Phenylene Ring Motions In Isomeric Glassy Epoxy Networks and Their Contributions to Thermal and Mechanical Properties
Document Type
Article
Publication Date
3-24-2015
School
Polymer Science and Engineering
Abstract
Cross-linked epoxies prepared from diglycidyl ether of bisphenol A (DGEBA) exhibit substantial property differences due to isomeric structures of the diamine curatives, 3,3′- and 4,4′-diaminodiphenyl sulfone (DDS). Here, the motions of phenylene rings on both the bisphenol A (BPA) and DDS structures of the networks were investigated through solid-state NMR 2H line shape analysis to trace the molecular origins. Ring deuterated monomers, namely, DGEBA-d8, 33DDS-d8, and 44DDS-d8, were synthesized, and four deuterated networks were prepared. The line shapes of the ring motions were interpreted using a motional model that described both ring π-flips and main-chain fluctuations. The contributions of different ring motions to mechanical relaxations are elucidated, and the molecular origins of property differences are identified.
Publication Title
Macromolecules
Volume
48
Issue
6
First Page
1748
Last Page
1758
Recommended Citation
Tu, J.,
Tucker, S.,
Christensen, S.,
Sayed, A.,
Jarrett, W.,
Wiggins, J.
(2015). Phenylene Ring Motions In Isomeric Glassy Epoxy Networks and Their Contributions to Thermal and Mechanical Properties. Macromolecules, 48(6), 1748-1758.
Available at: https://aquila.usm.edu/fac_pubs/18651