Thermal Energy Storage using Phase Change Materials Nicole Ozminkowski 3.014 Materials Laboratory Introduction Thermal energy systems take advantage of material properties to collect energy, store it, and make it available for retrieval. Phase change materials can be used for a variety of thermal energy storage applications. Some include building insulation, jackets and outerwear, and blood test incubation systems in developing countries. In order to determine which materials are good phase change materials, properties such as specific heat capacity, latent heat of fusion, and melting temperature must be studied. Theoretical Background Thermal energy systems use three types of heat storage: sensible heat storage, thermochemical heat storage, and latent heat storage. Sensible heat storage can be measured by specific heat capacity, which is the amount of heat required to raise the temperature of a material 1 degree Kelvin. Thermochemical heat storage is heat stored through chemical reactions. Latent heat is the amount of heat required or released through a phase change. In this experiment, we focus on latent heat of fusion: how much heat is required to melt the material. Successful phase change materials have high specific heats and latent heats of fusion: they can store a larger amount of energy without a large change in temperature. Another important characteristic of phase change materials is melting temperature. Since the material will stay at about a constant melting temperature during the phase change, it is important that the temperature required for the application is very close to the melting temperature. This is one reason why even though water has a high specific heat capacity, it is not good for keeping buildings at a comfortable temperature: it’s melting point is too low. Phase change materials can be pure materials or mixtures. However, when two materials are mixed, their melting characteristics are not just the average of the two mixtures. The mixture’s melting point will be lower than that of the each of the pure substances. Melting points of binary mixtures are modeled using a phase diagram. The upper boundary, called the liquidus, is the temperature at which the entirety of the mixture became liquid. The bottom boundary, called the solidus, is the temperature at which the entirety of the mixture became solid. At the eutectic point, the liquidus and solidus intersect. Materials and Methods Melting and Freezing Points for All Materials4 1. 2-8 mg of the following materials were added into aluminum pans, which were then crimped closed: 1. Mixtures of Lauric and Stearic Acid of various compositions were created by mixing the solids together and heating at a temperature above 69C and allowing the mixture to equilibrate for 10 minutes. 2. PCM paraffin products: n-Hexadecane: MPCM 18-D n-Octadecane: MPCM 28-D 3. Tempertex continuous climate control interlinings: NWH-38 – thermally enhanced nonwoven style. 4. Sapphire calibration standard for calculating specific heat. Specific Heat of Lauric/Stearic Acid Mixtures3 2. Differential Scanning Calorimetry (DSC) was used to measure the heat flux involved in melting each of the materials in comparison to a reference aluminum pan. Thermal profiles were obtained for single and cyclical scans. Binary Phase Diagram3 Results 1. Thermal profiles for each material were obtained. From each, the latent heat of melting and melting temperature could be read directly. Discussion • As temperature rises, specific heats for all materials also rises, due to the increased vibrations and movements of atoms. • Specific heat for all Lauric/Stearic Acid mixtures remains about constant at between 1400 and 2600 J/ kgK. It mainly changes with temperature, not composition. • The binary mixture between Lauric Acid and Stearic Acid shows a eutectic point at a Lauric Acid composition of about .8. The eutectic composition is ideal because the temperature remains completely constant during the phase change. • Tempertex has a much lower latent heat of melting than any other substance, probably due to the fact that it is not completely composed of PCM, so the mass measured was larger than the actual PCM mass. • The extent of supercooling was between 5-10C for all materials, but was largest for MPCM-18D and 50% wt Lauric Acid. • Most runs showed good thermal stability after the first cycle. The first cycle si probably different because of inconsistincies in the packing of the material. Conclusion Tm Phase change materials work best when their melting temperatures are at the desired temperature and when latent heat of fusion is high. Although materials like rocks have high latent heats of fusion, their melting points are too high for that to be valuable. Both n-Hexadecane and n-Octadecane are good PCM candidates, and due to melting point similarities, it is clear that n-Octadecane is used in Tempertex. In the future, materials with different melting points should be tested as phase change materials for different applications. Binary Phase Diagram2 Latent Heat of Melting for Various Materials 250 ΔHfusion 200 Latent Heat of Melting (J/g) 2. Thermal profiles for sapphire were used to calculate specific heat values for each material using the following equation: 3 150 References 1. Berera, Geetha “Entropy of Phase Change & Thermal Energy Balance,” 3.014 Materials Laboratory (2014) 2. Armstrong, Kathleen. “Foothill College Chemistry.” (2014) http://www.foothill.edu/psme/armstrong/ meltingpoints.shtml 3. Created by Christopher Klingshirtn 4. Created by Jennie Glerum 100 50 0 Tempertex 100% Lauric 90% Lauric 75% Lauric 60% Lauric 40% Lauric 20% Lauric 0% Lauric MPCM 28D MPCM 18D Acknowledgements Thank you to Geetha Berera and Vivek Singh for meeting with me outside of class and furthering my understanding of this topic. Thank you to my lab group members for helping with data analysis. nicoleoz
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