Abstract
It is widely accepted that the growth of protective α-Al2O3 scales on Ni-based alloys is governed by the inward diffusion of oxygen through the oxide grain boundaries (GB). However, there is also some outward diffusion of metal ions to the surface, but it is difficult to quantify. In this work we apply atomic force microscopy, scanning electron microscopy and transmission electron microscopy to investigate the outward flux of Al, which manifests as the growth of small ridges along the alumina GBs after the removal of the outermost oxide layer by mechanical polishing or focused ion beam techniques followed by additional oxidation. As a model alumina-former, NiAl with Hf and Zr additions was investigated. In comparison to Zr, Hf was found to reduce the outward Al diffusion. This outward diffusion was six orders of magnitude smaller than the O inward diffusion.
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Introduction
Alumina is important as a structural material, as well as a functional material in electronics and as a thermally grown external oxide or scale on Al-containing high-temperature alloys. For the past 25 years, it has been generally recognized that transport through a growing α-Al2O3 scale takes place predominantly by the inward diffusion of O along grain boundaries when a reactive element (RE) is present [1–11]. Without a RE addition, a mixed Al and O growth was observed for α-Al2O3. Some prior growth mechanism studies were confounded by the formation of cubic alumina phases such as θ-Al2O3 [7], which grow by outward transport [12]. Recent studies have noted that some concurrent outward Al diffusion along grain boundaries does occur in RE-doped α-Al2O3 [13–15]. While O transport is readily studied by 18O tracers, it is much more difficult to study Al transport. There is only one stable isotope, and its radioactive isotope, Al26, has a lifetime of only about 25 h. The diffusivity of Al26 in alumina was investigated by Fielitz et al. [16]. However, in order to study outward diffusion, the isotope must be in the alloy or in the oxide beneath a previously formed oxide.
There is still some debate about the exact mechanism by which alloy additions like REs affect diffusional fluxes [6]. It is well known that alloy chemistry can dramatically affect the scale performance, including RE additions and S [17–21]. However, most explanations for such observations are only qualitative. Ideally, the most protective, slow-growing scale will contain large α-alumina grains adjacent to the metal, i.e., one with few grain boundaries where transport occurs. In many cases, on top of these large columnar grains, smaller grains also are present. For NiAl, these grains result from the transformation of cubic Al2O3 phases (γ- and/or θ), which form during the initial exposure. Due to the difference between the stable and transient alumina lattice parameters, a layer containing voids is formed between the two regions [2, 6, 22–25].
This study describes the initial work aimed at improving the understanding of transport processes in alumina by conducting well-controlled oxidation exposures and applying high-resolution microscopy techniques for characterization of grain boundary chemistry. Two NiAl alloys were studied with different RE additions. Similar to prior studies [13, 14], the outward transport was studied by removing the outermost part of the scale, created during a longer exposure, and re-oxidizing the samples for a short time. Several different strategies were used that avoid the issue of loss of constraint in the scale, which was an issue in the prior work. Characterization of the regrown scale combined with modeling was used to quantify the very low level of outward transport observed in this study.
Experimental Procedures
Basic Idea
To calculate the outward flux J Al of aluminum atoms along GBs, an earlier study [14] relied on AFM of ridges on top of GBs of an outward growing oxide. Because the oxidation process produced small grains and voids (Fig. 1a) in the outer oxide and a rough topography (Fig. 2a), observation of ridges was difficult and it was necessary to remove this layer. The three-step process presented in Fig. 1 was applied: (a) formation of a protective oxide in the 1st exposure, (b) removal of the outer layer with small grains and voids, with concomitant smoothing of the surface, and (c) a 2nd exposure followed by measuring ridge formation. Due to the strong local variations of the oxide thickness (Fig. 2b), we have to perform a very local analysis using cross-section TEM. The top view in Fig. 1 shows that removing the oxide results in a much easier to interpret topography due to the large grain size. The general idea then is to calculate the flux from the volume of outward diffused material on top of a GB.
