Next Article in Journal
Tuning Crystallization Pathways via Phase Competition: Heat-Treatment-Induced Microstructural Evolution
Next Article in Special Issue
Effect of Fe Content on the Microstructure and Properties of 5083 Aluminum Alloy
Previous Article in Journal
The Modulated Hot Spot Formation of Void Defects During Laser Initiation in RDX Energetic Crystals
Previous Article in Special Issue
The Typical Microstructure of Twin-Roll Cast 2139 Alloy and Its Impact on Mechanical Properties
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Crystals
Volume 16
Issue 1
10.3390/cryst16010028
crystals-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effect of Yttrium on Iron-Rich Phases and Mechanical Properties of As-Cast Al-Fe Alloy with Low Si Concentration

by
Wenjie Wu
,
Wenxia Lai
,
Ziteng Cao
,
Chengdong Li
* and
Mei Zhao
*
College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266000, China
*
Authors to whom correspondence should be addressed.
Crystals 2026, 16(1), 28; https://doi.org/10.3390/cryst16010028
Submission received: 15 December 2025 / Revised: 26 December 2025 / Accepted: 28 December 2025 / Published: 30 December 2025
(This article belongs to the Special Issue Design, Development and Processing of Aluminium Alloys and Their Composite Materials)
Browse Figures
Versions Notes

Abstract

In Al–Fe alloys, the mechanical properties are determined by the morphology of iron-rich phases. In this work, AA8176(Al-1Fe)-nY (n = 0, 0.3, 0.5, 0.7, and 0.9 wt.%) alloys were prepared by the cast method. The effects of yttrium (Y) addition on the microstructure and mechanical properties of AA8176 alloy were studied using various techniques including optical microscopy (OM), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), cooling curve analysis and tensile tests. The results revealed that the optimal refinement effect was achieved when the amount of Y content was 0.5 wt.%. When the Y content increased from 0 to 0.5 wt.%, the coarse needle-like Al13Fe4 phases were gradually transformed into short rod-like morphology and some fine Al10Fe2Y phases were formed around the Al13Fe4 phases. The average length of iron-rich phases was decreased from 10.01 μm to 2.65 μm. Additionally, as the Y content increased from 0 to 0.5 wt.%, the secondary dendrite arm spacing (SDAS) of AA8176 alloy was reduced from 31.33 μm to 20.24 μm. Furthermore, the mechanical properties of the AA8176 alloy were improved due to the modified microstructure. With the addition of 0.5 wt.% Y, the ultimate tensile strength, yield strength, elongation, and Vickers hardness were improved to 96.86 MPa, 57.21 MPa, 23.1%, and 30.55 HV, respectively, compared to 84.47 MPa, 50.71 MPa, 18.6%, and 27.28 HV for the unmodified AA8176 alloy. It is proposed that the growth of α-Al dendrite and Al13Fe4 phases were effectively inhibited by segregation of Y atoms around α-Al dendrite and Al13Fe4 phases during solidification. And the Al10Fe2Y phases were formed by these Y atoms with Al and Fe elements. However, the formation of coarse Al10Fe2Y phases was promoted by excessive Y content, resulting in a substantial degradation in mechanical properties.

1. Introduction

For Al-Fe-based aluminum (Al) alloys, excellent heat and wear resistance are achieved, and the high specific strength and low density of Al alloys are maintained [1,2,3]. The advantages of Al-Fe-based alloys are predominantly derived from various iron-rich phases (formed by Fe, Al, and other alloying elements such as Si, Mg, Mn) during solidification and heat treatment processes, which is attributed to the intentional addition of Fe [4,5]. Among these alloying elements, Si plays the most important role in determining the types of iron-rich phases. In Al-Fe alloy with high Si content, the iron-rich phases are mainly composed of α-AlFeSi (Al8Fe2Si) and β-AlFeSi (Al5FeSi). In contrast, in Al-Fe alloy with low Si content, the iron-rich phases are composed of Al13Fe4 (Al3Fe), Al6Fe, and AlmFe phases [6].
Owing to the extremely low solubility of Fe in the Al matrix, a sharp increase in the size of iron-rich phases is achieved when the Fe content exceeds 0.1 wt.%. And their morphologies are gradually transformed from fine fibrous to large needle-like, flake-like, and plate-like structures [7,8]. These coarse iron-rich phases act as crack initiation sites, which lead to stress concentration during plastic deformation and thereby deteriorate the alloy’s mechanical performance. Furthermore, the flow of melt is hindered by coarse iron-rich phases precipitated in the solidification, consequently inducing casting defects [9]. Therefore, it is essential to develop effective methods for modifying the morphology of iron-rich phases in Al-Fe Al alloys.
The 8000 series Al alloys, including AA8076, AA8079, AA8176 and other grades, belong to Al-Fe Al alloys with low Si concentration, which are mainly used in packaging, containers, cables and other fields. Currently, research on the refinement of iron-rich phases in such low-Si Al-Fe alloys remains insufficient.
Some strategies such as rapid solidification [10], mechanical alloying [11], applied magnetic field [12], and severe plastic deformation [13,14] have been employed to modify the iron-rich phases in Al alloys. However, for these methods, stringent equipment conditions and entail higher costs are required, which limit their applicability in industrial production.
In comparison to common refiners such as Mn, Ti, Ni, and Cr, the addition of rare earth elements, including La, Ce, Er, Sc, and Sm, is more attractive for Al casting alloys [15,16,17,18,19,20,21,22,23,24,25]. It has been demonstrated that the addition of rare earth elements significantly enhances alloy properties through the formation of thermally stable intermetallics, the promotion of grain refinement, and the modification of texture evolution. In contrast, non-rare-earth elements may not always match the performance improvements of RE elements [26,27]. Meanwhile, the melt is purified, and the content of gases and inclusions is reduced [28]. Among these rare earth elements, the widespread application of high-value rare earth elements such as Er, Sc, and Sm in large-scale Al alloy manufacturing is frequently hindered by their high costs. Additionally, in comparison to rare earth elements such as La and Ce, Y exhibits a stronger tendency to combine with Fe in Al-Fe alloys to form Al-Fe-Y ternary phases [29,30,31]. On the one hand, a portion of Fe atoms are consumed by the formation of the Al-Fe-Y ternary phases, thereby reducing the volume fraction of needle-like iron-rich phases. On the other hand, more favorable morphologies are typically exhibited by the Al-Fe-Y ternary phases, which results in an increase in the number of strengthening secondary phases.
The beneficial effect of Y addition on both the microstructure and the mechanical properties of Al alloys has been demonstrated by several studies [32,33]. Ding et al. [34] reported that a significant refinement effect on 6063 Al alloy was achieved by Y addition. The size of Mg2Si particles was reduced by the addition of Y, and the β-AlFeSi phases were transformed into the α-AlFeSi phases. Furthermore, both tensile strength and elongation of the AA6063 alloy were improved by the combined addition of Y and the Al–Ti–B master alloy. Liu et al. [35] found that the microstructure of as-cast ADC12 Al alloy was significantly refined by Y addition, resulting in a notable decrease in the average size of the α-Al phase, as well as the coarse Si and iron-rich phases. And the mechanical properties of the ADC12 Al alloy were notably enhanced by the combination of Y addition and heat treatment. Wan et al. [36] reported on the effects of adding different contents of Y on the microstructure and tensile properties of recycled A356 cast alloy. When the Y content was 0.3 wt.%, the average length of the β-Fe phases was reduced from 78 μm to 20 μm and the finest α-Al phases were obtained. Meanwhile, the eutectic silicon was fully modified in morphology.
While these studies have enhanced comprehension of Y modification for Al alloys, limited attention has been paid to the addition of Y in Al-Fe alloys with low Si concentration. Consequently, the underlying modification mechanism and the associated mechanical property response need to be further studied.
As described above, AA8176 was selected as the matrix material and Y was utilized as the refiner in this study to explore effective approaches for refining iron-rich phases in Al-Fe alloys with low Si concentration. Y was added to AA8176 alloys by the cast method. The influence of varying Y additions (0, 0.3, 0.5, 0.7, and 0.9 wt.%) on the evolution of the iron-rich phases, α-Al dendrite, and mechanical properties of as-cast AA8176 alloys was systematically studied. The aim of this study is to reveal the refinement mechanism of Y on the microstructure and the strengthening mechanism of mechanical properties of AA8176 Al alloys, and to propose a new strategy for achieving effective refinement of iron-rich phases in Al-Fe alloys with low Si concentration.

