Abstract No.:
6364

 Scheduled at:
Wednesday, June 10, 2020, Hall D 3:50 PM
Session Young Professionals


 Title:
Aluminium oxide dispersion strengthened CoNiCrAlY coatings for high-temperature sliding wear applications

 Authors:
Giovanni Bolelli* / Department of Engineering "Enzo Ferrari", University of Modena and Reggio Emilia, Italy
Robert Vaßen / Forschungszentrum Jülich, Germany
Christoph Vorkötter/ Forschungszentrum Jülich GmbH, Institute of Energy and Climate Research, IEK- 1, Germany
Luca Lusvarghi/ Department of Engineering Enzo Ferrari, University of Modena and Reggio Emilia, Italy
Stefania Morelli/ University of Modena and Reggio Emilia, Italy
Veronica Testa/ Department of Engineering Enzo Ferrari, University of Modena and Reggio Emilia, Italy

 Abstract:

Coating materials for sliding wear protection at high temperature should include an oxidation-resistant metal matrix, which confers ductility and thermal expansion matching to stainless steel or superalloy substrates, and a refractory hard phase to provide hot hardness. Based on these criteria, oxide dispersion strengthened (ODS) CoNiCrAlY powders containing 2, 10 and 30 wt.% of fine Al2O3 particles were manufactured by high-energy ball milling. These powders were processed into approx. 300 micron-thick coatings by vacuum plasma spraying (VPS). The unreinforced CoNiCrAlY powder was also sprayed as a reference. Ball-on-disc sliding tests performed in air at 750 °C against an Al2O3 counterpart show that, in comparison to the uncoated substrate, the wear rates of the coatings decrease with increasing Al2O3 content, except for the sample containing 10 wt.% Al2O3. The wear mechanisms of all coatings include adhesion and tribo-oxidation. Specifically, the coatings tend to develop thick (>1 micron) oxidized tribo-layers, also termed glazes, which play a key role in restrain adhesive wear of the metal phase. The composite coating with 30 wt.% Al2O3, in particular, develops a particularly stable and uniform glaze, which minimizes the wear rate. The mechanisms by which Al2O3 particles affect glaze stability are investigated and discussed.



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