High-field dielectric properties of polyethylene in the high-temperature region

Nonpolar polymers such as polyethylene or polypropylene are widely used as insulation materials, often under conditions involving strong electric fields and high temperatures. Under these conditions, the conduction loss due to DC-like carrier transport may give rise to a high-field AC dissipation factor (tan δ). This paper describes the high-field dielectric properties of polyethylene films at frequencies from 50 to 400 Hz and temperatures from room temperature to 100°C, as measured with a new type electrode design developed by the authors. In the high-temperature region, the AC dissipation current waveform at 50 Hz was also measured. At room temperature, the electric-field dependence of tan δ is almost unaffected by the frequency of the applied field. But at high temperatures and strong electric fields, tan δ tends to have a large field dependence and to be almost inversely proportional to the frequency. Thus the AC conductivity becomes independent of the frequency of the applied field in the region of strong fields and high temperatures. A theoretical analysis shows that the high-field dielectric loss is governed by two processes, namely, the dielectric relaxation loss inherent to the AC field and the DC-like carrier transport loss that becomes prominent in the high-temperature region, where AC dissipation current waveform becomes significantly nonsinusoidal.     

Raman Spectroscopy of Laser‐Shocked Nitrobenzene

A technique for in situ Raman spectroscopy of laser‐shocked nitrobenzene was developed. Raman spectra of shocked nitrobenzene are obtained up to ∼3.5 GPa, and peak shifts at particular frequencies are observed. The shifts are plotted as a function of density and compared with the data under isothermal compression. Both data provide the same results. This indicates that the numbers of peak shifts of nitrobenzene depend solely on material density.     

Measurements of acoustic waves generated by electrical breakdown in a polypropylene film

Electrical breakdown of a polymer film generates a pressure wave that is believed to include information about the breakdown initiation point. We measured the breakdown pressure wave and the space charge distribution up to the electrical breakdown field by using the pulsed electro‐acoustic method in a 30 µm thick polypropylene film. We discuss electrical breakdown phenomena based on the breakdown pressure wave and the dependence of the space charge distribution on the applied field and temperature. At room temperature, the observed breakdown pressure wave had a pulse‐like shape with a width that depended on the polarity of the applied field. Positive space charge accumulation was observed near the cathode as a hetero space charge near the electrical breakdown field. At 60 °C, the width of the breakdown pressure wave showed no dependence on the applied field polarity and positive space charge accumulation was observed inside the film near the electrical breakdown field. These experimental results suggest that electrical breakdown phenomena are affected by hetero space charge accumulation and that the initiation point of electrical breakdown corresponds to the position of hetero space charge accumulation in 30 µm thick polypropylene film. ©1999 Scripta Technica, Electr Eng Jpn, 126(3): 1–8, 1999     

Evolution of patinas on copper exposed in a suburban area

Copper plates were exposed under sheltered outdoor conditions for up to one year, starting in September 2001 in Musashino City, Tokyo, a suburban area. Following various periods of exposure, the patinas on the plates were characterized to investigate their evolution by using X-ray fluorescence analysis, X-ray diffraction, field emission scanning electron microscopy, and glow discharge optical emission spectroscopy. The difference in the roles of sulfur and chlorine in the early stages of copper patination were identified by analyzing the depth profiles of these two elements. Sulfur was found on top of the patina as cupric sulfates such as posnjakite (Cu₄SO₄(OH)₆ · H₂O) or brochantite (Cu₄SO₄(OH)₆). Brochantite appeared only after 12 months of exposure. In contrast, chlorine was found on the surface after only one month of exposure. It gradually penetrated the patina as the exposure period lengthened, forming copper chloride complexes. Chloride ions accumulated at the patina/copper interface, forming nantokite (CuCl), which promoted corrosion.     

