Abstract
This paper describes the oxidation behavior of low-carbon steel samples in binary gas mixtures of oxygen and nitrogen, at oxygen concentrations ranging between 1% and 15% and temperatures ranging between 1000 and 1250°C. Sample weight gains versus time were analyzed, along with measurements and calculations of sample heating rates due to exothermic heat of reaction at the sample surface. It was found that initial rates of oxidation depended on oxygen content in the gasmixture and that these reaction rates were linear up to oxide thicknesses of 0.4 to 0.5 mm. Calculations of linear oxidation rate constants based on equations for mass transport of oxygen in the gas mixture to the sample surface showed good agreement with those measured experimentally, indicating that the initial period of oxidation is controlled by the mass transport of oxygen to the reaction interface. The linear rate constants showed little dependency on temperature, an activation energy of approximately 17kJ/mole being obtained. Measurements of sample surface temperatures have shown that within this linear-oxidation regime, interfacial temperatures of the samples increase with increasing oxygen contents in the gas mixture, owing to exothermic heats of oxidation. Subsequent oxidation kinetics were found to be parabolic. Measured parabolic rates constants were in good agreement with previous investigations, with activation energy values of approximately 127kJ/mole.
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