4.7 Article

Thermal and mechanical properties of nanofibers-based form-stable PCMs consisting of glycerol monostearate and polyethylene terephthalate

期刊

JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
卷 114, 期 1, 页码 101-111

出版社

SPRINGER
DOI: 10.1007/s10973-012-2856-7

关键词

Form-stable PCMs; Thermal energy storage; Glycerol monostearate; Electrospinning; Thermal properties; Mechanical properties

资金

  1. National High-tech R&D Program of China [2012AA030313]
  2. Changjiang Scholars and Innovative Research Team in University [IRT1135]
  3. National Natural Science Foundation of China [51006046, 51203064]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions
  5. Industry-Academia-Research Joint Innovation Fund of Jiangsu Province [BY2012068]
  6. Science and Technology Support Program of Jiangsu Province [SBE201201094]
  7. Natural Science Fundation of Jiangsu Province [BK2010140]
  8. Doctor Candidate Foundation of Jiangnan University [JUDCF12023]
  9. Innovation Program for Graduate Education in Jiangsu Province [CXZZ12_0747]

向作者/读者索取更多资源

An innovative type of nanofibers-based form-stable composite phase change materials for the storage and retrieval of thermal energy was successfully prepared by encapsulating glycerol monostearate (GMS) into the porous structure of polyethylene terephthalate (PET)-supporting matrices on the nanoscale through electrospinning. The field-emission scanning electron microscopy and transmission electron microscopy images revealed that the composite nanofibers possessed desired morphologies with the average fiber diameters ranging from about 290 to 1000 nm which increased with the contents of GMS. The two phase separation (e.g., GMS phase and PET phase) was clearly observed from the images. When GMS content reached 60 %, the amount of the GMS distributing on the surface of the composite nanofibers was significantly increased during the electrospinning. The Fourier transform infrared spectroscopy spectrum proved that the PET supporting matrices were physically combined with GMS molecules. The differential scanning calorimetry analysis indicated that the GMS/PET composite nanofibers had reversible phase change behaviors, and the melting enthalpies increased from 32.63 to 66.99 kJ kg(-1) with increasing GMS amount. The TG results showed that both the onset thermal degradation temperature and charred residue of the GMS/PET composite nanofibers at 700 A degrees C were higher than those of pristine GMS powder owing to the better thermal stability of the PET molecules. The tensile testing revealed that the averaged tensile strength and elongation at break of the all GMS/PET composite nanofibers varied from 3.29 to 10.30 MPa and from 2.42 to 42.30 %, respectively.

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