A method to determine direct‐ and quadrature‐axis inductances of permanent magnet synchronous motors

The equivalent circuit constants of permanent magnet synchronous motors are needed in the calculation of operation characteristics, construction of a control system, etc. These constants can be computed from the data on structural form and materials. However, measurements are necessary to obtain highly precise values. Methods for measurement of the d‐ and q‐axis inductances can be roughly divided into rotational and standstill methods. The standstill methods have the advantage that they are easy to carry out. However, it is difficult to consider magnetic saturation and distortion of the change in the armature winding inductance. The accuracy of the standstill method can be improved if these effects can be readily taken into account. This paper describes a standstill method for measuring accurate d‐ and q‐axis synchronous inductances of permanent magnet synchronous motors. By utilizing the fact that the EMF interference terms in the motor voltage equation considering the distortion of the inductance change are equal to zero when the rotor is in a specific position, the proposed method determines the inductances considering both magnetic saturation and inductance distortion effects from simple off‐line standstill testing. In addition, this method is capable of taking cross‐magnetic saturation into account when used with the necessary testing equipment. The proposed method was implemented on a 0.4‐kW interior permanent magnet synchronous motor with concentrated stator winding. The validity of the proposed method was demonstrated by comparing the measured and calculated results of the no‐load and on‐load characteristics. © 2010 Wiley Periodicals, Inc. Electr Eng Jpn, 171(3): 41–50, 2010; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20969     

Thermal desorption and pyrolysis direct analysis in real time mass spectrometry of Nafion membrane

Perfluorosulfonic acid ionomer membranes have been widely used as proton conducting membranes in various electrochemical processes such as polymer electrolyte fuel cells and water electrolysis. While their thermal stability has been studied by thermogravimetry and analysis of low molecular weight products, their decomposition mechanism is little understood. In this study a newly developed methodology of thermal desorption and pyrolysis in combination with direct analysis in real time mass spectrometry is applied for Nafion membrane. An ambient ionization source and a high-resolution time-of-flight mass spectrometer enabled unambiguous assignment of gaseous products. Thermal decomposition is initiated by side chain detachment above 350°C, which leaves carbonyls on the main chain at the locations of the side chains. Perfluoroalkanes are released above 400°C by main chain scission and their further decomposition products dominate above 500 °C. DFT calculation of reaction energies and barrier heights of model compounds support proposed decomposition reactions.     

Stromal CCL5 Promotes Breast Cancer Progression by Interacting with CCR3 in Tumor Cells

Chemokines secreted from stromal cells have important roles for interactions with carcinoma cells and regulating tumor progression. C-C motif chemokine ligand (CCL) 5 is expressed in various types of stromal cells and associated with tumor progression, interacting with C-C chemokine receptor (CCR) 1, 3 and 5 expressed in tumor cells. However, the expression on CCL5 and its receptors have so far not been well-examined in human breast carcinoma tissues. We therefore immunolocalized CCL5, as well as CCR1, 3 and 5, in 111 human breast carcinoma tissues and correlated them with clinicopathological characteristics. Stromal CCL5 immunoreactivity was significantly correlated with the aggressive phenotype of breast carcinomas. Importantly, this tendency was observed especially in the CCR3-positive group. Furthermore, the risk of recurrence was significantly higher in the patients with breast carcinomas positive for CCL5 and CCR3 but negative for CCR1 and CCR5, as compared with other patients. In summary, the CCL5-CCR3 axis might contribute to a worse prognosis in breast cancer patients, and these findings will contribute to a better understanding of the significance of the CCL5/CCRs axis in breast carcinoma microenvironment.     

Analytical and Experimental Evaluation of Dispersive Mixing Performance of Special Rotor Segments in a Corotating Twin-Screw Extruder

An intermeshing corotating twin-screw extruder is often used for producing polymer composites. In this study, we discussed mixing performance of special rotor segments in molten zone. These rotor segments have several tip clearances for achievement of self-cleaning and effective mixing, and these are named various clearance mixing technology. We studied about dispersive mixing performance of configuration, which consists of various clearance mixing technologys (various clearance mixing technology configuration) using numerical analyses and experiments. For the analytical evaluation of mixing performance, we have adopted a particle tracking method. As evaluation indices of dispersive mixing performance, we focused on following three values (1) maximum value in a history of first principal stress of each particle, (2) time-integrated shear rate of each particle, and (3) time-integrated first principal stress of each particle. And we made the probability distributions of the indices. We adopted weighted probability as approximation of volume probability in each region. The results were compared with those of kneading disk segments configuration (kneading disk configuration). Furthermore, we validated the accuracy of the analytical evaluation by performing experiments under same conditions as those of numerical analyses. For the experimental evaluation of mixing performance, we used twin-screw extruder. Polypropylene was selected as suspending media. And CaCO₃ was selected as filler. To compare just the mixing performance of various clearance mixing technology configuration with that of kneading disk configuration, side feeding and screw configuration which had third mixing segments zone were adopted. From the experimental result, it is found that various clearance mixing technology configuration dispersed better than kneading disk configuration. And from the comparison between the experimental evaluation and the analytical evaluation, it is found that the first principal stress is more appropriate for evaluation index of dispersive mixing. Finally, it can be mentioned that various clearance mixing technology configuration has better mixing performance than kneading disk configuration, and large stress is important for dispersive mixing.     

