Sound velocity in alumino-silicate liquids determined up to 2550 K from Brillouin spectroscopy: glass transition and crossover temperatures

Hypersonic longitudinal sound velocities in five silicate and alumino-silicate liquids have been measured between 293 and 2550 K by Brillouin spectroscopy. Together with previous observations for four other glasses and liquids of the system SiO₂-Al₂O₃-CaO-MgO, these results are used to discuss changes in hypersonic velocities in three adjacent temperature domains, i.e., below, in, and above the glass transformation range. The temperature dependence of Brillouin velocities is consistent with the observed variations with temperature of viscosity, density, and mean heat capacity for the same three temperature domains. These variations of physical properties of alumino-silicate liquids are qualitatively in agreement with the Inherent Structure Theory for liquids.     

A new general-purpose isothermal microcalorimeter for use at temperatures up to 200 °C

The design and some properties of a new general-purpose isothermal microcalorimeter are reported. The instrument is a twin thermopile heat conduction calorimeter, which is designed for use up to 200 °C. The calorimetric units and surrounding heat sink are suspended inside a hollow aluminium construction, which is thermostated. Above that unit a second thermostated block is positioned and the whole assembly is suspended inside a Dewar vessel. When the instrument is used at room temperature and below, the thermostated units are cooled by use of an insertion Peltier effect cooler. The instrument can be used with a wide range of different reaction vessels (diameter 14 mm). Baseline experiments have been conducted in the temperature range 15-200 °C. Typical values obtained during 10 h periods at 200 °C are ±3 and ±10 nW for the baseline drift and baseline fluctuations, respectively. The heat detection limit, determined by release of electrical energy, is about 2 μJ. Preliminary stability measurements have been conducted at 100 °C on samples of stabilised and non-stabilised polyamide film.     

Glycosidases of turnip leaf tissues

Four myrosinase (β-thioglucosidase EC. 3.2.3.1) and seven disaccharase (β-fructofuranosidase, EC. 3.2.1.26) isoenzymes were isolated from turnip leaves. The most active enzymes were isolated in pure form. Myrosinase and disaccharase mol wt was 62.0 × 10³ and 69.5 × 10³ dalton, respectively, on the basis of gel filtration on Sephadex G-200. Myrosinase pH profile showed high activity between pH 5 and 7 with the optimum at pH 5.5. The purified enzyme was heat-stable for 60 min at 30°C with only loss of 24% of activity. Its activity is strongly inhibited (100%) by Pb²⁺, Ba²⁺, Cu²⁺ and Ca²⁺ ions, and activated (70%) by EDTA at 0.04M. The pure enzyme failed to hydrolyze amylose, glycogen, lactose, maltose, and sucrose. TheK _m andV _max values of myrosinase using sinigrin as specific substrate was 0.045 mM and 2.5 U, respectively. The maximal activity of disaccharase enzyme was obtained at pH 4–5 and 35–37°C. The enzyme was heat-stable at 30°C for 30 min with only 10% loss of its activity. Its activity is strongly activated (70–240%) by Ca²⁺, Ba²⁺, Cu²⁺, and EDTA at 0.01M. The enzyme activity is specific to the disaccharide sucrose and failed to hydrolyze other disaccharides (maltose and lactose). TheK _m andV _max of disaccharase were 0.123 mM and 3.33 U, respectively.     

A critical reappraisal of recent communications on the hydrodynamic characterization of silica (aerosil) hydrosols

Different results from recent communications on the hydrodynamic characterization of ultrasonicated silica (®Aerosil) hydrosols led to a critical reappraisal of the data.It can be concluded that the degree of dispersion achievable in pyrogenic (Aerosil) hydrosols by ultrasonication is highly sensitive to the detailed parameters of the dispersion process. Characterization in terms ofabsolute numbers of a limiting particle morphology, corresponding to minima of aggregate size, porosity and number of primary particles in the aggregate is not possible.The most straightforward approach for hydrodynamic characterization seems to be a combination of sedimentation and diffusion data.Other approaches using a combination of sedimentation and viscosity data underestimate the particle dimensions. Moreover, they are quite arbitrary since the final result depends upon the proper choice between several equations for fitting the viscosity concentration dependence; the most rigorous approach seems to be an extended Einstein equation which has recently been adapted to particle aggregates.     

