Abstract
We present a study on the electrochemical behavior of magnesium hydroxide (MgOH+) reduction on a tungsten (W) cathode in molten chloride salt (MgCl2-KCl-NaCl) across the temperature range of 475 °C–525 °C. MgOH+, which forms within the salt upon exposure to moisture, is a leading cause of corrosion. Corrosion is a major barrier to deployment of chloride salts across a number of applications, including concentrating solar power plants and nuclear power plants. While pre-purification protocols have been developed to ensure MgOH+ is removed from molten chloride salts prior to deployment, MgOH+ forms in situ during operation of chloride-salt based plants. Thus, methods for continuous purification during plant operation are needed. Continuous electrochemical purification via electrolysis using a Mg anode and W cathode has been proposed, but little has been done to assess scalability. Here, we assess fundamental properties of electrochemical removal of MgOH+ to enable future scale up of this method.
Funder
Solar Energy Technologies Program
Publisher
The Electrochemical Society
Subject
Materials Chemistry,Electrochemistry,Surfaces, Coatings and Films,Condensed Matter Physics,Renewable Energy, Sustainability and the Environment,Electronic, Optical and Magnetic Materials