SinoTechIntel Academic Portal
Open AccessDOI: 10.1007/s12613-024-2942-4Original Research

Effects of high-entropy alloy binders on the microstructure and mechanical/thermal properties of cemented carbides

Jialin Sun¹,Xiao Li¹,Le Zhao¹,Jun Zhao¹

School of Mechanical, Electrical & Information Engineering, Shandong University, Weihai 264209, China

Read Executive PreviewQuick FAQ
Effects of high-entropy alloy binders on the microstructure and mechanical/thermal properties of cemented carbides
Graphical Abstract / Figure
Published In
Int. Journal of Minerals, Metallurgy and Materials (矿物冶金与材料学报)
Published:January 15, 2025Edition:Vol. 32, Issue 5 • pp. 1190Citation:Jialin Sun et al. (2025), Int. Journal of Minerals, Metallurgy and Materials (矿物冶金与材料学报)
Sponsored Research Partner
Keywords & Index Terms:mechanical propertiesthermal conductivityhardnessfracture toughness

Key Takeaways & Executive Findings

  • • Six HEA binders (e.g., CoCrFeNiMn) were successfully used to fabricate WC–HEA cemented carbides via mechanical alloying and two-step spark plasma sintering. • WC–HEA hardmetals exhibit superior hardness and fracture toughness compared to WC–metal or WC–intermetallic counterparts, overcoming the traditional hardness-toughness trade-off. • Thermal conductivity of WC–HEA is significantly lower than that of conventional WC–Co, which may be advantageous for thermal barrier applications. • The excellent HV–KIC relationship of WC–HEA suggests potential for engineering structural applications where both wear resistance and toughness are critical.
Sponsored Research Highlight

Abstract

The binder phase performs critically on the comprehensive properties of cemented carbides, especially the hardness (HV) and fracture toughness (KIC) relationship. There are strong motivations in both research community and industry for developing alternative binders to Co in cemented carbide system, due to the reasons such as price instability, property degeneration, and toxicity. Herein, six kinds of high entropy alloys (HEA) including CoCrFeNiMn, CoCrFeMnAl, CoCrFeNiAl, CoCrNiMnAl, CoFeNiMnAl, and CrFeNiMnAl were employed as the alternative binder for the preparation of WC–HEA cemented carbides through mechanical alloying and two-step spark plasma sintering. The impacts of HEA on the microstructures, mechanical properties, and thermal conductivity of WC–HEA hardmetals were determined and discussed. WC–HEA hardmetals exhibited both superior HV and KIC to WC–metal or WC–intermetallic cemented carbides, indicating that HEA alloys were not only harder but also tougher in comparison with traditional metal or intermetallic binders. The HEA bonded hardmetals yielded thermal conductivities much lower than that of traditional WC–Co cemented carbide. The excellent HV–KIC relationship of WC–HEA facilitated the potential engineering structural application of cemented carbides.

1. Introduction

Cemented carbides, also named as hardmetals, were considered as one of the most successful engineering composite materials by means of powder metallurgy since it was firstly developed by Karl Schroeter in 1923, which has been widely used as metal and wood machining tools, moulds, as well as wear-resistant mechanical parts [1–3]. Generally, cemented carbide is essentially a composite of hard carbide phase and soft metal phase. The carbide phase is responsible to the high hardness, while the metal phase critically influences the fracture toughness of cemented carbide. It is the combination of hardness and fracture toughness that makes the cemented carbide system uniquely different from either brittle ceramics or ductile metal alloys. Specifically, the cemented carbide is tougher and more impact resistance than ceramic matrix, whereas it is much harder in comparison with metal alloys. The metallic binder plays a critical role for cemented carbide achieving superior combination of mechanical properties.

