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The effect of ZrB2, Y2O3, and/or graphene nanoplatelet incorporation on densification, microstructural evolution, and compressive deformation of W-0.7Ni-0.3Fe alloys ZrB2、Y2O3和/或石墨烯纳米板掺入对W-0.7Ni-0.3Fe合金致密化、显微组织演化和压缩变形的影响
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-01-22 DOI: 10.1016/j.ijrmhm.2026.107694
Deepak Adhikari , Suvam Sarthak Tripathy , Suresh Chandra Adhikari , Ashirbad Nayak , Alok Kumar Prusty , Tapas Kumar Sahoo , Mayadhar Debata , Pradyut Sengupta
In recent times, dispersion strengthening has been given prime importance by researchers to modify the microstructure and enhance the mechanical properties of tungsten alloys for their applications in strategic sectors. The present study focuses on the incorporation of Y2O3, ZrB2, and graphene nanoplatelet (GNP) in W-0.7Ni-0.3Fe alloys to improve their overall characteristics. To achieve the same, the selected alloy compositions were blended, compacted, and then sintered at 1500 °C for 75 min in H2 atmosphere. It was observed that the addition of nano Y2O3 and GNP increases the sintered density of the WHAs. FESEM and EPMA analysis exhibit the uniform distribution of dispersoids in WHAs. It was noticed that the maximum compressive strength of 1985.6 MPa was obtained in 1 wt% Y2O3 incorporated W-0.7Ni-0.3Fe alloy, followed by Y2O3 + GNP, base alloy, GNP, and ZrB2 incorporated alloys. The maximum bulk hardness of ∼347 HV was obtained in the Y2O3 + GNP incorporated WHAs. Overall, the combined incorporation of Y2O3 and GNP was effective in improving the densification, microstructure and mechanical properties of sintered W-based systems.
近年来,为了改善钨合金的显微组织,提高其力学性能,弥散强化已成为钨合金在战略领域应用的重要手段。本研究的重点是在W-0.7Ni-0.3Fe合金中掺入Y2O3、ZrB2和石墨烯纳米板(GNP),以改善其整体性能。为了达到这一目的,将选定的合金成分混合、压实,然后在1500℃的H2气氛中烧结75 min。结果表明,纳米Y2O3和GNP的加入提高了合金的烧结密度。FESEM和EPMA分析表明,弥散体分布均匀。结果表明,Y2O3含量为1 wt%的W-0.7Ni-0.3Fe合金抗压强度最大,达到1985.6 MPa,其次是Y2O3 + GNP、基体合金、GNP和ZrB2合金。Y2O3 + GNP掺入的WHAs的最大体硬度为~ 347 HV。总体而言,掺加Y2O3和GNP可有效改善烧结w基体系的致密化、显微组织和力学性能。
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引用次数: 0
Correlation between microstructure, phase evolution, and high-temperature wear resistance of HVOF-sprayed Cr3C2-NiCr composite coatings subjected to superalloy aging treatment 高温合金时效处理下hvof喷涂Cr3C2-NiCr复合涂层组织、相演化与高温耐磨性的关系
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-02-12 DOI: 10.1016/j.ijrmhm.2026.107727
Pejman Zamani, Meysam Khakian, Saeed Lak, Mohammad Amin Amjadi
The sequence of aging heat treatment for superalloy base metals and the application of hardface coatings pose significant challenges in the refurbishment of gas turbine blades. This study investigates the influence of an aging heat treatment of IN738 superalloy (845 °C, 24 h) on the microstructural features, mechanical characteristics, and tribological performance of HVOF-sprayed Cr₃C₂–NiCr coating. Microstructural and phase analyses were performed utilizing XRD, SEM, and EDS, while microhardness, fracture toughness, and ball-on-disc wear tests were conducted at room temperature and 550 °C. The as-sprayed coating consisted of Cr₃C₂, Cr₇C₃, and NiCr phases, whereas aging promoted the formation of Ni₃Cr, Cr₂₃C₆, and Cr₂O₃ phases through carbide coarsening and oxidation. These transformations resulted in a synergistic effect, leading to approximately a 20% reduction in hardness and a 50% decrease in fracture toughness, accompanied by a moderate increase in wear rate. At room temperature, the as-sprayed and aged coatings exhibited wear rates of 3.1 × 10−15 and 4.1 × 10−15 m3/N·m, respectively, whereas at 550 °C these values decreased to 2.0 × 10−15 and 3.0 × 10−15 m3/N·m. The as-sprayed coating exhibited predominantly abrasive and mild oxidative–adhesive wear, while the aged one showed adhesive transfer and oxide-assisted delamination. The findings suggest that the aging heat treatment of turbine superalloys should precede HVOF coating deposition to maintain the coating's microstructural integrity and high-temperature wear resistance.
