Comparative study of the influences of different water tank shapes on thermal energy storage capacity and thermal stratification

2016 ◽  
Vol 85 ◽  
pp. 31-44 ◽  
Author(s):  
Zheng Yang ◽  
Haisheng Chen ◽  
Liang Wang ◽  
Yong Sheng ◽  
Yifei Wang
2020 ◽  
Vol 197 ◽  
pp. 01001
Author(s):  
Abdullah Bamoshmoosh ◽  
Gianluca Valenti

Thermal energy storage is of great interest both for the industrial world and for the district heating and cooling sector. Available technologies present drawbacks that reduce the margin of application, such as low energy density, limited temperature range of work, and investment costs. Phase transition is one of the main phenomena that can be exploited for thermal energy storage because of its naturally high energy density. Constant-volume vapor-liquid transition shows higher flexibility and increased heat transfer properties with respect to available technologies. This work presents a description of the behavior of these types of systems. The analysis is carried out through a generalized approach using the Corresponding State Principle. Variation of internal energy as a function of temperature over a fixed range is calculated at constant volume at different values of specific volume. It is shown that, for lower specific volumes, larger temperature ranges of work can be achieved without occurring in the steep pressure increase typically given by the expansion of liquid. Maximum operating temperature range is increased by up to 20% of the critical temperature with minimal energy loss. In optimal subsets of these ranges of temperature, the energy storage capacity of vapor-liquid systems increases at lower volumes, with energy storage capacity increasing to up to 40% with a 50% increase of the reduced volume. This is especially valid for more complex fluids, which are more interesting for these applications because of their higher heat capacity.


Author(s):  
Yuchen Mao ◽  
Jin Gong ◽  
Meifang Zhu ◽  
Hiroshi Ito

In this paper, we synthesized MC(BeA-co-MMA) copolymer microcapsules through suspension polymerization. The pendent n-behenyl group of BeA is highly crystalline, and it acts as the side-chain in the structure of BeA-co-MMA copolymer. The highly crystalline n-behenyl side-chain provides BeA-co-MMA copolymer thermal-energy-storage capacity. In order to investigate the correlation between thermal properties and crystal structure of BeA-co-MMA copolymer, the effects of monomer ratio, temperature changing and changing rate, as well as synthesis method were discussed. The monomer ratio influenced crystal transition behavior and thermal properties greatly. The DSC results proved that when the monomer ratio of BeA and MMA was 3:1, MC(BeA-co-MMA)3 showed the highest average phase change enthalpy ΔH (105.1 J·g–1). It indicated that the n-behenyl side-chain formed relatively perfect crystal region, which ensured a high energy storage capacity of copolymer. All the DSC and SAXS results proved that the amount of BeA had a strong effect on the thermal-energy-storage capacity of copolymer and the long spacing of crystals, but barely on the crystal lamella. It was found that MMA units worked like defects in the n-behenyl side-chain crystal structure of BeA-co-MMA copolymer. Therefore, a lower fraction of MMA, that is, a higher fraction of BeA contributed to a higher crystallinity of BeA-co-MMA copolymer for providing a better energy storage capacity and thermoregulation property. ST(BeA-co-MMA) copolymer sheets with the same ingredients as microcapsules were also prepared through light-induced polymerization aiming at clarifying the effect of synthesis method. The results proved that synthesis method mainly influenced the copolymer chemical component, but lightly on the crystal packing of n-behenyl side-chain.


2019 ◽  
Vol 2019 ◽  
pp. 1-15 ◽  
Author(s):  
Loubna Bousselamti ◽  
Mohamed Cherkaoui

Based on the examination of the efficiency of solar plants, this study focuses on three main plants: a photovoltaic (PV) plant, a concentrated solar power (CSP) plant, and a hybrid PV/CSP plant. The modelling of the three plants has been implemented to evaluate the influence of design parameters (orientation angles, solar multiple (SM), thermal energy storage capacity (TES), and fraction of hybridization) on them. Several simulations have been recreated and discussed in details to study the optimal configuration of the two first plants and the profitability of the PV/CSP plants for Ouarzazate (Morocco) location. The findings demonstrate that the optimal orientation angles and TES/SM, respectively, affect the performances of PV and CSP plants, and they also reveal that PV/CSP systems have the benefits to increase the annual energy produced, reduce the cost, and offer a high dispatchability to supply a baseload. The implementing of optimal PV/CSP plant has a great economic impact on Ouarzazate city.


Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1512 ◽  
Author(s):  
Yuchen Mao ◽  
Jin Gong ◽  
Meifang Zhu ◽  
Hiroshi Ito

In this paper, we synthesized MC(BeA-co-MMA) copolymer microcapsules through suspension polymerization. The pendent n-behenyl group of BeA is highly crystalline, and it acts as the side-chain in the structure of BeA-co-MMA copolymer. The highly crystalline n-behenyl side-chain provides BeA-co-MMA copolymer thermal-energy-storage capacity. In order to investigate the correlation between the thermal properties and crystal structure of the BeA-co-MMA copolymer, the effects of monomer ratio, temperature changing and the changing rate, as well as synthesis method were discussed. The monomer ratio influenced crystal transition behavior and thermal properties greatly. The DSC results proved that when the monomer ratio of BeA and MMA was 3:1, MC(BeA-co-MMA)3 showed the highest average phase change enthalpy ΔH (105.1 J·g–1). It indicated that the n-behenyl side-chain formed a relatively perfect crystal region, which ensured a high energy storage capacity of the copolymer. All the DSC and SAXS results proved that the amount of BeA had a strong effect on the thermal-energy-storage capacity of the copolymer and the long spacing of crystals, but barely on the crystal lamella. It was found that MMA units worked like defects in the n-behenyl side-chain crystal structure of the BeA-co-MMA copolymer. Therefore, a lower fraction of MMA, that is, a higher fraction of BeA, contributed to a higher crystallinity of the BeA-co-MMA copolymer, providing a better energy storage capacity and thermoregulation property. ST(BeA-co-MMA) copolymer sheets with the same ingredients as microcapsules were also prepared through light-induced polymerization aiming at clarifying the effect of the synthesis method. The results proved that the synthesis method mainly influenced the copolymer chemical component, but lightly on the crystal packing of the n-behenyl side-chain.


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