Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-19T10:29:12.531Z Has data issue: false hasContentIssue false

Enhanced Thermal Conductivity of Phase Change Materials Modified by Exfoliated Graphite Nanoplatelets

Published online by Cambridge University Press:  31 January 2011

Jinglei Xiang
Affiliation:
xiangjin@egr.msu.edu, Michigan State University, Chemical Engineering and Materials Science, East Lansing, United States
Lawrence Drzal
Affiliation:
drzal@egr.msu.edu, Michigan State University, Chemical Engineering and Materials Science, East Lansing, United States
Get access

Abstract

Composite phase change materials (PCM) were prepared by mixing exfoliated graphite nanoplatelets (xGnP) into paraffin wax. The two types of graphite nanoplatelets that were investigated were xGnP-1 having thickness of 10 nm and a diameter of 1 um and xGnP-15 having the same thickness with a platelet diameter of 15 um. Direct casting and two roll milling were used to prepare samples. Scanning electron microscopy images show that the nanofillers disperse very well in paraffin matrix without noticeable agglomeration. Paraffin/xGnP-15 PCM consistently exhibited higher thermal conductivity than xGnP-1 PCM. The improvement in thermal conductivity was as high as 5 fold for xGnP-15 composites and 2 fold for xGnP-1 composites at 4 vol%. The aspect ratio, particle orientation, and interface density between the conductive particles and the polymer matrix were found to be the critical parameters in determining the conductivities of the resulting nanocomposites. The thermal physical properties of the nanocomposites were investigated by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). It was found that the latent heat of nanocomposites was not negatively affected in the presence of xGnP particles and the thermal stability improved.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1 Hasnain, S.M.. Energy Convers. Manage, 39, 1127 (1998)Google Scholar
2 Hasnain, S.M..; in Energy '93. Proc.5th Intl. Energy Conference, Seoul, Korea 1993 Google Scholar
3 Pillai, K.K..; Brinkworth, B.J.. Appl. Energy. 2, 205 (1976)Google Scholar
4 Luyt, A.S., eXpress Polym. Lett, 2, 3, 147 (2008)Google Scholar
5 Velraj, R..; Seeniraj, R.V..; Hafner, B..; Faber, C..; Schwarzer, K.. Sol.Energy. 60, 281 (1997)Google Scholar
6 Hasnain, S.M..; in Proc. COMSTECH NIST Workshop on New Trends and Break-throughs in Solar Energy Research. Islamabad, Pakistan, 1994 Google Scholar
7 Fukai, J.. Energy Convers. Manage. 41, 1543 (2000)Google Scholar
8 Elgafy, A..; Lafdi, K.. Carbon, 43, 3067 (2005)Google Scholar
9 Pincemin, S.., Sol. Energy Mater. Sol. C 92, 603 (2008)Google Scholar
10 Kim, S..; Drzal, L.T..; Sol. Energy Mater. Sol. C 93, 136 (2009)Google Scholar
11 Fukushima, H..; Ph.D Thesis, Michigan State University, East Lansing, MI, USA, 2003 Google Scholar
12KKalaitzidou, ., Ph.D. Thesis, Michigan State University, East Lansing, MI, USA, 2006 Google Scholar
13 Kalaitzidou, K..; Fukushima, H..; Drzal, L.T., Carbon, 45 1446 (2007)Google Scholar