Fabrication and characterization of phase change material-SiO2 nanocomposite for thermal energy storage in buildings
Introduction
Energy is an essential requirement for the economic growth and development of any country. High global energy demand and concern about the fossil fuels depletion, besides environmental impacts of these fuels consumption headed to the huge attention to conserve energy [1,2].
The utilization of latent heat of phase change materials (PCMs) for energy storage is considered one of the most promising and useful techniques for increasing energy efficiency and energy saving [3,4]. PCMs are characterized by storage and release of large amounts of thermal energy during phase transition processes at a certain temperature and high density of latent heat [5], [6], [7]. However, two major drawbacks of PCMs are low thermal conductivity and large volume change during their phase change processes which cause leakage of PCM, limit their practical applications in thermal energy storage [8,9]. The shape-stabilization is an effective strategy to prevent the leakage and enhance the energy storage capacity of PCM. Hence, selecting an appropriate inorganic carrier matrix for PCMs is a promising idea to enhance their performance. Various supporting materials including polymers [10,11], carbon materials [1,12], diatomite [13], metal oxide nanoparticles [14,15] have been used to overcome these challenges.
Amongst these, SiO2 nanoparticles as a vital inorganic amorphous material are promising as a supporting material for PCMs owing to its great thermal stability, flame-retardant feature, suitable thermal conductivity, non-toxicity, outstanding compatibility with construction materials, and excellent mechanical properties [16].
A review of the previous researches indicates that there has no report on the n-heptadecane-SiO2 nanocomposite fabrication and evaluation as a thermal energy storage material. Thus, in this paper, we used n-heptadecane as a PCM with wide range of mass fractions and SiO2 nanoparticle as a supportive material to form n-heptadecane – SiO2 nanocomposite through impregnation method (Fig. 1). The morphology and structural investigations of the nanocomposite were performed by XRD, FTIR and SEM techniques. Thermal storage capacity of the nanocomposite was searched using DSC analysis and thermal cycling test was made to study the thermal reliability and reusability of the nanocomposite. The thermo-regulating performances of the PCM nanocomposite in gypsum was also measured and evaluated by developing the small test room to simulate a building.
Section snippets
Materials
Absolute ethanol was supplied from R&M Chemicals (UK). SiO2 nanoparticle (20–30 nm) was obtained from US Research Nanomaterials, Inc, while n-heptadecane (C17H36, molecular weight 240.475 g/mol) was acquired from Merck (Germany).
Fabrication of PCM-SiO2 nanocomposite
The synthesis of n-heptadecane- SiO2 nanocomposite was done through impregnation technique. The melted n-heptadecane was dissolved in absolute ethanol. Around 0.5 g, SiO2 nanoparticles were also dispersed in absolute ethanol and then dissolved n-heptadecane was slowly
Powder X-ray diffraction
Fig. 3 exhibits the XRD pattern of SiO2 nanoparticle (A), and n-heptadecane-SiO2 nanocomposites with different weight percentages of n-heptadecane, A1-A5 (B-F). The XRD pattern of SiO2 nanoparticle (Fig. 3A) demonstrates an amorphous structure with a broad peak at 2θ = =15–27◦ [16,17]. It can be seen from the XRD pattern of A5 nanocomposite (Fig. 3F) that the presence of n-heptadecane was reflected by the observation of two peaks at 2Ɵ = 21.2 and 22.9° [18], while the diffraction peak of SiO2
Conclusion
A novel PCM nanocomposite with improved thermal conductivity and great phase change behaviour, and excellent thermal stability was fabricated based on n-heptadecane core and SiO2 nanoparticles framework. DSC analysis indicated that A5 nanocomposite had an enthalpy of 123.8 and 120.9 J/g for melting and crystallization, respectively, and accelerated thermal cycling test certified that A5 nanocomposite showed a good thermal reliability, even after 500 melting/freezing cycles. In addition, the
CRediT authorship contribution statement
Samira Golestani Ranjbar: Formal analysis, Data curation. Ghodratollah Roudini: Conceptualization, Formal analysis, Supervision, Validation. Farahnaz Barahuie: Conceptualization, Formal analysis, Supervision, Validation, Writing - original draft, Writing - review & editing.
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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