Estimation of N-ethyl O-isopropyl Thionocarbamate (Dow: 2-200) in Mine Wastes by GLC

Abstract

Dow 2200 is a selective ore flotation agent, consisting mainly of Nethyl, 0-isopropyl thionocarbamate (IF'ETC). This paper describes a GLC method for the estimation of IPETC, and compares it with the conventional U.V. spectrophotometric procedure.

An aliquot of a cyclohexane extract of IPETC (prepared for spectrophotometric analysis) is chromatographed on a column of SE-30 or OV-17/QF-1 at 125°C and the IPETC peak is estimated in a ³H electron capture detector (ECD). The ECD is superior in sensitivity and linearity of response to the flame photometric detector operated in the S-mode. The ECD-GLC procedure is comparable in sensitivity to the conventional U.V. absorbance method, and offers an independent and complementary procedure useful for confirmation of low levels of IPETC.     

An efficient synthesis of pyrazole chalcones under solvent free conditions at room temperature

An easy,safe,solvent free and effective method for the synthesis of pyrazole-substituted chalcones has been achieved by grinding pyrazole aldehydes and acetophenones in the presence of activated barium hydroxide(C-200) in high yield within short span of time.All reactions were carried out just by grinding the two reactants in the presence of activated barium hydroxide(C-200). Results are also compared with sodium hydroxide and potassium hydroxide.     

Thermal quenching of thermoluminescence in TLD-200, TLD-300 and TLD-400 after β-irradiation

The dosimetric characteristics of many TL materials are influenced by changes in location, size and shape of the glow curves due to changes in the heating rate. In this study, the effect of heating rate on the integrated peak areas of CaF₂:Dy (TLD-200), CaF₂:Tm (TLD-300) and CaF₂:Mn (TLD-400) crystals have been investigated after β-irradiation. It was observed that the peak temperatures of all peaks shifted to the high temperature sides and the integrated peak areas decrease as the heating rate increases due to thermal quenching, whose efficiency increases as temperature increases.     

Fine structure of the isoscalar giant quadrupole resonance in Ca due to Landau damping?

The fragmentation of the Isoscalar Giant Quadrupole Resonance (ISGQR) in ⁴⁰Ca has been investigated in high energy-resolution experiments using proton inelastic scattering at Ep=200 MeV$E_{\mathrm{p}}=\mathrm{<font\; color="red">200</font>}\text{MeV}$. Fine structure is observed in the region of the ISGQR and its characteristic energy scales are extracted from the experimental data by means of a wavelet analysis. The experimental scales are well described by Random Phase Approximation (RPA) and second-RPA calculations with an effective interaction derived from a realistic nucleon–nucleon interaction by the Unitary Correlation Operator Method (UCOM). In these results characteristic scales are already present at the mean-field level pointing to their origination in Landau damping, in contrast to the findings in heavier nuclei and also to SRPA calculations for ⁴⁰Ca based on phenomenological effective interactions, where fine structure is explained by the coupling to two-particle–two-hole (2p–2h) states.     

The photochemical metal organic deposition of manganese oxide films from films of manganese(II) 2-ethylhexanoate: a mechanistic study

The photochemistry of thin films of manganese(II) 2-ethylhexanoate to produce manganese oxide films is presented. Thin films of manganese(II) 2-ethylhexanoate can be cast onto silicon wafers by spin coating. The FTIR spectroscopy of these films suggests they exist as chains or clusters with the manganese(II) centers linked by bridging 2-ethylhexanoate ligands. The initial photochemical reaction results in the loss of the bridging 2-ethylhexanoate ligands and the formation of monomeric manganese(II) 2-ethylhexanoate. In this process approximately 60% of the bridging 2-ethylhexanoate ligand is converted to chelating 2-ethylhexanoate while the other 40% fragments to form CO₂, heptane and heptene. Further photolysis resulted in the conversion of the remaining 2-ethylhexanoate ligand to form CO₂, heptane and heptene. The film consisted of manganese(II) oxide although the surface of the film was more oxidized and had carbon impurity on it. Annealing the film resulted in the conversion to polycrystalline α-Mn₂O₃.     

Defect levels in the band gap of amorphous selenium

Energy locations in the band gap have been determined for the thermally accessible levels of the negative-U defect centers in amorphous selenium. Both the temperature dependence of the steady-state photocurrents, and an analysis of emission currents in the post-transit regime of a time-of-flight transient photoconductivity experiment on the same samples, agree on the presence of defect levels at (0.42 ± 0.04) eV above the valence band mobility edge and (0.53 ± 0.06) eV below the conduction band. Both measured current levels and the resolved energy positions of the defects are subject to the Poole-Frenkel effect.