標題: Synthesis and characterization of amorphous octakis-functionalized polyhedral oligomeric silsesquioxanes for polymer nanocomposites
作者: Sheen, Yuung-Ching
Lu, Chu-Hua
Huang, Chih-Feng
Kuo, Shiao-Wei
Chang, Feng-Chih
應用化學系
Department of Applied Chemistry
關鍵字: amorphous;nanoparticles;nanocomposites
公開日期: 26-八月-2008
摘要: We have synthesized the polyhedral oligomeric silsesquioxane (POSS) derivatives OS-POSS and OA-POSS through the hydrosilylation of styrene and 4-acetoxystyrene, respectively, with octakis(dimethylsiloxy)-silsesquioxane (Q(8)M(8)(H)). We then prepared OP-POSS through acetoxyl hydrazinolysis of OA-POSS with hydrazine monohydrate. The chemical structures of these POSS derivatives were characterized using FTIR and H-1 NMR spectroscopy and MALDI-TOF mass spectrometry. Unlike Q(8)M(8)(H), which is crystalline, these three hydrosilylated POSS derivatives are liquids at 25 degrees C. Through DSC and XRD analyses, we found that they exhibit polymer-like glass transitions and amorphous halos. These octakis-functionalized POSS derivatives can be regarded as amorphous glasses possessing low glass transition temperatures, the values of which depend on the intermolecular interactions of their outer organic groups. To investigate the dispersion of these POSS derivatives in polymer nanocomposites, we blended OS-POSS, OA-POSS, and OP-POSS with polystyrene, poly(4-acetoxystyrene), and poly(4-vinylpyridine), respectively, and investigated the effects of the resulting intermolecular aromatic hydrophobic, dipole-dipole, and hydrogen-bonding interactions, respectively. Dipole-dipole interactions provided the best dispersion of OA-POSS in poly(4-acetoxystyrene), in which the POSS-polymer intermolecular interactions were of similar strength to the POSS-POSS interactions. (C) 2008 Elsevier Ltd. All rights reserved.
URI: http://dx.doi.org/10.1016/j.polymer.2008.06.055
http://hdl.handle.net/11536/8447
ISSN: 0032-3861
DOI: 10.1016/j.polymer.2008.06.055
期刊: POLYMER
Volume: 49
Issue: 18
起始頁: 4017
結束頁: 4024
顯示於類別:期刊論文


文件中的檔案:

  1. 000259113900022.pdf

若為 zip 檔案,請下載檔案解壓縮後,用瀏覽器開啟資料夾中的 index.html 瀏覽全文。