Advanced investigations on high temperature stability of commercial prealloyed ceria-yttria-zirconia powder, suitable for the manufacturing of Thermal Barrier Coatings (TBC), have been carried out by means of X-ray Photoelectron Spectroscopy (XPS), Scanning Transmission Electron Microscopy (STEM), Differential Thermal Analysis (DTA), and Thermogravimetry (TGA) with a view to foresee their behaviour in the plasma iet atmosphere and oxidizing service environment. Thermal treatments of the powder were performed in a thermobalance in both oxidizing (static air) and reducing (flowing N2/H2 = 10%) atmospheres up to 1873 K and then cooled down under static air conditions, two exothermal reactions taking place at 700 and 1300 K were disclosed by DTA experiments. On the contrary, under reducing conditions the powder was affected by a weight loss owing to the Ce (IV) reduction to Ce (III) in the outermost layers and after thermal treatments, it was either fully reduced to Ce (III) or fully oxidized to Ce (IV).

HIGH TEMPERATURE STABILITY OF CeO2-Y2O3 STABILIZED ZIRCONIA PLASMA SPRAY POWDER. XPS, STEM AND DTA INVESTIGATIONS

FIERRO G;INGO GM;
1990

Abstract

Advanced investigations on high temperature stability of commercial prealloyed ceria-yttria-zirconia powder, suitable for the manufacturing of Thermal Barrier Coatings (TBC), have been carried out by means of X-ray Photoelectron Spectroscopy (XPS), Scanning Transmission Electron Microscopy (STEM), Differential Thermal Analysis (DTA), and Thermogravimetry (TGA) with a view to foresee their behaviour in the plasma iet atmosphere and oxidizing service environment. Thermal treatments of the powder were performed in a thermobalance in both oxidizing (static air) and reducing (flowing N2/H2 = 10%) atmospheres up to 1873 K and then cooled down under static air conditions, two exothermal reactions taking place at 700 and 1300 K were disclosed by DTA experiments. On the contrary, under reducing conditions the powder was affected by a weight loss owing to the Ce (IV) reduction to Ce (III) in the outermost layers and after thermal treatments, it was either fully reduced to Ce (III) or fully oxidized to Ce (IV).
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/212715
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