Development of high voltage harmonic measuring instruments for distribution systems using optical voltage sensor and current sensor

Application of an optical measuring technique was attempted in order to develop harmonic voltage and current measuring instruments for distribution systems. To develop the harmonic voltage measuring system using a Bi₁₂GeO₂₀ crystal as a sensing Pockels cell for high‐voltage distribution lines, zinc oxide elements were adopted as a voltage divider. Also, an optical current sensor system was improved on the harmonic current measuring system using an R₃Fe₅O₁₂ film as a Faraday device. In practical three‐phase distribution systems, the developed high voltage harmonic measuring devices using the optical voltage sensor and current sensor were compared with conventional harmonic analyzers for low voltage. As a result, it was confirmed that the developed high voltage harmonic measuring devices had satisfactory characteristics for practical use. © 1999 Scripta Technica, Electr Eng Jpn, 128(4): 84–93, 1999     

The adhesion between electrolessly deposited copper and a photoimageable polymer

We investigated the relationship between the peel adhesion of copper, deposited by electroless plating, to a photoimageable polymer and the time of chemical etching before plating. Mechanical interlocking is generally considered as being the adhesion mechanism between deposited metals and substrates. However, we found that the peel strength decreased with an increase in the etching time though the polymer roughness did not change. The glass transition temperature of the photoimageable polymer became lower as the etching time increased. The pretreatment not only roughened the surface of the photoimageable polymer, but also affected the bulk polymer and the adhesion.     

Water Vapor Permeability of Poly(L‐lactide)/Poly(D‐lactide) Stereocomplexes

PLLA/PDLA blend films with only stereocomplex crystallites as a crystalline species together with pure PLLA and PDLA films with only homo‐crystallites as a crystalline species were prepared, and the effects of enantiomeric polymer blending, crystalline species, and crystallinity on the water vapor permeability were investigated. The WVT coefficient P of PLLA/PDLA blend films was 14–23% lower than that of pure PLLA and PDLA films in the crystallinity X_c range of 0–30%. Amorphous PLLA/PDLA blend films have a much lower P than pure PLLA and PDLA films. The dependence of P on X_c for blend films was stronger for X_c = 0–30% than for X_c = 30–100%. This dependence is discussed using the Nielsen model and the concept of “restricted” (or “restrained”) and “free” amorphous regions.

     

Morphological reason for enhancement of electrochemical double layer capacitances of various acetylene blacks by electrochemical polarization

Enhancement of electrochemical capacitance and morphological variations of various acetylene blacks caused by electrochemical polarization are presented. Acetylene blacks of different mean particle diameters were modified by air-oxidation and heat treatment to diversify the morphologies of the acetylene blacks before electrochemical polarization. The various acetylene blacks were electrochemically oxidized at 1.6 V (vs. Ag/AgCl) for 10 s and the polarization step was repeated until the capacitance values did not change any longer. These polarization steps enhanced the capacitances of the acetylene blacks and the specific enhancement factors range from 2 to 5.5. Such an enhancement is strongly related to morphological modification as revealed by transmission electron microscopic observations. The electrochemical polarization resulted in formation of tiny graphene sheets on the wide graphitic carbon surfaces, which were most responsible for the observed capacitive enhancement. Although the pseudo-capacitance increased after polarization by forming oxygenated species on the surfaces, its contribution to the total capacitance was less than 10%. The mechanism of the formation of the tiny graphene sheets during the electrochemical oxidation is described schematically.     

Ingestion of gelatinized potato starch containing a high level of phosphorus decreases serum and liver lipids in rats

