Quantitative visualization of temperature field in non-luminous flame by flame reaction technique

Abstract  

An experimental technique for measuring a temperature field in an axisymmetric non-luminous flame is developed using the flame reaction technique combined with the inverse Abel transformation. Flame visualization is carried out using alkali metal solution of Potassium (K), which is supplied to a premixed methane/air flame in a form of spray mist. The basic principle of this technique is based on the measurement of local emission intensity distribution visualized by the flame reaction, which is a function of temperature according to the Maxwell–Boltzmann statistics of thermodynamics. The relationship between the local intensity and the temperature is obtained from the calibration study, in which the local intensity is evaluated from the line of sight intensity by the inverse Abel transformation, and the temperature is measured by thermocouple. This technique is successfully applied to the measurement of local temperature distribution in steady and flickering premixed methane/air flame. The temperature field in the flickering flame indicates that the local temperature oscillates periodically with the flickering frequency, and the highest temperature is found along the flame front and in the merging region.     

Photoelectric pulse interval distribution of gaussian-lorentzian light

The time interval distribution of two successive photoelectric pulses depends not only upon the spectral linewidth but also on the correlation factor. The distribution is derived in the case of gaussian-lorentzian light under the condition of a markovian process and is also applied to the analysis of the counting loss of a circuit with dead time, from which information on the spectral linewidth is obtained. The theoretical counting loss is compared with the experimental one.     

O-selectivity and utility of phosphorylation mediated by phosphite triester intermediates in the N-unprotected phosphoramidite method

Previously, O-selective phosphorylation on polymer supports in the N-unprotected phosphoramidite method could not be carried out because the amino groups of dA and dC have high reactivity toward tervalent phosphorus(III)-type phosphitylating reagents. In this paper, we developed a new coupling strategy named the "activated phosphite method" in which the phosphitylation is mediated by phosphite triester intermediates 1. Application of 1-hydroxybenzotriazole as the promoter to the solid-phase synthesis resulted in excellent O-selectivity of more than 99.7%. This O-selectivity was explained by the frontier molecular orbital interactions between the reactive intermediates and the nucleophiles such as the amino or hydroxyl groups of nucleosides. Furthermore, longer oligonucleotides were synthesized not only by a manual operation but also by a DNA synthesizer. The utility of our new method was demonstrated by the successful synthesis of a base-labile modified oligodeoxyribonucleotide having 4-N-acetyldeoxycytidine residues. Finally, DNA 20-mers containing dA or dC could be synthesized in good yields by use of a combined reagent of 6-trifluoromethyl-1-hydroxybenzotriazole and benzimidazolium triflate.     

Reduction of propagation and bending losses of heterostructured photonic crystal waveguides by use of a high-delta structure

We describe the fabrication and evaluation of a low-loss, high-delta optical waveguide consisting of heterostructured photonic crystals. The waveguide is composed of a multilayer stack of Ta2O5/SiO2 and is prepared by use of the autocloning technique. Light is guided in the waveguide by the difference in the effective refractive indices of the constituent photonic crystals. By improving the design of the core region so that is has a flat multilayer structure, we achieve delta = 3.09% for the in-plane direction and net propagation loss of 0.56 dB/mm at lambda = 1.6 microm. Experiments also suggest that the bending loss of the waveguide can be reduced to less than 0.1 dB if the curvature radius is larger than 700 microm.     

Reduction of ion thermal diffusivity associated with the transition of the radial electric field in neutral-beam-heated plasmas in the large helical device

Recent large helical device experiments revealed that the transition from ion root to electron root occurred for the first time in neutral-beam-heated discharges, where no nonthermal electrons exist. The measured values of the radial electric field were found to be in qualitative agreement with those estimated by neoclassical theory. A clear reduction of ion thermal diffusivity was observed after the mode transition from ion root to electron root as predicted by neoclassical theory when the neoclassical ion loss is more dominant than the anomalous ion loss.     

Observation of the "self-healing" of an error field island in the large helical device

It was observed that the vacuum magnetic island produced by an external error magnetic field in the large helical device shrank in the presence of plasma. This was evidenced by the disappearance of flat regions in the electron temperature profile obtained by Thomson scattering. This island behavior depended on the magnetic configuration in which the plasmas were produced.     

Barrier-wave-internal-wave interference and airy minima in 16O16+O elastic scattering

Taking 16O+16O elastic scattering at 124 MeV as an example, we show that a barrier-wave-internal-wave decomposition of the elastic scattering amplitude provides valuable information on the light heavy-ion interaction and complements the more conventional nearside-farside decomposition. In particular, we show that the Airy minima present in the angular distributions are due to a barrier-wave-internal-wave interference mechanism, which sheds additional light on the exceptional transparency displayed by some light heavy-ion scattering systems. Extension of these ideas to other fields, like atomic and molecular collision physics, could prove rewarding.     

Potent 2,2-diphenyl-1-picrylhydrazyl radical-scavenging activity of novel antioxidants, double-stranded tyrosine residues conjugating pyrocatechol

New potent antioxidants conjugating the catechol (=pyrocatechol; pyrCat) group to two N-termini of modified double-stranded tyrosine residues were synthesized and showed radical scavenging activity with 2,2-diphenyl-1-picrylhydrazyl radical (DPPH radical, DPPH˙) as a free radical model, second-order rate constants for the DPPH˙ scavenging reaction, and the results from electron spin resonance (ESR) studies. It was found that the tyrosine (Tyr) residue and pyrCat containing new antioxidants developed in the study have about 3-20 times more potent antioxidative activity than Trolox, pyrCat, and L-ascorbic acid (VC). In order to elucidate the relationship between antioxidant activity and the molecular orbital states, and to design potent antioxidants we present an interesting approach using an absolute hardness (η)-absolute electronegativity (χ) diagram based on chemical hardness. It was shown that quantum chemicals were required to develop potent antioxidants.