“Concentrated solar power” (CSP) and thermal energy storage (TES) are promising renewable energy technologies, which have gained increasing interest and practical application in recent years. CSP and TES systems typically utilize molten salts such as the so-called “solar salt”, a mixture of 60 wt.% NaNO3 and 40 wt.% KNO3, for heat transfer and storage. The overall efficiency of commercially operating CSP and TES systems is currently limited, because of solar salt thermal stability, which prevents process temperatures higher than 600 °C. Even at these temperatures, corrosion of the structural materials applied in salt guiding pipework, tubes and containers is a matter of concern in long-term operation, which necessitates careful material selection. This paper outlines the superior salt corrosion behavior of a novel low-cost, Al2O3-forming, ferritic, Laves phase-strengthened (i.e., structural) steel in NaNO3/KNO3 solar salt at 600 °C. Directions for the further development of the LB2230 trial steel towards improved structural properties are derived in comparison to its predecessor Crofer®22 H.
Concentrating solar power (CSP) and thermal energy storage (TES) based on molten salts still lacks economic feasibility, with the material investment costs being a major drawback. Ferritic stainless steels are a comparatively cheap class of materials that could significantly contribute to cost reductions. The addition of aluminum to ferritic steel can result in self-passivation by forming a compact Al2O3 top layer, which exhibits significantly higher corrosion resistance to solar salt compared to the Cr2O3 surface layers typically formed on expensive structural alloys for CSP and TES, such as austenitic stainless steels and Ni-base super alloys. However, to date, no ferritic stainless steel combining Al2O3 formation and sufficient structural strength is available. For this reason, cyclic salt corrosion tests under flowing synthetic air were carried out on seven Laves phase-forming, ferritic model alloys (17Cr2-14Al0.6-1Nb2.6-4W0.25Si), using “solar salt” (60 wt. % NaNO3 and 40 wt. % KNO3). The Al content was varied to investigate the influence on the precipitation of the mechanically strengthening Laves phase, as well as the impact on the formation of the Al-oxide top layer. The W and Nb contents of the alloys were increased to examine their influence on the precipitation of the Laves phase. The salt corrosion experiments demonstrated that simultaneous self-passivation against a molten salt attack and mechanical strengthening by precipitation of fine Laves phase particles is possible in novel ferritic HiperFerSCR (salt corrosion-resistant) steel. Microstructural examination unveiled the formation of a compact, continuous Al2O3 layer on the surface of the model alloys with Al contents of 5 wt. % and higher. Furthermore, a stable distribution of fine, strengthening Laves phase precipitates was achieved in the metal matrix, resulting in a combination of molten salt corrosion resistance and potentially high mechanical strength by a combination of solid solution and precipitation strengthening. These results show that high-strength ferritic alloys are suitable for use in CSP applications.
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