Formation of phase structure and crystallization behavior in blends containing polystyrene–polyethylene block copolymers

The microphase separation structure in the molten state and the structure formation in crystallization from such ordered melt were investigated for the blends of polystyrene–polyethylene block copolymers (SE) with polystyrene homopolymer (PS) and polyethylene homopolymer (PE) and for the blends consisting of two kinds of SE with different copolymer compositions from each other, using synchrotron small-angle X-ray scattering techniques (SAXS). The copolymer compositions of SE block copolymers employed were 0.34, 0.58 and 0.73 wt. fraction of PE, and their melt morphologies were cylindrical, lamellar and lamellar, respectively. Macrophase separation or the morphology change in the melt occurred depending on the molecular weight and the blend composition, as reported so far. In crystallization from such macrophase-separated and microphase-separated melts, the melt morphology was completely kept for all the blends. Crystallization behavior was also investigated for the blends. The crystallization within the spherical and cylindrical domains surrounded by glassy PS was not observed for SE/PS blends. In the crystallization from the macrophase-separated melt, two exothermal peaks were observed in the DSC measurements, while a single peak was observed for other blends. For the blends with PS, the degree of crystallinity was depressed and the apparent activation energy of crystallization was high, compared to those for the corresponding neat SE. For SE/PE and SE/SE blends, those were changed depending on the blend composition.     

Differences between corrosion products formed on copper exposed in Tokyo in summer and winter

We analyzed the copper corrosion products that formed during a month in summer and a month in winter at three sites in Tokyo using several analytical techniques. The X-ray diffraction patterns revealed that cuprite Cu₂O and posnjakite Cu₄SO₄(OH)₆·H₂O formed on copper exposed in summer. By contrast, only cuprite was found in winter exposed copper. The X-ray fluorescence results indicated that the amounts of sulfur and chlorine on the copper plates exposed in summer were much greater than those in winter. This could be explained by the change in particulate sulfate and sea salt concentrations. Depth profiling analysis by Auger electron spectroscopy revealed that the oxide layer formed in summer was thicker than that in winter. This difference in oxide layer thickness could have been due to the differences in temperature, relative humidity, and the amount of sulfur and chlorine on the copper plate.     

Estimation of source contribution to nitrate loading in road runoff using stable isotope analysis

The nitrogen load was determined in road runoff during rainfall events. Moreover, nitrate isotopes analysis was conducted to determine the contribution of nitrates from atmospheric deposition and leaching from road dust. The concentrations of NO₃-N in road runoff were higher than those in atmospheric deposits for each rainfall event, except one event with a long antecedent dry weather period. The δ¹⁸O-NO₃ in road runoff was lower than in atmospheric deposits and higher than in leachate from road dust; however, no difference in δ¹⁵N-NO₃ was observed. By using δ¹⁸O-NO₃ as an indicator for evaluating NO₃-N sources in road runoff, contribution ratios of NO₃-N from road dust were estimated to be 14–22%, 23–25%, and 22–34% for Event 1 to Event 3, respectively. These results indicated that the NO₃-N from the atmosphere accounts for more than half of the NO₃-N in road runoff.     

Bacteriophages isolated from activated sludge processes and their polyvalency

In this study, bacteriophages were isolated from activated sludge and their host range was studied. Bacterial isolates were obtained from an activated sludge process treating urban sewage, and bacteriophages were obtained by plaque assay using the bacterial isolates obtained in this study as the host. Out of 15 bacteria isolated, 9 supported plaque formation. The host range test was conducted with a combination of 8 bacteriophage isolates and 9 bacterial isolates. All of the 8 bacteriophages tested were found to form plaques on more than 1 host, and 4 of them formed plaques on both gram-positive and gram-negative bacterial isolates. Three of the 8 bacteriophages failed to form plaques on their original bacterial host. The experimental result indicates that bacteriophages are an active part of the activated sludge microbial ecosystem, having a very close ecological relationship with their host bacteria.     

Geometric aspects of composite pulses

Unitary operations acting on a quantum system must be robust against systematic errors in control parameters for reliable quantum computing. Composite pulse technique in nuclear magnetic resonance realizes such a robust operation by employing a sequence of possibly poor-quality pulses. In this study, we demonstrate that two kinds of composite pulses-one compensates for a pulse length error in a one-qubit system and the other compensates for a J-coupling error in a two-qubit system-have a vanishing dynamical phase and thereby can be seen as geometric quantum gates, which implement unitary gates by the holonomy associated with dynamics of cyclic vectors defined in the text.