Analysis of red phosphorus in resins using pyrolysis-gas chromatography/mass spectrometry.

Although red phosphorus is used as a flame retardant for polymer materials, no analysis methods for it in resins has been established. Analysis methods for red phosphorus in resins were investigated using pyrolysis-gas chromatograpy/mass spectrometry (Py-GC/MS) by paying attention to the fact that it has a sublimation property. We found that the mass spectrum of red phosphorus shows a series of ions at m/z=62, 93 and 124, and a fragment pattern indicating that red phosphorus (P4=124, P=31) was pyrolytically decomposed. The coefficient of the correlation between the content of red phosphorus in the resin and the peak intensity in Py-GC/MS was 0.9781. The relative standard deviations of this analysis method was 6.29% (n=5). Py-GC/MS was applicable not only to qualitative analysis but also to the quantitative analysis of red phosphorus.     

A novel anthracene-based fluorescent colorimetric sensor for the simple naked-eye diagnosis of methylmalonic aciduria

A novel molecular sensor using anthracene bearing two amidopyridines emits blue fluorescence in the presence of succinic acid and green fluorescence in the presence of malonic acid, and its fluorescence intensity increased upon binding. Using this molecular sensor, we succeeded in detecting the difference of one carbon atom between succinic acid and malonic acid with the naked-eye. Furthermore, when methylmalonic acid was dissolved in urine to provide a model system for methylmalonic aciduria, the fluorescence changed from blue to green, and methylmalonic acid was successfully detected with the naked-eye.     

Water-soluble supramolecular porphyrin dimer: self-organization of mono(imidazolyl)-substituted Zn porphyrin to a special-pair type dimer in water

Tris(4-carboxylphenyl)-mono(N-methylimidazolyl)-substituted Zn porphyrin was synthesized as a precursor for a water-soluble supramolecular porphyrin dimer. The dimer formation was performed in a NaHCO₃ aq solution (pH 8.4) and phosphate buffer solutions (pH 7.4-9.0). The split Soret bands of Zn porphyrin observed in the absorption spectra clearly showed self-organization to a special-pair type slipped cofacial dimer via metal coordination of imidazole even in water.     

Determination of Ubiquinone in Blood by High-Performance Liquid Chromatography with Post-Column Fluorescence Derivatization Using 2-Cyanoacetamide

It was shown that ubiquinone (CoQ₁₀) and ubiquinol (CoQ₁₀H₂) produce fluorescence products under alkaline conditions when reacted with 2-cyanoacetamide. The reaction mixture from CoQ₁₀ gave fluorescence with excitation and emission maximum wavelengths at 442 nm and 549 nm, respectively. This reaction was considered to proceed via Craven’s reaction. Moreover, 2-cyanoacetamide was shown to be a useful reagent for high-performance liquid chromatography (HPLC) with post-column fluorescence derivatization of CoQ₁₀ and CoQ₁₀H₂ in blood. CoQ₁₀ showed a linear response in the range of 0.32–1276 ng, and the detection limit (S/N = 3) was 0.16 ng. Moreover, the sample pretreatment by deproteinization and extraction of CoQ₁₀ and CoQ₁₀H₂ from plasma using 1-propanol with potassium formate was effective for excellent separation of CoQ₁₀ and CoQ₁₀H₂ from other fluorescent substances in the blood. This simple and rapid pretreatment was considered to minimize the oxidation of CoQ₁₀H₂. On the other hand, CoQ₁₀ and CoQ₁₀H₂ in plasma samples obtained by finger prick were detected, as in venous blood obtained by venipuncture. Our method involving the simple and rapid collection of plasma by finger prick and sample pretreatment is thought to be applicable for the determination of CoQ₁₀H₂/total CoQ₁₀ ratio as a biomarker of oxidative stress.     