For an infinitesimal small time \(\Delta t\), the flux through a GB with lateral length \(L_{\text{GB}}\) can be defined from the number \(N_{\text{GB}}^{\text{Al}}\) of transported atoms as \(J_{Al} = N_{\text{GB}}^{\text{Al}} /(L_{\text{GB}} \Delta t)\). Since the volume \(V_{\text{u}}\) = 2.54 × 10−22 cm3 of the Al2O3 unit cell, which contains 12 Al atoms, is known and the volume V of the ridge is \(V = N_{\text{GB}}^{\text{Al}} V_{\text{u}} /12\), and the flux can be calculated directly from the cross-sectional area A of the ridge as \(J_{\text{Al}} = 12 A/V_{\text{u}}\), where A was obtained from the height and width of the resulting triangle. The obtained flux will depend on the vertical length of the GB, which we consider as the oxide thickness h of the oxide, which is the direct line between the grain boundary exit at the metal to and the upper end of the ridge (Fig. 1c).
Materials and Methods
Two different NiAl alloys with additions of Hf and Zr were studied. Their composition (Table 1) was determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES) and combustion analyses. The materials were subjected to an initial exposure in O2 at 1100 °C for 100 h. After this treatment, called 1st exposure in the following text, the outermost oxide layer was removed using focused ion beam milling or mechanical polishing. The samples were then re-exposed to O2 at 1100 °C for 10 h, which is referred to as the 2nd exposure.
For the mechanical polishing, P2400 polishing paper was used, followed by diamond spray with decreasing grain sizes of 15, 3, 1, and 0.25 µm. The polishing was performed at a small angle to the surface by applying more pressure to one side of the sample. For the ion beam preparation, a plasma-focused ion beam (FIB) from Tescan (Xe-FIB) and a Versa 3D (Ga-FIB) from FEI were used to ion mill circle-shaped patterns into the oxide with depths between 0.3 and 2 µm. Table 2 presents the investigated conditions of the two alloys. Scanning electron microscopy (SEM) characterization and high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) lamella production also were performed in the Versa 3D. For STEM and energy dispersive spectroscopy (EDS) mapping, a FEI Titan or Tecnai was used. For atomic force microscopy (AFM), a Digital Instruments Nanoscope IIIa was used.
Results
Scanning Electron Microscopy and Atomic Force Microscopy
The specimens showed the expected [2] outer region consisting of relatively small alumina grains with some Zr or Hf oxide precipitates and voids. Underneath is a layer with larger Al2O3-oxide grains. Because of the initial surface roughness (Fig. 2a), the removal of the oxide was not homogeneous, and the position on the sample could only be qualitatively related to the remaining oxide’s thickness. After ion milling, an overview of the sample surface was made by SEM and suitable areas for further studies by either AFM or STEM after the 2nd exposure was identified. Backscattered electron (BSE) imaging enabled the observation of GB RE enrichment (Fig. 3a). The bright areas in this figure are regions of exposed metal strongly oxidized after the 2nd exposure (Fig. 3b). Bright areas after the 2nd exposure are most likely Hf-rich precipitates below the oxide. After the 2nd exposure, the GBs were much more prominent, indicating that ridge growth occurred. This behavior was observed for all preparation methods (mechanical polishing, Xe-FIB and Ga-FIB) and both dopants.
Height profiles were obtained by AFM. Before the 2nd exposure, surface roughness (Fig. 4a, d) partially correlated with GB positions, especially for the Ga-milled samples. This made it harder to observe the ridge growth (Fig. 4b, e). This suggested that the higher ion mass of Xe plus defocusing of the beam [attained by the Tescan (Xe-FIB)] helped to produce smoother surfaces. This can be further complicated close to areas where the metal was visible before the 2nd exposure, since the oxide grew more quickly there during re-oxidation. For all of the samples, ridge growth was observed. For the mechanical polished samples, well-defined ridges were observed due to a very smooth initial surface (Fig. 4c, f). On the other hand, it was not possible to find a quantitative difference among the different samples using AFM alone since the ridge height (typically in the range of 50 nm) was dependent on the thickness of the underlying oxide. AFM does not allow determination of the local oxide thickness so a quantitative analysis of GB transport could not be performed.