高温合金基体金属的时效热处理顺序和硬面涂层的应用对燃气轮机叶片的翻新提出了重大挑战。研究了对IN738高温合金进行时效热处理(845℃,24 h)对hvof喷涂Cr₃C₂-NiCr涂层的组织特征、力学特性和摩擦学性能的影响。利用XRD、SEM和EDS进行了显微组织和物相分析,并在室温和550℃下进行了显微硬度、断裂韧性和球盘磨损测试。喷涂后的涂层由Cr₃C₂、Cr₇C₃和NiCr相组成,而时效通过碳化物粗化和氧化促进了Ni₃Cr、Cr₂₃C₆和Cr₂O₃相的形成。这些转变产生了协同效应,导致硬度降低约20%,断裂韧性降低50%,同时磨损率适度增加。在室温下,喷涂态和时效态涂层的磨损率分别为3.1 × 10−15和4.1 × 10−15 m3/N·m,而在550℃时,磨损率分别为2.0 × 10−15和3.0 × 10−15 m3/N·m。喷态涂层主要表现为磨粒磨损和轻度氧化-粘接磨损,而时效涂层则表现为粘接转移和氧化辅助脱层。研究结果表明,为了保持涂层的显微组织完整性和高温耐磨性,应先对涡轮高温合金进行时效热处理,然后再沉积HVOF涂层。
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引用次数: 0
Optimization of mechanical properties and cost-reduction of potential orthopedic Zr alloys maintaining favorable biocompatibility through impurity utilization and microalloying 通过杂质利用和微合金化优化潜在矫形用Zr合金的力学性能和降低成本以保持良好的生物相容性
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-01-20 DOI: 10.1016/j.ijrmhm.2026.107687
X.K. Liu , Z.C. Yin , S.X. Liang, Z.K. Zhou, Z.Y. Yuan, B.Y. Liu, Y.X. Guo, S.Z. Zhang, J.S. Zhang, X.Y. Zhang, R.P. Liu
Zirconium (Zr) shows great promise for next-generation orthopedic implants due to its excellent biocompatibility, low elastic modulus, and low magnetic susceptibility. However, it is clinically constrained by high production costs and insufficient yield strength. Herein, a novel “impurity utilization + microalloying” strategy is proposed to optimize mechanical properties and reduce costs of Zr-based alloys while preserving biocompatibility and magnetic resonance imaging (MRI) compatibility. By leveraging the β-stabilizing effect of inherent impurities (Hf, Fe) in sponge zirconium (SZr) and atomic mobility inhibition by microalloying elements (Fe, Si, Mg), the brittle ω phase is suppressed in SZr-xNb-0.2 Mg-0.15Fe-0.1Si (SZNx) alloys, promoting formation of the intermediate β' phase (from β → ω transformation). Ultrafine/nanoscale β' plates induce precipitation and boundary strengthening, synergizing with solid solution strengthening from impurities and microalloying elements to enhance strength while maintaining low Young's modulus and good ductility. Consequently, SZNx alloys outperform ZrNb alloys fabricated from high-purity Zr (NZr) or unalloyed SZr in strength. Notably, the Zr-15Nb-0.25 Mg-0.15Fe-0.1Si (SZN15) alloy exhibits exceptional comprehensive properties: Young's modulus (E) = 58 ± 3 GPa, yield strength (YS) = 750 ± 18 MPa, elongation (EL) = 15.5 ± 1.6%. In vitro biocompatibility assessments show SZN15 cell viability exceeds 92% over all test periods, comparable to or better than clinically used Ti–6Al–4 V (TC4) and NZr. The mass magnetic susceptibility of SZNx alloys (1.27–1.90 × 10−6 cm3/g) is ∼50% that of TC4, ensuring excellent MRI compatibility. Most importantly, the cost of SZNx alloys is reduced by over 80% versus NZr-based alloys. This work offers an efficient, cost-effective strategy for developing low-cost, high-performance Zr-based orthopedic alloys, addressing the strength-modulus-ductility trade-off and cost barriers limiting clinical translation. .
