant, copper is almost completely bound in the T-phase, which is consistent with the objective of alloy development. In AlZn4Mg3Cu(Fe), only approximately half of the copper is bound in the T-phase, and the remainder is dissolved in Al6Mn, αAl, and η-(MgZn2). The higher silicon content in AlZn4Mg3Cu(Fe) provides a higher proportion of Mg2Si; thus, a decrease in free magnesium is induced. Since this is accompanied by an increase in Zn/Mg ratio, the formation of the η-phase is promoted. The distribution of copper into several phases should significantly affect the material properties, which can be very critical with regard to corrosion.

Table 6 Calculation of 0.5 wt.% of Copper in an Equilibrium State at 300°C in %

The experimental tests can be summarized by two main points. First, it has been possible to process two extremely difficultly casted alloys by high-pressure die casting with no hot cracks observed in any product. Second, good mechanical properties were achieved in an energy-efficient manner, as shown in Figure 3. Although the mechanical properties of both alloys are similar as cast and in the T6* condition, the T73 variant of the alloy AlZn5Mg4Cu shows a significantly higher strength. Furthermore, the elongation of AlZn5Mg4Cu as cast is higher than that of AlZn4Mg3Cu(Fe). However, in the artificially aged conditions, the elongation of both materials drops to the same level. For a comparison, the standard die-cast alloy AlZn10Si8Mg17 and artificially aged alloys AlZn5Mg18 and AlZn8Mg2.6Cu2.619 are used, as shown in Figure 4. These reference alloys were not processed by high-pressure die casting but have higher contents of alloying elements or were subjected to energy-intensive heat treatment procedures (Table 7). The die-cast alloys AlZn4Mg3Cu(Fe) and AlZn5Mg4Cu achieve yield strengths of 208 MPa and 236 MPa, respectively, by an energy- and time-saving T6* aging. With a heat treatment time of only 12 h, a growth factor of 1.14 and 1.45 is realized. By using the T73 variant, the yield strength increases to 288 MPa (1.58) and 357 MPa (2.19), respectively. This strength is 10–15% lower than the maximum strength of an optimal T6 condition.20 The contents of zinc and magnesium increase the solid solution strengthening and precipitation strengthening; hence, the higher hardening potential of AlZn5Mg4Cu can be explained. Since there is an alloy-specific temperature dependency of the nucleation rate, at low temperatures, a multitude of finely distributed, small, coherent precipitates are formed and at high temperatures, there are rare, coarse, incoherent particles, as shown in Figure 5.21,22 According to this, the maximum strength values are achieved at comparatively low aging temperatures and long aging times. For example, the wrought alloy 7075 attains its maximum strength at a temperature of 120 °C and an aging time of 24 h.23 At higher temperatures, the achievable strengths are lower, but the aging time is significantly reduced.2,24 As a result, the control of both temperature and time is extremely important. This approach has great economic importance. However, the combination of high temperature and short aging time explains the T6* aging, which does not present the peak hardness of the alloys. During T73 aging, small, coherent precipitates are formed in the 1st stage at low temperature but grow to partially coherent particles in the 2nd stage. Therefore, the T73 condition is described as overaged. Although the T73 heat treatment process is energy- and time-intensive, it is particularly relevant for AlZnMg(Cu) alloys, since the highest resistance to stress corrosion cracking is achieved in this condition.

Figure 3
figure 3

Mechanical properties: yield strength, ultimate tensile strength, and elongation of the tested alloys.

Figure 4
figure 4

Mechanical properties: comparative analysis of yield strength and hardness values with heat treatment times and growth factors.17,18,19

Table 7 Heat Treatment Parameters of the Reference Alloys AlZn5Mg and AlZn8Mg2.6Cu2.618,19
Figure 5
figure 5

Schematic graph of the temperature dependency of the nucleation rate in precipitation strengthening.22

In optical microscopic analysis, AlZn4Mg3Cu(Fe) shows block-like particles, which indicate AlFe compounds, as shown in Figure 6. Furthermore, the eutectic regions are likely to be subdivided into MgZn and MgSi phases. However, the microstructure of the variant AlZn5Mg4Cu is more homogeneous without coarse particles, as shown in Figure 7. The scanning electron microscopic analysis confirms block-like AlFeSiCrMn phases in AlZn4Mg3Cu(Fe), as shown in Figure 8, which also contain levels of titanium and copper (Figure 9, Table 8). Although titanium was alloyed to refine αAl by the formation of Al3Ti, it is mainly found in the AlFeSiCrMn particles. The solidification simulation provides a possible indication. According to this result, Al3Ti, Al7Cr, and Al6Mn form a complex phase before the solidification of α-aluminum starts, which can affect the grain refinement. Other works have shown an interaction between chromium and titanium25 and a grain coarsening effect caused by chromium.26 In any case, the effect of iron-containing particles on the mechanical properties of aluminum alloys has been widely published: With an iron increase of 0.15%, the yield strength is not affected or can even be slightly enhanced27, but the elongation is reduced by more than 35%.28,29 This fact can explain the elongation ratios of the tested alloys. Furthermore, the eutectics show significant levels of zinc and magnesium; hence, ~ T-(Al2Mg3Zn3) precipitates can be identified. In addition, other eutectics such as ~ Mg2Si phases are detected. The frequent occurrence of ~ T-(Al2Mg3Zn3) and ~ Mg2Si is consistent with the simulative results and literature data.30 The characterization of AlZn5Mg4Cu shows no coarse AlFeSiCrMn phases like no other AlFeCr particles, as shown in Figure 10. Moreover, ~ Mg2Si phases are detected but less frequently than in AlZn4Mg3Cu(Fe), as shown in Figure 11a, due to the reduction in iron, manganese, chromium, and silicon. In addition, a higher proportion of eutectic regions can be identified in AlZn5Mg4Cu, which is consistent with the thermodynamic calculations. Besides ~ T-(Al2Mg3Zn3), as shown in Figure 11b, other complex eutectic compositions with iron, manganese, and silicon contents are detected using the X-ray analysis (Figure 12, Table 9). Since less zinc, magnesium, and copper are located in these areas, a partial copper supersaturation and the formation of ~ Al7Cu2Fe phases may occur, as shown in Figure 11c. These particles also contain small amounts of manganese and have been known before.31,32

Figure 6
figure 6

OM: microstructure analysis of AlZn4Mg3Cu(Fe) as cast at (a) low and (b) high magnification.