Potato starch is known to have a higher concentration of phosphate than other starches. The presence of phosphate groups in amylopectin results in resistance to digestion by amylase. Therefore, there is a possibility that potato starch is slowly digested, inducing a physiological effect similar to that of resistant starch and indigestible oligosaccharides. The amount of phosphate group in starch differs with potato cultivar. In the present study, we investigated the effects of gelatinized potato starch containing a high level of phosphorus on lipid metabolism in rats. For this purpose, we determined lipid levels in the serum and liver in rats fed two kinds of gelatinized potato starches with different phosphorus contents. Four groups of male Sprague-Dawley rats were fed a 60% sucrose diet (control) or one of three diets containing cornstarch (CS), Benimaru (BM) potato starch or Hokkaikogane (HK) potato starch. Fat pad weight was slightly decreased in the HK diet group compared with that in the other groups. Free fatty acids in serum were significantly lowered by dietary HK starch compared with control, and serum triglyceride in rats fed the HK diet was also decreased. In the BM and HK diet groups, triglyceride levels in the liver were decreased compared with that in the control and CS groups. As for hepatic total cholesterol level, there were no significant differences among three starch diet groups. Fecal bile acid excretion was greater in the two potato starch groups than in the control group. On the other hand, there were no significant differences in cecal short-chain fatty acid content or pH. Thus, we conclude that dietary gelatinized potato starch reduces free fatty acid and triglyceride in serum and hepatic triglyceride, but does not affect cecal fermentation.     

Mathematical modelling of MAG welding

The development of laser welding technology has enabled the mass production of thin-walled structures, including steel sandwich panels. The technology of joining plating panels with stiffeners by welding allows us to create joints with a specific geometry and material properties. In comparison with other types of joints, laser welds are characterized by their specific behaviour under cyclic load and, as a consequence, a different model of fatigue damage. The basis of fatigue analysis of laser-welded joints was the determination of stress concentrations in the notches. For this purpose, a numerical finite element method model of a laser-welded joint was created. The article presents the main aspects of the numerical model and the results concerning the influence of the modelling method on the strain and stress distribution in the notches. For the weld root notch, the theoretical results have been compared with experimental data of strain distributions obtained by the laser extensometry grid technique.     

Oxygen Uptake and Release Mechanism of Lithium Manganese Ferrite in the Low Temperature Range of 573–773 K

Oxygen uptake and release of (Li,Mn) ferrite [LMF; (Li_0.60Mn_1.20Fe_1.20)_1−δO₄; δ= 0.007 to 0.033] was investigated concerning the relations between redox reactions of ferrite and cation migration. Mössbauer spectroscopy and X-ray diffractometry showed that some of the Li⁺ and Fe³⁺ ions migrated from the A sites to the B sites of the spinel-type structure and Mn⁴⁺ ions migrated from the B sites to the A sites during oxygen uptake at 573 K. The cation-deficient LMF formed by the oxygen uptake released oxygen molecules in He gas only at 660 K. The cation migration during the oxygen release was in the opposite direction of the movement during oxygen uptake at 573 K.     

High permittivity BaTiO3 and BaTiO3-polymer nanocomposites enabled by cold sintering with a new transient chemistry: Ba(OH)2∙8H2O

Cold sintering process (CSP) offers a promising strategy for the fabrication of innovative and advanced high permittivity dielectric nanocomposite materials. Here, we introduce Ba(OH)₂?8H₂O hydrated flux as a new transient chemistry that enables the densification of BaTiO₃ in a single step at a temperature as low as 150 °C. This remarkably low temperature is near its Curie transition of 125 °C, associated with a displacive phase transition. The cold sintered BaTiO₃ shows a relative density of 95 % and a room temperature relative permittivity over 1000. This new hydrated flux permits the fabrication of a unique dense BaTiO₃-polymer nanocomposite with a high volume fraction of ceramics ((1-x) BaTiO₃ – x PTFE, with x = 0.05). The composite exhibits a relative permittivity of approximately 800, at least an order of magnitude higher than previous reports on polymer composites with BaTiO₃ nanoparticle fillers that are typically well below 100. Unique high permittivity dielectric nanocomposites with enhanced resistivities can now be designed using polymers to engineer grain boundaries and CSP as a processing method opening up new possibilities in dielectric materials design.     

Particle velocity and solids circulation rate in a jet-spouted bed

Radial distribution of particle velocities, solids circulation rate and radial variation in bed voidage in a jet-spouted bed were investigated in a 0.2 m diameter conical-cylindrical column. The upward particle velocity is strongly dependent on gas velocity and its radial profile is the Gaussian. The solids circulation rates are of the same order of magnitude as those in a conventional spouted bed and are proportional to the gas velocity. Estimation of the variation in bed voidage in the radial direction revealed that the annulus voidage of about 0.90 was greater than the spout voidage of around 0.70. This tendency is contrary to that in a conventional spouted bed.