4.7 Article

C-276 nickel alloy corrosion in eutectic Na2CO3/NaCl molten salt under isothermal and thermal cycling conditions

Journal

SOLAR ENERGY MATERIALS AND SOLAR CELLS
Volume 240, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.solmat.2022.111695

Keywords

Molten salt corrosion; Thermal energy storage; Nickel superalloy; Thermal cycling

Funding

  1. Australian Solar Thermal Research Initiative (ASTRI)
  2. Australian Government, through the Australian Renewable Energy Agency (ARENA)
  3. CARF

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This study analyzed the corrosion of a nickel superalloy in high temperature molten salts and found that thermal cycling reduced corrosion thickness and oxide layers provided protection for the metal.
Thermal energy storage (TES) is a key component for the practical application of concentrating solar thermal power. Recently, a push for higher temperatures has increased interest in molten salts with melting points above 550 degrees C as phase change thermal energy storage media. Corrosion of a nickel superalloy (C-276) with a eutectic salt mixture (59.5 %wt Na2CO3/40.5 %wt NaCl) at 650 degrees C was analysed under both isothermal conditions and with thermal cycle between 600 and 650 degrees C. Corrosion rates of 400-500 mu m/year under isothermal conditions and 200-300 mu m/year under thermal cycling were determined by measuring thickness loss, and oxide growth was primarily responsible for the metal loss. Thermal cycling reduced corrosion thickness, however it remained intact with no cracking or buckling. Post-test analysis of the salt found that molybdenum, manganese and tungsten were most likely to be removed from the alloy. Isothermal conditions did not cause chromium to be removed from the alloy by the salt. However, chromium was present in the salt after thermal cycling, due to its removal from the oxide layer. Whilst the corrosion was above the maximum acceptable corrosion rate for a TES system, this study shows that oxide layers formed on alloy C-276 have protective capabilities in this salt, gaining maximum thickness after about 400 h and preventing the salt from attacking the metal directly. Longer testing with more samples is require to determine if the corrosion of this alloy is halted due to the oxide layer growth on the metal surface.

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