2. Materials and Methods

AA8176 alloy samples with varying Y additions (0, 0.3, 0.5, 0.7, and 0.9 wt.%) were fabricated using 99.7 wt.% pure Al ingots, Al-20 wt.% Fe master alloy, and Al-20 wt.% Y master alloy. The cast process was as follows: (1) 99.7 wt.% pure Al ingots, and Al-20 wt.% Fe master alloy were melted in furnace at 760 °C; (2) A suitable quantity of Al-20 wt.% Y master alloy was added at 730 °C and held for 15 min after addition; (3) The temperature of furnace was reduced to 720 °C for degassing and slag removal to obtain a purified melt; (4) The molten alloy was subsequently poured into a steel mold, thus producing the experimental cast samples for further analysis. Before the alloy was poured, the mold was placed in a muffle furnace for preheating, with the temperature set to 250 °C. The composition of the experimental alloys was determined using a direct reading spectrometer, as presented in Table 1.
To systematically analyze the effects of Y addition on the microstructural evolution and mechanical properties of AA8176 Al alloy, a comprehensive set of experimental procedures was established. The sizes of specimens for metallographic observation and tensile test are shown in Figure 1. Metallographic samples were taken from the prospective near-fracture zone of tensile specimens, with the sampling location illustrated in Figure 1. Before the metallographic observation, the samples were sequentially mechanically ground with SiC sandpapers of #180, #400, #800, #1200 and #2000, and subsequently followed by polishing with diamond paste to achieve a mirror-like surface finish. After that the samples were etched with a solution of Keller’s reagent (2.5 mL HNO3 + 1.0 mL HF + 1.5 mL HCl + 95 mL H2O) for 10 s.
Metallographic observation was carried out using a PA53MET (Panthera, Chengdu, China) optical microscope. The SDAS of alloys was measured by the line intercept method using Image J 1.46r software. Phase analysis was performed with X-ray diffractometer using a D/MAX-2500/PC X-ray diffractometer (Rigaku, Tokyo, Japan) equipped with a Cu Kα radiation source. The diffraction patterns were recorded over a 2θ range of 20° to 90° at a scanning speed of 5°/min. The microstructure and fracture morphology were examined using a Regulus8100 field emission scanning electron microscope (HITACHI, Tokyo, Japan). The Al13Fe4 and Al10Fe2Y phases were further characterized by FEI Tecnai F20 transmission electron microscopy (FEI Company, Hillsboro, OR, USA). The samples for TEM observation were prepared using a TJ100-BE automatic twinjet electropolisher (LEBO, Jiangyin, China). The cooling curves of the alloy during solidification were measured using a THMA010K temperature recorder (TengHui, Yuyao, China) coupled with a K-type thermocouple inserted into the melt center to ensure reliable temperature monitoring throughout solidification. Tensile tests were conducted on an AI-700 tensile testing machine (Gotech, Taiwan, China), following GB/T 228.1-2021, at room temperature with a tensile speed of 5 mm·min−1. As shown in Figure 1, the bone-shaped specimens were used for tensile property testing, with five tests conducted for each composition.

3. Results

3.1. The Microstructure of AA8176-xY

3.1.1. Metallographic Observation

The microstructures of as-cast AA8176 Al alloys with varying Y contents were characterized using optical microscopy, as presented in Figure 2a–e. The microstructure of unmodified AA8176 alloy is predominantly composed of α-Al and eutectic structure [37]. As shown in Figure 2a and Figure 3a, the eutectic iron-rich phases in the unmodified AA8176 alloys predominantly exhibited coarse needle-like morphology with an average length of 10.01 μm. These coarse needle-like iron-rich phases were located within interdendritic regions. And the stress concentration during plastic deformation is greatly promoted by these coarse needle-like iron-rich phases, leading to a decline in the mechanical properties.
With the Y content increasing from 0 wt.% to 0.5 wt.%, significant changes in the morphology of the iron-rich phases were observed. The average length of the iron-rich phases was decreased from 10.01 μm to 2.65 μm, transforming into short rod-like and particulate morphologies as shown in Figure 2b,c and Figure 3a. When the Y content was further increased to 0.7 wt.%, the average length of iron-rich phases exhibited an increasing trend as illustrated in Figure 2d. When the Y content was 0.9 wt.%, the average length of iron-rich phases was significantly increased to 7.87 μm, as shown in Figure 2e and Figure 3a. Concurrently, a notable increase in the number of secondary phases within the alloy was observed.
To further analyze the effect of Y addition on the microstructure of AA8176 alloy, the SDAS of the α-Al matrix was measured for all alloys using the line intercept method in Image J 1.46r software. For the unmodified AA8176 alloy, the α-Al dendrites were relatively coarse, corresponding to an SDAS value of approximately 31.33 μm as shown in Figure 3b. With the Y addition to AA8176 alloys, the SDAS values of the AA8176 alloy with 0.3–0.9 wt.% Y were 24.03 μm, 20.24 μm, 20.45 μm, and 20.38 μm, respectively. It is confirmed by these results that the addition of Y promotes the refinement of both the iron-rich phases and the α-Al dendritic structure. Notably, no further enhancement in the refinement effect of Y on α-Al was observed when the Y content exceeded 0.5 wt.%.