Figure 7
figure 7

OM: microstructure analysis of AlZn5Mg4Cu as cast at (a) low and (b) high magnification.

Figure 8
figure 8

SEM: AlZn4Mg3Cu(Fe) as cast, point analysis of an AlFeSiCrMn phase (Spectrum 1), ~ T-(Al2Mg3Zn3) phase (Spectrum 2), and ~ Mg2Si phase (Spectrum 3) in at.%.

Figure 9
figure 9

EDS point analysis: (a) AlFeSiCrMn phase (Spectrum 1), (b) ~ T-(Al2Mg3Zn3) phase (Spectrum 2), and (c) ~ Mg2Si phase (Spectrum 3) in AlZn4Mg3Cu(Fe) as cast.

Table 8 EDS Point Analysis of AlZn4Mg3Cu(Fe) As Cast in at.%
Figure 10
figure 10

SEM: AlZn5Mg4Cu as cast, point analysis of a complex Fe–Mn–Si-containing eutectic (Spectrum 1), ~ T-(Al2Mg3Zn3) phase (Spectrum 2) in at.%, line analysis of a ~ Mg2Si phase, ~ T-(Al2Mg3Zn3) phase, and ~ Al7Cu2Fe phase.

Figure 11
figure 11

EDS line analysis: (a) ~ Mg2Si phase, (b) ~ T-(Al2Mg3Zn3) phase, and (c) ~ Al7Cu2Fe phase in AlZn5Mg4Cu as cast.

Figure 12
figure 12

EDS point analysis: (a) Fe–Mn–Si-containing eutectic (Spectrum 1) and (b) ~ T-(Al2Mg3Zn3) phase (Spectrum 2) in AlZn5Mg4Cu as cast.

Table 9 EDS Point Analysis of AlZn5Mg4Cu As Cast in at.%

The electrolytic Barker etch allows a predication about the grain structures of the materials. In AlZn4Mg3Cu(Fe), as shown in Figure 13, the dendritic structures and grains are more inhomogeneous and tend to be larger than those in AlZn5Mg4Cu, as shown in Figure 14. On the one hand, the appliance of different grain refining elements must be considered. On the other hand, the findings of this work confirm that the formation of titanium-containing AlFeSiCrMn precipitates adversely affects the grain refinement of αAl. Thus, TiB2 may cause a more effective grain refinement under given conditions with increased accompanying element content. The effect of the grain size on mechanical properties is generally described by Hall–Petch relationship. This equation explains the interaction of dislocations with grain boundaries; hence, it explains a higher strength at smaller grain sizes.33 Hall–Petch is particularly valid for wrought alloys, but with dendritic structures and intermetallic phases, there are more complex microstructures in cast alloys. Furthermore, the secondary dendrite arm spacing is greatly important in castings.34 Hence, based on AlSi alloys, almost no correlation between grain size and strength was found as cast.35,36 However, other studies have shown the opposite and a higher strength with smaller grains.37,38 In this case, the yield strength was approximately 10% higher. This increase was achieved by a grain size reduction from ~ 600 to ~ 100 µm. Due to precipitation, the difference is higher after artificial aging with approximately 15%. As a consequence, this work also assumes a minor effect of the grain sizes on the mechanical properties. In general, large grains impair feeding, increase the risk of hot cracking, and indirectly downgrade the mechanical properties due to the coarse distribution of micropores and secondary phases.39,40

Figure 13
figure 13

OM: AlZn4Mg3Cu(Fe) as cast after Barker etching at (a) low and (b) high magnification.

Figure 14
figure 14

OM: AlZn5Mg4Cu as cast after Barker etching at (a) low and (b) high magnification.

Summary

The alloys AlZn4Mg3Cu(Fe) and AlZn5Mg4Cu achieved yield strengths of over 200 MPa in the modified T6* state. Therefore, these materials can be attractive for structural components, where they can challenge standard cast alloys such as AlZn10Si8Mg. Due to the special heat treatment T6*, the peak hardness was not achieved in this condition. The mechanical properties in the T73 state were significantly higher. These results were primarily based on the high levels of zinc and magnesium, and a subsequent high level of solid solution strengthening and precipitation strengthening. In addition, the mechanical properties of AlZn4Mg3Cu(Fe) were influenced by the tendency of larger grains and blocky phases. The analysis shows titanium contents in these particles, which probably affect the grain refinement effect of the element. Due to the observed grain size differences, lower grain boundary strengthening was also assumed in AlZn4Mg3Cu(Fe).

In this study, difficultly casted AlZnMg(Cu) alloys could be processed by high-pressure die casting. Moreover, convincing material properties were achieved without cost-intensive alloying elements using an energy- and time-efficient heat treatment. Hence, this work can provide a trend for the development of such high-strength die-cast alloys. However, to further improve the mechanical properties, the formation of block-like particles and possible interactions with grain refining elements, as in AlZn4Mg3Cu(Fe), should be avoided. For this purpose, thermodynamic simulations can also be used in the future. Finally, since the corrosion properties are crucial for the appliance of AlZnMg(Cu) alloys, future work should focus on their investigation.