The improvement in high-temperature oxidation resistance of Ni0.25Co0.25Cr0.22Mo0.14Re0.14 high entropy alloy via industrial chemical vapor aluminizing process

The effects of the protective coating (NiAl coating) on the high temperature isothermal oxidation resistance of Ni0.25Co0.25Cr0.22Mo0.14Re0.14 high entropy alloy (HEA) was discussed in this work. A nickel aluminide (NiAl) coating was obtained on the Ni0.25Co0.25Cr0.22Mo0.14Re0.14 HEA via the industr...

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Veröffentlicht in:Materials chemistry and physics 2024-10, Vol.325, p.129769, Article 129769
Hauptverfasser: Odabaş, Ömür Can, İnceyer, Ahmet Arda, Usta, Metin, Zeytin, Havva Kazdal, Yücel, Onuralp
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Sprache:eng
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Zusammenfassung:The effects of the protective coating (NiAl coating) on the high temperature isothermal oxidation resistance of Ni0.25Co0.25Cr0.22Mo0.14Re0.14 high entropy alloy (HEA) was discussed in this work. A nickel aluminide (NiAl) coating was obtained on the Ni0.25Co0.25Cr0.22Mo0.14Re0.14 HEA via the industrial chemical vapor aluminizing (CVA) process. Isothermal oxidation tests were applied to NiAl-coated and uncoated samples in ambient laboratory air for durations of up to 200 h at 1050 °C to investigate the effects of the NiAl coating on high-temperature isothermal oxidation resistance of Ni0.25Co0.25Cr0.22Mo0.14Re0.14 HEA. The results revealed that a protective and slowly growing α-Al2O3 oxide layer formed on the surface of the NiAl-coated HEA samples and remained stable even after 200 h of isothermal oxidation. For uncoated HEA samples, not only Cr2O3 but also non-protective spinel oxides (CoCr2O4 and NiCr2O4) were detected on the surface. Weight gain was observed in the NiAl-coated HEA samples due to the formation of a protective and slowly growing α-Al2O3 oxide layer on the NiAl coating. In contrast, the uncoated HEA samples experienced weight loss even after 6 h of isothermal oxidation, as Cr2O3 lost its stability at 1050 °C and non-protective spinel oxides formed. Therefore, it has been determined that the NiAl coating significantly enhance the isothermal oxidation resistance of the Ni0.25Co0.25Cr0.22Mo0.14Re0.14 HEA. The α-Al2O3 oxide layer has prevented severe oxidation of NiAl-coated samples due to its stability at 1050 °C over 200 h and its slow growth rate. [Display omitted] •The oxidation behavior of CVA-coated and uncoated Ni0.25Co0.25Cr0.22Mo0.14Re0.14 HEA at 1050 °C was investigated.•Protective and slowly growing α-Al2O3 oxide formed on the surface of the CVA-coated Ni0.25Co0.25Cr0.22Mo0.14Re0.14 HEAs.•Cr2O3 and non-protective oxides (NiCr2O4 and CoCr2O4) formed on the surface of the uncoated Ni0.25Co0.25Cr0.22Mo0.14Re0.14.•The high temperature oxidation resistance of Ni0.25Co0.25Cr0.22Mo0.14Re0.14 HEA was notably improved with CVA process.
ISSN:0254-0584
DOI:10.1016/j.matchemphys.2024.129769