Abstract

A simple method is described for measuring low rates of selective oxidation of Ag–Mg alloys at elevated temperatures when water vapor is used as oxidizing agent. It is found that the MgO layer builds up on the surface of the alloy according to a parabolic law over a range of the water vapor pressure from 7×10 -3 to 6×10 -2 mm Hg, and the oxide growth begins to follow a linear law rather than a parabolic law at a pressure of 1 mm Hg. In the region where the parabolic law holds, the growth of the oxide layer seems to be controlled by the diffusion of Mg through the layer. 20.7 kcal/mol is obtained as the activation energy of diffusion. Applyjng the transition state theory of gas-metal reaction, as developed by Gulbransen, the diffusion of Mg through the oxide layer is given by D (cm 2 /sec)=2.17×10 -9 exp (-20,700/RT).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.