Catalytic Aerobic Photo‐oxidation of a Methyl Group on a Heterocycle to Produce an Aldehyde via Homolytic C?I Bond Cleavage caused by Irradiation with Visible Light

A new catalytic method was developed for photo‐oxidizing the methyl group on aromatic heterocycles such as benzothiazole, benzoxazole, and quinoline to produce the corresponding aldehyde. This is the first report of the metal‐free catalytic synthesis of benzothiazole‐2‐carboxaldehydes using molecular oxygen as the terminal oxidant.

     

Surface improvement on water and oil affinities and absorption rate of PVA/Tung oil-coated paperboard and fiberboard

A novel coating material on paperboard and fiberboard from poly(vinyl alcohol) (PVA) modified with Tung oil was developed. The PVA/Tung oil coating was cured at several conditions: 25, 40, 50, and 60°C, in the presence of two types of catalysts, i.e., thermal catalyst using potassium persulfate (KPS) and redox catalyst using KPS and sodium thiosulfate. The chemical crosslinked structure of PVA/Tung oil-coating films was confirmed by FTIR. The result indicated the decrease in the double bonds of Tung oil by crosslinking reaction, especially at 60°C. In comparison with the same curing temperature, the films with redox catalyst showed more reduction in the number of double bonds of Tung oil. DMA results of the PVA/Tung oil-coating materials with redox catalyst showed the lowering of the heights of both β transition peak of Tung oil and α transition peak of PVA. FTIR and DMA results confirmed the more efficient crosslinking reaction of redox catalytic system than that of the thermal catalytic system. The water resistance and mechanical properties of these coating materials exhibited better values as projected to higher curing temperature and redox catalyst. SEM images showed the smooth surface of PVA/Tung oil covered on the paperboards with ~72 µm in thickness. The contact angle of water or oil drop and dynamic change in contact angle on the surfaces of PVA/Tung oil-coated paperboards and fiberboards were investigated. The results show the contact angles for both water and oil were lower than those of the uncoated ones, indicating the improvement of water and oil affinities of the PVA/Tung oil-coating materials. The dynamic changes in contact angle of the coated ones also decreased, suggesting the reduction in water and oil absorption rates of these coated substrates.     

Growth Morphology and Mechanism of a Hollow ZnO Polycrystal

When zinc oxide and graphite were placed into an alumina crucible, with a square hole (∼3 mm ×∼3 mm) near the top, and the crucible was covered by an alumina lid and heated at >1050°C, a hollow polycrystal composed of needlelike, ribbon(comb)-like, dendritic, and bulk zinc oxide crystals grew from the hole toward the outside of the crucible. The diameter and length of the polycrystal grown at 1050°C after 1 h were ∼2.2 mm and ∼20 cm, respectively. The diameter increased, while the length decreased, with increasing temperature. Most of the needlelike zinc oxide crystals in the hollow polycrystal were elongated along the c -axis.     

Effect of α-substituents on molecular motion and wetting behaviors of poly(fluoroalkyl acrylate) thin films with short fluoroalkyl side chains

The effect of α-substituent on the molecular motion and wetting behavior of poly{2-(perfluorobutyl)ethyl acrylate} [PFA-C₄], poly{2-(perfluorobutyl)ethyl methacrylate} [PFMA-C₄], poly{2-(perfluorobutyl)ethyl α-fluoroacrylate} [PFFA-C₄], and poly{2-(perfluorobutyl)ethyl α-chloroacrylate} [PFClA-C₄] films were characterized by dynamic contact angle measurement, lateral force microscopy (LFM), wide angle X-ray diffraction (WAXD), and X-ray photoelectron spectroscopy (XPS). WAXD of oriented PFClA-C₄ fiber suggested the presence of rod-like chain due to the presence of bulky α-substituent. The glass transition temperature (T_g) of PFFA-C₄ and PFClA-C₄ were well above the room temperature. The water repellencies of PFFA-C₄ and PFClA-C₄ were as high as that of PFMA-C₄ and their oil repellency of PFFA-C₄ and PFClA-C₄ was higher than the PFMA-C_4. This result was originated from the low main chain mobility of PFFA-C₄ and PFClA-C₄ due to the presence of bulky α-substituents. The effect of molecular motion on water repellency was clarified by the results of temperature dependence studies of dynamic contact angle, LFM, and surface chemical composition measured by XPS.     

Nanostructured poly(3-hexylthiophene-2,5-diyl) films with tunable dimensions through self-assembly with polystyrene

Poly(3-hexylthiophene-2,5-diyl) is among the most widely used conjugated polymers for opto-electronic applications. To enhance its properties, researchers have attempted to nanostructure this polymer using various processes including breath figure arrays, nanolithography and elaborated organic synthesis. We here demonstrate a simple process to nanostructure the conjugated polymer using self-assembly with polystyrene and selective removal of one of the phases. The influence of the molecular weight of each polymer on the thin film morphology was systematically studied by atomic force microscopy. Using this approach, we observe two types of nanostructure, namely, nanoporous and nanoisland structures, of which the dimensions can be tuned by modifying the molecular weight of each polymer in the blend. This simple process introduces a cost-effective alternative to produce thin films of conjugated polymer with average nano-features from 100 nm up to 500 nm which could be used in a wide range of applications.