In the past decades, the metal Co has been considered as the most popular binder phase for cemented carbide, as a function of the excellent wettability of Co on WC, high yield strength and work hardening ability of Co, the plasticity of Co in the system, as well as the interfacial strength between Co and WC [4–6]. However, because of the combined influence of raising cost, hardness/corrosion/oxidation resistances deterioration, and negative effects on health, there is a strong motivation in both academia and industry for investigating alternative binder to Co in cemented carbides [7–8]. In other words, the design of WC–Co materials must balance a host of properties with respect to the intended applications. Up to now, metal, intermetallic compound, and ceramics (metal carbide and oxide) have been used to replace Co in cemented carbide systems [9–14]. However, whilst initially appealing, none of them, to date has been commercialized and produced on an industrial scale. Generally, the WC–metal exhibited unsatisfactory hardness and wear resistance, while WC–intermetallic and WC–ceramics yielded poor fracture toughness. For example, WC–9.6wt%Ni–0.4wt%Co possessed an excellent fracture toughness of 12.5 MPa·m1/2 with a poor hardness of 11.6 GPa [15], whereas WC–10vol% Fe3Al and WC–10wt%Al2O3 exhibited high hardness of 24.1 and 20 GPa but inferior fracture toughness of 7.5 and 5.9 MPa·m1/2 [16–17]. Advanced alternative binder to Co should be effective not only in facilitating the densification of WC, but also overcoming the balance between hardness and fracture toughness of cemented carbides.

Very recently, high entropy alloy (HEA), also named as multiple principal element alloy or compositionally complex alloy, has been attempted to be employed as the rather potential substitute binder for Co in cemented carbides, due to its superior thermal stability, room/high temperature mechanical properties, and tunable properties.

SinoTechIntel Interactive Document Reader
Page 1–5 of Preview
100%
Download Full PDF

Loading authentic research manuscript (Pages 1–5)...

Sponsored Research Partner
Cite This Research Paper
Jialin Sun, Xiao Li, Le Zhao, Jun Zhao (2025). Effects of high-entropy alloy binders on the microstructure and mechanical/thermal properties of cemented carbides. Int. Journal of Minerals, Metallurgy and Materials (矿物冶金与材料学报). https://doi.org/10.1007/s12613-024-2942-4
SinoTechIntel Academic & Legal Disclaimer

Research & Educational Purpose Only:The translations, structured abstracts, analytical annotations, and data reports provided by SinoTechIntel are intended exclusively for academic research, internal corporate R&D, and educational benchmarking. They do not constitute formal engineering, chemical safety, legal, or professional advice.

Copyright & Intellectual Property Notice: Original copyright of the underlying source articles and experimental data remains with the respective authors, institutions, and original publishing journals. SinoTechIntel claims intellectual property only over its proprietary translations, analytical syntheses, and AEO structured enhancements in accordance with international fair use and academic citation principles.

Frequently Asked Questions

What are high-entropy alloy (HEA) binders in cemented carbides?

High-entropy alloy binders are multi-principal element alloys (e.g., CoCrFeNiMn) used as substitutes for traditional cobalt (Co) in cemented carbides. They aim to improve mechanical properties and overcome issues like cost and toxicity associated with Co.

How are WC-HEA cemented carbides fabricated?

WC-HEA cemented carbides are typically fabricated via mechanical alloying of WC and HEA powders followed by two-step spark plasma sintering (SPS), which allows densification while controlling grain growth.

What are the advantages of using HEA binders over Co?

HEA binders can provide superior hardness and fracture toughness compared to traditional metal or intermetallic binders, potentially overcoming the hardness-toughness trade-off. They also offer better thermal stability and may reduce health and environmental concerns.

How does the thermal conductivity of WC-HEA compare to WC-Co?

WC-HEA hardmetals exhibit significantly lower thermal conductivity than conventional WC-Co cemented carbides, which could be beneficial for applications requiring thermal insulation.

What are the potential applications of WC-HEA cemented carbides?

Due to their excellent combination of hardness and toughness, WC-HEA cemented carbides are promising for engineering structural applications such as cutting tools, molds, and wear-resistant parts, especially where both wear resistance and impact resistance are required.

