Abstract

Curing agents for epoxy resins play a significant role in initiating crosslinking reactions resulting in the hardened and durable material with enhanced properties as per end-user applications. The industrial world still lacks efficient, environmentally friendly, and cheap curing agents for epoxy resins. Here, we report the development of deep eutectic solvents (DESs) based on N, N’-Bis(2-aminoethyl)ethane-1,2-diamine (commonly known as triethylenetetramine, TETA) as hydrogen bond donor (HBD), and salicylic acid (SA) and choline chloride (CC) as hydrogen bond acceptor (HBA). The formulated DESs are suggested to be relatively safe, affordable, and eco-friendly and the active groups in the DESs are capable of initiating crosslinking reactions. The physical stability of the formulated deep eutectic solvents was examined by polarizing optical microscopic (POM) analysis, which confirmed the absence of any crystals or residues. The purity was ensured by 13C nmr spectroscopy. Additionally, supportive evidence for the hydrogen bond formation between the constituents was gained from the outcomes of FTIR, 1H nmr, and mass spectrometry. Deep depression in melting points was confirmed from DSC studies, and TGA suggested better thermal stability for DESs than its constituents. Density functional theory (DFT) at B3LYP6-31G* of Gaussian computational framework was applied to energetically optimize the isolated structure and determine the bond lengths in angstroms. The structural characteristics and nonbonding interactions of DESs were investigated by the same. In addition, the density and rheological characteristics were assessed for the ideal utilization of the formulated DESs as epoxy resin curing agents. The detailed comparative studies demonstrated the advantages of deep eutectic solvents over conventional curing agents. The efficacy of the formulations as a curing agent was primarily confirmed from FTIR analysis and the curing behavior was investigated by DSC studies.

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