锆(Zr)由于其优异的生物相容性、低弹性模量和低磁化率,在下一代骨科植入物中显示出巨大的前景。但由于生产成本高,屈服强度不足,在临床上受到限制。本文提出了一种新的“杂质利用+微合金化”策略,以优化zr基合金的力学性能和降低成本,同时保持生物相容性和磁共振成像(MRI)相容性。利用海绵锆(SZr)中固有杂质(Hf, Fe)的β稳定作用和微合金化元素(Fe, Si, Mg)的原子迁移抑制作用,SZr- xnb -0.2 Mg-0.15Fe-0.1Si (SZNx)合金中的脆性ω相被抑制,促进中间β′相的形成(从β→ω转变)。超细/纳米级β′板诱导析出和边界强化,与杂质和微合金元素的固溶体强化协同作用,在保持低杨氏模量和良好延性的同时提高强度。因此,SZNx合金在强度上优于由高纯度Zr (NZr)或非合金化SZr制成的ZrNb合金。Zr-15Nb-0.25 Mg-0.15Fe-0.1Si (SZN15)合金表现出优异的综合性能:杨氏模量(E) = 58±3 GPa,屈服强度(YS) = 750±18 MPa,伸长率(EL) = 15.5±1.6%。体外生物相容性评估显示,在所有测试期间,SZN15的细胞存活率超过92%,与临床使用的Ti-6Al-4 V (TC4)和NZr相当或更好。SZNx合金的质量磁化率(1.27-1.90 × 10−6 cm3/g)是TC4的约50%,确保了出色的MRI相容性。最重要的是,与nzr基合金相比,SZNx合金的成本降低了80%以上。这项工作为开发低成本、高性能的zr基骨科合金提供了一种高效、经济的策略,解决了强度-模量-延性权衡和限制临床转化的成本障碍。
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引用次数: 0
Friction and wear behavior of NiCu-diamond composites fabricated by defect-controlled powder bed fusion (PBF) process 缺陷控制粉末床熔合制备nicu -金刚石复合材料的摩擦磨损行为
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-01-22 DOI: 10.1016/j.ijrmhm.2026.107691
Ruochong Wang , Yunan Fan , Zihan Yang , Weiwei He , Li Wang , Bin Liu , Yang Lu , Yong Liu
The influences of printing process on metallurgical quality and wear resistance of NiCu-diamond composites were quantitatively analyzed. The NiCu-diamond composite with low porosity (∼1.6 vol%) and low loss of diamond particles (only 0.5 vol%) was successfully fabricated, at an electron beam current of 2.4 mA, and a scanning rate of 1 m·s−1. The wear rate of the NiCu-diamond composite was as low as 5.0 × 10−7 mm3·N−1·m−1, and coefficients of friction (COFs) within 0.02–0.05. These values represent a substantial reduction compared to the corresponding values of 43.7 × 10−7 mm3·N−1·m−1 and 0.18–0.28. The dense tribofilm formed during wet friction (in 3.5 wt% NaCl solution) hinders further wear of the substrate, leading to lower COFs and wear rates than those of dry friction. The PBF-ed NiCu-diamond composites show excellent wet friction and wear properties with COFs lower than 0.04 and a wear rate of 1.6 × 10−7 mm3·N−1·m−1.
