Photocatalytic water splitting into H2 and O2 over various tantalate photocatalysts

Photocatalytic water splitting into H₂ and O₂ over various tantalates was reviewed and factors affecting photocatalytic activities of tantalates were discussed from a viewpoint of the crystal structure and the energy structure. Many tantalates, K₃Ta₃Si₂O₁₃, alkali and alkaline earth tantalates, were highly active photocatalysts for water splitting. The high activities were mainly due to the high conduction band level consisting of Ta5d orbitals. NiO-loaded NaTaO₃ with the distorted perovskite structure showed the highest activity among tantalates. Moreover, the activity of the NiO/NaTaO₃ photocatalyst was remarkably improved by doping of lanthanoids. The apparent quantum yield of NiO/NaTaO₃ doped with lanthanum was ca. 50% at 270 nm.     

100 Å-thick tunnel junction by double impurity doping liquid phase epitaxy for V-band TUNNETT oscillation

The tunnel injection transit time (TUNNETT) diodes with p⁺p⁺n⁺n⁻n⁺ structure were fabricated by liquid phase epitaxy (LPE). About 100 Å tunnel junction (p⁺n⁺) was successfully prepared by the double impurity diffusion of Ge and S during LPE growth. Continuous wave (CW) oscillation was realized at 51.520 GHz in the V-band cavity with the phase noise of −60 dBc/Hz at 1 kHz bandwidth.     

Aortic valve prolapse and aortic regurgitation associated with subpulmonic ventricular septal defect

The natural development of aortic valve deformity was studied in 315 patients with subpulmonic ventricular septal defect. The patients with early development of aortic regurgitation had a pulmonary-to-systemic flow ratio of > 1.5, normal right ventricular pressure, and severe aortic regurgitation.     

Developmental changes in the effect of acidosis on contraction, intracellular pH, and calcium in the rabbit mesenteric small artery

The purpose of the present study was to determine developmental changes in the effect of respiratory acidosis on vascular smooth muscle contraction. Vessel diameter, intracellular pH (pHi), and calcium concentration ([Ca]i) were measured in a cannulated preparation of the small mesenteric artery of newborn and adult rabbits. In the artery precontracted by high KCl, acidosis caused a vasorelaxation both in the newborn and the adult; the vasorelaxation was greater in the newborn than in the adult. The fura-2 fluorescence ratio, an indicator of [Ca]i, decreased transiently during acidosis and the decrease was similar in the two age groups. In the artery precontracted by norepinephrine, acidosis caused a transient vasoconstriction in the adult and a vasorelaxation in the newborn. In these vessels, the fura-2 fluorescence ratio increased transiently during acidosis; the increase was similar in the two groups. Upon induction of acidosis, pHi fell rapidly in the artery precontracted by norepinephrine or high KCl, and the depression of pHi was similar in the two groups. In the skinned smooth muscle preparation, a tension-[Ca] relationship curve at pH 7.1 was not significantly different from that at pH 6.8 in the adult. In the newborn, the tension-[Ca] curve at pH 6.8 was shifted to the right, compared with that at pH 7.1. These data suggest that the vasorelaxant effect of respiratory acidosis in the premature vessel is greater than in the adult. The greater vasorelaxation in the newborn cannot be explained by the age-related difference in pHi or [Ca]i during acidosis. The greater sensitivity of myofibrils to low pHi in the newborn may, at least in part, be responsible for the greater vasorelaxation in this age group.     

Distributed memory implementation of KLIC

This paper describes external reference management and distributed unification in a distributed implementation of a concurrent logic programming language KL1. This implementation is based on the KLIC system. KLIC has a feature calledgeneric objects that enable easy modification and extension of the system without changes in the core implementation. This distributed implementation is built upon the same core and external references are represented using generic objects. Unification operations are defined as methods of generic objects. Since creation of interprocessor reference loops cannot be avoided, we studied a new unification scheme that can cope with interprocessor reference loops. We built several experimental distributed systems that all demonstrate reasonable efficiency.     

