Ultrashort X-ray pulse generation using subpicosecond electron linac

As a promising tool for ultrafast material analyses, we propose to utilize the X-ray pulse which may be generated in a quite simple manner using subpicosecond electron linacs. The properties of the X-ray were numerically studied with the EGS4 code. Verification of the X-ray generation was also conducted at the Nuclear Engineering Research Laboratory (NERL) linac and clear diffraction patterns of characteristic X-ray were obtained for typical single crystals.     

The Fusion Science Research Plan for the Major U.S. Tokamaks

This is the May 1996 report of a subpanel of the US Department of Energy Fusion Energy Sciences Advisory Committee (FESAC), charged with conducting a review of the progress, priorities and potential near-term contributions of TFTR, DIII-D and Alcator C-MOD (and other facilities as appropriate) as part of the transition to a Fusion Energy Sciences Program and produce an optimum plan for obtaining the most scientific benefit from them.     

Forecasting electric power generation in a photovoltaic power system for an energy network

Recently, there has been an increase in concern about the global environment. Interest is growing in developing an energy network by which new energy systems such as photovoltaic and fuel cells generate power locally and electrical power and heat are controlled with a communication network. We developed the power generation forecast method for photovoltaic power systems in an energy network. The method makes use of weather information and regression analysis. We carried out forecasting power output of the photovoltaic power system installed in Expo 2005, Aichi Japan. As a result of comparing measurements with prediction values, the average prediction error per day was about 26% of the measured power. © 2009 Wiley Periodicals, Inc. Electr Eng Jpn, 167(4): 16–23, 2009; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20755     

DISTRIBUTION OF N- AND ISO- BUTYRALDEHYDES BETWEEN TRI-N-BUTYL PHOSPHATE/ N-DODECANE AND NITRIC ACID

ABSTRACT

The distribution of n- and iso-butyraldehydes between tri-n-butyl phosphate(TBP) n-dodecane(nDD) and HNO₃ were measured. The distribution ratio of n-butyraldehyde in the TBP/nDD and HNO₃ system was nearly the same as that of iso-butyraldehyde. The distribution ratios of n- and iso-butyraldehydes increased with TBP concentration in the organic phase. The equilibrium constant of the extraction reaction was about 2. In a uranium, neptunium and plutonium separation process, most of the n- and iso-butyra1dehydes fed into theNp separation stepor into thePu/U partition will be left with the TBP solvent. The two compounds will be partly back-extracted to the aqueous phase in the U purification and in the solvent washing steps of the PUREX process.     

Applications of hydrothermal electrolysis for conversion of 1-butanol in wastewater treatment

Hydrothermal electrolysis of organic compound in the presence of electrolyte was conducted for a woody biomass model compound. The reaction behavior of 1-butanol as a woody biomass model compound was studied in subcritical conditions at 200-250 °C and 8-12 MPa with a batch autoclave. The autoclave volume was 500 mL and equipped system with agitation stirrer, electric current control, electric heating and temperature control and a pressure gauge. The chemical species in aqueous products were identified by gas chromatography mass spectrometry (GC-MS) and quantified using gas chromatography flame ionization detector (GC-FID). The gaseous products were analyzed by gas chromatography with a thermal conductivity detector (GC-TCD). The effects of reaction temperature, pressure and applied constant current on the conversion process of 1-butanol were presented. The main products from the conversion of 1-butanol were butanal, butyric acid, hydrogen and carbon dioxide. Additionally, the values of reaction rate constant for butanal and butyric acid formation were calculated at 200 and 250 °C by kinetic study.     

