This article describes the changes in the microstructure, cooling curve characteristics and mechanical properties of cast Nickel Aluminium Bronze alloy (NAB) alloy that were produced by the addition of various amounts of Tin (Sn). The solidification parameters were recorded using a computer-aided cooling curve analysis setup, and optical and scanning electron microscopes were utilised to study the evolution of the microstructure. The chemical composition of different phases generated in the NAB alloy with and without Tin was investigated using an X-ray diffraction technique. With the addition of tin, the alloy's microstructure changed from columnar to equiaxed grain structures, and the ideal microstructure was produced at a Tin concentration of roughly 1.0 weight percent. The formation of the high temperature α and the grain boundary Sn rich phases across the alloy microstructure as a result of further addition has a considerable impact on the alloy's increased hardness (upto 69%) and tensile strength (upto 28.4%) compared to untreated NAB alloy. Influence of Sn on microstructure transformation is confirmed by the decline in alloy nucleation temperatures, the reduction in undercooling intensity, and the decrease in cooling rate during solidification. The addition of Tin to the NAB alloy caused morphological changes in the kappa (K) phases, which are also reported in the this article. In addition to this, the research makes an attempt to describe the mechanism underlying the formation of equiaxed grains and phase transformations in Sn-treated NAB alloys.

Polymer nanocomposites have been of great interest to packaging, energy, molding, and transportation industries due to several favorable properties including a higher resistance to stress and cracking even under flexed conditions, and also a chemical resistance to water, acids, and alkalis. The current work disseminates the studies on the mechanical and thermal properties of the polypropylene HHR102 polymer reinforced with nano dispersoids of silicon dioxide at varied weight fractions. The nanocomposites, fabricated via melt processing followed by injection molding, were tested for tensile strength, % elongation, tensile modulus, and impact toughness. Further, the samples were also subjected to dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA) to determine the dynamic storage modulus and thermal stability. The addition of nano-silica in polypropylene HHR102 resulted in enhanced ductility and well-balanced tensile modulus; however, the tensile strength and impact toughness were found to be decreased. On the other hand, the storage modulus was significantly increased for all nano-silica (NS)-containing polypropylene HHR102 matrices. With the increased nano-silica content, the storage modulus was optimal. Further, with the lower weight loss of 30% and 50%, the thermal stability of the increased silica content PP nanocomposites was much affected. However, it improved at a weight loss of 30% for the lower silica content PP nanocomposite (PP-1%NS). The imbibition was found to increase with the increase in NS. The increase in imbibition is attributed to the micro-voids generated during ageing. These micro-voids act as channels for water absorption. Further, the degree of crystallinity of the nanocomposites was decreased as a result of inhibition by the nano-particles on the regular packing of polymer molecules. The structure–property correlations were explicated based on the achieved mechanical properties.