New Route to Improve Thermal Property of Phenolic Resin

Article Preview

Abstract:

A new route for improving the thermal property of phenolic resin was described. Firstly, a soluble preceramic polymer was synthesized by condensation polymerization of zirconium oxychloride, salicyl alcohol and acetylacetone in the presence of triethylamine at room temperature. A modified phenolic resin was then obtained via blending the preceramic polymer and phenolic resin in solution. The preceramic polymer was characterized by FTIR, NMR and GPC. The thermal property of the modified phenolic resin was also investigated by TGA. It was found that the preceramic polymer was composed of Zr-O-Zr as the main chain and the ligands (salicyl alcohol and acetylacetone) as the side chain. It pyrolyzed completely at 600°C and formed ZrO2 in nitrogen atmosphere. The results of TGA indicated that 5 wt% preceramic polymer could increase the thermal decomposition temperature and the char yield of the modified phenolic resin by 18°C and 25%, respectively. Moreover, the preceramic polymer allowed the char formation from phenolic resin at relatively low temperature.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

1047-1051

Citation:

Online since:

December 2012

Authors:

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Periadurai T, Vijayakumar C T and Balasubramanian M: J. Anal. Appl. Pyrol. Vol 89 (2010), p.244.

Google Scholar

[2] Srikanth I, Daniel A, Kumar S, Padmavathi N, Singh V, Ghosal P, Kumar A and Devi G R: Scripta. Mater. Vol 63 (2010), p.200.

DOI: 10.1016/j.scriptamat.2010.03.052

Google Scholar

[3] Liu L andYe Z P: Polym. Degrad. Stabil. Vol 94 (2009), p. (1972).

Google Scholar

[4] Wang D-C, Chang G-W and Chen Y: Polym. Degrad. Stabil. Vol 93 (2008), p.125.

Google Scholar

[5] Wang J G, Jiang N and Jiang H Y: Mater. Chem. Phys. Vol 120 (2010), p.187.

Google Scholar

[6] Jr C U P, Li G Z and Cho H S: J. Inorg. Organomet. P. Vol 16 (2006), p.43.

Google Scholar

[7] Zhang Y D, Lee S H, Yoonessi M, Toghiani H and Jr C U P: J. Inorg. Organomet. P. Vol 17 (2007), p.159.

Google Scholar

[8] Abe Y, Kudo T, Tomioka H, Junji T, Nagao Y and Misono T: J. Mater. Sci. Vol 33 (1998), p.1863.

Google Scholar

[9] Pan M, Liu J-R, Lu M-K, Xu D, Yuan D-R, Chen D-R, Yang P and Yang Z-H: Thermochim. Acta. Vol 376 (2001), p.77.

Google Scholar

[10] Takahiro G, Hiroshi Y, Takaaki H, Kyoko B K and Yoshimoto A: Appl. Organomet. Chem. Vol 14 (2000), p.119.

Google Scholar

[11] Babonneau F J. Eur. Ceram. Soc. Vol 8 (1991), p.29.

Google Scholar

[12] Preiss H, Schierhorn E and Brzezinka K-W: J. Mater. Sci. Vol 33 (1998), p.4697.

Google Scholar

[13] Zhao J K, Han X W, Liu X M, Bao X H, Hang J F and Jiang B: Sci. China Ser. B Vol 43 (2000), p.40.

Google Scholar