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Thermal Characterization of Epoxy Nanocomposites Containing Polyhedral Oligomeric Silsesquioxane: Glass Transition Temperature and Chemical Conversion

Authors
Gu, PuzhongYang, GuangLee, Sang CheolLee, Jong Keun
Issue Date
Jan-2017
Publisher
KOREAN FIBER SOC
Keywords
Epoxy; Polyhedral oligomeric silsesquioxane (PUSS); Glass transition temperature; Chemical conversion; Differential scanning calorimetry (DSC)
Citation
FIBERS AND POLYMERS, v.18, no.1, pp 131 - 139
Pages
9
Journal Title
FIBERS AND POLYMERS
Volume
18
Number
1
Start Page
131
End Page
139
URI
https://scholarworks.bwise.kr/kumoh/handle/2020.sw.kumoh/26723
DOI
10.1007/s12221-017-6573-5
ISSN
1229-9197
1875-0052
Abstract
An epoxy resin (diglycidyl ether of bisphenol-A) was blended with different loadings of a glycidyl-polyhedral oligomeric silsesquioxane (POSS) and isothermally cured with an amine hardener at varying temperatures and times. The glass transition temperature (T-g) of the samples was measured at different chemical conversions (a) using differential scanning calorimetry (DSC). Time-temperature shifts were made for T-g vs. ln(time) data to be superposed at an arbitrary reference temperature in the kinetically controlled reaction regime, and these shift factors were used to obtain an Arrhenius activation energy. The influence of POSS on different reaction systems was investigated in terms of the T-g-alpha relationship, which was fitted with two models; DiBenedetto and Venditti/Gillham equations. It was found that POSS molecules played different roles at different stages of the curing process. At lower conversions, the inorganic cage of the incorporated POSS (up to 20 wt%) reduced the mobility of the molecular segments, giving rise to an increase in T-g. However, above the 20 wt% POSS, there was a depression of T-g, which may be associated with a plasticizing effect of organic substituents of the POSS molecules. Moreover, the effect of POSS on T-g became less pronounced when the conversion reached 0.8.
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