The effects of monophenol chain terminators on the structure–property relationships of controlled epoxy networks
Autor: | Lisa Allen, Anamari Laboy‐Bollinger, K. James Hrovat, James C. Buck, James A. Rabon, Carol L. O'connell, Nikhil E. Verghese, Maurice J. Marks |
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Rok vydání: | 2008 |
Předmět: |
Polymers and Plastics
Chemistry Thermodynamics Concentration effect Dynamic mechanical analysis Epoxy Condensed Matter Physics Mole fraction Thermal expansion visual_art Polymer chemistry Materials Chemistry visual_art.visual_art_medium Thermomechanical analysis Thermal stability Physical and Theoretical Chemistry Glass transition |
Zdroj: | Journal of Polymer Science Part B: Polymer Physics. 46:1632-1640 |
ISSN: | 1099-0488 0887-6266 |
DOI: | 10.1002/polb.21503 |
Popis: | Five families of new controlled epoxy thermosets (CENs) using three monophenol chain terminators were prepared to study systematic changes in the structure and amount of the monophenol and the initial molecular weight between crosslinks (M c,i ) on the properties of epoxy thermosets. Glass transition temperature (T g ) decreases with monophenol mole fraction (χ) in proportion to both the concentration and flexibility of the chain terminator. Distinct serial relations for T g depression were observed for the three M c,i families. Dynamic mechanical analysis (DMA) shows significant perturbations of the relaxation behavior with added terminator as evidenced by decrease in peak tan δ and in post T g damping. The rubbery coefficients of thermal expansion (CTE) increases with monophenol concentration only at χ> 0.05 and shows distinct curvature versus temperature, but is largely invariant with monophenol flexibility. The thermal stability of terminated CENs decreases only slightly with χ and little difference was found with monophenol structure. Most surprisingly, fracture toughness decreases markedly and discontinuously with χ c depending on M c,i . The values of the critical monophenol concentration at which fracture toughness markedly decreases (χ c ) are inversely proportional to M c,i but are independent of monophenol flexibility. No correlation of χ c with any of the calculated network structure parameters was apparent. |
Databáze: | OpenAIRE |
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