Double-Negative Mechanical Metamaterials Displaying Simultaneous Negative Stiffness and Negative Poisson’s Ratio Properties

Intuitively, materials become both shorter and wider when compressed along their length. Here we show how a composite material or structure can display a simultaneous reversal in the direction of deformation for both the axial and transverse dimensions, corresponding to negative values of effective stiffness and effective Poisson’s ratio, respectively. A negative Poisson’s ratio[1] (NPR or auxetic[2]) host assembly stabilising (otherwise unstable) embedded negative stiffness[3] (NS) elements is presented and modelled analytically. Composite assemblies containing 3 alternative NS elements are demonstrated experimentally, confirming both NPR and NS responses under quasi-static loading over certain strain ranges and in good agreement with model predictions. We report systems demonstrating NS values over two orders of magnitude, ranging from -1.4 N mm-1 to -160 N mm-1. Such systems are scalable and are expected to lead to increased enhancements in other useful properties such as vibration damping, finding application across transport, healthcare, defence and space sectors, amongst others

Effect of cross-linkers on the processing of lignin/polyamide precursors for carbon fibres

This work reports the use of cross-linkers in bio-based blends from hydroxypropyl-modified lignin (TcC) and a bio-based polyamide (PA1010) for possible use as carbon fibre precursors, which, while minimising their effects on melt processing into filaments, assist in cross-linking components during the subsequent thermal stabilisation stage. Cross-linkers included a highly sterically hindered aliphatic hydrocarbon (Perkadox 30, PdX), a mono-functional organic peroxide (Triganox 311, TnX), and two different hydroxyalkylamides (Primid® XL-552 (PmD 552) and Primid® QM-1260 (PmD 1260)). The characterisation of melt-compounded samples of TcC/PA1010 containing PdX and TnX indicated considerable cross-linking via FTIR, DSC, DMA and rheology measurements. While both Primids showed some evidence of cross-linking, it was less than with PdX and TnX. This was corroborated via melt spinning of the melt-compounded chips or pellet-coated TcC/PA1010, each with cross-linker via a continuous, sub-pilot scale, melt-spinning process, where both Primids showed better processability. With the latter technique, while filaments could be produced, they were very brittle. To overcome this, melt-spun TcC/PA1010 filaments were immersed in aqueous solutions of PmD 552 and PmD 1260 at 80 °C. The resultant filaments could be easily thermally stabilised and showed evidence of cross-linking, producing higher char residues than the control filaments in the TGA experiments

Effect of cross-linkers on the processing of lignin/polyamide precursors for carbon fibres

This work reports the use of cross-linkers in bio-based blends from hydroxypropyl-modified lignin (TcC) and a bio-based polyamide (PA1010) for possible use as carbon fibre precursors, which, while minimising their effects on melt processing into filaments, assist in cross-linking components during the subsequent thermal stabilisation stage. Cross-linkers included a highly sterically hindered aliphatic hydrocarbon (Perkadox 30, PdX), a mono-functional organic peroxide (Triganox 311, TnX), and two different hydroxyalkylamides (Primid® XL-552 (PmD 552) and Primid® QM-1260 (PmD 1260)). The characterisation of melt-compounded samples of TcC/PA1010 containing PdX and TnX indicated considerable cross-linking via FTIR, DSC, DMA and rheology measurements. While both Primids showed some evidence of cross-linking, it was less than with PdX and TnX. This was corroborated via melt spinning of the melt-compounded chips or pellet-coated TcC/PA1010, each with cross-linker via a continuous, sub-pilot scale, melt-spinning process, where both Primids showed better processability. With the latter technique, while filaments could be produced, they were very brittle. To overcome this, melt-spun TcC/PA1010 filaments were immersed in aqueous solutions of PmD 552 and PmD 1260 at 80 °C. The resultant filaments could be easily thermally stabilised and showed evidence of cross-linking, producing higher char residues than the control filaments in the TGA experiments