Degradation at 1200°C of a SiC coated 2D-Nicalon/C/SiC composite processed by SICFILL® method

The thermal stability of a 2D-Nicalon/C/SiC composite was studied through the variation of both mechanical properties and microstructure occurring during heat treating. The composite was processed by infiltration of SiC preforms according to SICFILL® method. The material toughness was enhanced by a carbon interphase put between the fibers and the matrix. In order to improve the thermal stability a CVI layer was deposited on the carbon interphase and the specimen surfaces were CVD covered by an external SiC seal coating about 165 μm thick. The aging tests were carried out at 1200°C in air or in non oxidizing environment (vacuum). Other specimens were thermally cycled between 25 and 1150°C. Three point bending tests and Charpy impact measurements were performed before and after these treatments. The composite microstructure was investigated by scanning electron microscope (SEM), electron probe microanalysis (EPMA), X-ray diffraction (XRD), reflectance infrared spectroscopy (FTIR) and surface area BET measurements. The as-processed material showed a modulus of rupture (MOR) of 483 MPa and appreciable toughness. These characteristics were retained after aging (200 h at 1200°C) under vacuum. Air thermal treatments caused heavy loss of strength and increase of brittleness. Strong oxidation occurred during these last treatments at both the carbon interlayer and the matrix, while the SiC external sample coating was not oxidized. The oxygen needed for composite bulk oxidation flowed through the SiC coating due to the occasional presence of very few structural defects. (C) 2000 Elsevier Science Ltd. All rights reserved. The thermal stability of a 2D-Nicalon/C/SiC composite was studied through the variation of both mechanical properties and microstructure occurring during heat treating. The composite was processed by infiltration of SiC preforms according to SICFILL method. The material toughness was enhanced by a carbon interphase put between the fibers and the matrix. In order to improve the thermal stability a CVI layer was deposited on the carbon interphase and the specimen surfaces were CVD covered by an external SiC seal coating about 165 μm thick. The aging tests were carried out at 1200 °C in air or in non oxidizing environment (vacuum). Other specimens were thermally cycled between 25 and 1150 °C. Three point bending tests and Charpy impact measurements were performed before and after these treatments. The composite microstructure was investigated by scanning electron microscope (SEM), electron probe microanalysis (EPMA), X-ray diffraction (XRD), reflectance infrared spectroscopy (FTIR) and surface area BET measurements. The as-processed material showed a modulus of rupture (MOR) of 483 MPa and appreciable toughness. These characteristics were retained after aging (200 h at 1200 °C) under vacuum. Air thermal treatments mused heavy loss of strength and increase of brittleness. Strong oxidation occurred during these last treatments at both the carbon interlayer and the matrix, while the SiC external sample coating was not oxidized. The oxygen needed for composite bulk oxidation flowed through the SiC coating due to the occasional presence of very few structural defects.