Systematic study on synthesis and structural, electrical transport and magnetic properties of Pb-substituted Bi-Ca-Co-O misfit-layer cobaltites

Single-phases of Pb-substituted Bi-Ca-Co-O misfit-layer cobaltites with various Pb concentrations have been synthesized and the Pb-substitution effects on the structural, electrical and magnetic properties have been systematically investigated. Powder X-ray diffraction analysis showed that the single-phases of Bi_1.8−x/2Pb_xCa₂Co₂O_z were obtained up to x=0.6-0.7 under the optimized synthesis conditions. The lattice parameters of Bi_1.8−x/2Pb_xCa₂Co₂O_z continuously changed with increasing Pb concentration. The electron diffraction analysis suggested that the structure consisted of two different sublattices with a rock salt structure (RS) and a hexagonal CdI₂ structure (H), respectively, without modulation. In combined with the chemical composition analysis, the chemical formulas of the x=0 and x=0.6 samples were determined approximately as [Bi_1.74Co_0.31Ca_2.01O₄]^RS[CoO₂]_1.69 and [Bi_1.47Pb_0.38Co_0.29Ca_1.98O₄]^RS[CoO₂]_1.71, respectively. The electrical resistivity became more metallic with increasing the Pb concentration up to x=0.6. Moreover, the Pb-substitution simultaneously increased the antiferromagnetic Weiss temperatures and decreased the effective magnetic moments of the Co ions.     

Uptake of transition metal ions using liposomes containing dicetylphosphate as a ligand.

The uptake of Cu2+ was investigated using various types of liposomes composed of phosphatidylcholine (PC), cholesterol (Chol) and dicethylphosphate (DCP). DCP played a role as a ligand for Cu2+. Multilamellar vesicles (MLVs) were more effective for the uptake of Cu2+ compared to unilamellar vesicles prepared by the extrusion technique. The uptake efficiency of MLVs for Cu2+ was dependent on the molar ratio of DCP in MLVs. The uptake percent of Cu2+ was 92% using MLVs having a PC:DCP:Chol molar ratio of 4:3:3; 95% of the total vesicle Cu2+ was bound to DCP of the outer membrane surface of the MLVs, and the remaining 5% of the total Cu2+ was distributed into the interior side of the MLVs. MLVs having a PC:DCP:Chol molar ratio of 4:3:3 were also effective as separation media for Mn2+, Co2+, Ni2+ and Zn2+. The uptake efficiency of the MLVs for the transition-metal ions increased in the order Co2+ < Zn2+ < Ni2+ < Mn2+ < Cu2+.     

Error bounds for asymptotic expansions of the distribution of the MLE in a GMANOVA model

Summary In this paper we obtain asymptotic expansions for the distribution function and the density function of a linear combination of the MLE in a GMANOVA model, and for the density function of the MLE itself. We also obtain certain error bounds for the asymptotic expansions.     

Degradation of aliphatic-aromatic copolyesters by bacteria that can degrade aliphatic polyesters

The degradation activities of bacteria that can degrade aliphatic polyesters on various aliphatic-aromatic copolyesters (PBSTIL, PBST, and Ecoflex™) were investigated. Among the bacteria examined, strain TB-71 showed the best degradation activity. An HPLC analysis of the degradation products revealed that PBST55 and Ecoflex™ are degraded into monomers by strain TB-71. In the case of PBSTIL, an unknown peak was detected by the HPLC analysis and was considered to be derived from water-soluble oligomers containing isophthalic acid segments. This finding seemed to be attributed to the chemical structure of the aromatic segments of the copolymers.     

Possible time-variability of the fine-structure constant expected from the accelerating universe

We present a theoretical calculation on the time-variability of the fine-structure constant to fit the result of the recent precise analysis of the measurement of the QSO absorption lines. We find the parameters of the scalar-tensor theory to be determined much more accurately than fitting the accelerating universe itself, but leading not to easy detections of the effect on the equation of state of the dark energy in the earlier epochs.     

