Effects of the porcelain-fused-to-metal firing process on the surface and corrosion of two Co–Cr dental alloys

The aim of this study was to evaluate the effects of a simulated porcelain-fused-to-metal (PFM) firing process on the surface, corrosion behavior, and cell culture response of two cobalt–chromium (Co–Cr) dental alloys. Two Co–Cr dental alloys were tested—a high and a low molybdenum (Mo)-containing alloys. Before PFM firing, as-cast alloy specimens were examined for their microstructure, surface composition, and hardness. Corrosion behavior was evaluated using electrochemical impedance spectroscopy tests. Mouse 3T3 fibroblasts were exposed indirectly to specimens and MTT cell proliferation assays were performed after 3 and 6 days. The cell culture medium exposed to specimens was analyzed for metal ion release. After firing, similar alloy specimens were examined for the same properties. The tests showed that the PFM firing changed both alloys’ microstructures and hardness values. After PFM firing, the corrosion resistance of the low Mo-containing Co–Cr alloy decreased statistically, which corresponded with a reduction of Cr and oxygen levels in the surface oxides via X-ray photoelectron spectroscopy. Also, the MTT assay of this alloy decreased significantly corresponding with an obvious increase of Co release after the firing. For the high Mo-containing Co–Cr alloy, the surface composition, corrosion resistance, and cell culture response were not significantly changed after PFM firing. The results suggested that the corrosion resistance and biocompatibility of the low Mo-containing Co–Cr alloy decreased after PFM firing, whereas the firing process had little effect on the same properties of the high Mo-containing Co–Cr alloy.     

Surface modification of Scots pine: the effect of process parameters on the through thickness density profile

This study evaluated the significance of different process parameters (press temperature, closing time, holding time, moisture content and compression ratio) on solid wood surface densification and its effect on the density profile generated in Scots pine sapwood. Changes in the microstructure of the wood were also evaluated microscopically. The results showed that with a shorter closing time, densification occurred closer to the sample surface than with an extended closing time. At a compression temperature of 150 °C, the vertical density profile exhibited a sharp peak in density that was close to the wood surface. A higher temperature of 200 °C resulted in a slightly broader density peak that was less intense and further from the surface. A holding time of 10 min resulted in the wood compressing to a slightly greater extent than when using a holding time of 1 min. Higher moisture content led to more extensive deformation. The results indicate that surface modification by densification is a viable method of enhancing wood properties.     

Zirconia-modified exfoliated graphite

Zirconia has been incorporated into exfoliated graphite (EG) through the anodic polarization in the natural graphite-ZrO(NO₃)₂-HNO₃-H₂O system, followed by flash heating. The thermal properties of the oxidized graphites employed as precursors to EG have been studied by thermogravimetry in combination with differential scanning calorimetry, and the distribution of ZrO₂ particles in the EG has been assessed by scanning and transmission electron microscopy. Conditions are described for the preparation of EG with bulk densities in the range 1.3–4.7 g/l and ZrO₂ contents in the range 4–34 wt %.     

Probing of wood–cement interactions during hydration of wood–cement composites by proton low-field NMR relaxometry

Proton NMR T ₂ relaxometry has been applied to investigate phenomena involved in wood–cement composites during hydration. The transformation of capillary pore water into hydrates and gel pore water, as well as the microstructural changes occurring in the cement matrix, was continuously monitored during the first 28 days of hydration. Water in wood and its transfer into the matrix as cement hardens were also evidenced with the method. It has been found, for example, that some of the water in the mixture is retained in wood in the form of bound or free water, depending on the initial water content. By measuring the area under the different peaks, the consumption of water during hydration can be measured and the advancement of the hydration process can be evaluated via the hydration advancement coefficient α. The cement hardening within the composite has been also studied in the presence of calcium chloride, an accelerating agent. The acceleration was clearly evidenced at the early stage of the hydration process. The influence of extractives has been evaluated by comparing the hydration behaviour of composites prepared from Eucalyptus saligna (low extractives content) and Afzelia bipendensis (high extractives content), and a new compatibility index based on NMR relaxometry measurements has been proposed.     

The influence of oxygen and nitrogen contamination on the densification behavior of cryomilled copper powders during spark plasma sintering

It has been found difficult to fully densify some mechanically milled pure metal powders by spark plasma sintering (SPS). In this study, the densification behavior of cryomilled, nanostructured (NS) Cu powders during SPS was related to changes to the chemistry of the powders. The results showed that the presence of very small amounts of O and N in the powders, which were introduced during cryomilling and handling, significantly influenced the densification response. Moreover, reduction/removal of O/N via thermal annealing of the powders before SPS led to complete densification of the powders during subsequent SPS. The mechanisms responsible for this behavior were ascertained: O and N existed in the cryomilled powders in the form of thermally unstable compounds, and the subsequent thermal decomposition of these compounds during SPS generated the gaseous species, leading to porosity formation and incomplete densification; annealing of the powders before SPS removed the gases which resulted from thermal decomposition, thereby facilitating complete consolidation during subsequent SPS.     

