Examining the quasi-static uniaxial compressive behaviour of commercial high-performance epoxy matrices

Four commercial high-performance aerospace aromatic epoxy matrices, CYCOM®890, CYCOM®977-2, PR520, and PRISM EP2400, were cured to a standardised 2 h, 180 °C cure cycle and evaluated in quasi-static uniaxial compression, as well as by dynamic scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The thermoplastic toughened CYCOM®977-2 formulation displayed an overall increase in true axial stress values across the entire stress-strain curve relative to the baseline CYCOM®890 sample. The particle-toughened PR520 sample exhibited an overall decrease in true axial stress values past the yield point of the material. The PRISM EP2400 resin, with combined toughening agents, led to true axial stress values across the entire plastic region of the stress-strain curve, which were in line with the stress values observed with the CYCOM®890 material. Interestingly, for all formulations, the dilation angles (associated with the volume change during plastic deformation), recorded at 0.3 plastic strain, were close to 0°, with the variations reflecting the polymer structure. Compression data collected for this series of commercial epoxy resins are in broad agreement with a selection of model epoxy resins based on di- and tetra-functional monomers, cured with polyamines or dicarboxylic anhydrides. However, the fully formulated resins demonstrate a significantly higher compressive modulus than the model resins, albeit at the expense of yield stress

Evaluation of healable epoxy matrices as covalent adaptive networks in uniaxial compression

Vitrimers provide dynamic bonding that can allow a degree of self-healing capability in cross-linked resins. A commercial amine-cured epoxy resin, Prime 27, showed a compressive yield stress, measured in compression, of 88 ± 2 MPa and a compression modulus of 3.41 ± 0.03 GPa. This base resin was modified by incorporating various proportions of two commercial vitrimers, either Thioplast EPS35 (an aliphatic epoxy-terminated polysulfide) or Vitrimax T130 (an imine-cured DGEBA epoxy resin). The addition of increasing amounts of Thioplast EPS35 into the resin led to a rapid drop in the glass transition temperature of the matrices and also a reduction in compressive performance. After an initial test in quasi-static, uniaxial compression, samples containing vitrimers were heated for 1 h at 100 °C and then subjected to a second compression test; all of the matrices loaded with Thioplast EPS35 were able to recover their full initial compression performance. Addition of increasing amounts of Vitrimax T130 to the same commercial epoxy resin did not cause any change in its glass transition temperature. However, after initial compression testing, followed by heating (1 h at 100 °C), only the formulation containing 40 wt% Vitrimax T130-loaded matrix regained its full initial compressive performance. Optimal results in terms of healing capability, measured as the recovery of the initial compression performance during a second identical test, following a heating step, were achieved by incorporating 10 wt% of EPS35 or 40 wt% Vitrimax T130, with little to no drop in glass transition temperature. For these selected formulations, the incorporation of 10% Thioplast EPS35 in Prime 27 gave a yield stress of 83 ± 2 MPa and a compression modulus of 3.13 ± 0.02 GPa, while the addition of 40% Vitrimax T130 gave a yield stress of 79 ± 2 MPa and a compression modulus of 3.30 ± 0.02 GPa

Experimental characterisation of the dilation angle of polymers

Despite the wide use of Drucker-Prager plasticity-based models on polymers, the experimental measurement of the dilation angle, a critical parameter to fully describe the plastic potential, has been rarely reported in existing literature. This paper shows, for the first time, the experimental characterisation of the dilation angle of polymers over a wide range of plastic strain. These measurements were obtained from uniaxial compression experiments conducted on poly(methyl methacrylate) (PMMA) and an untoughened epoxy resin. The calculation of the dilation angle relied on the measurements of the compressive force and the strain components obtained via Digital Image Correlation (DIC). Lower values of dilation angle were obtained for the epoxy resin, suggesting that resistance to volumetric change during plastic deformation could be associated to molecular structure and internal forces. The methodology and results presented in this study can be applied to different types of materials and employed for developing and validating constitutive models that incorporate plastic dilation