Kinetic aspects of aluminium titanate layer formation on titanium alloys by plasma electrolytic oxidation
Kinetic aspects of aluminium titanate layer formation on titanium alloys by plasma electrolytic oxidation
复制标题
DOI:
10.1016/s0169-4332(02)00848-6
复制
发表时间:
2002-11
影响因子:
6.7
通讯作者:
A. Yerokhin;A. Leyland;A. Matthews
中科院分区:
文献类型:
--
作者:
A. Yerokhin;A. Leyland;A. Matthews
The paper reports on a systematic investigation into the effects of process parameters on the growth kinetics and associated changes in the structure, phase composition and mechanical properties of surface layers formed on Ti–6Al–4V alloy by plasma electrolytic oxidation (PEO) treatment in 0.05–0.2moll−1solutions of sodium aluminate. Methods of gravimetric, SEM and XRD analysis, as well as microhardness and scratch testing, are employed to investigate mass transfer and phase-structure transformations in the surface layer. The probable mechanisms of layer formation are discussed, which comprise electrochemical oxidation of the Ti-electrode by OH−anions, complimented by chemical precipitation of Al(OH)3and plasma-induced transformations in the surface discharges. Running with a total yield efficiency of 20–30%, these processes lead to the formation of predominantly the Al2TiO5phase with heterogeneous precipitation of Al2TiO5·TiO2and 3Al2TiO5·Al2O3eutectics. Al- and Ti-enriched constituents of this structure show hardnesses of 1050–1480 and 300–845HK,0.02, respectively. The layer growth rate increases with increasing electrolyte concentration, providing a maximum thickness of over 60μm and a surface roughness (Ra) of 3–4μm. Increasing the electrolyte pH from 12.0 to 12.8 results in smoothing and thickening of the surface layer but a lower sample weight gain, associated with an enhancement of the Ti electro-oxidation process. Morphological changes during PEO formation of the surface layer include gradual transformation of the original fine grained but porous structure into a dense, fused morphology which is adversely affected by discharge-induced thermal stresses, causing a degradation of the layer adhesion strength.