Reducing treatment of coppersmelting slag: Thermodynamic analysis of impurities behavior

A thermodynamic mathematical model, describing behavior of Pb, Zn, and As during reducing slag cleaning in the Vanyukov furnace has been developed. Using a developed model, the influence of different factors, such as temperature, oxygen partial pressure, the ratio of the formed phases on the behavior of impurities, was analyzed. It was found that arsenic can significantly move to the bottom phase, and zinc can be significantly vaporized under conditions in the Vanyukov furnace.     

Collagen scaffolds for orthopedic regenerative medicine

Collagen and collagen-based scaffolds offer distinct advantages when selected as biomaterials for use across a broad spectrum of regenerative medicine applications. However, relatively poor mechanical properties are often perceived to limit their usefulness for orthopedic applications. These problems can be overcome through enhanced crosslinking mechanisms or through the addition of a second, stiffer phase such as hydroxyapatite, thus allowing tailored composite scaffolds to meet specific tissue requirements. This overview will highlight the current state of the art of these scaffolds, and consider the exciting prospects and future directions of collagen-based technologies for orthopedic regenerative medicine.     

Beneficial and technological analysis for the recycling of solar grade silicon wastes

In the current paper, different kinds of silicon wastes during the production of SoG-Si were summarized and the beneficial analyses, such as financial value, energy value, CO₂ emissions, and efficiency and energy payback time, were briefly discussed for the recycling of SoG-Si wastes. Possible technologies to recycle and purify SoG-Si wastes were reviewed: such as filtration, sedimentation, solidification control, electromagnetic separation, plasma oxidation, centrifugation, and high temperature remelting process, et al.     

Cation-promoted supramolecular assembly of bivalent metal tetra-15-crown-5-phthalocyaninates: Controlling the architecture of supramolecular aggregates

Cation-promoted supramolecular assembly of cobalt(II) and ruthenium(II) tetra-15-crown-5-phthalocyaninates is comparatively studied using the electronic absorption and infrared spectroscopy. The effects of the nature of the receptor and substrate on the architecture of the supramolecular aggregates formed are discovered. By contrast to Cu(II), Zn(II), and Ni(II) tetra-15-crown-5-phthalocyaninates, Co(II) and Ru(II) complexes are found to demonstrate sodium-potassium selectivity determined by the peculiarities of supramolecular structures formed upon the interaction with the cations.     

Modeling of microstructure effects on the mechanical behavior of ultrafine-grained nickels processed by hot isostatic pressing

Bulk ultrafine-grained nickel specimens having grain sizes in the range of 0.25-5 μm were consolidated by hot isostatic pressing technique. The resulting microstructures were characterized by transmission electron microscopy and X-ray diffraction analysis. Compression tests were carried out at room temperature and at strain rate of 1.6×10⁻⁴ s⁻¹. It was found that the measured yield strength does not follow the Hall-Petch law as a consequence of the presence of oxide phase. Therefore, the use of micromechanics based model, which takes into account only the Hall-Petch relationship at grain level for predicting the grain sized effects on mechanical behavior of this kind of materials, is not accurate yet. In this study, a modification made to the generalized self-consistent model was proposed for studying both grain size and oxide phase dependence of ultrafine-grained materials behavior. Because of the novel modification, an optimization procedure with two steps was required to identify the parameters of micromechanical model. An acceptable agreement between experimental and numerical results was achieved. Moreover, the influence of texture on the yield strength and the application of the proposed model to the spark plasma sintering processed materials were also discussed.     

Amphiphilic and photocatalytic behaviors of TiO2 nanotube arrays on Ti prepared via electrochemical oxidation

Amphiphilic TiO₂ nanotube arrays (TiO₂ NTs) were fabricated through electrochemical oxidation of Ti in solution containing H₃PO₄ and NaF. Scanning electron microscopic analysis shows that the as-prepared TiO₂ NTs have an average pore diameter of 100 nm and a wall thickness of 15 nm. The electrochemical oxidation of Ti can be divided into four stages. In the first stage, when the potential is very low, oxygen formation and Ti dissolution are the major reactions. The second stage corresponds to a slightly higher potential, but less than 2.5 V. In this stage, the formation of TiO₂ film occurs. When the potential is increased to the even higher range from 2.5 V to 6 V, the TiO₂ film dissolves and nanoporous surface structure is generated. This is the third stage. Further increase of the potential enters stage four. The high potentials cause the self-organization of the nanostructure and allow the formation of well-aligned TiO₂ NTs. We also found that the change in surface condition of Ti by annealing heat treatment affects the film dissolution kinetics. As compared with TiO₂ thin film, the TiO2 NTs show higher photocatalytic activity on decomposing Rhodamine B. The surface of the TiO₂ NTs can be wetted by both water and oil. Such an amphiphilic property comes from the capillary effect of the nanochannel structure of the TiO₂ NTs. Because of the amphiphilic property and the photocatalytic activity, we conclude that the TiO₂ NTs have the capability of self-cleaning.     

Infrared emission properties and energy transfer in ZnO-SiO2:Yb composites

Intense near-infrared emission at 1 μm has been obtained in ZnO-SiO₂:Yb³⁺ composites via a facile sol-gel method upon broadband ultraviolet light excitation. Systematic optical measurements including static and time-resolved photoluminescence have been performed to elucidate the energy transfer from ZnO quantum dots to Yb³⁺ ions. The dependence of energy transfer efficiency on Yb³⁺ concentration has been investigated in detail. Codoping with Li⁺ ions leads to about twice enhancement of the near-infrared luminescence intensity around 1 μm at room temperature. The enhancement in the luminescence intensity could be mostly attributed to the modification of the local symmetry around Yb³⁺ ions by codoping with Li⁺ ions.     

Dynamic behavior of a Zr-based metallic glass at cryogenic temperature

The dynamic behavior of a Zr-based bulk metallic glass at cryogenic temperature is investigated by a miniaturized split Hopkinson pressure bar apparatus. As that at room temperature, the failure stress decreases suddenly and then tends to hold steady along with increasing strain rate at cryogenic temperature, but the strain rate regime corresponding to the sudden decrease of the failure stress moves up. The failure stress also increases along with decreasing temperature, whereas there is no obvious change for the plasticity.