Latent heat storage systems are gaining the attention of researchers as possible substitutes to conventional sensible heat storage systems due to their compactness and their ability to absorb and release heat almost isothermally. Among the Phase Change Materials (PCM) for energy storage studied so far, esters are believed to show promising properties. In particular, a broad range of melting temperatures, little to no supercooling, low corrosivity, chemical and thermal stability, and high enthalpies of fusion are reported. Many esters have the advantage of being bio-based and biodegradable, making them more sustainable in comparison to other popular PCM. Still, a clear lack of experimental data exists in regards to this class. In the present study, esters derived from saturated fatty carboxylic acids (myristic, palmitic, stearic, behenic), coupled with primary linear alcohols of different length (methanol, 1-decanol) were synthesized through Fischer esterification and their properties were investigated. Purities higher than 89% were obtained for all cases as proven by gas chromatography coupled with mass spectroscopy and nuclear magnetic resonance analysis. Additionally, the esters' formation and reaction kinetics were characterized by attenuated total reflectance infrared spectroscopy. The esters produced showed to possess relatively high enthalpies of fusion above 190 J/g and thermal stability over three repeated cycles with differential scanning calorimetry. The melting points measured ranged between 20 • C and 50 • C, therefore proving to be interesting candidates for low-medium temperature applications such as heating and cooling in buildings. A correlation could be observed between the chemical structure and melting point of the produced esters. Additionally, thermogravimetric analysis revealed a higher thermal resistance for esters with longer aliphatic chains in comparison to shorter-chained ones.

No abstract

As global energy demand increases while primary sources and fossil fuels’ availability decrease, research has shifted its focus to thermal energy storage systems as alternative technologies able to cover for the mismatch between demand and supply. Among the different phase change materials available, esters possess particularly favorable properties with reported high enthalpies of fusion, low corrosivity, low toxicity, low supercooling, thermal and chemical stability as well as biodegradability and being derived from renewable feedstock. Despite such advantages, little to no data on the thermal behavior of esters is available due to low commercial availability. This study constitutes a continuation of previous works from the authors on the investigation of fatty esters as novel phase change materials. Here, methyl, pentyl and decyl esters of arachidic acid, and pentyl esters of myristic, palmitic, stearic and behenic acid are synthesized through Fischer esterification with high purities and their properties are studied. The chemical structures and purities are confirmed through Attenuated Total Reflectance Infrared Spectroscopy, Gas Chromatography coupled with Mass Spectroscopy and Nuclear Magnetic Resonance Spectroscopy, while the determination of the thermal properties is performed through Differential Scanning Calorimetry and Thermogravimetric Analysis. In conclusion, some correlations between the melting temperatures and the chemical structures are discovered, and the fatty esters are assessed based on their suitability as phase change materials for latent heat storage applications.

In the quest for a decarbonized energy system, the development of highly efficient technologies that allow the integration of renewables is of the utmost importance. Latent Heat Storage systems with Phase Change Materials (PCM) can contribute to solving the issue of the mismatch between demand and supply brought forward by renewable energies. Despite possessing promising thermal properties, organic PCMs and esters in particular have rarely been investigated. In the present study, eight commercial aromatic esters are assessed as possible PCM candidates. To do so, their thermal properties, such as phase change temperature, enthalpy of fusion, density, and thermal conductivity, alongside sustainability and toxicity issues, are considered. The aromatic esters are found to possess phase change temperatures between −16 ∘C and 190 ∘C and maximum enthalpies of fusion of 160 J/g. This, alongside densities above 1 g/mL, makes them interesting candidates for high-temperature applications, where, typically, salts and ceramics or metals dominate as PCMs.

An important prerequisite to select a reliable phase change material (PCM) for thermal energy storage applications is to test it under application conditions. In the case of solid–liquid PCM, a large amount of thermal energy can be stored and released in a small temperature range around the solid–liquid phase transition. Therefore, to test the long-term stability of solid–liquid PCM, they are subjected to melting and solidification processes taking into account the conditions of the intended application. In this work, 18 experimental devices to investigate the long-term stability of PCM are presented. The experiments can be divided into thermal cycling stability tests, tests on PCM with stable supercooling, and tests on the stability of phase change slurries (PCS). In addition to these experiments, appropriate methods to investigate a possible degradation of the PCM are introduced. Considering the diversity of the investigated devices and the wide range of experimental parameters, further work toward a standardization of PCM stability testing is recommended.