3.1.2. SEM and XRD Analysis

Figure 4 and Table 2 display SEM images and corresponding EDS analysis results for the AA8176 alloys with different Y contents. According to the X-ray diffraction patterns shown in Figure 5, except for α-Al matrix, the presence of the Al13Fe4 phases was detected in all AA8176 alloys with different Y contents, which is consistent with the reference code from the Joint Committee on Powder Diffraction Standards (JCPDS) Card No. 29-0042 reference code [38].
As illustrated in Figure 4a, the microstructure of the as-cast AA8176 alloy was primarily composed of α-Al matrix and coarse needle-like Al13Fe4 phases distributed along the grain boundaries. When the Y content was increased to 0.5 wt.%, the iron-rich phases were refined into short rod-like and particulate morphologies instead of the coarse needle-like structures, as shown in Figure 4b. Furthermore, EDS results for points B and C (Table 2) indicated the presence of Al-Fe-Y ternary phases attached to Al13Fe4 phases in the Alloy 05Y. Statistical analysis was performed on the iron-rich phase sizes in Figure 4b. The results show that the average size of the Al13Fe4 phases is 2.41 μm, while that of the Al-Fe-Y ternary phases is 1.54 μm. In contrast, when the Y content exceeded 0.5 wt.%, the refinement efficiency of Y was diminished. As shown in Figure 4c, the average length of iron-rich phases in Alloy 09Y was increased, with an increase in both the quantity and size of the Al-Fe-Y ternary phases. The average size of the Al13Fe4 phases in Figure 4c is 6.75 μm, while that of the Al-Fe-Y ternary phases is 3.01 μm. Moreover, as illustrated in Figure 4d, a morphology characterized by the aggregation of extremely coarse Al13Fe4 and Al-Fe-Y ternary phases was observed in Alloy 09Y. And the average size of these coarse Al-Fe-Y ternary phases was increased to 5.82 μm. The formation of these Al-Fe-Y ternary phases around the coarse Al13Fe4 phases was confirmed by EDS results from points E and F (Table 2). And it was revealed by the comparison of the average sizes of the two iron-rich phases in alloys with different Y contents that the ternary Al-Fe-Y phases exhibit a finer average size than the Al13Fe4 phases.
According to the XRD patterns in Figure 5, the Al10Fe2Y phases were detected in the Alloy 05Y, Alloy 07Y, and Alloy 09Y, which is consistent with the JCPDS Card No. 53-0532 reference code [39]. Furthermore, in the XRD pattern of Alloy 09Y, the peak intensity of Al10Fe2Y phases was increased, while that of Al13Fe4 phases was decreased. This trend is mainly attributed to the consumption of Fe atoms by the formation of coarse Al10Fe2Y phases, which results in a reduction of Fe available for Al13Fe4 phases precipitation. Based on the elemental ratios obtained from EDS and XRD patterns, the Al-Fe-Y ternary phases observed in the SEM images (Figure 4) are most likely to be the Al10Fe2Y phases.

3.1.3. TEM Observation

Initial morphological characterization and EDS analysis were conducted on the secondary phases possibly containing Fe and Y elements in Alloy 05Y, as indicated by earlier SEM observations. The Y elemental mapping clearly reveals the enrichment of Y at the periphery of the Al13Fe4 phases, indicating the in situ formation of Al-Fe-Y ternary phases through its reaction with Al and Fe, as shown in Figure 6d.
To further identify the crystal structure of these phases, SAED patterns were collected from point A (corresponding to Al13Fe4 phases) and point B (corresponding to Al-Fe-Y ternary phases), as shown in Figure 6e,f, respectively. The SAED pattern acquired at point A can be indexed to the Al13Fe4 phases. Due to the greater sample thickness at point B, the SAED pattern obtained from this location contained contributions from more than one kind phase, which was confirmed to consist mainly of α-Al matrix and Al10Fe2Y phase, as illustrated in Figure 6f.

3.1.4. Cooling Curves

The cooling curves and differential curves for AA8176 alloy, Alloy 05Y and Alloy 09Y are shown in Figure 7 and the characteristic temperatures of the eutectic reaction summarized in Table 3. TEN, TEU, and TEG denote the eutectic nucleation temperature, eutectic minimum undercooling temperature and eutectic growth temperature, respectively. According to the Al-Fe alloy binary phase diagram, the eutectic temperature of Al-Fe alloys is approximately 655 °C [40], which is consistent with the characteristic values measured for the AA8176 alloy. With the addition of 0.5 wt.% Y, TEN was decreased to 649.9 °C and TEG was decreased to 643.6 °C, respectively, indicating the adsorption and hindering effects of Y during the nucleation and growth processes of Al13Fe4 eutectic phases [41]. Additionally, a new peak emerged in the cooling curve, with a nucleation temperature around 626.8 °C, corresponding to the nucleation and growth of the Al10Fe2Y phases [42]. When the Y content was increased to 0.9 wt.%, only minor changes were detected on the values of both TEN and TEG, indicating the adsorption and hindering effects of Y on the eutectic structure were not further enhanced. In contrast, the T′EN of Alloy 09Y was significantly increased, suggesting that the nucleation and growth of Al10Fe2Y phases were greatly promoted by higher Y content. This also directly explains the presence of numerous coarse Al10Fe2Y phases in Alloy 09Y.

