4.8 Article

Preparation and thermal properties of palmitic acid/polyaniline/exfoliated graphite nanoplatelets form-stable phase change materials

期刊

APPLIED ENERGY
卷 115, 期 -, 页码 603-609

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.apenergy.2013.10.061

关键词

Form-stable phase change materials; Solar energy; Thermal energy storage; Exfoliated graphite nanoplatelets; Thermal conductivity

资金

  1. National Natural Science Foundation of China [21003014, 21001017, 21275022]
  2. Natural Science Foundation of Hunan Province, China [13JJ3068, 10JJ5002]
  3. Scientific Research Fund of Hunan Provincial Education Department [12C0007]
  4. Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation (Changsha University of Science Technology) [2014CL05]

向作者/读者索取更多资源

Exfoliated graphite nanoplatelets (xGnP) were applied to enhance the thermal conductivity of polyaniline (PANI) based form-stable phase change materials (PCMs). The xGnP was first dispersed in palmitic acid (PA) uniformly under the assistance of ultra-sonication. The xGnP/PA mixture was then applied to prepare PA/PANI/xGnP form-stable PCMs, in which PANI was obtained by means of surface polymerization of aniline and acted as supporting material. The content of PA in the prepared form-stable PCMs was fixed as 75 wt%. The structure, thermal energy storage properties and thermal conductivity of the PA/PANI/xGnP form-stable PCMs were investigated. The results showed that the thermal conductivity of the prepared form-stable PCMs could be greatly improved by xGnP while the thermal energy storage capacity was maintained. The thermal conductivity and thermal energy storage capacity of the PA/PANI/xGnP form-stable PCM doped with 7.87 wt% of xGnP could attain 1.08 W/(m K) and 157.7 J/g, respectively. The thermal conductivity was 237.5% higher than that of PA/PANI form-stable PCM. The prepared PA/PANI/xGnP form-stable PCM is expected to exhibit better performance in solar thermal energy applications. (C) 2013 Elsevier Ltd. All rights reserved.

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