High yield polypyrrole: A novel approach to synthesis and characterization

An improved synthetic route to polypyrrole salt was accomplished using methanesulfonic acid as a novel dopant along with potassium persulfate as the oxidant employing inverted emulsion polymerization technique. Polypyrrole salt was obtained in high-weight percent yield (83.77%) with respect to the amount of monomer used and the reaction time was drastically reduced (1 h 10 min.) as compared to the previously reported synthesis methods. Characterization of the salt yielded satisfactory results. Inverted emulsion polymerization technique has several unique and distinct advantages over conventional techniques which facilitate the synthesis of fused five membered heterocyclic rings which are otherwise difficult to synthesize, and hence sparsely reported in the literature.     

Influence of oxides on the stability of zinc foam

The influence of oxides on the stabilisation of zinc foam made by foaming-compacted powder mixtures has been investigated by varying the oxide content in the zinc powder used by oxidation and reduction. Optical, scanning electron and transmission electron microscopy as well as energy dispersive X-ray mapping were used to determine the oxide distribution, morphology and structure in the foams. The study revealed that with increase in the oxide content of the foam, the maximum expansion and expansion rate increased. Small amount of nano-sized oxide particles and their cluster, which are randomly distributed, were observed within the bulk of foam. But the major fraction of oxides is observed on the surface of pores in the form of clusters. These clusters are distributed uniformly all over the surface. Effect of these oxides on the stability of foam is discussed. The formation of satellite pores, which is characteristic signature of zinc foams, and their stability, is investigated.     

Gold nanoparticle-coated biomaterial as SERS micro-probes

We report for the first time, on the utility of plant-based biomaterial as enhanced-Raman scattering probes. The bio-substrate used in this study are commonly found in plant extracts, and are cost-effective, mechanically robust, flexible and easily transportable. The probe was fabricated by coating the plant extract with gold nanoparticles and characterized. By employing a ‘single-touch contact’ method, we reveal the ability of these probes to detect routinely used Raman markers such as 2-napthalenethiol and rhodamine B, at nano-molar concentrations, in dry and liquid forms, respectively. Reproducibility of the signals with variation <5%, and the ability to detect biomolecules are demonstrated herein. We envision these bio-probes as potential candidates for enhanced Raman sensing in chemical, environmental, and archaeological applications. By further engineering the shape, morphology, and surface chemistry of these micro-probes, we foresee their utility as miniaturized, natural SERS substrates.     

Spray-drying of alumina powder for APS: effect of slurry properties and drying conditions upon particle size and morphology of feedstock

In this paper, effects of variables concerning slurry properties and drying conditions on the particle size and morphology of feedstock were discussed. The results indicated that, the increase of powder loading increased D ₅₀ and volume content but reduced recovery rate slightly. Other variables, such as inlet temperature, showed a maximum on the desired property. The particle size of resulting feedstock increased with the rise of feeding rate of slurry, however, decreased with the increase of atomization pressure based on the premise that atomization pressure was enough to force slurry to form the liquid membrane. For preparation of spherical feedstock, optimized variables were as follows: 60 wt.% powder in slurry, 2 wt.% PVA in slurry, inlet temperature of 60°C, atomization pressure of 13 × 10³ KPa and feeding rate of 12 ml min^?1. The volume content of feedstocks with 10–45 μm was above 65% and for D ₅₀ it was 15·42 μm. In addition, according to the heat and mass transfer equation, the drying mechanism was established, which was well in agreement with the experimental results.     

Structural characteristics of titanium coating on copper substrates

The growth characteristics of titanium films deposited on glass, silicon (100) and oxygen free high purity copper substrate using magnetron sputtering have been investigated using X-ray diffraction, electron microscopy and scratch indentation techniques. The study of interface between the titanium film and the substrate was carried out to determine coating thickness, as well as intermixing of the elements at the interface. Studies revealed that the interface is free from voids and intermixing of the film and the substrate. Microstructural and diffraction analysis showed that the Ti coating was polycrystalline and exhibited columnar growth. The Ti crystallite size varied between 24 and 58 nm depending on the substrate. The thickness of the films were typically about 4 μm. Scratch test indicated that the films are adherent and the first critical load to failure was observed to be 4·5 N ± 2 N.