Water vapour corrosion resistance of five rare earth monosilicates Y 2 SiO 5 , Gd 2 SiO 5 , Er 2 SiO 5 , Yb 2 SiO 5 , and Lu 2 SiO 5 was investigated during testing at 1350 ˚C for up to 166 h in static air with 90% water vapour. Four of the RE-silicates showed little weight gain (0.859 mg cm -2 ) after 166 h of exposure. Prior to testing the microstrucre consists of equiaxed grains of 4-7 ± 0.4 µm. XRD analysis showed that after 50 h exposure to water vapour corrosion Y, Er, Yb and Lu-silicates had both mono and disilicates present on their surfaces as a result of the reaction between monosilicate and water vapour to form disilicate, while Gd-silicate has converted completely to G 4.67 Si 3 O 13 making it less stable for environmental barrier coatings application. The microstructures of corroded Y, Er, Yb and Lu-silicates contain ridges and cracks, while that of Gd-silicate contains rounded grains suggesting melting along with striped contract grains.Keywords: Rare earth monosilicates, environmental barrier coating, water vapour resistance.
IntroductionSilicon carbide fibre-reinforced ceramic matrix composites (CMCs) possess high temperature (Abcr, Germany, 4 ± 0.2 µm particle size) and SiO 2 (Abcr, Germany, 4 ± 0.1 µm particle size). All RE-oxides powders were 99.9% pure, while the SiO 2 powder was 99.0% pure.Particle size measurements were conducted using Malvern hydro equipment (2000SM, UK) and the average value was obtained based on three measurements for each powder. The exact weight per gram of each powder was homogeneously mixed in a ball mill using silicon carbide media (Union process, USA, 5 mm diameter) in ethanol for 24 h. The slurries were dried for 24h at 110 ˚C. 13 mm diameter and 3 mm thick pellets were obtained using uniaxial cold pressing (50 MPa) at room temperature. Y, Gd, Yb and Lu monosilicates were sintered for 3 hours at 1580˚C at a heating rate of 10˚C min -1 in a box furnace in air. However, to produce Er 2 SiO 5 , 12h sintering was necessary to obtain dense samples [18].Water vapour corrosion tests were conducted at 1350 ˚C for 50, 100 and 166 h in 90% water:10% air ratio with flow rate of 40 ml/min in an alumina tube (50 mm diameter and 1200 mm length) furnace ((Lenton, Hope, UK) at a heating and cooling rate of 10 ˚C min -1 and 20 ˚C min -1 respectively. Sample dimensions were 10 mm diameter and 3 mm thick. Samples were placed on high purity alumina boats (Almath crucibles, Newmarket, UK) and their weight was recorded before and after the corrosion tests with an accuracy of ± 0.001 g to determine the weight change. To exclude the water vapour corrosion taking place at low temperature, the water vapour was introduced when the temperature reached 1350 ˚C and the flow was stopped after the desired testing period.Phases were identified by XRD (Bruker D2 Phaser, Germany) on sample's surface which was not in contact with the alumina boat during corrosion test using CuKα radiation with spectra recorded from 10-70˚. Crystalline phases were determined using Xpert High Score Plus softwa...