Electrochemical engineering considerations for gas evolution in molten sulfide electrolytes
Name
1117771440-MIT.pdf
Size
9.32 MB
Format
Adobe PDF
Checksum (MD5)
6a98458311a3ecff5a448e51e4fbf043
Author(s)
Chmielowiec, Brian John.
Advisor(s)
Antoine Allanore.
Date Issued
2019
Publisher
Massachusetts Institute of Technology
Abstract
The current interrupt and galvanostatic electrochemical impedance spectroscopy techniques were utilized to characterize the ohmic, charge transfer, and mass transfer over-potential behavior of gas evolving electrodes in aqueous, molten chloride, and molten sulfide electrolyte solutions under steady-state natural convective flow conditions as a means to gain access to thermodynamic, physicochemical, and hydrodynamic properties of these systems. Previous efforts purposely chose operating conditions under which one or more sources of overpotential were negligible to facilitate analysis of the total overpotential observed at the expense of maintaining operating conditions of industrial relevance. This work represents a preliminary effort to understand the fundamental material properties of a molten sulfide electrolyte, by application of materials-blind electrochemical techniques that were validated on previously well characterized systems-oxygen evolution in aqueous KOH and chlorine evolution in eutectic LiCl-KCl-CsCl. For the first time, values are reported for the saturation concentration of dissolved sulfur gas, an approximate range of Schmidt number for dissolved sulfur, and natural convection limiting current densities in a molten sulfide electrolyte consisting of Cu₂S-BaS-La₂S₃ at 1300°C.
Description
Thesis: Sc. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2019
Cataloged from PDF version of thesis.
Includes bibliographical references.
Subjects
Materials Science and Engineering.
MIT Department
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Terms of Use
MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.
Persistent DSpace Link