Changes in the amounts of water-soluble umami-related substances in porcine longissimus and biceps femoris muscles during moist heat cooking

Time course changes in amounts of glutamic acid, total free amino acid, inosine monophosphate (IMP), and 2%-trichloroacetic acid-soluble oligopeptides in whole, muscle only, and cooking juice during wet-heat cooking in pork longissimus and biceps femoris muscles were investigated because the movements of umami-relevant substances during cooking treatment had not previously been clarified in detail. The amounts of glutamic acid, total free amino acid, and IMP significantly (P<.05) decreased and increased in muscle and cooking juice during 180min of cooking, respectively. The whole amounts of glutamic acid and total free amino acid remained unchanged during cooking treatment. The whole amount of IMP, however, increased significantly at 10min of cooking (P<.05) and was maintained after the 10-min period. The extramuscular oligopeptides amount increased significantly in response to the cooking treatment (P<.05). The intramuscular amount of oligopeptides decreased at 30min of cooking but increased significantly (P<.05) after 60min. The whole meat oligopeptides amount increased significantly during a 180-min cooking treatment (P<.05). These results indicate that glutamate, total free amino acid, and IMP were released from the muscle during cooking, and that IMP levels increased in the initial phase of cooking. In addition, oligopeptides increased during wet-heat cooking of pork muscles.     

Beneficial effect of carbon–PVA colloid additives for lead–acid batteries

Based on the previous success of adding ultra-fine carbon–PVA (polyvinyl alcohol) colloid solution to restore performance of weak batteries, a large scale test programme of practical batteries including those used in forklift, golf cart, taxi cab, truck and bus applications from 150 companies was carried out. More than 95% of the tested batteries exhibited excellent recovery in performance parameters including the specific gravity (S.G.), voltage and operation time (Ah capacity). The work reported here includes basic research studies to understand better the beneficial action of the carbon–PVA colloid additive.     

Particle arrangement and its application

The method by which micrometer-sized particles are arranged, is described. An electrified pattern is drawn on a polished insulating substrate using a SEM with a CAD facility. The substrate is dipped in a suspension of particles. The particles adhere to the substrate and form the pattern corresponding to the electrified pattern by the electrostatic force. The arranged particles are fixed by coating with a fluoride polymer of thin film. The method is applicable to the production of an inflammable gas sensor.     

Supercritical CO2 extraction of pigment components with pharmaceutical importance from Chlorella vulgaris

BACKGROUND: Chlorella vulgaris is a green microalgae that contains various pigment components of carotenoids and chlorophylls. Supercritical CO₂ is widely used for extraction of pharmaceutical compounds because it is non‐oxic and easily separated from extracted material by simply depressurizing. In this work, pharmaceutical compounds from Chlorella vulgaris have been extracted using supercritical CO₂ with or without entrainer at various extraction conditions. RESULTS: Based on high performance liquid chromatography (HPLC) analysis, the extracts contained pigment components, such as lutein, β‐carotene, chlorophyll a and b. Higher extraction pressure and temperature promoted higher lutein extraction by supercritical CO₂. The optimum pressure and temperature for extraction were obtained as 50 MPa and 80 °C. Ethanol as an entrainer was more effective than acetone for the extraction of pigment components. Pigment components in the extract obtained by supercritical CO₂ with and without entrainer were compared with the extract obtained by a conventional extraction method. CONCLUSION: Supercritical CO₂ has been successfully applied for the extraction of pigment components from Chlorella vulgaris. Supercritical CO₂ enabled high selectivity for lutein extraction; however, the lutein yield was lower than that obtained by extraction using supercritical CO₂ with ethanol and soxhlet. Copyright © 2008 Society of Chemical Industry     

Fundamental welding R&D results for manufacturing vacuum vessel of JT-60SA

The real vacuum vessel (VV) manufacturing of JT-60SA has started since November 2009 at Toshiba. Prior to starting manufacturing, fundamental welding R&Ds had been performed by three stages. In the first stage, primary tests for screening welding method were performed. In the second stage, the trial welding for 1 m-long straight and curved double shell samples were conducted. The dependences of welding quality and distortion on the welding conditions, such as arc voltage and current, setting accuracy, welding sequence, and the shape of grooves were studied. In addition, welding condition with low heat input was explored. In the last stage, fabrication sequence was confirmed and established by the trial manufacturing of the 20° upper half mock-up [1]. This paper presents the R&D results obtained in the first and second stages.