The hot deformation behavior of an Al-Zn-Mg-Cu alloy was investigated by hot compression test at deformation temperatures varying from 320 to 440 °C with strain rates ranging from 0.01 to 10 s⁻¹. The results show that the Mg(Zn, Cu)₂ particles as a result of the sufficient static precipitation prior to hot compression have an influence on flow softening. A constitutive model compensated with strain was developed from the experimental results, and it proved to be accurate for predicting the hot deformation behavior. Processing maps at various strains were established. The microstructural evolution demonstrates that the dominant dynamic softening mechanism stems from dynamic recovery (DRV) and partial dynamic recrystallization (DRX). The recrystallization mechanism is continuous dynamic recrystallization (CDRX). The microstructure observations are in good agreement with the results of processing maps. On account of the processing map and microstructural observation, the optimal hot processing parameters at a strain of 0.6 are at deformation temperature range of 390–440 °C and strain rate range of 0.010–0.316 s⁻¹ with a peak efficiency of 0.390.

A dense alumina ceramic coating was formed on UNS A97075 Al alloy by plasma electrolytic oxidation (PEO). An efficient and environmentally friendly silane layer was prepared to seal the PEO coating. The scanning electron microscopy (SEM) results showed that the PEO coating was completely sealed by the silane layer. The electrochemical corrosion evolution of the silane sealed PEO composite coating was studied by electrochemical impedance spectroscopy (EIS). Based on the EIS data, the corrosion evolution of the silane sealed composite coating could be divided to three stages during 576 h of immersion test, and the silane coating acted as a good physical barrier in the immersion test, effectively delayed the corrosion process and improved the corrosion resistance.

High temperature tensile properties and long-term thermal stability play an important role in practical applications of Al-Zn-Mg-Cu alloys. In order to evaluate the effect of Er addition on the properties of an Al-Zn-Mg-Cu alloy as potential high temperature structural materials, the heat resistance properties of an Al-Zn-Mg-Cu alloy were investigated at various temperatures. After high temperature tensile testing and long periods of heat exposure testing, the microstructures of Al-Zn-Cu-Mg alloys with and without small Er addition is intentionally investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), and quantitative transmission electron microscopy (TEM) characterization to explore the potential effect of Er on the tensile properties. The experimental results reveal that the heat resistance of T76-tempered Al-Zn-Cu-Mg alloy is obviously improved by adding trace Er. The Al₈Cu₄Er phase is found to segregate at the localized regions along grain boundaries and strengthens the grain boundaries at elevated temperatures. The η′ and η precipitation is obviously promoted by adding trace Er, and dispersed nano-sized Al₃(Er, Zr) precipitates were formed in the Er-containing alloys after homogenization, thereby enhancing the strength of Al-Zn-Mg-Cu. In addition, precipitates in both alloys gradually coarsen with the increase in thermal exposure temperature and the extension of thermal exposure time. The influence of precipitates on mechanical properties of the investigatived alloy after thermal exposure is also discussed.

Altering the content of an alloying element in alloy materials will inevitably affect the content of other elements, while the effect is frequently disregarded, leading to subsequent negligence of the common influence on the physical properties of alloys. Therefore, the correlation between alloying elements and physical properties has not been adequately addressed in the existing studies. In response to this problem, the present study focuses on the Al₁₀Ti₁₅Ni_x1Cr_x2Co_x3 alloys and investigates the competitive interplay among Ni, Cr, and Co elements in the formation of physical properties through a single-element (SE) analysis and a multi-element (ME) analysis based on the first principles calculations and the partial least squares (PLS) regression. The values of C₁₁ and C₄₄ generally increase with the incorporation of Ni or Cr content in light of SE analysis, which is contrary to the inclination of ME analysis in predicting the impact of Ni and Cr elements, and the Ni element demonstrates a pronounced negative competitive ability. The overall competitive relationship among the three alloying elements suggests that increasing the content of Ni and Cr does not contribute to enhancing the elastic constants of alloys, and the phenomenon is also observed in the analysis of elastic moduli. The reason is that the SE analysis fails to account for the aforementioned common influence of multiple alloying elements on the physical properties of alloys. Therefore, the integration of SE analysis and ME analysis is more advantageous in elucidating the hidden competitive mechanism among multiple alloying elements, and offering a more robust theoretical framework for the design of alloy materials.

The impact of variations in the content of single alloying element on the properties of alloy materials has been extensively discussed, but the influence of this change on the content of multiple alloying elements in the alloy materials has been disregarded, as the performances of alloy materials should be determined by the collective influence of multiple alloying elements. To address the aforementioned issue, the present study conducted a comprehensive investigation into the impact of variations in the content of alloying elements, namely Ni, Cr, and Co, on the structural and mechanical properties of L1₂-(Ni_x1Cr_x2Co_x3)₃Al precipitates using the high-throughput first-principles calculations and the partial least squares (PLS) regression, and the competitive mechanism among these three elements was elucidated. The findings demonstrate that the same alloying element may exhibit opposite effects in both single element analysis and comprehensive multi-element analysis, for example, the effect of Ni element on elastic constant C₁₁, and the influence of Cr element on Vickers hardness and yield strength. The reason for this is that the impact of the content of other two alloying elements is ignored in the single element analysis. Meanwhile, the Co element demonstrates a significant competitive advantage in the comparative analysis of three alloying elements for different physical properties. Therefore, the methodology proposed in this study will facilitate the elucidation of competition mechanisms among different alloy elements and offer a more robust guidance for experimental preparation.

In order to enhance the performance of 20# steel, this study successfully fabricated AlCoCrFeNi high-entropy alloy coatings with different WC contents (x = 0, 10, 20, 30 wt%) on its surface using plasma cladding technology. The effects of WC content on the microstructure, mechanical properties, and corrosion resistance of the coatings were systematically investigated. The results indicate that without WC addition, the coating consists of a dual-phase structure comprising BCC and FCC phases. With the incorporation of WC, the FCC phase disappears, and the coating evolves into a composite structure based on the BCC matrix, embedded with multiple carbide phases such as W₂C, M₇C₃, M_xC_γ, and Co₆W₆C. These carbides are predominantly distributed along grain boundaries. As the WC content increases, significant grain refinement occurs and the volume fraction of carbides rises. The coating exhibits a mixed microstructure of equiaxed and columnar crystals, with excellent metallurgical bonding to the substrate. The microhardness of the coating increases markedly with higher WC content; however, the rate of enhancement slows when WC exceeds 20 wt%. The hardness of 1066.36 HV is achieved at 30 wt% WC. Wear test results show that both the friction coefficient and wear rate first decrease and then increase with increasing WC content. The optimal wear resistance is observed at 20 wt% WC, with a friction coefficient of 0.549 and a wear mass loss of only 0.25 mg, representing an approximately 40% reduction compared to the WC-free coating. Electrochemical tests demonstrate that the coating with 20 wt% WC facilitates the formation of a dense and stable passive film in NaCl solution, effectively inhibiting Cl⁻ ion penetration. This coating exhibits the best corrosion resistance, characterized by the lowest corrosion current density of 1.349 × 10⁻⁶ A·cm⁻² and the highest passive film resistance of 2764 Ω·cm².