3.2. Mechanical Property

The mechanical properties of cast AA8176 alloys with different Y contents are presented in Figure 8 and Table 4. In unmodified AA8176 alloy, the ultimate tensile strength of the alloy was 84.47 MPa, the yield strength was 50.71 MPa, and the elongation was 18.6%. Optimal mechanical properties were achieved when the Y content was increased to 0.5 wt.%. The ultimate tensile strength was increased to 96.86 MPa, the yield strength was increased to 57.21 MPa and elongation was increased to 23.1%. However, further increase in Y content to 0.9 wt.% led to a reduction in ultimate tensile strength, yield strength and elongation. Therefore, it can be deduced that the ultimate tensile strength, yield strength and the elongation of the AA8176 alloys exhibited a trend of firstly increasing and then decreasing with rising Y content. As shown in Figure 8c and Table 4, the Vickers hardness of AA8176 alloy with varying Y content also followed a similar trend. When the Y content was increased from 0 to 0.5 wt.%, the Vickers hardness was increased from 27.28 HV to 30.55 HV. And the Vickers hardness was decreased to 28.74 HV with further Y addition to 0.9 wt.%.
Figure 9 presents the fracture surfaces of the as-cast AA8176 alloys with different Y contents. In the unmodified AA8176 alloy, shallow and irregularly sized dimples are observed with coarse iron-rich phase particles within the dimples (point A), as shown in Figure 9a. This is attributed to the presence of coarse, brittle iron-rich phases in AA8176 alloy. During deformation, stress concentration and rapid crack propagation, promoted by these coarse iron-rich phases, significantly inhibit the growth of dimples. Consequently, the non-uniform size and distribution of the iron-rich phases directly resulted in variability in dimple sizes. For Alloy 05Y, deeper and more uniformly distributed dimples were observed, with modified iron-rich phases observed within the dimples (point B), as shown in Figure 9c. The refined iron-rich phases mitigate stress concentration during deformation. This allows dimples to undergo more extensive growth, leading to the formation of deeper dimples. Moreover, the uniform size and distribution of these refined phases result in a corresponding uniformity in dimple size. However, when the Y content exceeded 0.5 wt.%, the weakening refinement effect of Y on the Al13Fe4 phases and formation of coarse Al10Fe2Y phases resulted in a subsequent reduction in the ductility. Correspondingly, the fracture surfaces exhibited a tendency toward shallower dimples and an increased presence of coarse iron-rich phases (point C). Figure 9f shows the morphology of the tensile fracture side of Alloy 05Y. It reveals that obvious microcrack initiate at iron-rich phases and propagate along the interface between the iron-rich phases and the matrix. This behavior is consistent with the phenomenon observed in the AA8176 alloy shown in Supplementary Figure S1.

4. Discussion

4.1. Effect of Y Addition on α-Al Dendrite

As the total solid–liquid interface area between dendritic arms in the system is gradually decreased, neighboring dendritic arms are grown and merged, resulting in the formation of coarse dendritic structures during the solidification process. The atomic radii of the rare earth element Y and Al are 0.182 nm and 0.143 nm [35], respectively, resulting in a difference of 27%. According to the Hume-Rothery rule, the formation of solid solutions is inhibited by a radius difference exceeding 15% between solvent and solute [43]. Consequently, Y exhibits extremely low solubility in the Al matrix (less than 0.035 mol.% at 573 K [44]), and enrichment of Y atoms at the dendritic fronts tends to occur during solidification. The growth and merging of dendritic arms are restricted by this enrichment, thereby refining the SDAS of α-Al matrix [45]. The growth induced by element enrichment is described based on the growth restriction factor ( G R F ) as follows [20,46]:
G R F = C Y · m · ( k − 1 )
where C Y is the concentration of solute Y in the alloy melt, m is the liquidus slope, and k is the equilibrium partition coefficient [20]. For the Al–Y alloy system, m = 4.98 and k = 0.5 are given by the Al–Y binary phase diagram. For the AA8176 alloy with 0.5 wt.% Y, the calculated G R F is approximately 1.25 K, the growth of α-Al is effectively inhibited by the addition of Y.

4.2. Effect of Y Addition on Iron-Rich Phases

The Al13Fe4 phases prefer to grow along the [010] orientation, resulting in the formation of coarse needle-like and plate-like morphologies during solidification [24]. The influence of active solute atoms on crystal growth is theoretically explained through doping (substitutional incorporation) and adsorption (surface segregation). There exists a significant difference in atomic radius between Y atoms and Al/Fe atoms—specifically, the atomic radius of Y, Al, and Fe are 0.182 nm, 0.143 nm, and 0.128 nm, respectively [35,47]. Owing to this remarkable size mismatch, Y atoms cannot easily substitute Al or Fe atoms in the Al13Fe4 phases. According to result of EDS, rare Y element was detected in the eutectic Al13Fe4 phase, which directly confirms that the doping of Y atoms into Al13Fe4 phases is not the main mechanism for the refinement of Al13Fe4 phases. This experimental observation is consistent with the theoretical calculation results reported by Pang et al. [31], which show that Y doping into Al13Fe4 phases increases their formation enthalpy. In contrast, the adsorption of Y on the (010) plane is an exothermic reaction, Y atoms are easily adsorbed on the (010) plane during the solidification process. The adsorption of Y atoms modifies the surface structure of the (010) plane and impedes the preferential growth along the [010] direction. In the final solidification stage, Y atoms eventually form Al10Fe2Y ternary phases [31,42]. When the Y content reaches 0.9 wt.%, excessive aggregation of Y atoms significantly increases the nucleation temperature of the Al10Fe2Y phases. The nucleation and growth of coarse Al10Fe2Y phases leads to a massive consumption of Y atoms. This reduces the amount of Y atoms for inhibiting the preferential growth of the Al13Fe4 phases, resulting in a weakened refinement effect [20].

4.3. Strengthening Mechanism

Due to the extremely low solid solubility of Y and Fe in the Al matrix and the fact that the mechanical test specimens used in this study underwent no plastic deformation processing, solid solution strengthening and dislocation strengthening are not considered to be the primary mechanisms responsible for the enhancement in mechanical properties. Thus, the enhancement of ultimate tensile strength can be attributed to two factors. First, Al13Fe4 intermetallic compounds are second phases with high hardness and brittleness, distributing on the α-Al matrix. During tensile process, deformation of the alloy is hindered by the Al13Fe4 phases distributed between the grains, resulting in the formation of dislocations [48].
However, in the AA8176 alloy without Y addition, the coarse Al13Fe4 phases can induce stress concentrations, which adversely affects the mechanical properties of the alloy. When the Y addition was increased to 0.5 wt.%, the morphology of the Al13Fe4 phases was transformed into short rod-like and particulate with an average length of 2.65 μm. Consequently, the stress concentration during plastic deformation is effectively mitigated by this refinement for Al13Fe4 phases. Meanwhile, the number of secondary phases in the alloy matrix is further increased by the formation of Al10Fe2Y phases, which grow around the Al13Fe4 phases. The mechanical properties of the AA8176 alloy with 0.5 wt.% Y are enhanced by this dual effect. When the Y addition exceeded the optimal content of 0.5 wt.%, no further enhancement in the adsorption effect of Y on Al13Fe4 phases was observed. However, the nucleation and growth temperature of the Al10Fe2Y phases was increased by the excessive addition of Y. The Y atoms that would otherwise inhibit the growth of Al13Fe4 are consumed by the growth of the Al10Fe2Y phases, eventually leading to the formation of coarse Al13Fe4 and Al10Fe2Y phases, which consequently results in the degradation of mechanical properties.
Secondly, the SDAS of the AA8176 alloys was significantly reduced by the addition of Y, leading to a more refined microstructure. Secondly, the addition of Y significantly reduces the SDAS of the AA8176 alloys, resulting in a more refined microstructure. Generally, finer grains lead to a higher density of grain boundaries. Dislocation movement is effectively hindered and dislocation pile-up is induced by this increased boundary density, resulting in a significant improvement in the strength of the AA8176 alloys.
Gerbe et al. [49] proposed that in hypoeutectic alloys, the dendritic regions are regarded as behaving similarly to grain boundaries in polycrystalline alloys, since the eutectic zones between dendrites are traversed by slip planes. The SDAS is considered analogous to grain size in the Hall–Petch relationship, whereby a reduction in the mean free path of dislocation motion during plastic deformation is produced by smaller dendritic regions, thus further enhancing the strength of the AA8176 alloys.

