In-situ X-ray diffraction study on β-CrOOH at high pressure and high-temperature

ABSTRACT

High pressure hydrous phases with distorted rutile-type structure have attracted much interest as potential water reservoirs in the Earth’s mantle. An in-situ X-ray diffraction study of β-CrOOH was performed at high pressures of up to 6.2?GPa and high-temperatures of up to 700?K in order to clarify the temperature effect on compression behaviors of β-CrOOH. The P-V-T data fitted to a Birch–Murnaghan equation of state yielded the following results: isothermal bulk modulus K_T0?=?191(4)?GPa, temperature derivative (?K_T/?T)_P?=??0.04(2)?GPa?K^?1, and volumetric thermal expansion coefficient α?=?3.3(2)?×?10^?5?K^?1. In this study, at 300?K, the a-axis became less compressible at pressures above 1–2?GPa. We found that the pressure where the slopes of a/b and a/c ratios turned positive increased with temperature. This is the first experimental study indicating the temperature dependence of the change in the axial compressibility in distorted rutile-type M³⁺OOH.     

Synthesis of Al–Cr decagonal quasicrystal nanoparticles and their temperature of phase transformation to stable crystal phase

The synthesis of Al–Cr single quasicrystal (QC) nanoparticles of the decagonal phase was achieved by introducing an advanced gas flow evaporation method. By obtaining successive electron diffraction patterns for single-QC nanoparticles, the phase transformation temperature of a single-QC nanoparticle was determined to be 700 °C. It was also determined that part of the QC nanoparticle decomposed into hex-Al₈Cr₅ and Al during the phase transformation. Since the grain growth did not occur during the phase transformation in the present experiment, the inherent phase transformation temperature could be measured.     

Characterization of calcium carbonate polymorphs with Ca K edge X-ray absorption fine structure spectroscopy

Ca K edge X-ray absorption fine structure (XAFS) spectroscopy was utilized for the characterization and quantification of calcium carbonate polymorphs and their mixtures. The advantage of the XAFS is the small sample quantity required for measurements, and a flexible sample environment. The near-edge XAFS spectra of calcite, aragonite and vaterite were measured with the conversion electron yield (CEY) method, and the obtained spectra showed characteristic features that can be utilized as fingerprints. The quantification of mixed polymorphs was examined by using a linear combination fitting of reference XAFS spectra. Though the quality of the fits was satisfactory, discrepancies in the evaluated values were observed between those with X-ray diffraction (XRD) and XAFS. The nonuniformity of samples may be enhanced by the surface sensitivity of the CEY method.     

13C-Spingitter-Relaxationszeiten von verschiedenen Polymethacrylaten in Lösung

Ohne Zusammenfassung     

Einstein-de Haas effect in dipolar Bose-Einstein condensates

The general properties of the order parameter for a dipolar spinor Bose-Einstein condensate are discussed based on symmetries of interactions. An initially spin-polarized dipolar condensate is shown to dynamically generate a nonsingular vortex via spin-orbit interactions--a phenomenon reminiscent of the Einstein-de Haas effect in ferromagnets.     

FePt L10 ordering and grain growth using millisecond pulse laser processing

The structural and magnetic properties of ∼12 nm thick FePt thin films grown on Si substrates annealed using a 1064 nm wavelength laser with a 10 ms pulse have been examined. The A1 to L1₀ ordering phase transformation was confirmed by electron and X-ray diffraction. An order parameter near 50% and a maximum coercivity of 12 kOe were obtained with laser energy densities of 25-32 J/cm². Grain growth, quantified by dark field transmission electron microscopy, occurred during chemical ordering at the laser pulse widths studied.     

Wilsonian RG Analysis of the P-wave Nucleon–Nucleon Scattering Including Pions

We perform a Wilsonian renormalization group analysis for the nucleon–nucleon scattering in the P waves in the nuclear effective field theory including pions, in a similar way to the one done for the S-waves in our previous paper. We emphasize that the one-pion exchange interaction with large momentum transfer is of the same order as the leading contact interaction, so that there is no mismatch of the power counting. It is explicitly shown by obtaining consistent sets of renormalization group equations, that the cutoff dependence generated by the loop diagrams containing pion exchanges can be compensated by the cutoff dependence of the coupling constants of the contact interactions.     

Pions in Nuclear Effective Field Theory: How They Behave Differently at Different Scales and How They Decouple at Very Low Energies

We explain how the Wilsonian renormalization group (RG) can determine the power counting of the nuclear effective field theory (NEFT) including pions. We emphasize that the separation of pion exchange into the short-distance part and the long-distance part is essential since they behave differently in the RG analysis; we found that the latter is perturbative whereas the a part of the former is nonperturbative. As for the contact interactions power counting turns out to be the same as that for pionless NEFT: pion exchange does not affect the scaling property of contact operators. Our RG equations for NEFT including pions connect smoothly with those for the pionless NEFT: pions decouple at very low energies as we expect.     

Halichonic acid,a new rearranged bisabolene-type sesquiterpene from a marine sponge Halichondria sp.

A new compound, halichonic acid (1), was isolated from a marine sponge Halichondria sp., together with (6R,7S)-7-amino-7,8-dihydro-α-bisabolene (2). The structure of 1 was elucidated by spectroscopic analysis and ECD spectrum calculation to be a rearranged bisabolene-type sesquiterpene having a 3-azabicyclo[3.3.1]nonene moiety. Compound 2 was cytotoxic against HeLa cells with an IC₅₀ value of 50?μM, whereas 1 did not show cytotoxicity even at 50?μM. It is possible that 1 is biosynthesized from farnesyl pyrophosphate and glycine, with rearrangement.