定量分析了印刷工艺对镍钴-金刚石复合材料冶金质量和耐磨性的影响。在2.4 mA的电子束电流和1 m·s−1的扫描速率下,成功制备了低孔隙率(~ 1.6 vol%)和低金刚石颗粒损耗(仅0.5 vol%)的nicu -金刚石复合材料。nicu -金刚石复合材料的磨损率低至5.0 × 10−7 mm3·N−1·m−1,摩擦系数(COFs)在0.02 ~ 0.05之间。与相应的43.7 × 10−7 mm3·N−1·m−1和0.18-0.28值相比,这些值有了很大的降低。湿摩擦(在3.5 wt% NaCl溶液中)形成的致密摩擦膜阻碍了基体的进一步磨损,导致COFs和磨损率低于干摩擦。PBF-ed nicu -金刚石复合材料具有优异的湿摩擦磨损性能,COFs < 0.04,磨损率为1.6 × 10−7 mm3·N−1·m−1。
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引用次数: 0
Effects of Co addition on the microstructure and properties of multi-elemental NbSi based ultrahigh temperature alloys Co添加对多元素Nb - Si基超高温合金组织和性能的影响
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-02-11 DOI: 10.1016/j.ijrmhm.2026.107732
Xiya He, Xiping Guo, Ying Li, Chenyu Hu
Five multi-elemental NbSi based ultrahigh temperature alloys with nominal compositions of Nb-22Ti-14.8Si-4Cr-2.5Al-xCo (x = 0, 1, 2, 4, and 8 at.%) were prepared via vacuum non-consumable arc-melting. The effects of Co addition on the microstructure, nanoindentation hardness, compressive strength and isothermal oxidation resistance at 1250 °C of the alloys were investigated. The results reveal that the content of both the Nbss/γ(Nb,X)5Si3 eutectic and the Nbss phase decreases with increasing Co content in the alloys and Co addition promotes the morphological transformation of Nbss toward a dendritic structure. Meanwhile, the addition of Co promotes the formation of new polymorphs of silicide phases; the increase in Co content changes the phase fractions of the alloys. In alloys with 0, 1, and 2 at.% Co, the only silicide phase is γ(Nb,X)5Si3, but in alloys with Co content above 2 at.%, two other types of silicide phases (α(Nb,X)5Si3 and β(Nb,X)5Si3) also exist except for γ(Nb,X)5Si3. Furthermore, Co addition promotes the formation of low-melting-point phases such as Cr2(Nb,X), Tiss and Ti2Co between Nbss/γ(Nb,X)5Si3 eutectic cells and along the Nbss boundaries, which degrades the compressive strength at 1250 °C of the alloys. However, Co addition increases the nanoindentation hardness of both Nbss and γ(Nb,X)5Si3 due to the solid solution strengthening effect of Co. The addition of Co has no significant effect on the oxidation resistance at 1250 °C of the alloys.
5种多元素NbSi基超高温合金,标称成分为Nb-22Ti-14.8Si-4Cr-2.5Al-xCo (x = 0、1、2、4和8 at)。%)通过真空非耗材电弧熔炼制备。研究了Co的加入对合金显微组织、纳米压痕硬度、抗压强度和1250℃等温抗氧化性能的影响。结果表明:随着Co含量的增加,Nbss/γ(Nb,X)5Si3共晶和Nbss相的含量均降低,Co的加入促进了Nbss向枝晶组织转变;同时,Co的加入促进了硅化物相新晶型的形成;Co含量的增加改变了合金的相分数。在具有0、1和2 at的合金中。% Co,唯一的硅化物相是γ(Nb,X)5Si3,但在Co含量大于2 at的合金中。%,除γ(Nb,X)5Si3外,还存在另外两种硅化物相(α(Nb,X)5Si3和β(Nb,X)5Si3)。此外,Co的加入促进了Nbss/γ(Nb,X)5Si3共晶胞间及Nbss晶界上Cr2(Nb,X)、Tiss和Ti2Co等低熔点相的形成,降低了合金在1250℃时的抗压强度。然而,由于Co的固溶强化作用,Co的加入提高了Nbss和γ(Nb,X)5Si3的纳米压痕硬度,而Co的加入对合金在1250℃时的抗氧化性能没有显著影响。
{"title":"Effects of Co addition on the microstructure and properties of multi-elemental NbSi based ultrahigh temperature alloys","authors":"Xiya He,&nbsp;Xiping Guo,&nbsp;Ying Li,&nbsp;Chenyu Hu","doi":"10.1016/j.ijrmhm.2026.107732","DOIUrl":"10.1016/j.ijrmhm.2026.107732","url":null,"abstract":"<div><div>Five multi-elemental Nb<img>Si based ultrahigh temperature alloys with nominal compositions of Nb-22Ti-14.8Si-4Cr-2.5Al-xCo (x = 0, 1, 2, 4, and 8 at.