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Polyethylene Glycol-Carbon Nanotubes/Expanded Vermiculite Form-Stable Composite Phase Change Materials: Simultaneously Enhanced Latent Heat and Heat Transfer
Polyethylene Glycol-Carbon Nanotubes/Expanded Vermiculite Form-Stable Composite Phase Change Materials: Simultaneously Enhanced Latent Heat and Heat Transfer
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Polyethylene Glycol-Carbon Nanotubes/Expanded Vermiculite Form-Stable Composite Phase Change Materials: Simultaneously Enhanced Latent Heat and Heat Transfer
Polyethylene Glycol-Carbon Nanotubes/Expanded Vermiculite Form-Stable Composite Phase Change Materials: Simultaneously Enhanced Latent Heat and Heat Transfer

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Polyethylene Glycol-Carbon Nanotubes/Expanded Vermiculite Form-Stable Composite Phase Change Materials: Simultaneously Enhanced Latent Heat and Heat Transfer
Polyethylene Glycol-Carbon Nanotubes/Expanded Vermiculite Form-Stable Composite Phase Change Materials: Simultaneously Enhanced Latent Heat and Heat Transfer
Journal Article

Polyethylene Glycol-Carbon Nanotubes/Expanded Vermiculite Form-Stable Composite Phase Change Materials: Simultaneously Enhanced Latent Heat and Heat Transfer

2018
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Overview
Polyethylene glycol (PEG)-carbon nanotubes (CNTs) with expanded vermiculite (EVM) form-stable composite phase change materials (PCE-CPCMs) were constructed via the efficient synergistic effect between EVM and CNTs. The resultant material demonstrated simultaneously enhanced latent heat and heat transfer. The unique EVM pore structure and CNTs surfaces contributed to the form stability of PCE-CPCMs. The adsorption capacity was 77.75–81.54 wt %. The latent heat of the PCE-CPCMs increased with increasing CNTs content due to the decreasing inhibition effect of EVM and the increasing adsorption capacity of PEG, which was 83.9 J/g during melting and 104.2 J/g during solidification for PCE7.09. The pore confinement and surface EVM interactions inhibited the heat storage capacity of the PCE-CPCMs. Moreover, the inhibition effect on the heat storage capacity of PCE-CPCMs during the melting process was stronger than during solidification due to the crystallization-promoting effect. The heat transfer of PCE-CPCMs was significantly enhanced by the CNTs filler (0.5148 W/(m·K) for PCE7.09) due to the decrease in interfacial thermal resistance and the formation of rapid thermally conductive pathways. Fourier transform infrared spectroscopy, thermogravimetric analysis, and thermal cycles test results confirmed that the PCE-CPCMs exhibited excellent chemical compatibility, thermal stability, and reliability.
Publisher
MDPI

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