Design and tribological performance of short S-Glass fibre reinforced biocomposites on the influence of fibre length and concentration.

Fibre-reinforced biocomposites usage has gained prominence over the past decade. Although higher fracture toughness was observed when fibres were added to biocomposites, material degradation could occur due to filler and fibre content intolerance in the biocomposite matrix. Optimisation of resin-fibre-filler ratios helps in increasing the tribological performance of high load-bearing applications. However, the tribological performance is less understood due to limited in-vitro studies on the effect of fibre microstructures. A comprehensive investigation of the reciprocating and rotary wear behaviour of different compositions was carried out by varying fibre (0%, 5%, 10% and 15%) to particulate filler (40%, 45%, 50%, and 55%) weight fractions. The investigation aimed to identify the optimal composition of fibre-reinforced biocomposites based on the in-vitro ball-on-disc reciprocating and rotary wear tests in the presence of modified Fusayama solution. The cross-sectional areas of wear tracks were analysed using laser microscopy and scanning electron microscopy techniques to assess the surface morphology and subsurface damage of the wear tracks on biocomposites and the antagonist. The numerical results were statistically analysed using two-way ANOVA followed by a posthoc Tukey's test (p = 0.05). The results showed a combination of adhesive, abrasive and fatigue wear for all the tested Groups. The friction coefficient had a longer transient period for the 5 wt% and 10 wt% Groups. Based on the surface roughness, coefficient of friction, SEMs, specific wear rate, and ease of manufacturing, the threshold limit for fibre loading was found to be 10 wt%. The rotary test had a considerably lower specific wear rate compared to the reciprocating test. Fibre weight fraction was found to be the influencing factor of the abrasive wear behaviour compared to fibre length for the tested Groups.

Role of Ca2+ doping on the enhancement of dielectric properties of Sr2-xCaxNiWO6 for energy storage device application.

In this paper, Sr2-xCaxNiWO6 (x = 0.00, 0.02, 0.04, 0.06) were synthesized using a solid-state reaction method. The crystal structure, optical and dielectric properties of the compounds were examined using X-ray diffraction (XRD), scanning electron microscope (SEM) with energy dispersive (EDX) analysis, Ultraviolet-visible (UV-vis) diffuse reflectance spectroscopy and electrochemical impedance spectroscopy respectively. The Rietveld refinement of XRD confirmed that the compounds crystallized in a tetragonal structure with a space group I4/m. According to the SEM images, the grain sizes of the compounds decreased as the dopant increased. The UV-vis analysis revealed that the band gap energy of the compounds decreased from 3.17 eV to 3.13 eV as the amount of doping increased from x = 0.00 to x = 0.06. A dielectric characterization showed that the dielectric constant (ε') and dielectric loss (tan δ) for all compounds possessed a similar trend where it was higher in low-frequency area (~ 1 Hz) and dropped instantaneously with the enhancement of frequency up to 1 MHz until it reached constant values.