Abstract:Poly(methyl methacrylate) (PMMA)/copper hydroxy methacrylate (CHM) composites were prepared via solution blending and bulk polymerization. Addition of 3% by weight of the CHM additive using solution blending resulted in a significant increment (∼45°C) in thermogravimetric NOT THE PUBLISHED VERSION; this is the author's final, peer-reviewed manuscript. The published version may be accessed by following the link in the citation at the bottom of the page. Technology, Vol. 17, No. 4 (April 2006): pg. 312-319. DOI. This article is © Wiley and permission has been granted for this version to appear in e-Publications@Marquette. Wiley does not grant permission for this article to be further copied/distributed or hosted elsewhere without the express permission from Wiley.
Polymers for Advanced2 analysis (TGA) T50, the temperature at which 50% of the original polymeric mass is lost. The value T50 increased by 30°C for a PMMA composite with 4% CHM, synthesized via bulk polymerization. Activation energies, Ea, were calculated as a function of conversion fractions (TGA decomposition profile) for the polymeric materials. Analysis of multiple heating rate data using the Flynn-Wall-Ozawa method resulted in Ea values that were 50 kJ mol −1 higher for conversions above 0.5 in the solution blended composite compared to a reference sample of pure PMMA recrystallized from the same solvent. Similar results were obtained for bulk polymerization process with differences in Ea values > 30 kJ mol −1 relative to pure PMMA. However, in contrast to previous studies of bulk polymerized samples, the solution-blended composite exhibited no improvement in cone calorimetry determination of total heat release as compared with the reference PMMA sample