Date of Award

5-2026

Degree Type

Dissertation

Degree Name

Doctor of Philosophy (PhD)

School

Polymer Science and Engineering

Committee Chair

Dr. Derek Patton

Committee Chair School

Polymer Science and Engineering

Committee Member 2

Dr. Tristan Clemons

Committee Member 2 School

Polymer Science and Engineering

Committee Member 3

Dr. Sergei Nazarenko

Committee Member 3 School

Polymer Science and Engineering

Committee Member 4

Dr. James Rawlins

Committee Member 4 School

Polymer Science and Engineering

Committee Member 5

Dr. Jeffrey Wiggins

Committee Member 5 School

Polymer Science and Engineering

Abstract

This dissertation relates to ester-containing aromatic epoxy monomers and thermosets formed via reaction of those monomers with either ester-containing or non-ester-containing amine comonomers.  Due to the wide array of potential reactants (many bioderivable) to form ester-containing epoxy monomers that are closely related in structure, fundamental study of structure-property relationships was highly practical for this platform of materials.

Though properties of aromatic epoxy thermosets of relatively high-crosslink density and network strand rigidity vary widely with chemical composition and architecture, relatively low fracture toughness and impact resistance due to lack of ductility are typical. Integration of ester functionality and aliphatic spacers/connectors for the ester groups permitted regulation of molecular mobility of thermosets described herein. Aromatic ester functionality (vs. aliphatic), connection by spacers of limited-length, and the use of structurally-analogous ester-containing amine comonomers to uniformly distribute mobility were useful approaches to augment ductility yet limit loss in properties typically associated with highly-crosslinked aromatic epoxy thermosets (high strength, modulus, etc.). The widespread and uniform placement of ester linkages also permitted depolymerization via hydrolysis and alcoholysis – useful from a material end-of-use standpoint.

ORCID ID

0009-0007-2417-4821

Available for download on Saturday, August 01, 2026

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