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The phase change enthalpy of the SA/a-CNTs composite could also be tailored by changing the mass ratio of SA and a-CNTs.
The heating cycle phase change enthalpy is 137.4 J/g, and the cooling cycle phase change enthalpy is 127.6 J/g.
60 wt% PEG/CNIC PCM has a relatively larger phase change enthalpy of 45.8 J g−1.
The effects of different EG mass fractions associated with different phase change enthalpy and thermal conductivity are investigated firstly under high-rate discharge condition.
Thermal gravimetrical and differential scanning calorimeter analyses showed the phase change enthalpy of 80.9 kJ kg−1 or 120.0 MJ m−3.
The thermal conductivity of modified plasters is greatly improved, as well as the heat storage capacity, the additional phase change enthalpy being up to 13 J/g.
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The phase change enthalpies increase with higher PEG content.
Acree and Chickos [1], recently published a comprehensive compilation of phase change enthalpies, including vaporization enthalpies of pure organic compounds.
The DSC analyses indicate that the melting temperatures are between 44 °C and 60 °C with phase change enthalpies above 180 kJ/kg.
A review on polyols as PCM for TES shows that polyols have phase change temperatures in the range of −15 to 245 °C, and considerable phase change enthalpies of 100 413 kJ/kg.
Phase change enthalpies of the microcapsules produced with n-hexadecane core were obtained as 137 J g−1 at 22 26 °C and the microcapsules produced with n-octadecane core were obtained as 168 J g−1 at 33 35 °C even after hundred cycles.
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