Transmission Electron Microscopy
Before the 2nd exposure, the average oxide thickness was ~1 µm (Fig. 2b), but the exposed metal suggested considerable variation in that thickness. In our RE-doped NiAl samples (Fig. 2), the exposed grain sizes were several µm laterally, exceeding the thickness of the oxide scale. In Fig. 2b, the HAADF-STEM image indicated ridge growth on top of the GBs (inset in Fig. 2b) as a result from the 2nd exposure Ridges that overlapped where two GBs were very close were ignored. The variation in oxide thickness carried over to all milled and mechanical polished samples. In the case of the ion milled samples, the rough surface topography was maintained. The height and width of the ridges depended on the underlying grain boundary height, h, such that as h increased the ridge dimensions were reduced. In contrast, the ridge growth was larger for low h values as displayed in Fig. 5 for Xe-milled Hf-doped NiAl. Figure 6 shows mechanically polished Zr-doped NiAl where the ridge cross-section resembles a half sphere or a triangle where the oxide was thick. For both Hf- and Zr-doped NiAl, EDS elemental maps revealed that GBs were RE enriched (Figs. 5b, 6b). For Zr-doped NiAl, a Zr enrichment at the metal-oxide interface also was observed. For the Ga-milled samples, we could observe the formation of a Ga and Ni containing aluminum oxide, which seemed to grow from the surface into the oxide.
Al Transport Calculations
Using the procedure described above in the general concept section, the Al transport results for the different samples are displayed in Fig. 7 using a double-logarithmic plot of the flux J of Al against the thickness of the oxide, h. The Xe-FIB prepared Hf-doped NiAl sample followed Fick’s 1st law as indicated by the plotted line. The mechanical polished Hf-doped sample appeared to display a higher Al flux than was observed for Xe-milling.
Discussion
To remove the outer oxide, three different methods were used in this study to investigate the role of sample preparation: (a) mechanical polishing, (b) milling using Ga and (c) milling using Xe-ions. AFM studies of the re-exposed samples showed the formation of oxide ridges above oxide GBs in all cases. However, the non-uniform oxide allowed only a qualitative observation of the outward diffusion in comparison to Nychka et al. [14] and Yang et al. [15]. But yet, Nychka and Tolpygo used only a tapered sectioning technique, i.e., mechanical polishing. The problem with this technique is that there is a loss of constraint of the in-plane stresses in the scale. If this stress is important in affecting transport, as argued by Clarke [26], then the results from this method may not be valid. Nychka et al. found that MA956, an oxide dispersion strengthened FeCrAl alloy, had the least outward transport. This alloy also had the highest strength at temperature and would be least likely to deform under the stress state created by the polishing. Thus, the comparison with Ga and Xe milling in this study attempted to address that issue.
The mechanical polished Hf-doped sample generally seems to display a higher flux than the Xe-milled one, which could be caused by the chemically inert Xe ions remaining on the oxide GB in small quantities, not detectable by STEM-EDS, and acting as an additional obstacle to any diffusion. As another, more likely, explanation is that the strong mechanical deformation during the polishing could have induced additional dislocations, enabling faster diffusion for such samples. Comparing mechanical polished samples, the flux for the Zr-doped NiAl sample was about 5–10 times higher than for the Hf-doped NiAl sample. Generally, all observed fluxes were in the range of several atoms/(nm s), which seems to correlate well with the results of Nychka et al. [14] for Al outward diffusion through alumina on an Fe–Cr–Al alloy. In Nychka’s work, for a similar oxide thickness, fluxes were in the range of 1–100 atoms/(nm s) depending on the alloy composition.
A large variation in the outward flux, J, was observed. Errors in measurements of the ridge dimensions are not likely the largest source of error, accounting for <20% for the worst cases. (However, all measurements were obtained from cross-sections, which cannot capture the 3-dimensional ridge growth.) Of more importance are differences in morphologies of the investigated GBs. In several cases, the investigated GBs contained second phase precipitates or voids, which influenced diffusion and the accuracy of the GB height measurement. Another important issue is the difference between high- and low-angle GBs, which is known to have an impact on segregation [25, 27]. All these factors appear to contribute to the observed scatter of the calculated flux.