Influence of ordering change on the optical and thermal properties of inflation polyethylene films

Changes of thermal diffusivity inside femtosecond laser-structured volumes as small as few percent were reliably determined (with standard deviation less than 1%) with miniaturized sensors. An increase of thermal diffusivity of a crystalline high-density polyethylene (HDPE) inflation films by 10-20% from the measured (1.16 ± 0.01) × 10⁻⁷ m² s⁻¹ value in regions not structured by femtosecond laser pulses is considerably larger than that of non-crystalline polymers, 0-3%. The origin of the change of thermal diffusivity are interplay between the laser induced disordering, voids’ formation, compaction, and changes in molecular orientation. It is shown that laser structuring can be used to modify thermal and optical properties. The birefringence and infrared spectroscopy with thermal imaging of CH₂ vibrations are confirming inter-relation between structural, optical, and thermal properties of the laser-structured crystalline HDPE inflation films. Birefringence modulation as high as Δn ∼ ± 1 × 10⁻³ is achieved with grating structures.     

Two-band BCS mechanism of superconductivity in a Ba(Fe0.9Co0.1)2As2 high-temperature superconductor

Terahertz and infrared spectra of the conductivity, σ(ν), and dielectric constant, ?(ν), of a Ba(Fe_0.9Co_0.1)₂As₂ film (T _c = 20 K) have been analyzed together with previous specific-heat and angular resolved photoelectron spectroscopy data. It has been shown that the spectra σ(ν) and ?(ν) of Ba(Fe_0.9Co_0.1)₂As₂ in the superconducting phase at T = 5 K, as well as the magnetic field penetration depth, can be described well using the standard Bardeen-Cooper-Schrieffer (BCS) model with an additive contribution of electron and hole bands. It has been found that the measured temperature dependence of the magnetic field penetration depth in a wide temperature range 5 K < T < T _c can be described only with the introduction of interband pairing interaction. The coupling constant of electron and hole bands, λ_{1, 2} = 0.1, as well as the temperature dependences of superconducting gaps in the electron and hole subsystems, has been determined using the model of two-band superconductivity developed earlier for MgB₂.     

Beam profile measurement with CR-39 track detector for low-energy ions

A CR-39 track detector was successfully used to measure the outline of thin low-energy ion beams. After the etching, the surface of the detector was examined with an observation system composed of a Normarski microscope, a CCD camera and a digital image processing computer. Beam images obtained with the system were in good agreement on the outline of the beam formed with a beam aperture. Also, the resolving power in the beam outline measurement was roughly explained from the consideration of the ion range and the etch-pit growth in the chemical etching for the CR-39 detector.     

Mössbauer study on a two-dimensional triangular antiferromagnet YFeMnO4

Magnetic ordering of YFeMnO₄ has been studied with Mössbauer spectroscopy in the temperature range between 4.2 K and 300 K on the conditions of gamma rays parallel to and perpendicular to thec-axis. It is revealed that the spin system orders like a Heisenberg spin system in a triangular antiferromagnet with an anisotropic axis parallel to thec-axis.     

Optically induced mechanical interaction between semiconductor quantum dots under an electronic resonance condition

Assuming an electronic resonance condition, we study the shape-dependence of the radiation force (RF) on a semiconductor quantum dot (QD) floating in medium and the optically induced mechanical interaction (OIMI) between two QDs with Maxwell stress tensor (MST) method, where the response fields are calculated by the improved discrete dipole approximation (DDA). Main results are as follows: (1) Properties of the RF on an isolated QD drastically change due to its shape and polarization of an incident light, which can be used for shape-selective manipulation. (2) Anomalous OIMI between two QDs arises depending on the spatial structures of internal fields, which results from the interaction between polarizations in respective QDs when they are near each other.     

Enhancement of sonochemical reaction of terephthalate ion by superposition of ultrasonic fields of various frequencies

The ultrasonic reactor with dual frequency was used and the effect of frequency on the fluorescence intensity of terephthalate ion was experimentally investigated in the frequency range from 176 to 635 kHz. The sonochemical reaction fields were visualized by using sonochemical luminescence of luminol solution. Compared with the fluorescence intensity of terephthalate ion for single frequency, the fluorescence intensity for dual frequency increased. The fluorescence intensity ratio of dual frequency to single frequency had maximum value when the frequency of transducer attached at the bottom wall was comparable in magnitude to that at the side wall. In the case of dual frequency, the sonochemical reaction fields became more extensive in the reactor and more intensive around the center of the reactor.