%) were prepared via vacuum non-consumable arc-melting. The effects of Co addition on the microstructure, nanoindentation hardness, compressive strength and isothermal oxidation resistance at 1250 °C of the alloys were investigated. The results reveal that the content of both the Nbss/γ(Nb,X)<sub>5</sub>Si<sub>3</sub> eutectic and the Nbss phase decreases with increasing Co content in the alloys and Co addition promotes the morphological transformation of Nbss toward a dendritic structure. Meanwhile, the addition of Co promotes the formation of new polymorphs of silicide phases; the increase in Co content changes the phase fractions of the alloys. In alloys with 0, 1, and 2 at.% Co, the only silicide phase is γ(Nb,X)<sub>5</sub>Si<sub>3</sub>, but in alloys with Co content above 2 at.%, two other types of silicide phases (α(Nb,X)<sub>5</sub>Si<sub>3</sub> and β(Nb,X)<sub>5</sub>Si<sub>3</sub>) also exist except for γ(Nb,X)<sub>5</sub>Si<sub>3</sub>. Furthermore, Co addition promotes the formation of low-melting-point phases such as Cr<sub>2</sub>(Nb,X), Tiss and Ti<sub>2</sub>Co between Nbss/γ(Nb,X)<sub>5</sub>Si<sub>3</sub> eutectic cells and along the Nbss boundaries, which degrades the compressive strength at 1250 °C of the alloys. However, Co addition increases the nanoindentation hardness of both Nbss and γ(Nb,X)<sub>5</sub>Si<sub>3</sub> due to the solid solution strengthening effect of Co. The addition of Co has no significant effect on the oxidation resistance at 1250 °C of the alloys.</div></div>","PeriodicalId":14216,"journal":{"name":"International Journal of Refractory Metals & Hard Materials","volume":"138 ","pages":"Article 107732"},"PeriodicalIF":4.6,"publicationDate":"2026-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146160482","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Potter orientation relationship: The key to the origin of {101¯1} α martensitic twinning and the unusual β precipitation in Zr alloys 波特取向关系:Zr合金中{10.1¯1}α马氏体孪晶和异常β析出的关键
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-02-11 DOI: 10.1016/j.ijrmhm.2026.107730
Xinu Tan , Yushun Liu , Risheng Qiu , Xuan Zhang , Liang Zhang , Jiateng Ma , Wangrui Ren , Feitao Li
Two types of orientation relationship (OR) Burgers and Potter can be observed during the phase transformation between the α and β phases in Zr alloys. In this work, electron back scatter diffraction and high-resolution transmission electron microscopy were carried out to characterize Potter OR in the solution-treated and subsequently annealed Zr alloys. Our results reveal the presence of Potter OR between parent β-Zr and {101¯1}α twinning Martensite, elucidating the unique variant selection of {101¯1} twins with in a single α-Zr grain in solution-treated samples. Significantly, a novel, non-stress induced, twinning mechanism was proposed via direct phase transformation based on Potter OR in Martensite. Upon annealing, the OR between β-Zr within the twinning Martensite and α-Zr retains Potter OR, independent of the element segregation at twin boundary. The occurrence of Potter OR instead of Burgers OR is attributed to the lower formation energy of Potter OR upon twinning based on our calculation. These results demonstrate an intrinsic association between Potter OR and the formation of {101¯1} twins, shedding light on the designing of novel high-performance Zr alloys.