5. Conclusions

For the as-cast AA8176 alloys, an optimal microstructure was achieved by the addition of 0.5 wt.% Y. In the unmodified AA8176, the microstructure is predominantly composed of the α-Al phases and the eutectic structure. The SDAS of α-Al phases was measured to be approximately 31.33 μm, and a needle-like morphology with an average length of 10.01 μm was exhibited by the iron-rich phases. In contrast, after the addition of 0.5 wt.% Y, the SDAS of the alloy was decreased to 20.24 μm, and the iron-rich phases were transformed into short rod-like and particulate forms with an average length of 2.65 μm. When the Y content exceeded 0.5 wt.%, no significant change in the SDAS of α-Al phases was observed, while an increase in both the number and average size of the iron-rich phases occurred.
In the unmodified AA8176 alloy, the iron-rich phases consist of Al13Fe4 phases. The refinement of the Al13Fe4 phases is primarily attributed to the adsorption effect of Y atoms around these phases. Microstructural observations revealed that small-size Al10Fe2Y ternary phases were attached to the surfaces of Al13Fe4 phases in the AA8176 alloy with 0.5 wt.% Y content. When the Y content exceeded 0.5 wt.%, the coarse Al10Fe2Y phases were formed. And a substantial consumption of Y atoms is caused by the growth of these Al10Fe2Y phases, resulting in a weakening of the refinement effect.
With the Y content increased, a trend of initially increasing and then decreasing was exhibited by the mechanical properties of the cast AA8176 alloys. When the Y content was 0.5 wt.%, an optimal balance of strength and ductility was achieved, with ultimate tensile strength, yield strength, elongation, and Vickers hardness measured at 96.86 MPa, 57.21 MPa, 23.1%, and 30.55 HV, respectively. The primary strengthening mechanism of the AA8176 alloys is attributed to the refinement in the morphology of iron-rich phases and reduction in the SDAS of α-Al matrix. When the Y content exceeded 0.5 wt.%, coarse Al10Fe2Y phases were formed, and the refining effect was reduced. The deterioration in the mechanical properties of the alloy is attributed to both coarse Al13Fe4 phases and Al10Fe2Y phases lead to worse mechanical properties of the alloy.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/cryst16010028/s1, Figure S1. OM image of tensile fracture side of AA8176 alloy.

Author Contributions

Conceptualization, W.W. and C.L.; methodology, W.W.; formal analysis, W.W.; investigation, W.W., W.L. and Z.C.; resources, C.L. and M.Z.; data curation, W.W., W.L. and Z.C.; writing—original draft preparation, W.W.; writing—review and editing, W.W., C.L. and M.Z.; supervision, C.L. and M.Z.; funding acquisition, C.L. and M.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by National Natural Science Foundation of China under Grant Nos. 51672145, 52171229 and 51872034.

Data Availability Statement

The data presented in this study is available on request from the corresponding author. The data is not publicly available due to privacy restrictions.

