Quantitative analysis of collaborative and mobility networks

This study proposes a quantitative analysis of researcher mobility (i.e. transfer from one institution to another) and collaborative networks on the basis of author background data extracted from biographical notes in scientific articles to identify connections that are not revealed via simple co-authorship analysis. Using a top-ranked journal in the field of computer vision, we create a layered network that describes various aspects of author backgrounds, demonstrating a geographical distribution of institutions. We classify networks according to various dimensions including authors, institutions and countries. The results of the quantitative analysis indicate that mobility networks extend beyond the typical collaborative networks describing institutional and international relationships. We also discuss sectoral collaboration considering the mobility networks. Our findings indicate a limitation of collaborative analysis based on bibliometric data and the importance of tracing researcher mobility within potential networks to identify the true nature of scientific collaboration.     

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.     

Spatially resolved X-ray spectroscopy using a flat HOPG crystal

A novel design of a 1-D imaging X-ray spectrometer is implemented, using a high efficiency HOPG (highly oriented pyrolitic graphite) Bragg crystal and a double-entrance-slit. The double slit provides self-calibration of the imaging magnification. The spatial and spectral resolutions and dispersion are characterised both analytically and by ray tracing simulations. A key feature of this approach is that it enables the X-ray spectrum to be measured over different regions of the plasma source. The application of this instrument is demonstrated in high intensity laser-foil interaction experiments.     

Thermal conductivity measurement of the epoxies and composite material for low temperature superconducting magnet design

The thermal conductivities of solid materials were measured by a G-M cryo-cooler based apparatus in the temperature range of 2.6–21.0 K. The performance of this apparatus was verified by measuring the thermal conductivity of 304-stainless steel, and good reproducibility as well as accuracy was shown when compared with the certified values. The thermal conductivities of EC1017 and Stycast2850FT and a composite material were measured. Similar behavior to amorphous materials was shown for EC1017 and Stycast2850FT in that there was an apparent plateau, which could be ascribed to a very lower crystallinity of epoxy. An equivalent model was proposed to predict the thermal conductivity of the composite material.     

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 %.     

High-pressure volume magnetostriction in the diluted magnetic semiconductor Cd1 ? xMnxGeAs2 (x = 0.06–0.3)

The specific volume of the diluted magnetic semiconductor Cd_{1 − x} Mn _x GeAs₂ (x = 0.06–0.3) has been determined for the first time by strain measurements at pressures of up to 7 GPa. From the pressure dependences of the relative specific volume, we evaluated the volume magnetostriction (spontaneous magnetization coefficient). A scaling relation was used to estimate the bulk modulus of the magnetically ordered and disordered phases.     

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.