在Zr合金的α相和β相相变过程中,可以观察到两种取向关系(OR): Burgers和Potter。在这项工作中,电子背散射衍射和高分辨率透射电镜进行表征波特或在固溶处理和随后退火的Zr合金。我们的研究结果显示亲本β-Zr和{101¯1}α孪晶马氏体之间存在Potter OR,阐明了在溶液处理样品中具有单一α- zr晶粒的{101¯1}孪晶的独特变异选择。值得注意的是,基于马氏体的波特或直接相变,提出了一种新的、非应力诱导的孪生机制。退火后,孪晶马氏体内β-Zr与α-Zr之间的OR保持波特OR,与孪晶边界元素偏析无关。根据我们的计算,波特或而不是汉堡或的出现是由于波特或在孪生时的地层能量较低。这些结果证明了Potter OR与{101¯1}孪晶形成之间的内在联系,为设计新型高性能Zr合金提供了指导。
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引用次数: 0
Microstructure and properties of spark plasma sintered WC–Cu–based in situ composites containing graphite 火花等离子烧结wc - cu基石墨原位复合材料的组织与性能
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-02-05 DOI: 10.1016/j.ijrmhm.2026.107722
Tomila M. Vidyuk , Dina V. Dudina , Alexander I. Gavrilov , Arina V. Ukhina , Vladislav S. Shikalov , Igor S. Batraev , Sergey Yu. Usynin , Boris B. Bokhonov
In this study, in situ WC–Cu–based composites containing graphite were fabricated from a mixture of W, C(graphite) and Cu powders by high-energy mechanical milling and subsequent reactive spark plasma sintering (SPS). The synthesis of the carbides occurred during the SPS stage. In order to investigate the effect of graphite concentration on the structure and properties of the composites, the W–C(graphite)–Cu mixtures with three different molar ratios of elements (1:1:3, 1:1.3:3 and 1:1.7:3) were prepared. The graphite not converted into carbides remained unreacted in the sintered compacts. The combination of mechanical milling and SPS resulted in the formation of unconventional microstructures. The Cu-rich regions of re-solidified material are located between the composite areas, in which the WC and W2C particles are distributed uniformly. As the concentration of graphite was increased, the hardness and electrical conductivity of the composites decreased. The concentration of graphite in the composites influenced the morphology of the worn surfaces formed under dry sliding conditions. The WC–W2C–Cu-graphite composite (processing conditions: W–C(graphite)–3Cu mixture, 15 min of milling, SPS at 980 °C) shows an attractive combination of properties: a hardness of 250 HV, an electrical conductivity of 25% of the International Annealed Copper Standard, a residual porosity of less than 5%, a coefficient of friction of 0.58 in a pair with a WC-6Co ball, and a specific wear rate of 0.6 × 10−5 mm3 N−1 m−1.
在本研究中,将W, C(石墨)和Cu粉末混合,通过高能机械铣削和随后的反应放电等离子烧结(SPS)制备了含有石墨的原位wc - Cu基复合材料。碳化物的合成发生在SPS阶段。为了研究石墨浓度对复合材料结构和性能的影响,制备了三种不同元素摩尔比(1:1:3,1:1.3:3和1:1.7:3)的W-C(石墨)-Cu混合物。未转化为碳化物的石墨在烧结坯中未发生反应。机械铣削与SPS的结合导致了非常规显微组织的形成。再固化材料的富cu区位于复合区之间,其中WC和W2C颗粒分布均匀。随着石墨浓度的增加,复合材料的硬度和电导率下降。复合材料中石墨的浓度影响了干滑动条件下形成的磨损表面的形貌。wc - w2c - cu -石墨复合材料(加工条件:W-C(石墨)-3Cu混合物,铣削15分钟,在980℃下SPS)显示出具有吸引力的性能组合:硬度为250 HV,电导率为国际退火铜标准的25%,残余孔隙率小于5%,与WC-6Co球对的摩擦系数为0.58,比磨损率为0.6 × 10−5 mm3 N−1 m−1。
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引用次数: 0
Microstructure and properties of tantalum deposited by laser melting deposition using non-spherical tantalum powder 非球形钽粉激光熔敷钽的组织与性能
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-01-12 DOI: 10.1016/j.ijrmhm.2026.107673
Jun Yang, Yanhang Shi, Liu He, Wei Wang, Guomin Le, Xinjian Zhang
The elevated cost of spherical tantalum powder utilized in additive manufacturing significantly hinders the development and application of tantalum components. In this study, three sets of tantalum thin-wall samples were fabricated using laser melting deposition (LMD) with varying laser power settings, employing non-spherical tantalum powder as the raw material. The samples were analyzed for their scanning electron microscopy (SEM) morphology, phase composition, density, hardness, mechanical properties, and impurity content. The findings indicate that the tantalum components produced via LMD exhibit columnar grains oriented along the deposition direction, achieving a high density of up to 98.7%. The LMD-fabricated tantalum components demonstrate moderate mechanical properties and elongation rate. This study demonstrates that non-spherical tantalum powder can be effectively utilized to produce tantalum components with superior performance through LMD. This approach offers a novel and cost-effective method for the preparation of tantalum components, which holds significant potential for the widespread adoption and application of tantalum.
