Numerical Simulation of the Effect of the Size of Suspensions on the Solidification Process of Nanoparticle-Enhanced Phase Change Materials

2013 ◽  
Vol 135 (5) ◽  
Author(s):  
Yousef M. F. El Hasadi ◽  
J. M. Khodadadi

Nanostructure-enhanced phase change materials (NePCM) have been widely studied in recent years due to their enhanced thermal conductivity and improved charge/discharge in thermal energy storage applications. In this study, the effect of the size of the nanoparticles on the morphology of the solid–liquid interface and the evolving concentration field during solidification is reported. Combining a one-fluid-mixture approach with the single-domain enthalpy-porosity model for phase change and assuming a linear dependence of the liquidus and solidus temperatures of the mushy zone on the local concentration of the nanoparticles subject to a constant value of the segregation coefficient, thermal-solutal convection as well as the Brownian and thermophoretic effects are taken into account. A square cavity containing a suspension of copper nanoparticles (diameter of 5 and 2 nm) in water was the model NePCM considered. Subject to a 5 °C temperature difference between the hot (top) and cold (bottom) sides and with an initial loading of the nanoparticles equal to 10 wt. % (1.22 vol. %), the colloid was solidified from the bottom. The solid–liquid interface for the case of NePCM with 5 nm particle size was almost planar throughout the solidification process. However, for the case of the NePCM with particle size of 2 nm, the solid–liquid interface evolved from a stable planar shape to an unstable dendritic structure. This transition was attributed to the constitutional supercooling effect, whereby the rejected particles that are pushed away from the interface into the liquid zone form regions of high concentration thus leading to a lower solidus temperature. Moreover, for the smaller particle size of 2 nm, the ensuing solutal convection at the liquid–solid interface due to the concentration gradient is affected by the increased Brownian diffusivity. Due to size-dependent rejection of nanoparticles, the frozen layer that resulted from a dendritic growth contains regions of depleted concentration. Despite the higher thermal conductivity of the colloids, the amount of frozen phase during a fixed time period diminished as the particle size decreased.

Author(s):  
Yousef M. F. El Hasadi ◽  
J. M. Khodadadi

Nanoparticle-enhanced phase change materials (NEPCM) were proposed recently as alternatives to conventional phase change materials due to their enhanced thermophysical properties. In this study, the effect of the size of the nanoparticles on the morphology of the solid-liquid interface and evolving concentration field, during solidification had been reported. The numerical method that was used is based on the one-fluid-mixture model. The model takes into account the thermal as well as the solutal convection effects. A square cavity model was used in the simulation. The NEPCM that was composed of a suspension of copper nanoparticles in water was solidified from the bottom. The nanoparticles size used were 5 nm and 2 nm. The temperature difference between the hot and cold sides was 5 degrees centigrade and the loading of the nanoparticles that have been used in the simulation was 10% by mass. The results obtained from the model were compared with those existing in the literature, and the comparison was satisfactory. The solid-liquid interface for the case of NEPCM with 5 nm particle size was almost planar throughout the solidification process. However, for the case of the NEPCM with particle size of 2 nm, the solid-liquid interface evolved from a planar stable shape to an unstable dendritic shape, as the solidification process proceeded with time. This was attributed to the constitutional supercooling effect. It has been observed that the constitutional supercooling effect is more pronounced as the particle size decreases. Furthermore, the freezing time increases as the particle size decreases.


2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
B. Heydari ◽  
F. Talati

Thermal energy storage units that utilize phase change materials have been widely employed to balance temporary temperature alternations and store energy in many engineering systems. In the present paper, an operational approach is proposed to the Tau method with standard polynomial bases to simulate the phase change problems in latent heat thermal storage systems, that is, the two-dimensional solidification process in rectangular finned storage with a constant end-wall temperature. In order to illustrate the efficiency and accuracy of the present method, the solid-liquid interface location and the temperature distribution of the fin for three test cases with different geometries are obtained and compared to simplified analytical results in the published literature. The results indicate that using a two-dimensional numerical approach can predict the solid-liquid interface location more accurately than the simplified analytical model in all cases, especially at the corners.


2019 ◽  
Vol 297 ◽  
pp. 187-194
Author(s):  
Izzeddine Saouane ◽  
Abla Chaker ◽  
Tarek Messai ◽  
Hichem Farh

The use of phase change materials must allow storage / destocking of energy from solar or internal gains. The applications in the case of light constructions will lead to an improvement in the thermal comfort of users and a reduction in energy consumption. The use of phase change materials (PCMs) in the energy-saving walls themselves makes it possible to substitute sensible heat storage for latent heat storage which requires a much lower volume and mass for the same amount of thermal energy. The objective of this work is the study of heat transfer by conduction during a phase change, and aims on the one hand to model and simulate the phase change behavior and on the other hand to approach the mechanism of heat exchange at the solid-liquid interface. The results obtained in 2D show the temporal evolution of the temperature, the position and the speed of the solid-liquid interface.


