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Melting temperature and enthalpy variations of phase change materials (PCMs): a differential scanning calorimetry (DSC) analysis

机译:熔化温度和相变材料的焓变化(PCM):差示扫描量热法(DSC)分析

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摘要

Differential scanning calorimetry (DSC) analysis is a standard thermal analysis technique used to determine the phase transition temperature, enthalpy, heat of fusion, specific heat and activation energy of phase change materials (PCMs). To determine the appropriate heating rate and sample mass, various DSC measurements were carried out using two kinds of PCMs, namely N-octadecane paraffin and calcium chloride hexahydrate. The variations in phase transition temperature, enthalpy, heat of fusion, specific heat and activation energy were observed within applicable heating rates and sample masses. It was found that the phase transition temperature range increased with increasing heating rate and sample mass; while the heat of fusion varied without any established pattern. The specific heat decreased with the increase of heating rate and sample mass. For accuracy purpose, it is recommended that for PCMs with high thermal conductivity (e.g. hydrated salt) the focus will be on heating rate rather than sample mass.
机译:差分扫描量热法(DSC)分析是一种标准的热分析技术,用于确定相变温度,焓,融合热,相变材料(PCMS)的比例的热量和活化能量。为了确定适当的加热速率和样品质量,使用两种PCM,即正八达丁烷石蜡和氯化钙六水合物进行各种DSC测量。在适用的加热速率和样品质量中观察到相变温度,焓,熔化,特异性热和活化能量的变化。发现相变温度范围随着加热速率和样品质量而增加;虽然融合的热量变化而没有任何既定的图案。随着加热速率和样品质量的增加,比热降低。为了准确目的,建议为具有高导热率的PCM(例如水合盐),焦点将在加热速率而不是样品质量上。

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