Conflicts of Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

References

  1. Medvedev, A.; Zhukova, O.; Enikeev, N.; Kazykhanov, V.; Timofeev, V.; Murashkin, M. The effect of casting technique and severe straining on the microstructure, electrical conductivity, mechanical properties and thermal stability of the Al–1.7 wt.% Fe alloy. Materials 2023, 16, 3067. [Google Scholar] [CrossRef]
  2. Zhao, Q.; Qian, Z.; Cui, X.; Wu, Y.; Liu, X. Optimizing microstructures of dilute Al–Fe–Si alloys designed with enhanced electrical conductivity and tensile strength. J. Alloys Compd. 2015, 650, 768–776. [Google Scholar] [CrossRef]
  3. Meignanamoorthy, M.; Ravichandran, M.; Mohanavel, V.; Afzal, A.; Sathish, T.; Alamri, S.; Khan, S.A.; Saleel, C.A. Microstructure, mechanical properties, and corrosion behavior of boron carbide reinforced Al alloy (Al-Fe-Si-Zn-Cu) matrix composites produced via powder metallurgy route. Materials 2021, 14, 4315. [Google Scholar] [CrossRef] [PubMed]
  4. Trink, B.; Weißensteiner, I.; Uggowitzer, P.J.; Strobel, K.; Pogatscher, S. High Fe content in Al-Mg-Si wrought alloys facilitates excellent mechanical properties. Scr. Mater. 2022, 215, 114701. [Google Scholar] [CrossRef]
  5. Wang, X.; Guan, R.G.; Wang, Y.; Misra, R.D.K.; Yang, B.W.; Li, Y.D.; Chen, T.J. Mechanistic understanding on the evolution of nanosized Al3Fe phase in Al–Fe alloy during heat treatment and its effect on mechanical properties. Mater. Sci. Eng. A 2019, 751, 23–34. [Google Scholar] [CrossRef]
  6. Que, Z.; Fang, C.; Mendis, C.L.; Wang, Y.; Fan, Z. Effects of Si solution in θ-Al13Fe4 on phase transformation between Fe-containing intermetallic compounds in Al alloys. J. Alloys Compd. 2023, 932, 167587. [Google Scholar] [CrossRef]
  7. Chen, J.; Lengsdorf, R.; Henein, H.; Herlach, D.M.; Dahlborg, U.; Calvo-Dahlborg, M. Microstructure evolution in undercooled Al–8 wt% Fe melts: Comparison between terrestrial and parabolic flight conditions. J. Alloys Compd. 2013, 556, 243–251. [Google Scholar] [CrossRef]
  8. Que, Z.; Wang, Y.; Mendis, C.L.; Fang, C.; Xia, J.; Zhou, X.; Fan, Z. Understanding Fe-containing intermetallic compounds in Al alloys: An overview of recent advances from the LiME research hub. Metals 2022, 12, 1677. [Google Scholar] [CrossRef]
  9. Zhao, Y.; Zhang, W.; Song, D.; Lin, B.; Shen, F.; Zheng, D.; Xie, C.; Sun, Z.; Fu, Y.; Li, R. Nucleation and growth of Fe-rich phases in Al-5Ti-1B modified Al-Fe alloys investigated using synchrotron X-ray imaging and electron microscopy. J. Mater. Sci. Technol. 2021, 80, 84–99. [Google Scholar] [CrossRef]
  10. Nayak, S.S.; Chang, H.J.; Kim, D.H.; Pabi, S.K.; Murty, B.S. Formation of metastable phases and nanocomposite structures in rapidly solidified Al–Fe alloys. Mater. Sci. Eng. A 2011, 528, 5967–5973. [Google Scholar] [CrossRef]
  11. Nayak, S.S.; Wollgarten, M.; Banhart, J.; Pabi, S.K.; Murty, B.S. Nanocomposites and an extremely hard nanocrystalline intermetallic of Al–Fe alloys prepared by mechanical alloying. Mater. Sci. Eng. A 2010, 527, 2370–2378. [Google Scholar] [CrossRef]
  12. Lan, Q.; Le, Q.; Liao, Q.; Bao, L.; Zhang, J.; Cui, J. Effect of AC magnetic field on Al3Fe phase by measuring thermoelectric power. Mater. Chem. Phys. 2018, 214, 383–390. [Google Scholar] [CrossRef]
  13. Duchaussoy, A.; Sauvage, X.; Edalati, K.; Horita, Z.; Renou, G.; Deschamps, A.; De Geuser, F. Structure and mechanical behavior of ultrafine-grained Al-iron alloy stabilized by nanoscaled intermetallic particles. Acta Mater. 2019, 167, 89–102. [Google Scholar] [CrossRef]
  14. Medvedev, A.; Murashkin, M.; Enikeev, N.; Medvedev, E.; Sauvage, X. Influence of morphology of intermetallic particles on the microstructure and properties evolution in severely deformed Al-Fe alloys. Metals 2021, 11, 815. [Google Scholar] [CrossRef]
  15. Song, D.; Zhao, Y.; Jia, Y.; Li, X.; Fu, Y.; Zhang, W. Synergistic effects of Mn and B on iron-rich intermetallic modification of recycled Al alloy. J. Mater. Res. Technol. 2023, 24, 527–541. [Google Scholar] [CrossRef]
  16. Watanabe, Y.; Mihara-Narita, M.; Sato, H. Grain refinement of cast Al by heterogeneous nucleation site particles with high lattice matching. Mater. Trans. 2023, 64, 1083–1097. [Google Scholar] [CrossRef]
  17. Qin, L.; Tang, P.; Meng, S. Effect of Ni addition on the microstructure, conductivities and mechanical properties of as-cast Al-Fe alloys. J. Alloys Compd. 2024, 986, 174160. [Google Scholar] [CrossRef]
  18. Song, X.; Gao, M.; Yang, B.; Guan, R. Modification and refinement of Fe-containing phases, mechanical properties and strengthening mechanisms in Al–Fe alloys via Cr alloying and continuous rheo-extrusion. Mater. Sci. Eng. A 2022, 850, 143557. [Google Scholar] [CrossRef]
  19. Xu, H.; Jia, H.; Ji, Z.; Li, M.L.; Yu, H.; Jiang, B.; Wang, Y.; Hu, M.L. Effect of La content on microstructure, tensile properties, and electrical conductivity of cast Al-Mg-Si-xLa alloys. China Foundry 2025, 22, 385–394. [Google Scholar] [CrossRef]
  20. Liao, H.C.; Liu, Y.; Lü, C.L.; Wang, Q.G. Effect of Ce addition on castability, mechanical properties and electric conductivity of Al–0.3 Si–0.2 Mg alloy. Int. J. Cast Met. Res. 2015, 28, 213–220. [Google Scholar] [CrossRef]
  21. Mahmoud, M.G.; Mosleh, A.O.; Mohamed, M.S.; El-Moayed, M.H.; Khalifa, W.; Pozdniakov, A.V.; Salem, S. The impact of Ce-containing precipitates on the solidification behavior, microstructure, and mechanical properties of Al-6063. J. Alloys Compd. 2023, 948, 169805. [Google Scholar] [CrossRef]
  22. Liang, Y.H.; Shi, Z.M.; Li, G.W.; Zhang, R.Y.; Zhao, G. Effects of Er addition on the crystallization characteristic and microstructure of Al-2wt% Fe cast alloy. J. Alloys Compd. 2019, 781, 235–244. [Google Scholar] [CrossRef]
