Resinification Behavior of Regenerated Feather Keratin Powder

A preliminary study was performed on the resinification behavior of regenerated feather keratin powder by changing the sintering conditions, and the thermal and mechanical properties for the obtained resin were investigated. It was confirmed that the molding at 140°C was enough to complete the resinification. The resin obtained was amorphous and its glass transition temperature could be raised to 93°C. In addition, the hardness of the resin could be increased from 20–25 HV to 90 HV by leaving the as-sintered compact resin in ambient air at room temperature for 133 days. Crosslinking agents that work even at room temperature seem to be synthesized during the molding.     

On the thermal conductivity of bimodal SiC/A356 composites fabricated via powder metallurgy route

The present study investigates the thermal conductivity of bimodal SiC particulate distribution in aluminum matrix composites fabricated via powder metallurgy route. The effects of the SiC_p reinforcement size distribution and processing parameters such as sintering time and temperature on the thermal conductivity have been examined. The Box–Behnken experimental array was employed to identify the effects of selected variables on the thermal conductivity of the composite. A reasonable augmentation in the thermal conductivity was observed with an increase in sintering time and %volume fraction of fine SiC particulates. It has been demonstrated that the matrix doped with fine SiC particulates (37?µm) occupied interstitial positions and formed continuous SiC–matrix network resulting in minimizing the micropores that contributed for good thermal conductivity, that is, 235?W/mK. Scanning electron microscopy (SEM) and x-ray diffraction (XRD) were conducted to evaluate the microstructure architecture and interfacial phase formation.     

Mechanical Properties of an Fe‐Based SAM2×5‐630 Metallic Glass Matrix Composite with Tungsten Particle Additions

We present the role of tungsten additions on the mechanical properties of a Fe‐based structural amorphous metal (SAM2×5‐630) containing crystalline tungsten. Matrix cracking by microindentation is inhibited by the addition of tungsten and indicates that tungsten improves the fracture toughness. Response surfaces from nanoindentation arrays indicate that the hardness and modulus of the matrix phase are increased by tungsten additions. Bulk composites with 30 vol% tungsten subjected to 4‐point flexure exhibited brittle fracture behavior and the characteristic strength and Weibull modulus were 165 and 8.7 MPa, respectively. The addition of tungsten did not cause devitrification of the matrix phase.     

The design and assessment of bio-inspired additive manufactured stab-resistant armour

The performance of modern fibre-based or polycarbonate armour has significantly improved since their introduction, providing protection against a range of low- and high-velocity threats. While this is so, users of such armour frequently report of issues relating to their operational suitability resulting in impaired performance and physiological effects. Recently, researchers have focused on how naturally occurring protective mechanisms could be utilised to enhance the protective and operational performance of wearers of engineered body armour. The research presented within this paper therefore utilises a series of key design characteristics exhibited within naturally occurring elasmoid scale armour, coupled with established laser sintering manufacturing parameters, for the realisation and assessment of a scale-based stab-resistant armoured structure to internationally recognised test standards.     

Turning Industrial Residues into Resources: An Environmental Impact Assessment of Goethite Valorization

Goethite is a metals-rich residue that occurs during zinc production. The feasibility of metal recovery from goethite has been demonstrated, but is not economically viable on an industrial scale. Therefore, goethite is landfilled with considerable economic costs and environmental risks. The goal of this study is to evaluate the environmental performance of a new valorization strategy for goethite residues from zinc production, with the aims of: ① recovering the valuable zinc contained in the goethite and ② avoiding the landfilling of goethite by producing a clean byproduct. The presented goethite valorization strategy consists of a sequence of two processes: ① plasma fuming and ② inorganic polymerization of the fumed slag. Plasma fuming recovers the valuable metals by fuming the goethite. The metals-free fumed slag undergoes a process of inorganic polymerization to form inorganic polymers, that can be used as a novel building material, as an alternative to ordinary Portland cement (OPC)-based concrete. Life-cycle assessment (LCA) is used to compare the environmental performance of the inorganic polymer with the environmental performances of equivalent OPC-based concrete. The LCA results show the tradeoff between the environmental burdens of the fuming process and inorganic polymerization versus the environmental benefits of metal recovery, OPC concrete substitution, and the avoidance of goethite landfilling. The goethite-based inorganic polymers production shows better performances in several environmental impact categories, thanks to the avoided landfilling of goethite. However, in other environmental impact categories, such as global warming, the goethite valorization is strongly affected by the high-energy requirements of the plasma-fuming process, which represent the environmental hotspots of the proposed goethite recycling scheme. The key elements toward the sustainability of goethite valorization have been identified, and include the use of a clean electric mix, more effective control of the fumed gas emissions, and a reduced use of fumed slag through increased efficiency of the inorganic polymerization process.     

