TY - JOUR
T1 - Cleavable epoxy networks using azomethine-bearing amine hardeners
AU - Chanteli, Angeliki
AU - Conaire, Marcus
AU - Brannigan, Ruairi
AU - Heise, Andreas
AU - Weaver, Paul M.
AU - Manolakis, Ioannis
N1 - Publisher Copyright:
© 2022 The Authors
PY - 2022/9
Y1 - 2022/9
N2 - This work is a proof-of-concept of the use of azomethine-bearing diamines as novel hardeners of standard epoxy compounds to yield cleavable and thermoformable covalent adaptable networks (CANs), with functional properties otherwise comparable to conventional epoxy networks. A suitable aromatic diamine (TPA-o-PD) was synthesised at acceptable purity for the intended use and successfully reacted with DGEBA. The resulting azomethine-bearing cured epoxy networks exhibited glass transition temperature values and a thermal stability profile similar to conventional epoxy network counterparts. In contrast to their conventional counterparts however, the azomethine-bearing networks were shown to dissolve in mixtures of chloroform and methanesulfonic acid, due to acid hydrolysis of at least some of the azomethine bonds of the network. The resulting recyclate material after evaporating the solvent was consistent with the profile of a thermoplastic polymer of high molecular weight, suggesting limited depolymerisation/network cleavage during dissolution in the chloroform/methanesulfonic acid mixture. The recyclates were soluble in polar aprotic solvents and showed good thermal stability, high Tg and molecular weight values, consistent with the attributes of engineering thermoplastics. Lastly, the cured networks were shown to be thermoformable at 200 °C, yielding self-standing films with only minor reduction of properties.
AB - This work is a proof-of-concept of the use of azomethine-bearing diamines as novel hardeners of standard epoxy compounds to yield cleavable and thermoformable covalent adaptable networks (CANs), with functional properties otherwise comparable to conventional epoxy networks. A suitable aromatic diamine (TPA-o-PD) was synthesised at acceptable purity for the intended use and successfully reacted with DGEBA. The resulting azomethine-bearing cured epoxy networks exhibited glass transition temperature values and a thermal stability profile similar to conventional epoxy network counterparts. In contrast to their conventional counterparts however, the azomethine-bearing networks were shown to dissolve in mixtures of chloroform and methanesulfonic acid, due to acid hydrolysis of at least some of the azomethine bonds of the network. The resulting recyclate material after evaporating the solvent was consistent with the profile of a thermoplastic polymer of high molecular weight, suggesting limited depolymerisation/network cleavage during dissolution in the chloroform/methanesulfonic acid mixture. The recyclates were soluble in polar aprotic solvents and showed good thermal stability, high Tg and molecular weight values, consistent with the attributes of engineering thermoplastics. Lastly, the cured networks were shown to be thermoformable at 200 °C, yielding self-standing films with only minor reduction of properties.
KW - Azomethine bond
KW - Cleavable thermosets
KW - Composite recycling
KW - Diamine epoxy hardeners
KW - Epoxy covalent adaptable networks (CANs)
UR - http://www.scopus.com/inward/record.url?scp=85134322017&partnerID=8YFLogxK
U2 - 10.1016/j.reactfunctpolym.2022.105338
DO - 10.1016/j.reactfunctpolym.2022.105338
M3 - Article
AN - SCOPUS:85134322017
SN - 1381-5148
VL - 178
JO - Reactive and Functional Polymers
JF - Reactive and Functional Polymers
M1 - 105338
ER -