Szala Mirosław, Chocyk Dariusz, Skic Anna, Kamiński Mariusz, Macek Wojciech, Turek Marcin
Department of Materials Engineering, Faculty of Mechanical Engineering, Lublin University of Technology, Nadbystrzycka 36D, 20-618 Lublin, Poland.
Department of Applied Physics, Faculty of Mechanical Engineering, Lublin University of Technology, Nadbystrzycka 36D, 20-618 Lublin, Poland.
Materials (Basel). 2021 Apr 29;14(9):2324. doi: 10.3390/ma14092324.
From the wide range of engineering materials traditional Stellite 6 (cobalt alloy) exhibits excellent resistance to cavitation erosion (CE). Nonetheless, the influence of ion implantation of cobalt alloys on the CE behaviour has not been completely clarified by the literature. Thus, this work investigates the effect of nitrogen ion implantation (NII) of HIPed Stellite 6 on the improvement of resistance to CE. Finally, the cobalt-rich matrix phase transformations due to both NII and cavitation load were studied. The CE resistance of stellites ion-implanted by 120 keV N ions two fluences: 5 × 10 cm and 1 × 10 cm were comparatively analysed with the unimplanted stellite and AISI 304 stainless steel. CE tests were conducted according to ASTM G32 with stationary specimen method. Erosion rate curves and mean depth of erosion confirm that the nitrogen-implanted HIPed Stellite 6 two times exceeds the resistance to CE than unimplanted stellite, and has almost ten times higher CE reference than stainless steel. The X-ray diffraction (XRD) confirms that NII of HIPed Stellite 6 favours transformation of the ε(hcp) to γ(fcc) structure. Unimplanted stellite ε-rich matrix is less prone to plastic deformation than γ and consequently, increase of γ phase effectively holds carbides in cobalt matrix and prevents CrC debonding. This phenomenon elongates three times the CE incubation stage, slows erosion rate and mitigates the material loss. Metastable γ structure formed by ion implantation consumes the cavitation load for work-hardening and γ → ε martensitic transformation. In further CE stages, phases transform as for unimplanted alloy namely, the cavitation-inducted recovery process, removal of strain, dislocations resulting in increase of γ phase. The CE mechanism was investigated using a surface profilometer, atomic force microscopy, SEM-EDS and XRD. HIPed Stellite 6 wear behaviour relies on the plastic deformation of cobalt matrix, starting at CrC/matrix interfaces. Once the CrC particles lose from the matrix restrain, they debond from matrix and are removed from the material. Carbides detachment creates cavitation pits which initiate cracks propagation through cobalt matrix, that leads to loss of matrix phase and as a result the CE proceeds with a detachment of massive chunk of materials.
在众多工程材料中,传统的司太立合金6(钴合金)表现出优异的抗气蚀性能(CE)。然而,钴合金离子注入对其CE行为的影响在文献中尚未完全阐明。因此,本工作研究了热等静压司太立合金6的氮离子注入(NII)对提高抗CE性能的影响。最后,研究了由于NII和气蚀载荷导致的富钴基体相变。对通过120 keV N离子注入两种注量(5×10¹⁷ cm⁻²和1×10¹⁸ cm⁻²)的司太立合金与未注入的司太立合金以及AISI 304不锈钢的抗CE性能进行了比较分析。根据ASTM G32标准采用固定试样法进行气蚀试验。侵蚀速率曲线和平均侵蚀深度证实,两次注入氮的热等静压司太立合金6的抗CE性能比未注入的司太立合金高出两倍,其CE基准比不锈钢高近十倍。X射线衍射(XRD)证实,热等静压司太立合金6的NII有利于ε(密排六方)结构向γ(面心立方)结构转变。未注入的司太立合金富ε基体比γ基体更不易发生塑性变形,因此,γ相的增加有效地将碳化物保持在钴基体中,并防止CrC脱粘。这种现象使CE潜伏期延长了三倍,减缓了侵蚀速率并减轻了材料损失。离子注入形成的亚稳γ结构消耗气蚀载荷进行加工硬化和γ→ε马氏体转变。在进一步的CE阶段,相的转变与未注入合金的情况相同,即气蚀诱导的回复过程、应变消除、位错导致γ相增加。使用表面轮廓仪、原子力显微镜、扫描电子显微镜-能谱仪(SEM-EDS)和XRD对CE机制进行了研究。热等静压司太立合金6的磨损行为依赖于钴基体的塑性变形,从CrC/基体界面开始。一旦CrC颗粒从基体约束中脱落,它们就会从基体上脱粘并从材料中去除。碳化物的脱离产生气蚀坑,引发裂纹通过钴基体扩展,这导致基体相的损失,结果CE以大量材料块的脱离而进行。