Effect of Nd3+ substitution on structural and magnetic properties of Mg–Cd ferrites synthesized by microwave sintering technique

Nd~(3+) substituted spinel ferrites with formula Mg_xCd_(1-x)Nd_(0.03)Fe_(1.97)O_4(x = 0.0.2,0.4,0.6.0.8 and 1.0)were prepared by oxalate co-precipitation method using novel microwave sintering technique. AR grade sulphates were used as starting chemicals. The samples were sintered at optimized power of 70 W for10 min in a microwave oven(800 W). The structural analysis of these samples was done by using X-ray diffraction, scanning electron microscope and Fourier transform IR techniques. The XRD analysis of the synthesized ferrite confirms the formation of cubic spinel structure of ferrite. The influence of Nd3+substitution on various structural parameters of Mg-Cd ferrites was reported. IR study indicates the spectra contain two intense absorption bands around 600 and 400 cm~(-1) in addition with four extra bands. The magnetic properties of all ferrites were studied by using a vibration sample magnetometer.The crystallite and grain size dependant magnetic properties are observed. The composition Mg_(0.6)Cd_(0.4)Nd_(0.03)Fe_(1.97)O_4 has better magnetic properties that can be used in recording media. The fast synthesis of spinel ferrites is yielded due to use of the microwave sintering technique.     

Thermoelectric performance of polycrystalline Sn1-xCuxSe (x = 0–0.03) prepared by high pressure method

P-type Sn_1-xCu_xSe (x = 0–0.03) polycrystal was prepared through melting synthesis and high pressure (6.0 GPa) sintering (HPS) method. The composition and microstructure of the samples was analyzed, and the thermoelectric transport properties were investigated in the temperature range of 303 K–823 K. The results indicate that the electrical conductivity increases as Cu content increases. An observable improvement is found for the Seebeck coefficient when x is 0.01. In addition, the total thermal conductivities (κ_tot) of all samples decrease with rising temperature, and reach its minimum values at 773 K. As a result, the maximum power factor (PF) and ZT_max value are 378 μW m⁻¹ K⁻² and 0.79 for Sn_0.97Cu_0.03Se at 823 K, respectively.     

Preparation of Copper Nanoparticles Using Dielectric Barrier Discharge at Atmospheric Pressure and its Mechanism简

Dielectric barrier discharge （DBD） cold plasma at atmospheric pressure was used for preparation of copper nanoparticles by reduction of copper oxide （CuO）. Power X-ray diffraction （XRD） was used to characterize the structure of the copper oxide samples treated by DBD plasma. Influences of H2 content and the treating time on the reduction of copper oxide by DBD plasma were investigated. The results show that the reduction ratio of copper oxide was increased initially and then decreased with increasing H2 content, and the highest reduction ratio was achieved at 20% H2 content. Moreover, the copper oxide samples were gradually reduced by DBD plasma into copper nanoparticles with the increase in treating time. However, the average reduction rate was decreased as a result of the diffusion of the active hydrogen species. Optical emission spectra （OES） were observed during the reduction of the copper oxide samples by DBD plasma, and the reduction mechanism was explored accordingly. Instead of high-energy electrons, atomic hydrogen （H） radicals, and the heating effect, excited-state hydrogen molecules are suspected to be one kind of important reducing agents. Atmospheric-pressure DBD cold plasma is proved to be an efficient method for preparing copper nanoparticles.