Geothermal resources of Hachijojima

Hachijojima is a gourd-shaped volcanic island in the Pacific Ocean. Nishiyama and Higashiyama volcanoes consist of basalt lava and associated pyroclastic rocks. A promising geothermal resource was found in south Higashiyama, associated with an uplift of Tertiary rocks consisting of mainly andesite lava and related pyroclastic rocks, overlain by Quaternary volcanic rocks. Steep high-temperature (over 250°C) and high-pressure gradients occur in the deeper portion of the system near the Tertiary–Quaternary contact, indicating the presence of a cap rock. The cap rock formed by deposition of hydrothermal minerals. Geothermal fluid ascends from the deeper portions to shallow depths along vertical fractures through the cap rock. These vertical fractures form the geothermal reservoir in the Tertiary formation. Three wells were drilled into these vertical fractures, and approximately 30 t/h of superheated steam was obtained from each well during flow tests. The geothermal fluid is mainly a mixture of seawater and meteoric water in an approximate ratio of 1 to 2, based on chemical analyses, with a portion of volcanic gas included. At present a 3.3 MW_e, geothermal power plant is being constructed here.     

Artifact reduction using reliability reasoning for image generation of FTV

In this paper, we present a new view synthesis method in multiview camera configurations of Free viewpoint TV (FTV) where potential depth errors are considered. The emphasis is on the artifacts eliminating for photorealistic synthesis especially near object boundaries. In contrast to conventional techniques which ignore geometry errors, we first categorize the artifact cases and depth modes. Furthermore, this paper infers the complementarity principle of the artifacts from left and right references. This complementarity guarantees the effectiveness of our reliability-based synthesis. The reliability reasoning is crucial for artifacts reduction. The reliable and unreliable areas from different views can be correctly labeled. Then artifacts caused by unreliable pixels from one reference can be replaced by the reliable pixels from the other reference. As a final result, artifacts of novel view are demonstrated to be significantly reduced on different multiview sequences.     

Kinetic and morphological study of a magnesium ethoxide‐based Ziegler–Natta catalyst for propylene polymerization

BACKGROUND: Kinetic and morphological aspects of slurry propylene polymerization using a MgCl₂‐supported Ziegler–Natta catalyst synthesized from a Mg(OEt)₂ precursor are investigated in comparison with a ball‐milled Ziegler–Natta catalyst. RESULTS: The two types of catalyst show completely different polymerization profiles: mild activation and long‐standing activity with good replication of the catalyst particles for the Mg(OEt)₂‐based catalyst, and rapid activation and deactivation with severe fragmentation of the catalyst particles for the ball‐milled catalyst. The observed differences are discussed in relation to spatial distribution of TiCl₄ on the outermost part and inside of the catalyst particles. CONCLUSION: The Mg(OEt)₂‐based Ziegler–Natta catalyst is believed to show highly stable polymerization activity and good replication because of the uniform titanium distribution all over the catalyst particles. Copyright © 2008 Society of Chemical Industry     

Fischer–Tropsch synthesis in slurry-phase reactors over Mn- and Zr-modified Co/SiO2 catalysts

Fischer–Tropsch (F–T) synthesis was carried out in a gas-flowed slurry-phase reaction system over Mn- and Zr-modified Co/SiO₂ catalysts. A 0.5 L stirred tank slurry reactor (STSR) was used for catalyst screening and a 12.5 L slurry bubble column reactor (SBCR) was used for trial pilot operation. While using the 0.5 L reactor for catalyst screening, Co supported on the SiO₂ with an average pore size of 10 nm showed a high catalytic performance for the F–T synthesis due to the suitable Co particle size in the catalyst. Zr promoter improved the activity and Mn promoter improved the stability of Co/SiO₂ catalyst for the F–T synthesis. H₂-TPR profiles indicated that Zr and Mn promoters improved the reduction degree of Co₃O₄ particles (on SiO₂ surface) to Co⁰ active species in H₂ flow at low temperature. While using the 12.5 L reactor for trial pilot operation over Mn–Zr–Co/SiO₂ catalyst, the space-time yield (STY) of C₅₊ hydrocarbons (liquid fuel) showed almost the same values when various solvents (n-C₁₆H₃₄, n-C₁₄H₃₀, diesel from petrol station, F–T crude oil) were used. Diesel and F–T crude oil are suitable for using in a large-scaled F–T synthesis plant owing to the low prices. Mn–Zr–Co/SiO₂ catalyst achieved a STY of C₅₊ hydrocarbons larger than 1000 g-C₅₊ kg-cat^? 1 h^? 1 in the 12.5 L reactor. The production capacity of liquid fuel from the 12.5 L reactor reached to 15.6 L per day (assumed for 24 h continuous operation). The stirring was very important for the F–T synthesis both reaction in the 0.5 L reactor and reaction in the 12.5 L reactor. The shape of slurry reactor also influenced the CO conversion for the F–T synthesis: reaction in the 12.5 L SBCR gave a higher CO conversion than that of reaction in the 0.5 L STSR (at the same W/F value under the same stirring speed) because the slender column reactor (SBCR) extended the residue time of reaction gas in the slurry-phase containing catalyst.     

A new method of controlling cavity-induced pressure oscillations using sub-cavity

A new passive control technique of cavity-induced pressure oscillations has been investigated numerically for a supersonic two-dimensional flow over open rectangular cavities at Mac h number 1.83 at the cavity entrance. A subcavity on the front wall of the cavity covered by a flat plate was evaluated for the effectiveness of controlling cavity-induced acoustic oscillations. The results showed that sub-cavity is very effective in reducing cavity-induced pressure oscillations. The results also showed that the resultant amount of attenuation of cavity-induced pressure oscillations was dependent on the length and thickness of the flat plate, and also on the depth of the sub-cavity used as an oscillation suppressor.     

