Suppr超能文献

纳米结构 Co-Cr-Mo 骨科植入合金:氮增强的纳米结构演变及其对相稳定性的影响。

Nanoarchitectured Co-Cr-Mo orthopedic implant alloys: nitrogen-enhanced nanostructural evolution and its effect on phase stability.

机构信息

Department of Materials Processing, Graduate School of Engineering, Tohoku University, Sendai, Japan.

出版信息

Acta Biomater. 2013 Apr;9(4):6259-67. doi: 10.1016/j.actbio.2012.12.013. Epub 2012 Dec 16.

Abstract

Our previous studies indicate that nitrogen addition suppresses the athermal γ (face-centered cubic, fcc)→ε (hexagonal close-packed, hcp) martensitic transformation of biomedical Co-Cr-Mo alloys and ultimately offers large elongation to failure while maintaining high strength. In the present study, structural evolution and dislocation slip as an elementary process in the martensitic transformation in Co-Cr-Mo alloys were investigated to reveal the origin of their enhanced γ phase stability due to nitrogen addition. Alloy specimens with and without nitrogen addition were prepared. The N-doped alloys had a single-phase γ matrix, whereas the N-free alloys had a γ/ε duplex microstructure. Irrespective of the nitrogen content, dislocations frequently dissociated into Shockley partial dislocations with stacking faults. This indicates that nitrogen has little effect on the stability of the γ phase, which is also predicted by thermodynamic calculations. We discovered short-range ordering (SRO) or nanoscale Cr2N precipitates in the γ matrix of the N-containing alloy specimens, and it was revealed that both SRO and nanoprecipitates function as obstacles to the glide of partial dislocations and consequently significantly affect the kinetics of the γ→ε martensitic transformation. Since the formation of ε martensite plays a crucial role in plastic deformation and wear behavior, the developed nanostructural modification associated with nitrogen addition must be a promising strategy for highly durable orthopedic implants.

摘要

我们之前的研究表明,氮的添加抑制了生物医学 Co-Cr-Mo 合金的非热 γ(面心立方,fcc)→ε(密排六方,hcp)马氏体相变,最终在保持高强度的同时提供了较大的断裂伸长率。在本研究中,我们研究了 Co-Cr-Mo 合金中马氏体相变的结构演变和位错滑移作为一个基本过程,以揭示由于氮的添加导致其增强的 γ 相稳定性的起源。制备了添加和未添加氮的合金样品。含氮合金具有单相 γ 基体,而无氮合金具有 γ/ε 双相微观结构。无论氮含量如何,位错经常分解为具有层错的肖克利部分位错。这表明氮对 γ 相的稳定性几乎没有影响,这也被热力学计算所预测。我们在含氮合金样品的 γ 基体中发现了短程有序(SRO)或纳米级 Cr2N 析出物,并且表明 SRO 和纳米析出物都作为部分位错滑移的障碍,从而显著影响 γ→ε 马氏体相变的动力学。由于 ε 马氏体的形成在塑性变形和磨损行为中起着至关重要的作用,因此与氮添加相关的纳米结构改性一定是制造高耐用骨科植入物的有前途的策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验