Prediction method of critical power by film flow rate measurement and subchannel analysis

This paper presents a method that can estimate the critical power of boiling water reactors, BWRs, with regard to spacer geometry. The current experimental method for estimating the critical power for BWR design requires many trained experts and expensive facilities to conduct the experiments. In the present method, the liquid film flow rate of adiabatic gas‐liquid two‐phase flow and a subchannel analysis of the actual BWR flow condition are measured experimentally and analyzed. In the experiment, deposition enhancement coefficients of three spacer geometries—a ferrule, an egg‐crate, and a ferrule spacer with twisted tape (CYCLONE spacer)—were estimated by measuring the liquid film flow rate of air‐water two‐phase flow flowing up in a vertical square (4 × 4) rod bundle that simulated the rod bundle of a BWR. Using these coefficients, the critical powers for bundles using each type of spacer geometry were calculated in the subchannel analysis. This method was validated using previous critical power data in the actual BWR flow condition. The critical powers predicted by this method agreed well with those of the experimental data. The result confirmed the effectiveness of this experiment‐simulation combined method, as well as the advantage over current experimental methods in terms of human and facility costs. © 2005 Wiley Periodicals, Inc. Heat Trans Asian Res, 34(5): 309–323, 2005; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/htj.20069     

Decomposition Characteristics of an Artificial Biogas in a Low‐Pressure DC Glow Discharge

The decomposition characteristics of an artificial biogas, which is a mixture of CH ₄, CO ₂, and H ₂ S, using a low‐pressure DC glow discharge have been investigated. It is found that H ₂, CO, C ₂ H ₂, H ₂ O, CS ₂, and COS are produced from the artificial biogas in the glow discharge. About 65% of the hydrogen atoms in CH ₄ are converted into H ₂ at an input energy of 800 J, at which CH ₄ is completely decomposed, and the decomposition characteristics of the artificial biogas are minimally dependent on the H ₂ S additive. Further, H ₂ S has a tendency to be decomposed earlier than the other components of the artificial biogas. When the glow discharge is generated in the artificial biogas with H ₂ S, some of the carbon atoms are found to deposit on the electrodes and the wall of the discharge chamber. © 2013 Wiley Periodicals, Inc. Electr Eng Jpn, 186(1): 26–33, 2014; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.22304     

Preparation of poly(N-isopropylacrylamide)–SiO2 hybrid gels and their thermosensitive properties

The swelling and adsorption behavior of poly(N-isopropylacrylamide)–SiO₂ hybrid gels, derived from copolymerization of N-isopropylacrylamide and 3-methacryloxypropyltrimethoxysilane (MPTMOS) and following hydrolysis and condensation, were investigated. The hybrid gels exhibited temperature dependence of both the swelling ratio and adsorption of solutes, and their temperature dependence of both the swelling ratio and adsorption of solutes, and their temperature dependence was related to the MPTMOS content in the hybrid gels. In addition, the modification of thermosensitive properties of the hybrid gels could be achieved by treatment with other silane compounds. © 1996 John Wiley & Sons, Inc.     

Phase Formation and Microstructure of Titanium Oxides and Composites Produced by Thermal Plasma Oxidation of Titanium Carbide

The phase formation and microstructure of titanium oxides and composites produced by Ar–O₂ thermal plasma oxidation of titanium carbide powders were investigated in detail by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Relationships between the phase compositions and microstructures of the oxides were established by combined structural and phase analyses, in correlation with synthesis conditions and phase formation mechanisms. It is revealed that vapor condensation favored the formation of anatase, which existed as smaller particles, while liquid/solid oxidation favored the formation of rutile, which appeared as larger particles or composites. A higher oxygen input in the plasma gases (Ar + O₂) enhanced the formation of anatase due to impeded oxidation and evaporation. A small amount of Ti₄O₇ and Ti₃O₅ was detected in the larger particles coexisting with rutile or TiC. These suboxides were formed as intermediates in solid oxidation of TiC or precipitated from the Ti–C–O melt during cooling. Furthermore, extensive cracks, dislocations and stresses were observed in the monolithic rutile and composites, in association with the rapid quenching in this high-temperature in-flight oxidation process.     

New kinetic aspects on the mechanism of thermal oxidative degradation of polypropylenes with various tacticities

Thermal oxidative degradation behavior of polypropylene (PP) with different tacticities was studied based on the activation energy (ΔE) data obtained by thermogravimetric analysis (TGA). The ΔE value showed a negative proportion to the content of meso pentad fraction (mmmm) in all of isotactic PP (iPP) samples, and that of syndiotactic PP sample considerably deviated from this negative proportion relationship. Since the value of mmmm was directly related to polymer chain conformation, the ΔE value was thought to have close connection with the concentration of 3₁ helix conformation in the iPPs. The ΔE changes would be caused by the competition between uni- and bimolecular hydroperoxide decomposition, which was controlled by concentration and character of conformations of PPs.     