To understand the relevance of the outward flux J Al of Al for the oxidation process, it is necessary to compare it to the inward flux J O of O into the metal. An approximate value for J O in dependence of the oxide thickness can be obtained from the mass gain curves. The thickness h of the oxide at every time of the oxidation is obtained by a measurement of the average thickness of the oxide in STEM images after the exposures, which is 0.9 µm (Fig. 2a), and assuming the initial thickness is zero. The development of the thickness between these two values is estimated to follow the mass gain curve. For thick scales, it can be assumed that the outward growth is negligible and that all oxygen is converted to α-Al203.
The flux through a 2-dimensional surface S is \(- \frac{\text{d}}{{{\text{d}}t}}N_{\text{O,tot}} (t)/S\). With the weight of one Al atom m O = 16 Da = 26.6 × 10−27 kg and the total number of reacted O-atoms N O,tot = m tot /m O depends on the gained mass m tot and thus the gained volume. To calculate the flux through the 1-dimensional GBs, it is necessary to know the grain boundary density ν. This density can be obtained from SEM images (Fig. 3b) by counting the number of GBs that intersect with randomly drawn lines. Additionally, we assume that the GBs form a grid with square meshes of equal size. For the Hf-doped NiAl alloy, ν = 1.26 · (14) × 10−4 nm−2. The inward GB flux is thus \(J_{\text{O}} = - \frac{\text{d}}{{{\text{d}}t}}N_{\text{O,tot}} (t)/(S_{\text{tot}} \nu )\) with the sample surface area \(S_{\text{tot}}\). Apart from the already mentioned approximations, this calculation also relies on the growth being homogeneous with uniform thickness, which is not the case as observed in TEM (Fig. 2a). The resulting values for \(J_{\text{O}}\) for the mechanical polished Hf-doped NiAl sample are in the range of 106 s−1 nm−1, which is six orders of magnitude larger than for the outward diffusion of Al. Thus, if Zr-doped NiAl is 10X higher, the outward transport still represents a tiny fraction of the total growth. Future work is planned to study undoped alumina formed on binary NiAl for comparison as well as RE-doped NiCrAl. Until present, we only investigated the influence of two dopants. To be able to judge the relevance of the outward growth for this type of alloys, we are planning to investigate both binary NiAl with no dopants and ternary Ni–Cr–Al alloys with additions of Y and Hf. Furthermore, since the quantification of faint segregation to the GB by TEM techniques is difficult, if not impossible, we are conducting at present atom probe tomography studies of GB and ridges.
Conclusions
Oxide ridges were observed to grow on Hf- and Zr-doped NiAl during a second oxidation period at 1100 °C after removal of the outermost oxide layer for all the removal methods: ion milling with Ga or Xe and mechanical polishing. This confirms previous studies that some outward grain boundary transport of Al occurs during the growth of alumina doped with a reactive element (i.e., Hf or Zr). However, the measured outward flux of Al was 5–6 orders of magnitude smaller than the flux for the inward diffusion of O, which was in the range of 106 s−1 nm−1. Thus, the contribution of the outward Al flux had negligible effect on the mass gain or the oxide thickness on doped NiAl. In this study, the oxide thickness was not uniform. However, using HAADF-STEM images, it was still possible to study the outward transport. An influence of the dopant on the outward flux was found: replacing Zr with Hf reduced the outward flux by a factor of 5–10 in NiAl.
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Acknowledgements
The authors would like to thank Patrik Alnegren and Kristina Hellström from Chalmers for help with the oxidations exposures and Tracie Lowe, Adam W. Willoughby, Michael S. Stephens from ORNL for assistance with experimental work. This research is supported by Swedish Energy Agency.
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Boll, T., Unocic, K.A., Pint, B.A. et al. Grain Boundary Chemistry and Transport Through Alumina Scales on NiAl Alloys. Oxid Met 88, 469–479 (2017). https://doi.org/10.1007/s11085-016-9697-x
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DOI: https://doi.org/10.1007/s11085-016-9697-x