Recommended Scientific Literature & Research Partners

Related Technical Papers & Translations

Research Paper
Direct Repair of the Crystal Structure and Coating Surface of Spent LiFePO4 Materials Enables Superfast Li-Ion Migration

Direct Repair of the Crystal Structure and Coating Surface of Spent LiFePO4 Materials Enables Superfast Li-Ion Migration

The rapid accumulation of spent LiFePO4 (LFP) cathodes from retired lithium-ion batteries necessitates the development of effective and environmental-friendly recycling strategies. In this context, direct regeneration has emerged as a promising approach for reclaiming LFP cathode materials, offering a streamlined pathway to restore their electrochemical functionality. We report an integrated regeneration protocol that simultaneously repairs the degraded crystal structure and reconstructs the damaged carbon coating in spent LFP. The regenerated cathode material had superfast lithium-ion diffusion kinetics and a stable cathode–electrolyte interface, giving a remarkable rate capability with specific capacities of 122 mAh g−1 at 5C and 106 mAh g−1 at 10C (1C = 170 mA g−1). It also maintained capacities of 110.7 mAh g−1 (5C) and 84.1 mAh g−1 (10C) after 400 cycles. It could be used in harsh environments and could be stably cycled at subzero temperatures (−10 and −20 °C) and in solid-state electrolyte batteries. Life cycle assessment combined with economic evaluation using the EverBatt model reveals that this direct regeneration approach has high economic and environmental benefits.

Read Abstract & PDF
Research Paper
Oxide Semiconductor for Advanced Memory Architectures: Atomic Layer Deposition, Key Requirement and Challenges

Oxide Semiconductor for Advanced Memory Architectures: Atomic Layer Deposition, Key Requirement and Challenges

Oxide semiconductors (OSs), introduced by the Hosono group in the early 2000s, have evolved from display backplane materials to promising candidates for advanced memory and logic devices. The exceptionally low leakage current of OSs and compatibility with three-dimensional (3D) architectures have recently sparked renewed interest in their use in semiconductor applications. This review begins by exploring the unique material properties of OSs, which fundamentally originate from their distinct electronic band structure. Subsequently, we focus on atomic layer deposition (ALD), a core technique for growing excellent OS films, covering both basic and advanced processes compatible with 3D scaling. The basic surface reaction mechanisms—adsorption and reaction—and their roles in film growth are introduced. Furthermore, material design strategies, such as cation selection, crystallinity control, anion doping, and heterostructure engineering, are discussed. We also highlight challenges in memory applications, including contact resistance, hydrogen instability, and lack of p-type materials, and discuss the feasibility of ALD-grown OSs as potential solutions. Lastly, we provide an outlook on the role of ALD-grown OSs in memory technologies. This review bridges material fundamentals and device-level requirements, offering a comprehensive perspective on the potential of ALD-driven OSs for next-generation semiconductor memory devices.

Read Abstract & PDF
Research Paper
Laser powder bed fusion of biodegradable Zn-4Cu alloy: Processing, microstructure and properties

Laser powder bed fusion of biodegradable Zn-4Cu alloy: Processing, microstructure and properties

Zn's natural degradability and biocompatibility make it a promising candidate for implants, however, its mechanical properties remain insufficient for bone applications. In this study, the performance of Zn was enhanced by developing Zn-Cu alloys via laser powder bed fusion (LPBF). Optimal LPBF parameters for forming stable tracks were achieved by adjusting laser power and scanning speed. Under optimized conditions of 100 W and 100 mm/s, high-density (99.58%) Zn-Cu alloys with improved hardness (68.2HV) and yield strength (160 MPa) were achieved. These improvements are attributed to solid solution strengthening, segregation strengthening, and grain refinement. The Zn-Cu alloys also demonstrated favorable degradation behavior, with a rate of 0.16 mm/year. This degradation is primarily driven by micro-galvanic corrosion between the CuZn5 phase and Zn matrix, along with refined grains and increased grain boundary density. This work demonstrates a viable strategy for fabricating Zn-based implants with enhanced structural integrity and mechanical performance via LPBF.

Read Abstract & PDF