在增材制造中使用的球形钽粉的高成本严重阻碍了钽组件的开发和应用。本研究以非球形钽粉为原料,采用激光熔化沉积(LMD)技术,在不同的激光功率设置下制备了三组钽薄壁样品。分析了样品的扫描电镜形貌、相组成、密度、硬度、力学性能和杂质含量。结果表明,通过LMD制备的钽组分呈现出沿沉积方向取向的柱状晶粒,密度高达98.7%。lmd制备的钽元件具有中等的力学性能和伸长率。本研究表明,通过LMD可以有效地利用非球形钽粉制备性能优异的钽组分。该方法为制备钽组分提供了一种新颖、经济的方法,对钽的广泛采用和应用具有重要的潜力。
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引用次数: 0
Design of novel sustainable cemented carbides strengthened by η-phase to replace critical raw materials 新型可持续发展的η相强化硬质合金的设计,以取代关键的原材料
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-01-22 DOI: 10.1016/j.ijrmhm.2026.107695
José García , Andrei Chychko , Christian Gold
Cemented carbide production is heavily reliant on critical raw materials (CRMs) such as tungsten (W), cobalt (Co), titanium (Ti), tantalum (Ta), niobium (Nb), and ruthenium (Ru), which face increasing supply risks, cost volatility, and environmental challenges. This study presents a sustainable alternative through the design of WC-based cemented carbides reinforced with finely dispersed η-phase carbides. The η-phase morphology and distribution are tailored to substitute conventional γ-phase formers (Ti, Ta, Nb), allowing the replacement of Co binder metal, and minimizing reliance on scarce elements such as Ru. The resulting microstructures exhibit enhanced high-temperature strength, hot hardness, and fracture resistance. Cutting performance tests under severe thermomechanical loading conditions confirm that the new η-phase–reinforced grades offer equivalent or superior performance compared to conventional grades. A detailed Product Carbon Footprint (PCF) analysis demonstrates significantly lower environmental impact and material criticality, establishing η-phase strengthening as a robust strategy for developing next-generation, high-performance cemented carbides with improved sustainability.
