Development of 72‐kV high‐pressure air‐insulated GIS with vacuum circuit breaker

SF₆ gas has excellent dielectric strength and interruption performance. For these reasons, it has been widely used for gas‐insulated switchgear (GIS). However, use of SF₆ gas has become regulated under agreements set at the 1997 COP3. Thus, investigation and development for GIS with a lower amount of SF₆ gas are being carried out worldwide. Presently, SF₆‐free GIS has been commercialized for the 24‐kV class. Air or N₂ gas is used as the insulation gas for this GIS. On the other hand, SF₆‐free GIS has not been commercialized for the 72‐kV‐class GIS. The dielectric strengths of air and N₂ gas are approximately one‐third that of SF₆ gas. To enhance the insulation performance of air and N₂ we have investigated a hybrid gas insulation system which has the combined features of providing an insulation coating and suitable insulation gas. We have developed the world's first 72‐kV SF₆‐free GIS. This paper deals with key technologies for SF₆‐free GIS, such as the hybrid insulation structure, a bellows for the high‐pressure vacuum circuit breaker, a newly designed disconnector and spacer, and prevention of particle levitation. Test results of the 72‐kV high‐pressure air‐insulated GIS with the vacuum circuit breaker are described. © 2006 Wiley Periodicals, Inc. Electr Eng Jpn, 157(4): 13–23, 2006; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20451     

Development of a hybrid catalytic combustor for a 1300°C class gas turbine

The hybrid catalytic combustor concept proposed by the authors has an advantage concerned with catalyst durability, because the catalyst is maintained below 1000°C even for application to 1300°C class gas turbines. A full-scale hybrid catalytic combustor has been designed for a 200 MW (1300°C) class gas turbine. The catalyst bed was 450 mm in diameter and consisted of a Pd/ alumina washcoat on a cordierite monolith. In experiments, the combustor has demonstrated the capability of meeting the NO_x emission level of SCR (selected catalytic reduction) during atmospheric pressure testing. To predict the catalyst performance at an elevated pressure, the characteristics of the catalyst were studied using a small scale reactor test, and a material property test using a DTA/TGA-Q.MASS system. The catalyst showed a higher activity in the oxidized state (PdO) than in the metallic state (Pd). This activity difference was governed by the equilibrium of the oxygen release from PdO in bulk. It was considered that oxidation rate of the metallic Pd in bulk was not so high and this caused self-oscillation for the Pd catalyst around the temperature of the oxygen release equilibrium. Even below the temperature of the oxygen release equilibrium, both surface and bulk (lattice) oxygen of the PdO was consumed by the methane oxidation reaction, and resulted in a lack of surface oxygen on the catalyst. This caused a reversible decrease in the catalyst activity during combustion testing, and indicated that the oxygen dissociation step was a rate limiting step in the catalytic combustion.     

Synergistic action of Sb2O3 with bromine-containing flame retardant in polyolefins. 1—the variance in their performance versus Sb/Br ratio

The synergistic action of antimony (Sb) with bromine (Br) was studied for polypropylene-2,3-dibromopropylpentabromophenyl ether–Sb₂O₃ systems at various Sb/Br molar ratios. Oxygen index, weight loss rate and heating value were used to evaluate the retardant effect. Bromine and antimony emission and their material balances were measured by gravimetric and X-ray fluorometric analysis of heated samples at each reaction time. Retarded HBr formation in the gaseous phase through SbBr₃, SbOBr and Sb₄O₅Br₂ was proved by X-ray diffraction analysis of heated residues and model products. SbBr₃ and HBr formation were greatest at Sb/Br ratios of 1/3 and 1/4, respectively, while the highest oxygen index and the lowest weight loss rate and heating value were obtained at 1/4. Consequently, HBr will most probably produce the retardant effect rather than SbBr₃. Effective synergistic action at the Sb/Br ratio of 1/4 is explained by presuming the formation of an acidic HBr.SbBr₃ complex in the molten phase for the particular reaction pattern of bromine in 2,3-dibromopropylpentabromophenyl either.     

The role of polyvinyl alcohol in emulsion polymerization

Emulsion polymerization of styrene (St) and vinyl acetate (VAc) in the presence of conventional polyvinyl alcohol (PVA), PVA modified with a terminal alkyl group or PVA modified with a terminal thiol group (HS-PVA) was compared. Whereas stable PVAc latexes were obtained, a stable PSt latex was obtained only in the case of HS-PVA. From the adsorption isotherms of these PVAs on the surface of PVAc and PSt latex particles, as well as the grafting efficiencies of VAc and St onto HS-PVA in relation to the stability of the polymerization process, the role of PVA in the emulsion polymerization was discussed.