Displacement substoichiometric separations in radioanalytical chemistry

The principle of displacement substoichiometry and the possibilities of its practical use have been outlined. The substoichiometric separation of lead, arsenic, and zinc can be carried out by applying diethyldithiocarbamate complexes and solvent extraction.     

NMR for equilateral triangular geometry under conditions of surface relaxivity—analytical and random walk solution

We consider analytical and numerical solution of NMR relaxation under the condition of surface relaxation in an equilateral triangular geometry. We present an analytical expression for the Green’s function in this geometry. We calculate the transverse magnetic relaxation without magnetic gradients present, single-phase, both analytically and numerically. There is a very good match between the analytical and numerical results. We also show that the magnetic signal from an equilateral triangular geometry is qualitatively different from the known solution: plate, cylinder, and sphere, in the case of a nonuniform initial magnetization. Nonuniform magnetization close to the sharp corners makes the magnetic signal very fast multiexponential. This type of initial configuration fits qualitatively with the experimental results by Song (Phys. Rev. Lett. 85, 3878 (2000)), Song et al. (Nature 406, 178 (2000)), Song (Mag. Reson. Imag. 19, 417 (2001)) and Lisitza and Song (Phys. Rev. B 65, 172406 (2002)). It should also be noted that the solution presented here can be used to describe absorption of a chemical substance in an equilateral triangular geometry (for a stationary fluid).     

On the viscosity of Fe<Subscript>79</Subscript>Cr<Subscript>21</Subscript> melt of congruent composition

The temperature and time dependences of the Fe₇₉Cr₂₁ melt viscosity have been investigated by the method of damping torsional vibrations of a crucible with one or two face surfaces. Anomalies in the viscosity polytherms at certain temperatures have been found for the first time. The display of these anomalies is determined by the melt structure and the melt-crucible interaction.     

CrO2 (1 0 0) and TiO2 (1 0 0) film heteroepitaxy on a BaF2 (1 1 1)/Si (1 0 0) substrate

Multi-domained heteroepitaxial rutile-phase TiO₂ (1 0 0)-oriented films were grown on Si (1 0 0) substrates by using a 30-nm-thick BaF₂ (1 1 1) buffer layer at the TiO₂–Si interface. The 50 nm TiO₂ films were grown by electron cyclotron resonance oxygen plasma-assisted electron beam evaporation of a titanium source, and the growth temperature was varied from 300 to 600 °C. At an optimal temperature of 500 °C, X-ray diffraction measurements show that rutile phase TiO₂ films are produced. Pole figure analysis indicates that the TiO₂ layer follows the symmetry of the BaF₂ surface mesh, and consists of six (1 0 0)-oriented domains separated by 30° in-plane rotations about the TiO₂ [1 0 0] axis. The in-plane alignment between the TiO₂ and BaF₂ films is oriented as [0 0 1] TiO₂ || BaF₂ or [0 0 1] TiO₂ || BaF₂ . Rocking curve and STM analyses suggest that the TiO₂ films are more finely grained than the BaF₂ film. STM imaging also reveals that the TiO₂ surface has morphological features consistent with the BaF₂ surface mesh symmetry. One of the optimally grown TiO₂ (1 0 0) films was used to template a CrO₂ (1 0 0) film which was grown via chemical vapor deposition. Point contact Andreev reflection measurements indicate that the CrO₂ film was approximately 70% spin polarized.     

Stacking faults and mechanisms strain-induced transformations of hcp metals (Ti,Mg) during mechanical activation in liquid hydrocarbons

The evolution of the structure and substructure of metals Ti and Mg with hexagonal close-packed (hcp) lattice is studied during their mechanical activation in a planetary ball mill in liquid hydrocarbons (toluene, n-heptane) and with additions of carbon materials (graphite, fullerite, nanotubes) by X-ray diffraction, scanning electron microscopy, and chemical analysis. The temperature behavior and hydrogen-accumulating properties of mechanocomposites are studied. During mechanical activation of Ti and Mg, liquid hydrocarbons decay, metastable nanocrystalline titanium carbohydride Ti(C,H) _x and magnesium hydride β-MgH₂ are formed, respectively. The Ti(C,H) _x and MgH₂ formation mechanisms during mechanical activation are deformation ones and are associated with stacking faults accumulation, and the formation of face-centered cubic (fcc) packing of atoms. Metastable Ti(C,H)x decays at a temperature of 550°C, the partial reverse transformation fcc → hcp occurs. The crystalline defect accumulation (nanograin boundaries, stacking faults), hydrocarbon destruction, and mechanocomposite formation leads to the enhancement of subsequent magnesium hydrogenation in the Sieverts reactor.

     

Inhibition of the oxygen evolution reaction during titanium passivation in aqueous phosphoric acid solution

Journal of Solid State Electrochemistry - The anodic oxide on titanium can be thickened by anodization, with the consequent corrosion properties of this oxide depending on many variables, including...     

The study of the electrochemical oxidation mechanism of diphenylamine derivatives in dipolar aprotic solvents: III. Effect of acids and bases of different strengths

The effect of addition of different acids and bases in a wide range of concentration on the voltammetric oxidation of both Variamine blue (VB) and 4-aminodiphenylamine (4-ADPA) was examined in acetonitrile (AcN). The oxidation potential values of either wave of both depolarizers were found to depend on the acid or base strength of the additive—relative to the depolarizer and solvent—and on their concentration in solution. Addition of strong acid as CH₃SO₃H resulted in a single oxidation wave at potentials either equal to or more positive than that of the original second wave. Relatively weak acids as picric and pyridinium ion only shifted the oxidation potential of the first wave to more positive values without affecting the general oxidation pattern.On the other hand, strong bases like ethanolamine, resulted in the formation of a preoxidation wave at more negative potential when present in low concentration and a single wave at identical negative potential at high enough concentrations. Bases of comparable strengths, as that of the depolarizer, like pyridine do not form prewaves but only shifted the final single oxidation wave to more negative potential values. Weaker bases like water and ethanol mainly shifted the oxidation potential of the second wave to less positive values.     

HPLC enantioseparation of amino acids and their protected derivatives used in peptide synthesis with pre-column chiral derivatization

Summary Indirect chiral separation methods based on enantiomeric derivatizations were developed in order to monitor optical purity of uncoded amino acids and a new series of amino acid derivatives. Marfey's reagent was used for derivatization of amino groups: whilst boxyl groups were derivatised with (1R, 2R)-or (1S, 2S)-2-amino-1(4-nitrophenyl)-1,3-propanediol reagents were used, respectively. The separations of diastereomeric derivatives formed via derivatization were optimized in RP-HPLC and NP-HPLC systems. Presented at Balaton Symposium on High Performance Separation Methods, Siófok, Hungary, September 1–3, 1999