  23. Li, Y.; Yu, Q.; Chen, F.; Yang, H.M.; Li, M.N. Effect of Sc on Al3Fe phase and mechanical properties of as-cast AA5052 Al alloy. China Foundry 2024, 21, 257–264. [Google Scholar] [CrossRef]
  24. Dai, K.; Ye, J.; Wang, Z.; Gao, M.; Chen, J.; Guan, R. Effects of Sc and Zr addition on the solidification and mechanical properties of Al–Fe alloys. J. Mater. Res. Technol. 2022, 18, 112–121. [Google Scholar] [CrossRef]
  25. Mo, L.; Jiang, M.; Zhou, X.; Zhao, Y.J.; Du, J. Modification mechanisms of hypereutectic Al-Fe alloys treated by Sm/Yb addition: Experiments and first-principles calculations. J. Alloys Compd. 2023, 948, 169786. [Google Scholar] [CrossRef]
  26. Tariq, H.M.R.; Ishtiaq, M.; Kang, H.H.; Chaudry, U.M.; Jun, T.S. A Critical Review on the Comparative Assessment of Rare-Earth and Non-Rare-Earth Alloying in Magnesium Alloy. Metals 2025, 15, 128. [Google Scholar] [CrossRef]
  27. Mansoor, A.; Zulfiqar, M.; Ishtiaq, M.; Hussain, M.A.; Younes, M.H.; Inam, A.; Afifi, M.A.; Khan, M.A.; Jabar, B. Tuning the microstructure and strength of Mg–RE alloys through the rare-earth elements. J. Mater. Sci. 2025, 60, 4808–4819. [Google Scholar] [CrossRef]
  28. Sahin, H.; Dispinar, D. Effect of rare earth elements erbium and europium addition on microstructure and mechanical properties of A356 (Al–7Si–0.3 Mg) alloy. Int. J. Met. 2023, 17, 2612–2621. [Google Scholar] [CrossRef]
  29. Luo, S.X.; Shi, Z.M.; Li, N.Y.; Lin, Y.M.; Liang, Y.H.; Zeng, Y.D. Crystallization inhibition and microstructure refinement of Al-5Fe alloys by addition of rare earth elements. J. Alloys Compd. 2019, 789, 90–99. [Google Scholar] [CrossRef]
  30. Pang, N.; Shi, Z.; Wang, C.; Lian, H.; Liu, J. Modification mechanisms of the primary Al13Fe4 phase in hypereutectic Al–Fe alloys by La element: Experiments and first–principles study. J. Cryst. Growth 2025, 659, 128136. [Google Scholar] [CrossRef]
  31. Pang, N.; Shi, Z.; Wang, C.; Wu, Y.; Zhang, J.; Sun, J. Doping and adsorption mechanism of the element Y modifying the primary Al13Fe4 phase in hypereutectic Al–Fe alloys from first-principles. CrystEngComm 2021, 23, 3802–3811. [Google Scholar] [CrossRef]
  32. Mao, G.; Liu, S.; Wu, Z.; Zhu, C.; Gao, W. The effects of Y on primary α-Al and precipitation of hypoeutectic Al-Si alloy. Mater. Lett. 2020, 271, 127795. [Google Scholar] [CrossRef]
  33. Mao, G.; Yan, H.; Zhu, C.; Wu, Z.; Gao, W. The varied mechanisms of yttrium (Y) modifying a hypoeutectic Al–Si alloy under conditions of different cooling rates. J. Alloys Compd. 2019, 806, 909–916. [Google Scholar] [CrossRef]
  34. Ding, W.; Zhao, X.; Chen, T.; Zhang, H.; Liu, X.; Cheng, Y.; Lei, D. Effect of rare earth Y and Al–Ti–B master alloy on the microstructure and mechanical properties of 6063 Al alloy. J. Alloys Compd. 2020, 830, 154685. [Google Scholar] [CrossRef]
  35. Liu, J.; Wu, Q.; Yan, H.; Zhong, S.; Huang, Z. Effect of trace yttrium addition and heat treatment on the microstructure and mechanical properties of as-cast ADC12 Al alloy. Appl. Sci. 2018, 9, 53. [Google Scholar] [CrossRef]
  36. Wan, B.; Chen, W.; Liu, L.; Cao, X.; Zhou, L.; Fu, Z. Effect of trace yttrium addition on the microstructure and tensile properties of recycled Al–7Si–0.3 Mg–1.0 Fe casting alloys. Mater. Sci. Eng. A 2016, 666, 165–175. [Google Scholar] [CrossRef]
  37. Jiang, H.; Li, S.; Zhang, L.; He, J.; Zheng, Q.; Song, Y.; Li, Y.; Zhao, J. The influence of rare earth element lanthanum on the microstructures and properties of as-cast 8176 (Al-0.5 Fe) Al alloy. J. Alloys Compd. 2021, 859, 157804. [Google Scholar] [CrossRef]
  38. Nemati, N.; Emamy, M. Evaluating Microstructure and High-Temperature Shear Behavior of Hot Extruded Al-Al13Fe4 Nanocomposite. Mater. Trans. 2016, 57, 1236–1245. [Google Scholar] [CrossRef][Green Version]
  39. Waerenborgh, J.C.; Salamakha, P.; Sologub, O.; Sério, S.; Godinho, M.; Gonçalves, A.P.; Almeida, M. Y–Fe–Al ternary system: Partial isothermal section at 1070 K: Powder X-ray diffraction and Mössbauer spectroscopy study. J. Alloys Compd. 2001, 323, 78–82. [Google Scholar] [CrossRef]
  40. da Silva Leal, J.R.; Saldanha, F.E.; Ganju, E.; Spinelli, J.E.; de Gouveia, G.L. Effect of cooling rate on AlFe primary and eutectic phase growth evolution in an Al-2Fe-1Mn alloy. J. Alloys Compd. 2025, 1010, 177870. [Google Scholar] [CrossRef]
  41. Mao, F.; Li, J.; Yan, G.; Zou, L.; Cao, Z.; Wang, T. Effect of Eu on the silicon phase in Al-40Zn-5Si alloys. J. Alloys Compd. 2017, 722, 116–130. [Google Scholar] [CrossRef]
  42. Wang, M.; Knezevic, M.; Chen, M. Effects of Fe content on microstructure and mechanical properties of Al-Y eutectic alloys. Mater. Sci. Eng. A 2023, 863, 144558. [Google Scholar] [CrossRef]
  43. Hume-Rothery, W.; Raynor, G.V. The Structure of Metals and Alloys. Nature 1936, 138, 7–8. [Google Scholar] [CrossRef]
  44. Li, B.; Wang, H.; Jie, J.; Wei, Z. Effects of yttrium and heat treatment on the microstructure and tensile properties of Al–7.5 Si–0.5 Mg alloy. Mater. Des. 2011, 32, 1617–1622. [Google Scholar] [CrossRef]
  45. Mao, F.; Yan, G.; Xuan, Z.; Cao, Z.; Wang, T. Effect of Eu addition on the microstructures and mechanical properties of A356 Al alloys. J. Alloys Compd. 2015, 650, 896–906. [Google Scholar] [CrossRef]
  46. Zheng, Q.; Zhang, L.; Jiang, H.; Zhao, J.; He, J. Effect mechanisms of micro-alloying element La on microstructure and mechanical properties of hypoeutectic Al-Si alloys. J. Mater. Sci. Technol. 2020, 47, 142–151. [Google Scholar] [CrossRef]
  47. He, J.; Liao, X.; Lan, X.; Qiu, W.; Yu, H.; Zhang, J.; Fan, W.; Zhong, X.; Liu, Z. Annealed Al-Cr coating: A hard anti-corrosion coating with grain boundary modification effect for Nd-Fe-B magnets. J. Alloys Compd. 2021, 870, 159229. [Google Scholar] [CrossRef]