Structural,Thermal and Magnetic Properties of Thin Metal Films and Adsorbate–Substrate Systems Studied by XAFS and XMCD

Thin metal films often exhibit interesting properties that are essentially different from the bulk ones. XAFS (X-ray absorption fine structure) and XMCD (X-ray magnetic circular dichroism) techniques are quite suitable to investigate structural, thermal and magnetic properties of thin metal films. In this proceeding, we will present following two topics concerning structural and magnetic properties of adsorbates on thin metal films. The first one is the adsorption geometry of SO₂ on a 1-monolayer (ML) Pd thin film grown on a Ni(111) single crystal. It was found by S K-edge XAFS that SO₂ is lying flat on 1-ML Pd/Ni(111). This result is not similar to the bulk Pd surface but to the bulk Ni one. This finding indicates significant modification of the electronic structure of the 1-ML Pd film compared to the bulk one. The second topic is the magnetic moment induced on CO adsorbed on Ni epitaxial films grown on Cu(001). The O K-edge XMCD results revealed that in the perpendicularly magnetized 10-ML Ni film the orbital moment of CO is parallel to the substrate Ni magnetization, while it is antiparallel in the in-planar magnetized 6-ML and thick (>100 ML) films. The origin of the induced orbital moment at CO is discussed.     

Vibrational Spectroscopic Study of Structural Evolution in the Coprecipitated Precursors to La2Sn2O7 and La2Ti2O7

Structural evolution in the X-ray amorphous precursors to La₂Sn₂O₇ and La₂Ti₂O₇ is examined using IR and Raman spectroscopy. These precursors are prepared by rapid coprecipitation from mixed aqueous solutions of the corresponding metal chlorides. Rapid coprecipitation from an SnCl²⁻₆ and La³⁺-containing aqueous solution yields microcrystalline particles of SnO₂· n H₂O and La(OH)₃, which instantaneously interconnect to form an ultimate, complex colloid particle. The Ti(OH)²⁺₂ and La³⁺ in the other solution system coprecipitate into a different, complex colloid (an unidentified phase), which is definitely not a mixed dispersion of single-component colloids. A comparative examination of the vibrational spectra of the coprecipitates heated to various temperatures indicates that the SnO₂ and anatase phases develop in the respective precursors before crystallization of the desired double oxides. Crystallization itself can be attributed to a solid-state reaction among the various microcrystallites of each single-metal oxide in a gel particle of the precursor.     

Effects of the degree of unsaturation of coexisting triacylglycerols on cholesterol oxidation

In order to evaluate the effects of the degree of unsaturation of triacylglycerols on cholesterol oxidation, mixtures of purified sardine oil triacylglycerols (iodine value, IV=182.6) and cholesterol; of partially hydrogenated sardine oil triacylglycerols (IV=174.5) and cholesterol; and of fully hydrogenated sardine oil triacylglycerols (IV=92.0) and cholesterol were incubated at 25°C in the dark. The oxidative stability of the samples decreased with increasing degree of unsaturation of the triacylglycerols in the sample mixtures; the induction period for peroxide values (PV) of the sardine oil triacylglycerols and cholesterol was shorter than that of the partially hydrogenated sardine oil triacylglycerols and cholesterol. Certain polyunsaturated fatty acids (PUFAs) in the constituent fatty acids of sardine oil triacylglycerols started to decrease after a shorter induction period compared with that of the partially hydrogenated triacylglycerols. The prominent cholesterol oxides accumulated in the samples were 7β-hydroxycholesterol, 7-ketocholesterol, β-epoxide and cholestane triol. The tendency for accumulation of cholesterol oxides in the time course coincided with the changes in PV as well as the decrease in PUFAs. Cholesterol was oxidized in conjunction with autoxidation of coexisting fish oil triacylglycerols. Although lowering the degree of unsaturation of fish oil triacylglycerols was effective in prolonging the induction period of cholesterol oxidation, the rate of cholesterol oxidation in the cholesterol oxides' formation phase after the induction period was not affected by the difference in the proportion of highly unsaturated fatty acids in the natural and partially hydrogenated triacylglycerols of fish oils.     

Terpendole E and its Derivative Inhibit STLC‐ and GSK‐1‐Resistant Eg5

Terpendole E is first natural product found to inhibit mitotic kinesin Eg5, but its inhibitory mechanism remains to be revealed. Here, we report the effects of terpendole E and 11ketopaspaline (a new natural terpendole E analogue) on the Eg5–microtubule interaction and in several Eg5 mutants. 11‐Ketopaspaline is a shunt product from terpendole E, and it shows potent inhibitory activity against the microtubule‐stimulated ATPase activity of Eg5. Unlike other Eg5 inhibitors, such as S‐trityl‐L ‐cysteine (STLC) and GSK‐1, both terpendole E and 11‐ketopaspaline only partially inhibited Eg5–microtubule interaction. Furthermore, terpendole E and 11‐ketopaspaline inhibited several Eg5 mutants that are resistant to STLC (Eg5^D130A, Eg5^L214A) or GSK‐1 (Eg5^I299F, Eg5^A356T), but with the same extent of inhibition against wild‐type Eg5. Because Eg5^D130A and Eg5^L214A show cross‐resistance to most known Eg5 inhibitors, which bind the L5 loop, these results suggest that terpendole E and its analogues have a different binding site and/or inhibitory mechanism to those for L5 loop‐binding type Eg5 inhibitors.