Reaction and Formation of Crystalline Silicon Oxynitride in Si–O–N Systems under Solid High Pressure

Oxidized amorphous Si₃N₄ and SiO₂ powders were pressed alone or as a mixture under high pressure (1.0–5.0 GPa) at high temperatures (800–1700°C). Formation of crystalline silicon oxynitride (Si₂ON₂) was observed from amorphous silicon nitride (Si₃N₄) powders containing 5.8 wt% oxygen at 1.0 GPa and 1400°C. The Si₂ON₂ coexisted with β-Si₃N₄ with a weight fraction of 40 wt%, suggesting that all oxygen in the powders participated in the reaction to form Si₂ON₂. Pressing a mixture of amorphous Si₃N₄ of lower oxygen (1.5 wt%) and SiO₂ under 1.0–5.0 GPa between 1000° and 1350°C did not give Si₂ON₂ phase, but yielded a mixture of α,β-Si₃N₄, quartz, and coesite (a high-pressure form of SiO₂). The formation of Si₂ON₂ from oxidized amorphous Si₃N₄ seemed to be assisted by formation of a Si–O–N melt in the system that was enhanced under the high pressure.     

Control of Oxidation State of Eu Ions in Na2O–Al2O3–SiO2 Glasses

Glasses doped with well‐controlled Eu³⁺ and Eu²⁺ ions have attracted considerable interest due to the possibility of tuning the wavelength range of the emitted light from violet to red by using their ⁵D₀→⁷F_j and 5d–4f electron transitions. Glasses were prepared to dope Eu³⁺ ions in a Na₂O–Al₂O₃–SiO₂ system, and the changes in the valence state of Eu³⁺ ions and the glass structure surrounding the Eu atoms during heating under H₂ atmosphere were investigated using fluorescence spectroscopy, X‐ray absorption fine‐structure spectroscopy, and ²⁷Al magic‐angle spinning solid‐state nuclear magnetic resonance spectroscopy. The reduction behavior of Eu³⁺ ions was dependent on the Al/Na molar ratio of the glass. For Al/Na < 1, the Al³⁺ ions formed the AlO₄ network structure accompanied by the Na⁺ ions as charge compensators; the Eu³⁺ ions occupied the interstitial positions in the SiO₄ network structure and were not reduced even under heating in H₂ gas. On the other hand, in the glasses containing Al₂O₃ with the Al/Na ratio exceeding unity, the Eu³⁺ ions commenced to be coordinated by the AlO₄ units in addition to the SiO₄ network structure. When heated in H₂ gas, H₂ gas molecules reacted with the AlO₄ units surrounding Eu³⁺ ions to form AlO₆ units terminated with OH bonds, and reduced Eu³⁺ ions to Eu²⁺ via the extracted electrons.     

Numerical analysis of a reactive extrusion process. Part II: Simulations and verifications for the twin screw extrusion

A newly designed extruder reactor for grafting vinyl monomers onto polyolefins was studied experimentally and theoretically. The process was made up of a self‐wiping co‐rotating twin screw extruder with a separated reaction zone and two vent zones. The reactive extrusion was performed using a linear low density polyethylene, vinyltrimethoxysilane and di‐t‐butylperoxide under different operation conditions. For the purpose of process analysis, we built a computer simulation based on the reaction kinetics and rheological models studied in the preceding paper. The flow field in the extruder was calculated by the flow analysis network (FAN) method with non‐isothermal non‐Newtonian flow conditions. The iterative procedure was organized to predict local pressure, filling factor, cumulative residence time and temperature along the extruder. Furthermore, we succeeded in representing the profiles of reaction conversion and shear viscosity. Calculated results showed good agreements with the experimental data.     

Principle and operation of a new type motor consisting of piezoelectric device and strain wave gearing

The authors have developed a new type of motor consisting of a piezoelectric device and strain wave gearing, and is called a piezoelectric motor. This is a first step in realizing a low-speed, small-size and lightweight motor. The principle of the motor is that the traveling wave is produced by piezoelectric devices and displacement conversion devices without mechanical resonance, and the torque to rotate the motor is generated by a mechanism of strain wave gearing (circular spline and flexspline) without using friction. The motor is operated at variable frequency and its rotational position (angle) is controlled in open-loop because it is basically a synchronous motor. In this paper, the structure and principle of the proposed motor are explained and the driving method and the mechanical characteristics of an experimental motor also are described. The results are as follows:

• 1 The realizability of the proposed piezoelectric motor is verified experimentally. The experimental motor operates at 2920 steps per revolution, and its speed range is 0 to 960 pps [or 0 to 20 (rpms)].
• 2 The torque characteristics are clarified qualitatively.
• 3 The generated torque of the experimental motor is small (less than 0.03 Nm) and therefore the improvement of the torque is an important subject hereafter.
• 4 It is possible to construct the motor with nonmetallic material. This fact is considered to facilitate obtaining a means to lighten the weight of the motor in the future.