Phase study on solid fission products,Ba, Sr and Zr in oxide fuel

Behavior of pseudo-fission products (Ba, Sr, and Zr) as oxides in UO₂ has been investigated by means of high-temperature X-ray diffraction and microprobe analysis. Two identifiable compounds were formed as reaction products in the mixed oxides which initially consisted of UO₂, BaO, SrO, and ZrO₂ powder. These compounds were present and were identified crystallographically as (Ba, Sr) ZrO₃ and (Ba, Sr)UO₃ after heat treatment of the powders at 1500°C for 30 min. Both compounds are isostructural with perovskite, CaTiO₃, and the lattice parameters of both (Ba, Sr)ZrO₃ and (Ba, Sr)UO₃ decrease with increasing content of Sr. (Ba, Sr)UO₃ is decomposed almost completely at 1800°C while (Ba, Sr) ZrO₃ is stable up to 2000°C. The behavior of Ba, Sr, and Zr in fuel under irradiation is discussed.     

Rheological interpretation of heat generation associated with fatigue of polycarbonate

Temperature change was measured of polycarbonate under monotonically increasing tensile and pulsating tensile loads. In the former case, the specimen temperature began to rise when an appreciable amount of viscoelastic strain was noticed on the stress—strain diagram. The rise, θ_v, could be formulated as a function of the viscoelastic strain, εv: In fatigue tests, the average temperature began to rise immediately after the decrease due to the thermoelastic effect. The amount of the heat generation, σ, was nearly constant for each cycle throughout the fatigue process and has a relation to the fatigue life, N_f, (α? a)·N_f = constant, where a is another adjustable constant. From a rheological aspect of dissipation energy, the equation is transformed to a relation between the viscoelastic strain and the fatigue life as εV^1/2 · N_f = constant, which is similar to the one for metals given by Manson and Coffin.⁶ The temperature rise in the fatigue was also related to the viscoelastic strain. The relation is of the same form as for static tension but less by a factor of one order.     

Ultrasonic-assisted pH Swing Method for the Synthesis of Highly Efficient TiO2 Nano-size Photocatalysts

A new route for the preparation of nanocrystalline TiO₂ particles based on the pH swing method assisted by ultrasonic irradiation in the presence of a surfactant (Pluronic P-123) has been successfully achieved. The prepared TiO₂ catalysts were calcined from 400 to 800 °C and characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transformed infra-red spectroscopy (FTIR), gas adsorption measurements (BET) and thermogravimetirc measurements (TAG/DTA) analyses. Characterization results revealed that the enhancement in the particle size of TiO₂ by the pH swing method could be controlled by combining the pH swing with ultrasonic irradiation. Increasing the calcination temperatures led to an increase in both the particle and pore size, whereas the surface area and pore volume gradually decreased. A synergistic effect was observed in the combined process of pH swing with ultrasonication, yielding small TiO₂ particles as well as high surface area, pore volume, pore diameter, and crystalline anatase phase. The activity of the catalysts was investigated for the oxidation of 4-chlorophenol (4-CP). TiO₂ prepared with 15 times pH swing and calcined at 700 °C was found to show the highest rate for the oxidative degradation of 4-CP when compared to the TiO₂ sample prepared with just 1 time pH swing and to the commercial P-25 TiO₂ Degussa photocatalyst. Thus, a novel approach in controlling the various physico-chemical parameters of TiO₂ nanoparticles was developed.     

Study on chemical structures of poly (tetrafluoroethylene-co-perfluoroalkylvinylether) by soft-EB irradiation in solid and molten state

Poly (tetrafluoroethylene-co-perfluoroalkylvinylether) (PFA) was irradiated by soft electron beam (soft-EB) under nitrogen gas atmosphere in solid-state and its molten state, respectively. The changes of thermal property and chemical structures of irradiated PFA in solid-state and molten state were studied by differential scanning calorimetric analysis (DSC) and solid-state ¹⁹F magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. By DSC analysis, the melting temperature shifted to lower temperatures, and crystallinity decreased with increasing soft-EB dose. By solid-state ¹⁹F MAS NMR spectroscopy, the new signals was observed and the detected new signals in irradiated PFA at 315 °C and at 30 °C were due to the tertiary carbon group with branching site (Y-type crosslinking site), perfluoro-propylene site and chain end methylene groups, respectively.Moreover, the molar ratio of perfluoroalkylvinylether (FAVE) structure to -CF₂- units decreased with increasing dose.     

