Elsevier

Intermetallics

Volume 13, Issue 2, February 2005, Pages 129-136
Intermetallics

Deposition of NiAl coating for improvement of oxidation resistance of cold-rolled Ni3Al foils

https://doi.org/10.1016/j.intermet.2004.06.009Get rights and content

Abstract

β-NiAl, an important intermetallic compound in Ni–Al systems, together with γ′-Ni3Al, has been used as a coating material for Ni-base superalloys, because of its excellent oxidation resistance. In this study, NiAl-based coating through RF magnetron sputtering was selected for deposition on Ni3Al thin foils which were cold-rolled up to 96% without any intermediate annealing steps. The thickness of the coating on Ni3Al foils is restricted below 10 μm, which is much thinner than general coatings on bulk alloys. Insufficient coating thickness can induce rapid Al depletion in the NiAl coating layer. However, the addition of 3 at.% Ti was very effective in retarding atomic diffusion and Al depletion in the coating layer. The binary Ni–50Al coating did not form a stable α-Al2O3 oxide during cyclic oxidation tests at 1000 °C. Moreover, rapid Al diffusion between the coating layer and substrate was observed. Ni–47Al–3Ti–0.1Y was then selected as a modified coating composition. The Ni–47Al–3Ti–0.1Y coating showed superior oxidation resistance due to stable α-Al2O3 formation and effective retardation of Al diffusion from the coating layer. In addition, Ni-oxide and α-Al2O3 coexisted in the bare Ni3Al foil without any coating, and the bare Ni3Al foil exhibited more stable oxidation behavior than the bulk Ni3Al alloy.

Introduction

Ni3Al has received strong interest as a high temperature material because of its anomalous strengthening with increasing temperature [1], [2]. However, the very small room temperature ductility of polycrystalline Ni3Al due to its severe intergranular brittleness [3] has been an obstacle to the development of this intermetallic compound. It is well known that the brittleness of the grain boundaries, which is a common problem in intermetallics, can be greatly improved by a small addition of boron [4].

As an alternative approach, directional solidification using the floating zone (FZ) method provides significant ductility improvement for Ni3Al without any boron addition [5], [6]. The FZ method makes it possible to fabricate binary Ni3Al thin foils below 100 μm in thickness with smooth and crack-free surfaces by cold rolling without any intermediate annealing steps [7], [8], [9]. Moreover, through annealing of the cold-rolled foils at temperatures over 1000 °C, the recrystallized foils can attain some room temperature ductility (3.0–14.6%) in air and they can be bent plastically around TD more than 100° without cracking [7]. These results demonstrate that Ni3Al thin foils can be utilized for lightweight, high-temperature structural materials through forming honeycomb structures.

For the practical application of Ni3Al foils, the oxidation properties at high temperature as well as their mechanical properties should be considered. In particular, the oxidation resistance of cast Ni3Al alloys is inhibited because they form non-protective Ni-oxides such as NiO and NiAl2O4 at high temperature and spalling of the oxide scale occurs under a cyclic oxidation environment [11], [12], [13]. β-NiAl, an important intermetallic compound in Ni–Al systems, together with γ′-Ni3Al, has been used for coating materials of Ni-base superalloys because of its excellent oxidation resistance. In addition to oxidation resistance at high temperature, coating materials should display chemical compatibility with the substrate [10]. Therefore, NiAl is considered a good candidate for a coating material of Ni3Al foils.

When Ni3Al foils are utilized for a honeycomb structure, the thickness of Ni3Al foils should be less than 100 μm [14]. Therefore, it is generally considered that the thickness of the coating on the Ni3Al foils is restricted below 10 μm, which constitutes a very thin deposition level relative to the general oxidation-resistant coating of over 100 μm in thickness on bulk alloys [10]. Insufficient coating thickness, however, can induce rapid Al depletion in the NiAl coating layer at high temperature because the scale-forming element Al is consumed continuously by the formation of Al2O3 scales and interdiffusion with the Ni3Al substrate. In this study, we attempt to determine a suitable coating composition to address the limitation of thin coating. For the modification, the Al diffusion behavior from the coating to substrate as well as the oxidation-resistant property of the coating should be considered.

Section snippets

Experimental procedures

The substrates of Ni3Al foils were produced from single-crystalline ingots of boron-free binary Ni3Al (Ni–24 at.% Al) by the investment casting method and subsequent cold rolling. The investment casting method has an advantage in growing large single crystals compared to the FZ method. The crystals (plate in shape) used in this study are 80–100 mm long, 55 mm wide and 5 mm thick, which are much larger than bar-like crystals grown by FZ method, 12 mm in diameter and 100 mm long. Therefore, it is

Modification of binary Ni–50Al coating

As noted in Section 1, the coating thickness on the Ni3Al foils is restricted below 10 μm, which is much thinner than general coatings of over 100 μm in thickness on bulk alloys [10]. The insufficient coating thickness can induce rapid Al depletion in the NiAl coating layer because the scale-forming element Al is consumed continuously during exposure to high temperature by interdiffusion with the Ni3Al substrate. Fig. 1 shows the surface and cross-section morphologies after heat-treatment at 1000 

Effect of Ti addition on interdiffusion between coating and substrate

Since the coating thickness on the Ni3Al foils is much thinner than general coatings on bulk alloys, it is necessary to relieve the consequent rapid Al depletion at high temperature. It has been reported that Ti addition to binary NiAl alloys, which undergo hot-extrusion and following annealing, raises the recrystallization temperature of the deformed NiAl alloys [20]. Moreover, 3 at.% Ti can preserve the columnar-grained structure of directionally solidified NiAl/Ni3Al alloys, even when the

Conclusions

When a NiAl coating is deposited on a Ni3Al foil in order to improve its oxidation resistance, a suitable coating composition should be selected. The coating should exhibit good oxidation resistance and, moreover, effectively suppress Al diffusion from the coating to substrate. The following conclusions were derived from the experiments and discussion.

  • (1)

    The thickness of the coating on Ni3Al foils is restricted below 10 μm, which is much thinner than general coatings on bulk alloys. Insufficient

Acknowledgements

This work was supported by grant No. R01-2003-000-10433-0 from the Basic Research Program of the Korea Science and Engineering Foundation.

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