硬质合金的生产严重依赖于关键原材料,如钨(W)、钴(Co)、钛(Ti)、钽(Ta)、铌(Nb)和钌(Ru),这些原材料面临着越来越大的供应风险、成本波动和环境挑战。本研究提出了一种可持续的替代方案,即设计以分散良好的η相碳化物为增强材料的wc基硬质合金。η相的形态和分布适合于传统的γ相形成物(Ti, Ta, Nb),允许替代Co结合金属,并最大限度地减少对稀有元素(如Ru)的依赖。由此产生的显微组织表现出增强的高温强度、热硬度和抗断裂性。在严格的热机械载荷条件下的切削性能测试证实,与传统牌号相比,新的η相增强牌号具有同等或更好的性能。一项详细的产品碳足迹(PCF)分析表明,该方法显著降低了对环境的影响和材料的临界性,确立了η相强化作为开发下一代高性能硬质合金的有力策略,并提高了可持续性。
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引用次数: 0
The development of W-Cr-Al alloys by spark plasma sintering and their oxidation behavior 放电等离子烧结制备W-Cr-Al合金及其氧化性能
IF 4.6 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-01 Epub Date: 2026-01-30 DOI: 10.1016/j.ijrmhm.2026.107713
Chunyan Li , Jie Chen , Andrey Litnovsky , Christian Linsmeier , Shuotong Zong , Yucheng Wu , Xuejiao Wang , Junwei Qiao
Tungsten-based self-passivating metal alloys with reduced thermo-oxidation (SMART), which using Cr or Si as oxidation-resistant elements, have exhibited great potential for oxidation resistance application at high temperature compared with pure W. In this work, aluminum (Al) was added to WCr SMART systems to further improve the oxidation resistance, and the novel W-17.8Cr-6.4Al alloys were successfully developed using spark plasma sintering (SPS) technique. The influence of sintering pressure and temperature on the densification process was systematically investigated, and the oxidation behaviors were studied at 800 °C and 1000 °C. The sintering curves exhibit that there is the liquidation of Al above around 630 °C, and the rapid densification of W-Cr-Al alloys starts above 923–950 °C. The intermetallic compounds of (WCr)Al12 and (WCr)Al4 are generated when sintered at 650 °C and 700 °C, respectively. When sintered above 1000 °C, W-Cr-Al alloys mainly consist of two BCC phases of W-Cr-Al solution. Dense bulk W-Cr-Al alloys, with a density of around 11.6 g/cm3, could be manufactured by sintering above 1200 °C at 20 MPa for 15 min. At the end of oxidation, the oxides formed at 800 °C mainly consist of WO3, Cr2WO6 and Al2W3O12, while WO3 disappears at 1000 °C due to the volatilization of WO3 and the reaction with Cr2O3. In addition, no obvious variation trend of mass gain is observed when oxidized at 800 °C compared with pure W, while a double parabolic trend of mass gain is found during oxidization at 1000 °C. The parabolic oxidation parameter, kp, is around (7–8) × 10−5 mg2/(cm4min) and (4–5) × 10−4 mg2/(cm4min), respectively. Compared to the linear oxidation behavior of pure W, W-Cr-Al alloys exhibit its potential for oxidation resistance application at high temperature.
以Cr或Si为抗氧化元素的钨基自钝化还原性热氧化金属合金(SMART)与纯w相比,在高温下表现出很大的抗氧化应用潜力。本研究将铝(Al)添加到WCr SMART体系中,进一步提高了其抗氧化性能,并利用火花等离子烧结(SPS)技术成功制备了新型W-17.8Cr-6.4Al合金。系统研究了烧结压力和温度对致密化过程的影响,并研究了800℃和1000℃下的氧化行为。烧结曲线表明,在630℃以上Al析出,在923 ~ 950℃以上W-Cr-Al合金开始快速致密化。(WCr)Al12和(WCr)Al4分别在650℃和700℃烧结时生成金属间化合物。在1000℃以上烧结时,W-Cr-Al合金主要由W-Cr-Al溶液的两个BCC相组成。在1200℃以上、20 MPa、15 min的烧结条件下,可制得密度约为11.6 g/cm3的致密块状W-Cr-Al合金。氧化结束时,在800℃时形成的氧化物主要为WO3、Cr2WO6和Al2W3O12,而在1000℃时由于WO3的挥发和与Cr2O3的反应,WO3消失。另外,在800℃氧化时,与纯W相比,质量增加没有明显的变化趋势,而在1000℃氧化时,质量增加呈双抛物线趋势。抛物氧化参数kp分别约为(7-8)× 10−5 mg2/(cm4∙min)和(4 - 5)× 10−4 mg2/(cm4∙min)。与纯W的线性氧化行为相比,W- cr - al合金显示出其在高温下抗氧化应用的潜力。
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International Journal of Refractory Metals & Hard Materials
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