Photocatalysts using hexa- and octa-titanates with different tunnel space for water decomposition

Photocatalytic activities for water decomposition were examined for photocatalysts using hexa- and octa-titanates and TiO2(B) with different tunnel space in the structure. Using RuO2 as promoter, M2Ti6O13 (M = Li, Na, K, Rb) showed the stoichiometric production of Hz and O₂ except for Li, whereas H₂Ti₈O₁₇ and TiO₂(B) had very low activity producing only hydrogen as a product. The effects of promoters on Na₂Ti₆O₁₃ showed that the activity increased in the order of RuO₂ > RuO₂ + IrO₂ > IrO₂ > RuO₂ + Pt > MnO₂. These effects along with other related ones are discussed: it emerges that the presence of the tunnels is important for the achievement of high photocatalytic activity.     

Motion analysis of a tripod parallel mechanism

A tripod parallel mechanism consists of three links of fixed length and a rigid platform, and these are connected by revolute joints. The platform can achieve sixdegrees-of-freedom (6-DOF) motion by the coordinated movement of the bottom ends of the three links on a horizontal plane. This mechanism has advantages over the more common six extendible parallel manipulators. It has a much larger work space and a simple structure. In this article, we show that the vector analysis for this tripod parallel mechanism and the derivation of the positions of the three bottom ends of the links in an arbitrary attitude of platform can be found by inverse kinematics and the conditions of geometrical constraint. Then, by a numerical simulation, the trajectories of the bottom ends of the three links are shown.     

铭琪加特纳维尔癌症关顾中心

正铭琪癌症关顾中心旨在为癌症患者以及他们的家人和朋友提供实际上和情绪上的支援服务。自1996年第一所铭琪中心在爱丁堡成立以来,铭琪癌症关顾中心基金会的规模日益扩展,并透过委托世界知名的建筑师发展一系列开创先河的建筑。不论是刻意还是偶然的,当代建筑有时难免会产生冷漠或拒人于千里之外的观感,但每一所铭琪中心——在格拉斯哥、伦敦抑或香港——都希望营造令人宾至如归的感觉,     

MgATP-induced conformational changes in a single myosin molecule observed by atomic force microscopy: periodicity of substructures in myosin rods

This paper discusses the conformational changes in a single myosin molecule directly observed using atomic force microscopy (AFM). The myosin molecules were pretreated in rigor solutions without MgATP or in relaxed solutions with various concentrations of MgATP. The images of these molecules were obtained using a tapping mode AFM. The results indicate that the orientation of the myosin's heads and tail strongly depend on the MgATP concentration. Without using MgATP, almost all of the myosin molecules are in the extended form; however, when MgATP is used, the molecules bend according to the level of MgATP concentration. The mean-square end-to-end distance of the myosin molecules is significantly shorter with p[MgATP] = 4 than with p[MgATP] = 6. The rod region did not show the same level of intensity along their length in the extended form. The rods exhibited clusters of discontinuity, which were identified as substructures. The size of these substructures change at intervals that are multiples of 14.3-14.5 nm, which reflects the periodicity of the alpha-helical coiled coils. The substructure clusters also correspond to the myosin crossbridge spacing in muscles (14.3 or 43 nm). These results suggest that the myosin's head bends in conjunction with the bending or tilting in the helical substructures. Conformational changes of the myosin molecule induced by MgATP seem to mimic the molecular motions in a muscle's force generation process.     

Computer-aided design of a factor Xa inhibitor by using MCSS functionality maps and a CAVEAT linker search

We have investigated a new approach to efficiently find a novel inhibitor against a serine protease (i.e. an activated coagulation factor X, FXa) by using de novo design programs and the X-ray crystal structure of the target enzyme. FXa is a coagulant enzyme that generates thrombin (a serine protease) and participates in both intrinsic and extrinsic coagulation pathways. We adopted multiple copy simultaneous search (MCSS) and CAVEAT linker search techniques, which disclosed a novel FXa inhibitor (T01312) consisting of two binding moieties (the benzamidinyl and adamantyl groups) and a linker unit (the carboxybenzylamine group). The inhibitory activity of T01312 against FXa was determined to be a small K(i)-value of 48nM, which is two orders of magnitude smaller than that against thrombin. An X-ray crystal analysis of T01312 complexed with trypsin (an analogue of FXa) and docking studies of T01312 with trypsin and FXa showed that: (i) the benzamidinyl group is a predominant binding moiety in the anionic pocket (S1 site) with an asparatic acid residue; (ii) a hydrophobic pocket (S4 site) is the binding site of the adamantyl group; (iii) the carboxylate group of the linker contributes to the selectivity for FXa against thrombin. Thus, the combination of the knowledge of the X-ray crystal structure of the target molecule with MCSS and CAVEAT linker search techniques proved to be an effective hit-finding method that does not require the screening of huge compound libraries.     