An application of the 2-nitrobenzenesulfenyl method to proteomic profiling of human colorectal carcinoma: A novel approach for biomarker discovery

In the development of novel biomarkers, the proteomic approach is advantageous because using it the cancer-associated proteins can be directly identified. We previously developed a 2-nitrobenzenesulfenyl (NBS) method to improve quantitative proteome analysis. Here, we applied this method to proteomic profiling of colorectal carcinoma (CRC) to identify novel proteins with altered expression in CRC. Each pair of tumor and normal tissue specimens from 12 CRC patients was analyzed, and approximately 5000 NBS-labeled paired peaks were quantified. Peaks with altered signal intensities (>1.5-fold) and occurring frequently in the samples (>70%) were selected, and 128 proteins were identified by MS/MS analyses as differentially expressed proteins in CRC tissues. Many proteins were newly revealed to be CRC related; 30 were reported in earlier studies of CRC. Six proteins that were up-regulated in CRC (ZYX, RAN, RCN1, AHCY, LGALS1, and VIM) were further characterized and validated by Western blot and immunohistochemistry. All six were found to be CRC-localized, either in cancer cells or in stroma cells near the cancer cells. These results indicate that the proteins identified in this study are novel candidates for CRC markers, and that the NBS method is useful in proteome mining to discover novel biomarkers.     

Low cycle fatigue behaviors of elbow pipe with local wall thinning

Low cycle fatigue tests were conducted using 100A elbow specimens made of STPT410 carbon steel with local wall thinning. Local wall thinning by erosion/corrosion was simulated by machined pipe wall thinning. The local wall thinning areas were located at three different areas, called extrados, crown and intrados. The elbow specimens were subjected to cyclic in-plane bending under displacement control without internal pressure. The effects of eroded conditions, such as eroded ratio, eroded angle and position, on the low cycle fatigue behavior and fatigue life were discussed by using experimental results and finite element analyses. Also the location of crack initiation and the crack growth direction could be predicted by three dimensional elasto-plastic finite element analyses. In addition, the safety margin of eroded elbows against seismic loading was discussed by comparing the fictitious stress of elbows with the allowable stress limit demanded by the design code.     

THz-wave absorption by field-induced carriers in pentacene thin-film transistors for THz imaging sensors

Innovative sensing systems based on THz electromagnetic waves have been attracting a great deal of attention. Although many THz detectors have been developed over the years, it is currently difficult to manufacture low-cost THz sensing/imaging devices. In the present study, we propose to use organic field-effect transistors (OFETs) and small potential fluctuation against the carriers within them (N. Ohashi, H. Tomii, R. Matsubara, M. Sakai, K. Kudo, M. Nakamura, Appl. Phys. Lett. 91 (2007) 162105). We use THz time-domain spectroscopy for OFETs in which the carrier density in the pentacene active layer is modulated by the gate bias. We found evidence that the accumulated free holes in pentacene films can be excited by THz photons to overcome the surrounding barriers in the fluctuating potential. The Drude–Lorentz model could not account for the shape of the absorption spectra, which suggests that the holes are weakly restricted by the potential fluctuation. The integrated absorption intensity was proportional to the transfer characteristics of the OFETs. The present findings represent an important step toward developing a new class of THz-wave sensors.     

Electrical Breakdown Properties and Space Charge Formation in High Temperature Region in Ultraviolet Ray Irradiated PVC

Polyvinyl chloride (PVC) is the most popular insulating material for electric wiring instruments. However, an exothermic reaction above 150 °C may cause deterioration of the insulating properties of PVC. Therefore, it is important to clarify the heat degradation in PVC, not only to investigate the ignition of electrical wiring products but also to use electrical products safely. It is known that ultraviolet (UV) irradiation causes chemical deterioration of PVC and an increase in its conductivity. Generally, it has been thought that the electrical breakdown properties, electrical conduction, and insulating performance are affected by space charge accumulation in an insulating material. A high temperature pulsed electroacoustic (PEA) system usable up to 250 °C has been developed, and the PEA system can measure the space charge distribution and conduction current in the high temperature range simultaneously. In this investigation, the space charge distribution and conduction current were measured up to electrical breakdown in a non‐UV irradiated sample (normal PVC) and in 353 nm and 253 nm UV‐irradiated PVC samples in the range from room temperature to 200 °C in a DC electric field. In the short wavelength UV irradiated PVC sample (253 nm, 300 h), a deterioration of breakdown strength at 90 °C to 150 °C and negative packet‐like charges were observed at 60 °C and 100 °C, a positive charge accumulated in front of both the anode and cathode above 90 °C, and a higher electric field near the cathode side because the positive charge of the cathode side was greater.