  48. Fuller, C.B.; Seidman, D.N.; Dunand, D.C. Mechanical properties of Al (Sc, Zr) alloys at ambient and elevated temperatures. Acta Mater. 2003, 51, 4803–4814. [Google Scholar] [CrossRef]
  49. Gerbe, S.; Krupp, U.; Michels, W. Influence of secondary dendrite arm spacing (SDAS) on the fatigue properties of different conventional automotive Al cast alloys. Fract. Struct. Integr. 2019, 13, 105–115. [Google Scholar] [CrossRef]
Crystals 16 00028 g001
Figure 1. Schematic of (A) microstructure observation and (B) tensile test specimen.
Figure 1. Schematic of (A) microstructure observation and (B) tensile test specimen.
Crystals 16 00028 g001
Crystals 16 00028 g002
Figure 2. OM images of as-cast AA8176 alloys with different Y contents: (a) AA8176; (b) Alloy 03Y; (c) Alloy 05Y; (d) Alloy 07Y; (e) Alloy 09Y.
Figure 2. OM images of as-cast AA8176 alloys with different Y contents: (a) AA8176; (b) Alloy 03Y; (c) Alloy 05Y; (d) Alloy 07Y; (e) Alloy 09Y.
Crystals 16 00028 g002
Crystals 16 00028 g003
Figure 3. (a) Distribution of the length of iron-rich phases in as-cast AA8176 alloys with different Y contents; (b) SDAS of AA8176 alloys with different Y contents.
Figure 3. (a) Distribution of the length of iron-rich phases in as-cast AA8176 alloys with different Y contents; (b) SDAS of AA8176 alloys with different Y contents.
Crystals 16 00028 g003
Crystals 16 00028 g004
Figure 4. SEM images of as-cast AA8176 alloys with different Y contents: (a) AA8176; (b) Alloy 05Y; (c) Alloy 09Y. (d) Extremely coarse Al13Fe4 and Al10Fe2Y phases in Alloy 09Y.
Figure 4. SEM images of as-cast AA8176 alloys with different Y contents: (a) AA8176; (b) Alloy 05Y; (c) Alloy 09Y. (d) Extremely coarse Al13Fe4 and Al10Fe2Y phases in Alloy 09Y.
Crystals 16 00028 g004
Crystals 16 00028 g005
Figure 5. XRD patterns of the AA8176 alloys with different Y contents.
Figure 5. XRD patterns of the AA8176 alloys with different Y contents.
Crystals 16 00028 g005
Crystals 16 00028 g006aCrystals 16 00028 g006b
Figure 6. TEM characterization of the as-cast Alloy 05Y: (a): TEM bright-field image of Alloy; (b–d): EDS mapping results of Al13Fe4 phase and Al10Fe2Y phase; (e,f): SAED patterns in the selected areas A and B, respectively.
Figure 6. TEM characterization of the as-cast Alloy 05Y: (a): TEM bright-field image of Alloy; (b–d): EDS mapping results of Al13Fe4 phase and Al10Fe2Y phase; (e,f): SAED patterns in the selected areas A and B, respectively.
Crystals 16 00028 g006aCrystals 16 00028 g006b
Crystals 16 00028 g007
Figure 7. Cooling curves of (a): AA8176; (b): Alloy 05Y; (c): Alloy 09Y.
Figure 7. Cooling curves of (a): AA8176; (b): Alloy 05Y; (c): Alloy 09Y.
Crystals 16 00028 g007
Crystals 16 00028 g008
Figure 8. (a) Engineering stress–strain curves (b) Mechanical properties of AA8176 alloys with different Y contents (c) Vickers hardness of AA8176 alloys with different Y contents.
Figure 8. (a) Engineering stress–strain curves (b) Mechanical properties of AA8176 alloys with different Y contents (c) Vickers hardness of AA8176 alloys with different Y contents.
Crystals 16 00028 g008
Crystals 16 00028 g009
Figure 9. SEM image of tensile fracture morphology: (a) AA8176; (b) Alloy 03Y; (c) Alloy 05Y; (d) Alloy 07Y; (e) Alloy 09Y; (f) SEM image of tensile fracture side of Alloy 05Y.
Figure 9. SEM image of tensile fracture morphology: (a) AA8176; (b) Alloy 03Y; (c) Alloy 05Y; (d) Alloy 07Y; (e) Alloy 09Y; (f) SEM image of tensile fracture side of Alloy 05Y.
Crystals 16 00028 g009
Table 1. Chemical composition of Al alloy samples (wt.%).
Table 1. Chemical composition of Al alloy samples (wt.%).
AlloyFeYSiAl
AA81761.02<0.01<0.05Bal.
03Y1.090.29<0.05Bal.
05Y1.040.52<0.05Bal.
07Y0.980.68<0.05Bal.
09Y1.010.91<0.05Bal.
Table 2. Composition of Al alloy samples (at. %).
Table 2. Composition of Al alloy samples (at. %).
PointAl KFe KY KPossible Phase
A74.4425.56—Al13Fe4
B89.906.493.61Al10Fe2Y
C78.1221.88—Al13Fe4
D76.8223.72—Al13Fe4
E84.219.706.09Al10Fe2Y
Table 3. Characteristic values of eutectic reaction.
Table 3. Characteristic values of eutectic reaction.
AlloyTEN (°C)TEU (°C)TEG (°C)T′EN (°C)
AA8176656.2646.9647.0—
Alloy 05Y649.9643.1643.5626.8
Alloy 09Y651.1642.6642.9634.7
Table 4. Mechanical properties of AA8176 alloys with different Y contents.
Table 4. Mechanical properties of AA8176 alloys with different Y contents.
AlloyUTS (MPa)YS (MPa)Elongation (%)Hardness (HV)
AA817684.4750.7118.627.28
Alloy 03Y92.8154.9221.229.13
Alloy 05Y96.8657.2123.130.55
Alloy 07Y91.5954.1420.929.28
Alloy 09Y87.1051.7818.828.74
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Wu, W.; Lai, W.; Cao, Z.; Li, C.; Zhao, M. Effect of Yttrium on Iron-Rich Phases and Mechanical Properties of As-Cast Al-Fe Alloy with Low Si Concentration. Crystals 2026, 16, 28. https://doi.org/10.3390/cryst16010028

AMA Style

Wu W, Lai W, Cao Z, Li C, Zhao M. Effect of Yttrium on Iron-Rich Phases and Mechanical Properties of As-Cast Al-Fe Alloy with Low Si Concentration. Crystals. 2026; 16(1):28. https://doi.org/10.3390/cryst16010028

Chicago/Turabian Style

Wu, Wenjie, Wenxia Lai, Ziteng Cao, Chengdong Li, and Mei Zhao. 2026. "Effect of Yttrium on Iron-Rich Phases and Mechanical Properties of As-Cast Al-Fe Alloy with Low Si Concentration" Crystals 16, no. 1: 28. https://doi.org/10.3390/cryst16010028

APA Style

Wu, W., Lai, W., Cao, Z., Li, C., & Zhao, M. (2026). Effect of Yttrium on Iron-Rich Phases and Mechanical Properties of As-Cast Al-Fe Alloy with Low Si Concentration. Crystals, 16(1), 28. https://doi.org/10.3390/cryst16010028

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop