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Showing papers by "Kenneth A. Mauritz published in 2003"


Journal ArticleDOI
TL;DR: In this article, diffusion-controlled polymer in situ sol-gel reactions for tetraethylorthosilicate (THS) and Surlyn®/silicate hybrid materials were examined with transmission electron (TEM), atomic force (AFM), and environmental scanning electron microscopic methods.
Abstract: Surlyn®/silicate hybrid materials were produced via diffusion-controlled polymer in situ sol–gel reactions for tetraethylorthosilicate. The heterogeneous morphologies of these materials were inspected with transmission electron (TEM), atomic force (AFM), and environmental scanning electron microscopic methods. The silicate uptake was highly dependent on the water affinity of the particular Surlyn® form (acid or ionic) rather than on the affinity of the solvent. The morphology consisted of silicate particles with diameters that were on the order of tens of nanometers. Hence, these materials can be classified as nanocomposites. The particle size distributions in both the TEM and AFM images for all composites appeared to be narrow, with un-neutralized Surlyn® exhibiting a broader distribution. Larger particles were found near the film surfaces, and the silicon elemental distribution across the film thickness indicated higher concentrations near the surfaces, which is most likely due to the fact that the sol–gel reaction is diffusion controlled in these polymeric media. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1563–1571, 2003

21 citations


Journal ArticleDOI
TL;DR: The first-scan differential scanning calorimetric thermogram for unfilled Surlyn® revealed the usual twin-melting endotherms as discussed by the authors, but the lower temperature endotherm was either not present or weak.
Abstract: Acid form Surlyn®/titanate hybrid materials were achieved by polymer insitu sol–gel reactions for a titanium alkoxide monomer. Atomic force microscopic images revealed arrays of titania nanoparticles having diameters of 10–30 nm. Fourier transform infrared spectra verified the presence of an internally polymerized titanate phase although unhydrolyzed TiOR groups were present. Carboxylic acid dimerization was complete at room temperature, but carboxylate anions appeared at higher titanate levels. The methylene rocking doublet persisted upon incorporation of the inorganic component, which supported the idea of largely undisrupted crystallinity. Thermogravimetric analysis showed that the degradation onset temperature of each hybrid is largely unaffected by the presence of the inorganic filler, which is consistent with the concept of an isolated titanate phase. The first-scan differential scanning calorimetric thermogram for unfilled Surlyn® revealed the usual twin-melting endotherms. In contrast, the primary, high-temperature melting endotherm was seen on the first scan for the Surlyn®/titanate hybrids, but the lower temperature endotherm was either not present or weak. Primary melting persisted after several cycles of heating above the melting temperature followed by cooling, demonstrating that primary crystallinity persisted despite titanate phase incorporation. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 11–22, 2003

20 citations