Eu-doped LiF-SrF2 eutectic scintillators for neutron detection

Eu²⁺ 0.05%, 0.1%, and 0.2% activated LiF-SrF₂ eutectic scintillators were prepared by the Bridgman method using ⁶Li enriched (95%) raw material. The α-ray-induced radio luminescence spectra showed intense emission peak at 430 nm due to an emission from Eu²⁺ 5d-4f transition in the Eu:SrF₂ layers. When excited by ²⁵²Cf neutrons, all the samples exhibited almost the same light yields of 5000-7000 ph/n with a typical decay times of several hundreds ns.     

Control of precipitation behaviour of Hastelloy-X through grain boundary engineering

Grain boundary engineering (GBE) was employed to control the precipitation behaviour of Hastelloy-X alloy. The precipitate characteristics and thermal stability of grain boundary character distribution (GBCD) were investigated by aging at 850°C. M₆C carbides and µ phases were observed in the matrix and on grain boundaries, respectively. It revealed that the formation of µ phase was closely related to the grain boundary structure. GBCD effectively suppressed the nucleation and coarsening of µ phases on the grain boundaries. Owing to the Mo depletion in the vicinity of random grain boundary, the formation of the precipitates was inhibited on the adjacent grain boundaries. The thermal stability of the GBE-optimised microstructure was confirmed at 850°C for 720?h without significant microstructural degradation.     

Effects of SO2 on selective catalytic reduction of NO with NH3 over a TiO2 photocatalyst

The effect of SO₂ gas was investigated on the activity of the photo-assisted selective catalytic reduction of nitrogen monoxide (NO) with ammonia (NH₃) over a TiO₂ photocatalyst in the presence of excess oxygen (photo-SCR). The introduction of SO₂ (300 ppm) greatly decreased the activity of the photo-SCR at 373 K. The increment of the reaction temperature enhanced the resistance to SO₂ gas, and at 553 K the conversion of NO was stable for at least 300 min of the reaction. X-ray diffraction, FTIR spectroscopy, thermogravimetry and differential thermal analysis, x-ray photoelectron spectroscopy (XPS), elemental analysis and N₂ adsorption measurement revealed that the ammonium sulfate species were generated after the reaction. There was a strong negative correlation between the deposition amount of the ammonium sulfate species and the specific surface area. Based on the above relationship, we concluded that the deposition of the ammonium sulfate species decreased the specific surface area by plugging the pore structure of the catalyst, and the decrease of the specific surface area resulted in the deactivation of the catalyst.     

Detection of relative and uniform motion

We measured the lowest velocity (velocity threshold) for discriminating motion direction in relative and uniform motion stimuli, varying the contrast and the spatial frequency of the stimulus gratings. The results showed significant differences in the effects of contrast and spatial frequency on the threshold, as well as on the absolute threshold level between the two motion conditions, except when the contrast was 1% or lower. Little effect of spatial frequency was found for uniform motion, whereas a bandpass property with a peak at approximately 5 cycles per degree was found for relative motion. It was also found that contrast had little effect on uniform motion, whereas the threshold decreased with increases in contrast up to 85% for relative motion. These differences cannot be attributed to possible differences in eye movements between the relative and the uniform motion conditions, because the spatial-frequency characteristics differed in the two conditions even when the presentation duration was short enough to prevent eye movements. The differences also cannot be attributed to detecting positional changes, because the velocity threshold was not determined by the total distance of the stimulus movements. These results suggest that there are two different motion pathways: one that specializes in relative motion and one that specializes in uniform or global motion. A simulation showed that the difference in the response functions of the two possible pathways accounts for the differences in the spatial-frequency and contrast dependency of the velocity threshold.     

Relationship between Ba atom emission and electrode temperature in a low-pressure fluorescent lamp

A relationship between emission characteristics of Ba atom as an emitter material and temperature distributions of an electrode in a fluorescent lamp is described, which is measured by using laser-induced fluorescence and black-body radiation method, respectively. In a virgin lamp, a hot spot observed at the electrode edge connected to the power supply is the main source of Ba atom emission. In a long-term-used lamp, it is shown that Ba atom emission, thermionic electron emission in cathode half-cycle and electron collection in anode half-cycle are most active on the hot spot appearing on the center of the electrode.     

Comparison of the relative stability of pharmaceutical cocrystals consisting of paracetamol and dicarboxylic acids

Objective: The aim of this study is to evaluate the relative stability of pharmaceutical cocrystals consisting of paracetamol (APAP) and oxalic acid (OXA) or maleic acid (MLA).

Significance: These observations of cocrystal stability under various conditions are useful coformer criteria when cocrystals are selected as the active pharmaceutical ingredient in drug development.

Method: The relative stability was determined from the preferentially formed cocrystals under various conditions.

Result: Cocrystal of APAP–OXA was more stable than that of APAP–MLA in a ternary cogrinding system and possessed thermodynamical stability. On the other hand, when grinding with moisture or maintaining at high temperatures and relative humidity conditions, APAP–MLA was more stable, and OXA converted to OXA dihydrate. In the slurry method, APAP–OXA was more stable in aprotic solvents because the APAP–OXA with low-solubility product precipitated.

Conclusions: The relative stability order was affected by preparing conditions of presence of moisture. This order might attribute to the small difference of crystal structure in the extension of the hydrogen bond network.     

Growth of emerald crystals from PbO · V2O5 flux

The flux growth of emerald crystals by slow cooling in the PbO · V₂O₅ flux is reported. The crystals exhibited the typical emerald-green colour, were up to 1.8 mm in size and transparent. Their form was a regular hexagonal rod bounded by the well-developed {0001} and {10ˉ10} faces. The solubility of emerald in PbO · V₂O₅ was also investigated; about 9.0 g emerald was dissolved in 100 g PbO · V₂O₅ at 1200 °C. The solubility decreased gradually with decreasing temperature. Taking the solubility data into account, the presence of undissolved particles in the solution was found to be a necessary condition for the growth of large emerald crystals. Unsaturated solution at a soak temperature produced good and relatively small emerald crystals in a subsequent cooling experiment. Advantages of the PbO · V₂O₅ flux are also mentioned. Emerald crystals showing various kinds of imperfections, and even good crystals, were also present.