1984 ◽  
Vol 34 ◽  
Author(s):  
Zhu Peiyue ◽  
Sha Rozeng ◽  
Li Yanxiang

ABSTRACTThe effect of twin/tilt initiated in the process of graphite growth making the graphite curling and change from flake to vermicular and spheroidal is discussed. With the developing of the solidification process,the modifying elements enrich in the front of solid-liquid interface, the amount of twin defects in the graphite increases,its tilt fashion changes and the graphite formed varies from flake to vermicular and spheroidal. The modifying elements promote the formation of twin/tilt. When the modifying elements are insufficient for spheroidizing,the tilt orientation of twins is changeable,and the graphite formed is twisted. When the modifying elements are sufficient enough, the tilt orientation of twins becomes singular, and the graphite formed tends to be round. According to the energy and kinetics consideration of the formation of twin/tilt boundary, it is predicted that the twin plane would firstly adopt (10Tm), especially the (10T2) plane. This result coincides well with the experimental observations. It is proposed that the formation of SG can be divided into two steps: growth of graphite nucleus into spherulite by twin/tilt mechanism and brancing on it in a spiral mode.


2012 ◽  
Vol 2012 ◽  
pp. 1-20 ◽  
Author(s):  
Hamid El Qarnia ◽  
Fayssal El Adnani ◽  
El Khadir Lakhal

This work reports an analytical solution for the solidification of a superheating phase change material (PCM) contained in a rectangular enclosure with a finite height. The analytical solution has been obtained by solving nondimensional energy equations by using the perturbation method for a small perturbation parameter: the Stefan number,ε. This analytical solution, which takes into account the effects of the superheating of PCM, finite height of the enclosure, thickness of the wall, and wall-solid shell interfacial thermal resistances, was expressed in terms of nondimensional temperature distributions of the bottom wall of the enclosure and both PCM phases, and the dimensionless solid-liquid interface position and its dimensionless speed. The developed solution was firstly compared with that existing in the literature for the case of nonsuperheating PCM. The predicted results agreed well with those published in the literature. Next, a parametric study was carried out in order to study the impacts of the dimensionless control parameters on the dimensionless temperature distributions of the wall, the solid shell, and liquid phase of the PCM, as well as the solid-liquid interface position and its dimensionless speed.


2020 ◽  
Vol 142 (6) ◽  
Author(s):  
Mohammad Parsazadeh ◽  
Xili Duan

Abstract This research investigates the melting rate of a phase change material (PCM) in the presence of Rayleigh–Benard convection. A scaling analysis is conducted for the first time for such a problem, which is useful to identify the parameters affecting the phase change rate and to develop correlations for the solid–liquid interface location and the Nusselt number. The solid–liquid interface and flow patterns in the liquid region are analyzed for PCM in a rectangular enclosure heated from bottom. Numerical and experimental results both reveal that the number of Benard cells is proportional to the ratio of the length of the rectangular enclosure over the solid–liquid interface location (i.e.,, the liquified region aspect ratio). Their effect on the local heat flux is also analyzed as the local heat flux profile changes with the solid–liquid interface moving upward. The variations of average Nusselt number are obtained in terms of the Stefan number, Fourier number, and Rayleigh number. Eventually, the experimental and numerical data are used to develop correlations for the solid–liquid interface location and average Nusselt number for this type of melting problems.


Author(s):  
Yannan Liang ◽  
Jiemin Zhou ◽  
Ying Yang ◽  
Ye Wu ◽  
Yanyan He

The use of phase-change materials for latent heat storage is a new type of environmentally-friendly energy-saving technologies. Molten salts, one kind of phase-change materials, which have high latent heats, and whose phase transition temperatures match the high temperatures of heat engines, are the most widely used high-temperature phase-change heat storage materials. However, the heat transfer at solid/liquid phase interface belongs to Micro/Nanoscale Heat transfer, lots of the thermal properties of molten salt at melting point is difficult to test. In this investigation, based on the theory that the thermal conductivity can be determined by measuring the speed of the propagation of the solid/liquid phase interface during phase change, a set of system is developed to investigate the thermal conductivity of molten salts at liquid/solid phase transformation point. Meanwhile, mathematical calculation is applied to intuitively simulate the melting and solidifying process in the phase change chamber, by which the error could be analyzed and partly corrected and the result precision could also be increased. And a series of verification experiments have been performed to estimate the precision and the applicability of the measuring system to evaluate the feasibility of the method and measuring system. This research will pave the way to the follow-on research on heat storage at high temperature in industry.


2015 ◽  
Vol 36 (10-11) ◽  
pp. 2897-2915 ◽  
Author(s):  
Soumaya Kadri ◽  
Belgacem Dhifaoui ◽  
Yvan Dutil ◽  
Sadok Ben Jabrallah ◽  
Daniel R. Rousse

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