LAUSR

Abstract A UV-curable polyurethane acrylate (PUA) oligomer was prepared from dimer acid (DA) based polyester polyol (DAPEP) with a monofunctional acrylate precursor which was developed upon isophorone diisocyanate (IPDI) reacted with 2-hydroxyethyl methacrylate (HEMA). The structural elucidation of synthesized dimer acid based PUA (DAPUA) oligomer was verified through Fourier-transform infrared spectroscopy (FT-IR) and Proton nuclear magnetic resonance (1H NMR). A series of UV cured coatings were prepared by adding trimethylolpropane triacrylate (TMPTA) and 1,6-hexanediol diacrylate (HDDA) reactive diluents in varying percentages (10−30 wt%) to PUA oligomer. The bio-coatings exhibited exceptional results, including the highest thermal degradation temperature of 382–422 °C, glass transition temperature (Tg) of 56.38–66.27 °C, the tensile strength of 17.3–30.6 MPa, volume shrinkage of 6.19–9.13 %, and surface roughness of 4.89–28.21 nm. Compared to vegetable oil based UV-curable coatings, long chain dimer acid based PUA oligomer coatings exhibited excellent flexibility, impact, hydrophobicity, and resistance to volume shrinkage.