Critical heat flux of binary mixtures in pool boiling and its correlation in terms of Marangoni number

Critical heat flux (CHF) in nucleate pool boiling of binary mixtures was newly measured with a horizontal platinum wire, 0.5 mm in diameter, and heated by DC, over the full range of concentrations. Seven mixtures were selected with the intent to cover various types of mixtures: methanol/water, ethanol/water, methanol/ethanol, ethanol/n-butanol, methanol/benzene, benzene/n-heptane and water/ethylene glycol, each in the saturated state at atmospheric pressure. Total 311 raw CHF data were obtained at 75 concentrations including pure components.Aqueous mixtures of methanol and ethanol revealed significant increase of CHF compared to either CHF linearly interpolated between pure components or CHF predicted from a single component correlation with use of the mixture properties. Three organic mixtures showed more or less the same level as an interpolated CHF, while the remaining two mixtures of methanol/benzene and water/ethylene glycol gave the reduced CHF by 20% and 50% at most, respectively. Marangoni number was introduced as a controlling variable to explain the observed increased, invariable, or reduced CHF, and an empirical correlation was developed.     

Ultrasonic irradiation on hydrolysis of magnesium hydride to enhance hydrogen generation

This paper describes the ultrasonic irradiation on the hydrolysis of magnesium hydride to enhance hydrogen generation; the effects of the ultrasonic frequency and the sample size on the hydrogen generation were mainly examined. In the experiments, three MgH₂ particle and nanofiber samples were soaked in distilled water and ultrasonically irradiated at frequencies of 28, 45, and 100 kHz. Then, the amount of hydrogen generated was measured. We found that the low frequency of ultrasonic irradiation and the relatively small sample size accelerated the hydrolysis reaction MgH₂ + 2H₂O = Mg(OH)₂ + 2H₂ + 277 kJ. In particular, the MgH₂ nanofibers exhibited the maximum hydrogen storage capacity of 14.4 mass% at room temperature at a frequency of 28 kHz (ultrasound irradiation). The results also experimentally validated that a combination of ultrasonic irradiation and MgH₂ hydrolysis is considerably effective for efficiently generating hydrogen without heating and adding any agent.     

Characteristics of the Mach Disk in the Underexpanded Jet in which the Back Pressure Continuously Changes with Time

When the high-pressure gas is exhausted to the vacuum chamber from the nozzle, the underexpanded supersonic jet contained with the Mach disk is generally formed. The eventual purpose of this study is to clarify the unsteady phenomenon of the underexpanded free jet when the back pressure continuously changes with time. The characteristic of the Mach disk has been clarified in consideration of the diameter and position of it by the numerical analysis in this paper. The sonic jet of the exit Mach number Me=1 is assumed and the axisymmetric conservational equation is solved by the TVD method in the numerical calculation. The diameter and position of the Mach disk differs with the results of a steady jet and the influence on the continuously changing of the back pressure is evidenced from the comparison with the case of steady supersonic jet.     

Structural Defects Control the Energy Level Alignment at Organic/Organic Interfaces

The dependence of the energy level alignment (ELA) on structural defects at an organic/organic heterojunction (OOH) of perfluoropentacene (PFP)‐on‐diindenoperylene (DIP) was investigated using X‐ray scattering and ultraviolet photoelectron spectroscopy. The density of structural defects near the interface between the PFP and DIP layers was varied by changing the growth temperature of the DIP film. A direct relationship was found between the defect density and the ELA at the OOH; the ELA together with the change in the electrostatic potential (quasi‐interface dipole layer) at the OOH varies systematically with the defect density near the interface. This indicates that a key factor affecting the ELA is the electrostatic potential change across the OOH interface, which is produced by electron transfer from DIP occupied gap states to PFP unoccupied gap states. These gap states originate from the defects and are effectively controlled by adjusting the growth conditions of the organic films. As a result, the ELA at OOH interfaces can be controlled by the density of structural defect, which is important for organic devices employing OOHs, such as organic photovoltaic cells.     

Ironmaking with ammonia at low temperature

This paper describes the reduction of hematite with ammonia for ironmaking, in which the effect of temperature on the products was examined. The results showed that the reduction process began at 430 °C during heating, and with an increase in temperature, the reduction mechanism changed apparently from a direct reduction of ammonia (Fe(2)O(3) + 2NH(3) → 2Fe + N(2) + 3H(2)O) to an indirect reduction via the thermal decomposition of ammonia (2NH(3) → N(2) + 3H(2), Fe(2)O(3) + 3H(2) → 2Fe + 3H(2)O) at temperatures over 530 °C. The final product obtained at 600 and 700 °C was pure metallic iron, in contrast with that formed at 450 °C, that is, a mixture of metallic iron and iron nitride. The results suggest the possibility of using ammonia as a reducing agent for carbonless ironmaking, which is operated at a much lower temperature than 900 °C in conventional coal-based ironmaking.