Degradation of polymers by high-speed stirring

Benzene solutions containing either poly(ethylene oxide) or poly(methyl methacrylate) or both of varying concentrations were prepared, stirred at a speed of 30,000 rpm, and the effects of concentrations of the same species or different species of polymers on the degradation of the polymers were investigated. Within experimental error little difference was observed in the [η] curves measured for each degraded polymer in spite of change in concentration. It is clear that the degradation of polymer with high-speed stirring in the concentration range 1–4% w/v is not caused by the interaction of polymer chains.     

Removal of lignin in a liquid system by an isolated fungus

The screening of a strain which could perform lignin removal was carried out. Based on taxonomic study the isolated strain (LM‐2) was identified as Penicillium sp. LM‐2 could decolorize 0.6 g dm^?3 lignin within 4 days in a shaking culture at 25 °C. The efficiency of decolorization of the lignin was over 80% in the pH range of 4.0–6.0, but was low above pH 6.2. The rise of temperature had a slight adverse effect on the lignin decolorization in the range of 25–35 °C. Lignolytic enzymes such as lignin peroxidase, manganese peroxidase and laccase were not detected in the culture broth or within the fungal cells. The lignin was removed from the high molecular weight fraction mainly by adsorption and accumulation inside the cells. © 2001 Society of Chemical Industry     

Electric dichroism studies of the bonding of Co(III) chelate with synthetic polyelectrolytes

The interactions of bis-2-(2-pyridylazo)-1-naphthol Co(III), [Co(III) (αPAN)₂⁺], with five kinds of synthetic polyelectrolytes have been studied by spectrophotometric and transient electric dichroism measurements. The polyelectrolytes were: poly(styrene sulphonic acid) (PSS); poly(acrylic acid) (PAA); poly(l-glutamic acid) (PLG); $\text{poly}\text{(N}{}^{\mathrm{<mtext>e</mtext>}}\text{,N}{}^{\mathrm{<mtext>e</mtext>}}\text{-}\text{dicarboxylmethyl-}\text{l}\text{-lysine}$ (PDCML); and poly(l-lysine) (PLL). The equilibrium constant of the reaction:

with P = polyelectrolyte residue was determined spectrophotometrically: K₁ is > 10⁷ M^?1 (PSS); (1.4 ± 0.2) × 10⁴ M^?1 (PAA); (4.0 ± 0.4) × 10³ M^?1 (PLG); (1.4 ± 0.2) × 10⁶ M^?1 (PDCML); and < 10² M^?1 (PLL) at pH 6–8. From transient electric dichroism, the angle (ψ) between the αPAN plane and the polymer axis was determined to be 65° (PSS); 52° (PAA); 55° (PLG); and 52° (PDCML). The large K₁ and ψ values for PSS are ascribed to the hydrophobic interaction between the aromatic αPAN ring and the styrene sulphonate residues of PSS. Using stopped-flow electric dichroism measurements, rapid transfer of a bound Co(III) chelate from the PDCML to PSS chains was shown to occur.     

Iodine-initiated,solid-state copolymerization of tetraoxane with 1,3-dioxolane in the presence of methylal. II. Properties of copolymer obtained by beaker-scale copolymerization

In order to elucidate the copolymerization mechanism, the properties of the copolymer obtained by the iodine-initiated copolymerization of the tetraoxane–1,3-dioxolane–methylal system have been studied using gas chromatography, microscopy, scanning electron microscopy, differential scanning calorimetry, and gel permeation chromatography. From the behavior of the thermal stability and gas chromatography of the reaction mixture, it was found that reactivity of 1,3-dioxolane with active center is larger than that of tetraoxane, i.e., more than 90% 1,3-dioxolane is consumed at an early stage of the polymerization. The results obtained by microscopy, DSC, and GPC of the copolymer suggested that the copolymerization proceeds from the surface to the center of the tetraoxane crystal as if it were a core model. It was also suggested that the heterogeniety in copolymer properties can be explained not only by heterogeneous dispersion of 1,3-dioxolane in tetraoxane crystal, but also by the difference of reactivity of 1,3-dioxolane with the active center.