In the master's thesis, we discussed the corrosion resistance of stainless steel THERMA 4828 and titanium alloy TIMETAL Exhaust XT. We experimentally studied high-temperature oxidation at test temperatures of 700 and 950 °C and corrosion in an aqueous medium. First, all examined samples were properly prepared for both parts of the tests. The high-temperature oxidation of the first set of samples was performed using a simultaneous thermal analysis device (STA 449 Jupiter from NETZSCH). The oxidation kinetics results were obtained based on tests conducted in the STA device and were compared with linear, parabolic, and cubic
mathematical models. After oxidation, the samples were sectioned and metallographically prepared, and the thicknesses of the resulting oxide layers were
measured using a digital optical microscope. This was followed by analysis using a scanning electron microscope (SEM) where an energy-dispersive spectroscopy (EDS) detector was used to determine the chemical composition of the samples and oxide layers. In calculations using the Thermo-Calc software, we modeled the fractions of individual oxides and their chemical compositions at specific temperatures. In parallel with high-temperature oxidation tests, corrosion resistance was also examined using electrochemical measurements. These were conducted with a system comprising a corrosion cell, a potentiostat, and a computer running
Nova 2.0 software. The second set of properly prepared samples was placed in the corrosion cell, with a 3.5% NaCl solution used as the corrosive medium. The measurement results were presented as open circuit potential (OCP) curves over time as Nyquist and Bode plots representing electrochemical impedance spectra and as potentiodynamic polarization curves. Based on the interpretation of the hightemperature oxidation measurement results, we concluded that the TIMETAL_XT titanium alloy oxidizes faster than THERMA 4828 stainless steel and forms a thicker
oxide layer compared to stainless steel. This was confirmed both by the oxidation mass curves over time where the greatest mass change was recorded in the hightemperature
oxidation of the titanium alloy at 950 °C and by the results of microscopic analysis. Electrochemical measurements indicated that the titanium alloy exhibits greater corrosion resistance in chloride solution than stainless steel.
This was determined based on OCP measurements, which showed a slower stabilization for the titanium alloy, indicating the gradual formation of a protective oxide layer. Potentiodynamic polarization curves also did not detect oxide layer breakdown in the titanium alloy whereas a clear breakdown was observed in the stainless steel.
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