Solar salt (SS), a well-known non-eutectic mixture of sodium nitrate (60% w/w) and potassium nitrate (40% w/w), is commonly used either as Thermal Energy Storage (TES) material (double tank technology) or Heat Transfer Fluid (HTF) (solar tower) in modern CSP plants worldwide. The specific heat (c_p, kJ kg⁻¹ °C⁻¹) of SS is a very important property in order to support the design of new CSP Plants or develop novel materials based on SS. A high scientific effort has been dedicated to perform a suitable thermophysical characterization of this material. However, there is still a great discrepancy among the c_p values reported by different authors¹. These differences may be due to either experimental errors (random or systematic) or divergences in the starting material (grade of purity, presence of impurities and/or water). In order to avoid the second source of uncertainty (the starting material), a Round Robin Test (RRT) was proposed starting from a common material. In this way, the different methods from each laboratory could be compared. The study should lay the foundations for the establishment of a systematic procedure for the measurement of the specific heat of this kind of materials. Nine institutions, research centers and companies, accepted the proposal and are contributing with their results. The initiative was organized within the Workshop SolarPACES Task III – Material activity.

Concentrating Solar Power (CSP) is one of the key electricity production renewable energy technologies with a clear distinguishing advantage: the possibility to store the heat generated during the sunny periods, turning it into a dispatchable technology. Current CSP Plants use an intermediate Heat Transfer Fluid (HTF), thermal oil or inorganic salt, to transfer heat from the Solar Field (SF) either to the heat exchanger (HX) unit to produce high pressure steam that can be leaded to a turbine for electricity production, or to the Thermal Energy Storage (TES) system. In recent years, a novel CSP technology is attracting great interest: Direct Steam Generation (DSG). The direct use of water/steam as HTF would lead to lower investment costs for CSP Plants by the suppression of the HX unit. Moreover, water is more environmentally friendly than thermal oils or salts, not flammable and compatible with container materials (pipes, tanks). However, this technology also has some important challenges, being one of the major the need for optimized TES systems. In DSG, from the exergy point of view, optimized TES systems based on two sensible heat TES systems (for preheating of water and superheating vapour) and a latent heat TES system for the evaporation of water (around the 70% of energy) is the preferred solution. This concept has been extensively tested [1, 2, 3] using mainly NaNO3 as latent heat storage medium. Its interesting melting temperature (Tm) of 306°C, considering a driving temperature difference of 10°C, means TES charging steam conditions of 107 bar at 316°C and discharging conditions of 81bar at 296°C. The average value for the heat of fusion (ΔHf) of NaNO3 from literature data is 178 J/g [4]. The main disadvantage of inorganic salts is their very low thermal conductivity (0.5 W/m.K) requiring sophisticated heat exchanging designs. The use of high thermal conductivity eutectic metal alloys has been recently proposed [5, 6, 7] as a feasible alternative. Tms of these proposed eutectic alloys are too high for currently available DSG solar fields, for instance the Mg49-Zn51 alloy melts at 342°C requiring saturated steam pressures above 160 bar to charge the TES unit. Being aware of this, novel eutectic metallic alloys have been designed reducing the Tms to the range between 285°C and 330°C (79bar and 145bar of charging steam pressure respectively) with ΔHfs between 150 and 170 J/g, and thus achieving metallic Phase Change Materials (PCM) suitable for the available DSG technologies.

The study of more efficient materials for thermal energy storage at high temperatures is a broad field of research. The use of the nanotechnology is a strategy recently considered to enhance the thermal properties of these materials. The nano-enhanced Molten Salts (neMS) are constituted by an inorganic salt where tiny quantities of nanoparticles (NPs) are dispersed. These nanomaterials possess a specific heat higher than that of the salt or the isolated NPs. This phenomenon is not still well understood and great research efforts are needed to describe the interactions on the material at a molecular level. The existence of a nanolayer at the interface between the NPs surface and the molten salt with superior thermal properties is the main mechanism proposed up to now. A high available surface of the NPs promotes the formation of higher quantities of these nanostructures. The available surface depends on the NPs size and shape and is strongly reduced if NPs are agglomerated. We have studied and compared the effect on the specific heat of embedding two different ceramic NPs on molten Solar Salt.

The use of nanofluids (NFs) based on Solar Salt (SS) and nanoparticles (NPs), either as Thermal Energy Storage (TES) material or as Heat Transfer Fluid (HTF), is attracting great interest in recent years. Many authors [1,3] have reported important improvements on the thermophysical properties (specific heat capacity cp,thermal conductivity k) of NFs based on SS and ceramic NPs. These improvements would lead to important savings and better performance of TES facilities on new Concentrated Solar Power (CSP) plants due to lower quantities of material required and smaller storage tanks. To achieve these advantageous features in the final NFs, it is essential to avoid NP agglomeration during their preparation. Different synthesis procedures have been reported: mixing of solid NPs within a SS solution by means of ultrasounds [1-3], direct mixing of solid NPs and molten salt [4]. In this work, NFs based on SS and 1% by wt. of silica NPs were synthetized from a SS-water solution and a commercial water-silica NF called Ludox HS 30% (Sigma-Aldrich). The influence of the mixing water volume (MW) on the cp of NFs was evaluated. With this aim, the cp of these samples was measured by Differential Scanning Calorimetry (DSC) both in the solid and the liquid state. In addition, the distribution of sizes was measured during the whole preparation process by Dynamic Light Scattering (DLS). Further information about sizes and uniformity of the final NFs was obtained from Scanning Electron Microscopy (SEM) images. X-ray Diffraction (XRD) patterns of the SS and final NF were performed.

Low melting point thermal energy storage (TES) materials have been proposed in the last years to reduce the storage cost in concentrating solar power (CSP) technology. One of the most interesting additive due to the enhancement in thermal properties is lithium nitrate. However, there is a lack of dynamic corrosion tests to simulate real operation conditions in CSP plants. In this work, we present a dynamic reactor set up where a mixture of 30 wt.% LiNO₃ + 57 wt.% KNO₃ + 13 wt.%. NaNO₃ is moved through a mechanical stirrer obtaining a lineal speed of 0.30 m/s. A commercial carbon steel A516 was tested as container material at 390 °C during 1000 h. Fe₂O₃ and Fe₃O₄ were obtained as the main corrosion products by scanning electron microscopy (SEM) and x-ray diffraction (XRD) with a metallographic corrosion rate of 0.015 mm/year.