4.7 Article

New approach for sol-gel synthesis of microencapsulated n-octadecane phase change material with silica wall using sodium silicate precursor

期刊

ENERGY
卷 67, 期 -, 页码 223-233

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.energy.2013.11.088

关键词

Microencapsulated n-octadecane; Silica wall; Phase change performance; Microstructure; Thermal conductivity; Phase change performance

资金

  1. National Natural Science Foundation of China [51173010]

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A new silica encapsulation technique toward n-octadecane PCM (phase change material) was developed through sal gel synthesis using sodium silicate as a silica precursor. Fourier transform infrared spectra confirm the chemical composition of the synthesized microcapsules, and wide-angle X-ray scattering patterns indicate good crystallinity for the n-octadecane inside silica microcapsules. Scanning electric micrographs demonstrate that the microencapsulated n-octadecane obtained at pH 2.95 similar to 3.05 presents a perfect spherical morphology and a well-defined core shell microstructure. Because the pH value of reaction solution determines the silica condensation rate and, thus, influences the balance between the self-assembly and polycondensation of silica precursors on the surface of n-octadecane droplets, the microcapsules could achieve a smooth and compact surface at pH 2.95 similar to 3.05. The microencapsulated noctadecane also exhibits good phase change performance and achieves a high encapsulation rate and high encapsulation efficiency in this synthetic condition. The encapsulation of n-octadecane with compact and thick silica wall can impart a high thermal conductivity and a good anti-osmosis property to the microcapsules, and can also improve the thermal stability of the microcapsules by preventing inside n-octadecane from thermally evaporating. Owing to the easy availability and low cost of sodium silicate, this synthetic technique indicates a high feasibility in industrial manufacture for the microencapsulated PCMs with inorganic walls. (C) 2014 Elsevier Ltd. All rights reserved.

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