Polarized Raman spectroscopic study of relaxed high density amorphous ices under pressure

We have made high density amorphous ice (HDA) by the pressure-induced amorphization of hexagonal ice at 77 K and measured the volume change on isobaric heating in a pressure range between 0.1 and 1.5 GPa. The volume of HDA on heating below ～0.35?GPa increases, while the volume of HDA on heating above ～0.35?GPa decreases. The polarized OH-stretching Raman spectra of the relaxed HDAs are compared with that of the unannealed HDA. The relaxed HDAs are prepared at 0.2 GPa at 130 K and 1.5 GPa at 160 K. It is found that the relatively strong totally symmetric OH-stretching vibration mode around 3100?cm(-1) exists in the depolarized reduced Raman spectrum χ(VH)(") of the unannealed HDA and that its intensity rapidly decreases by relaxation. The χ(VH)(") profiles of the relaxed HDA are similar to those of liquid water. These results indicate that the HDA reaches a nearly equilibrium state by annealing and the intrinsic state of HDA relates to a liquid state. The pressure-volume curve of the relaxed HDA at 140 K seems to be smooth in the pressure range below 1.5 GPa.     

Remark on the Helmholtz decomposition in domains with noncompact boundary

Let \(\varOmega \) be a domain in \(\mathbb {R}^{d+1}\) whose boundary is given as a uniform Lipschitz graph \(x_{d+1}=\eta (x)\) for \(x \in \mathbb {R}^d\) . For such a domain, it is known that the Helmholtz decomposition is not always valid in \(L^p(\varOmega )\) except for the energy space \(L^2 (\varOmega )\) . In this paper we show that the Helmholtz decomposition still holds in certain anisotropic spaces which include vector fields decaying slowly in the \(x_{d+1}\) variable. In particular, these classes include some infinite energy vector fields. For the purpose, we develop a new approach based on a factorization of divergence form elliptic operators whose coefficients are independent of one variable.     

Oblique-Incidence Characteristics of a Parallel-Aligned Nematic-Liquid-Crystal Spatial Light Modulator

We have developed optically-addressed and electrically-addressed liquid crystal spatial phase-only light modulators having no pixelized structures. We obtained a large depth of phase-only modulation and high diffraction efficiency based on the electro-optical characteristics of a parallel-aligned nematic liquid crystal. These spatial light modulators (SLM) are of the reflection type, so there would be a loss of power in the readout light from the half mirror, which was set up so as to separate the incident and reflected lights. To optimize the characteristics of a reflection type spatial phase-only light modulator, we have proposed an oblique incident optical readout setup. We have examined the effect of conditions such as the polarization direction and the incidence angle of the readout light, and the orientation of liquid crystal molecules in the SLM. High diffraction efficiency close to the theoretical maximum value was obtained by adjusting the above conditions. The simulation analysis can well explain the experimental results of phase modulation.     

Proton-coupled electron-transfer processes in photosystem II probed by highly resolved g-anisotropy of redox-active tyrosine YZ

The oxidation of a redox-active tyrosine residue Y(Z) in photosystem II (PSII) is coupled with proton transfer to a hydrogen-bonded D1-His190 residue. Because of the apparent proximity of Y(Z) to the water-oxidizing complex and its redox activity, it is believed that Y(Z) plays a significant role in water oxidation in PSII. We investigated the g-anisotropy of the tyrosine radical Y(Z)(?) to provide insight into the mechanism of Y(Z)(?) proton-coupled electron transfer in Mn-depleted PSII. The anisotropy was highly resolved by electron paramagnetic resonance spectroscopy at the W-band (94.9 GHz) using PSII single crystals. The g(X)-component along the phenolic C-O bond of Y(Z)(?) was calculated by density functional theory (DFT). It was concluded from the highly resolved g-anisotropy that Y(Z) loses a phenol proton to D1-His190 upon tyrosine oxidation, and D1-His190 redonates the same proton back to Y(Z)(?) upon reduction.