Search

Thermal Energy Storage Materials (TESMs) may be the missing link to the “carbon neutral future” of our dreams. TESMs already cater to many renewable heating, cooling and thermal management applications. However, many challenges remain in finding optimal TESMs for specific requirements. Here, we combine literature, a bibliometric analysis and our experiences to elaborate on the true potential of TESMs. This starts with the evolution, fundamentals, and categorization of TESMs: phase change materials (PCMs), thermochemical heat storage materials (TCMs) and sensible thermal energy storage materials (STESMs). PCMs are the most researched, followed by STESMs and TCMs. China, the European Union (EU), the USA, India and the UK lead TESM publications globally, with Spain, France, Germany, Italy and Sweden leading in the EU. Dissemination and communication gaps on TESMs appear to hinder their deployment. Salt hydrates, alkanes, fatty acids, polyols, and esters lead amongst PCMs. Salt hydrates, hydroxides, hydrides, carbonates, ammines and composites dominate TCMs. Besides water, ceramics, rocks and molten salts lead as STESMs for large-scale applications. We discuss TESMs’ trends, gaps and barriers for commercialization, plus missing links from laboratory-to-applications. In conclusion, we present research paths and tasks to make these remarkable materials fly on the market by unveiling their potential to realize a carbon neutral future.

Latent heat storage (LHS) represents a valuable technology for the integration of intermittent renewable energy sources in existing and future energy systems. Improvements in LHS can be sought by enhancing heat transfer efficiency, compactness and diminishing the environmental impact of storage systems. In this paper, direct contact latent heat storage (DC-LHS) using esters as phase change material (PCM) is proposed as a promising compact storage technology to achieve high performance both in terms of heat transfer and sustainability. The technology allows for the heat transfer fluid (HTF) to flow directly through the PCM, forming a large amount of small droplets and thus providing a large heat exchange surface area between the two materials. At the same time, using biobased esters as PCM, gives the technology clear ecological advantages when compared to alternative types of compact energy storage. Furthermore, no complex heat transfer enhancing structures are necessary in a DC-LHS, further reducing the environmental impact and enabling very high energy densities. In this paper, the feasibility of this concept is explored for the first time by developing and testing an experimental DC-LHS device using methyl palmitate as PCM and water as HTF. The thermal performance and stability of the material combination are analysed by different melting–solidification experiments and distinctive effects are identified and comprehensively discussed for the first time. The basic concept as well as the novel material combination are validated. The study finds the critical challenges that must be overcome in order for this highly promising technology to be successfully implemented.

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.

Latent Heat Storage (LHS) with Phase-Change Materials (PCMs) represents a high energy density storage technology which could be applied in a variety of applications such as waste heat recovery and integration of renewable energy technologies in energy systems. To increase the sustainability of these storage solutions, PCMs have to be developed with particular regard to bio-origin and biodegradability. Triglycerides represent an interesting class of esters as the main constituents of animal and vegetable fats, with attractive thermal properties. In order to be used as PCMs, the thermal behaviour of triglycerides has to be fully understood, as in some cases they have been reported to show polymorphism and supercooling. This study assesses the suitability of triglycerides as PCMs by reviewing the literature published so far on their behaviour and properties. In particular, melting points, enthalpies of fusion, polymorphism, thermal conductivities, heat capacities and thermal cycling stabilities are considered, with a focus on LHS and thermal energy storage applications. In addition, the efforts conducted regarding modelling and the prediction of melting points and enthalpies based on chemical structures are summarized and assessed.

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.

In the presented work, five bio-based and bio-degradable cyclic esters, i.e. lactones, have been investigated as possible phase change materials for applications in latent heat storage systems. Commercial natural lactones such as ε-caprolactone and γ-valerolactone were easily purchased through chemical suppliers, while 1,2-campholide, oxa-adamantanone and dibenzochromen-6-one were synthesized through Baeyer-Villiger oxidation. The compounds were characterized with respect to attenuated total reflectance spectroscopy and gas chromatography coupled with mass spectroscopy, in order to confirm their chemical structures and identity. Subsequently, thermogravimetric analysis and differential scanning calorimetry were used to measure the phase change temperatures, enthalpies of fusion, degradation temperatures, as well to estimate the degree of supercooling. The lactones showed a wide range of phase change temperatures from −40 °C to 290 °C, making them a high interest for both low and high temperature latent heat storage applications, given the lack of organic phase change materials covering phase change temperature ranges below 0 °C and above 80 °C. However, low enthalpies of fusion, high degrees of supercooling and thermal degradations at low temperatures were registered for all samples, rendering them unsuitable as phase change materials.

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.

The problem of emulsification between Phase Change Material (PCM) and Heat Transfer Fluid (HTF) in direct contact latent heat storage systems has been reported in various studies. This issue causes the PCM to flow out of the storage tank and crystallize at unwanted locations and thus presents a major limitation for the proper operation of such systems. These anomalies become more pronounced when high HTF flow rates are employed with the aim to achieve fast heat transfer rates. The goal of this paper is to find a method which will enable the fast separation of the formed emulsion and thus the uninterrupted operation of the storage unit. In this study, three separation methods were examined and the use of superhydrophobic filters was chosen as the best candidate for the demulsification of the PCM and HTF mixtures. The filter was produced by processing of a melamine sponge with different superhydrophobic adhesives and was tested with emulsions closely resembling the ones formed in a real direct contact setup. The superhydrophobic filter obtained, was able to separate the emulsions effectively while presenting a very high permeability (up to 1,194,980 kg h−1 m−2 bar−1). This is the first time the use of a superhydrophobic sponge has been investigated in the context of demulsification in direct contact latent heat storage.

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.