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Sample records for rutenium tanji shokubai

  1. Hydrogenation of heteroaromatics by high pressure DTA techniques. 3; Koatsu DTA ho ni yoru hokozoku kagobutsu no suisoka (rutenium tanji shokubai ni yoru kakusuisoka datsu hetero hanno)

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    Yamamoto, M.; Yoshida, T. [Hokkaido National Industrial Research Institute, Sapporo (Japan); Kotanigawa, T. [Japan International Cooperation Agency, Tokyo (Japan)

    1996-10-28

    Ring-opening of heteroaromatics and heteroatom-removal reaction were studied experimentally using the acidic catalyst containing phosphoric acid for improvement of an upgrading method of coal derived oils. In experiment, some Ru-carrying metal oxide catalysts such as RMZ, RML and RMN catalyst, and MNP catalyst containing phosphoric acid were used as specimens. Nuclear hydrogenation reaction and hydro-denitrogenation reaction of dibenzothiophene and carbazole were compared with each other. The experimental results are as follows. Both RMN and RMNP catalysts offer a superior selectivity in nuclear hydrogenation reaction and hydro-denitrogenation reaction of carbazole. Although both catalysts offer an extremely high nuclear hydrogenation activity at 360{degree}C, these offer the high selectivity of denitrogenation products at 430{degree}C. In comparison of the activities of MN and MNP catalysts with the same Mn2O3:NiO ratio, MNP catalyst offers the higher denitrogenation activity than MN catalyst at 430{degree}C. 1 ref., 3 tabs.

  2. Influences of species of metals and supports on the hydrogenation activity of carbon-supported metal sulfides catalysts; Tanso biryushi tanji shokubai no suisoka kassei ni taisuru kassei kinzoku oyobi tantaishu no eikyo

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    Sakanishi, K.; Hasuo, H.; Taniguchi, H.; Nagamatsu, T.; Mochida, I. [Kyushu University, Fukuoka (Japan). Institute of Advanced Material Study

    1996-10-28

    In order to design catalysts suitable for primary liquefaction stage and secondary upgrading stage respectively in the multi-stage liquefaction process, various carbon-supported catalysts were prepared. Catalytic activities of them were investigated for the hydrogenation of 1-methylnaphthalene, to discuss the influences of metals and carbon species on the catalytic activity. Various water soluble and oil soluble Mo and Ni salts were used for NiMo supported catalysts. Among various carbon supports, Ketjen Black (KB) was effective for preparing the catalyst showing the most excellent hydrogenation activity. The KB and Black Pearl 2000 (BP2000) showing high hydrogenation activity were fine particles having high specific surface area more than 1000 m{sup 2}/g and primary particle diameter around 30 nm. This was inferred to contribute to the high dispersion support of active metals. Since such fine particles of carbon exhibited hydrophobic surface, they were suitable for preparing catalysts from the methanol-soluble metals. Although Ni and Mo added iron-based catalysts provided lower aromatic hydrogenation activity, they exhibited liquefaction activity competing with the NiMo/KB catalyst. 3 refs., 1 fig., 3 tabs.

  3. Photo catalyst; Ko shokubai

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    NONE

    1999-07-01

    While titanium oxide is excited by the light, electrons of titanium oxide are taken away by the light energy to form positive holes. Water will be decomposed into hydrogen ion and hydroxy radical (OH) by these positive holes. This hydroxy radical is a strong reactive substance called active oxygen, it decomposes organisms. Besides this photo- catalyst function, the titanium oxide can also make surface of a substance superhydrophilic. The super hydrophilicity results in not forming water drops on the glass surface but spreading all over the surface to prevent a covering of fog on the glass surface. The published patents concerning the photo catalysts were 593 from Jan. 1998 to Jan. 1999. The applicant order is the first TOTO 143, the second Daikin Industry 19, the third Toshiba Raitech, Nitto Denko, Hitachi 17 respectively. (NEDO)

  4. Deodorant ceramic catalyst. Dasshu ceramics shokubai

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    Arai, K. (Kobe Steel Ltd., Kobe (Japan)); Naka, R. (Hitachi Ltd., Tokyo (Japan))

    1993-07-01

    Concerning debromination to be used for the filter of deodorizing device, those of long life and high deodorizing performance are demanded a great deal. As one of this kind of debromination, a deodorant ceramic catalyst (mangantid) has been developed and put for practical use as deodorant for refrigerator. In this article, the information and knowledge obtained by the development of mangantid, the features as well as several properties of the product are stated. The deodorizing methods currently used practically are roughly divided into 6 kinds such as the adsorption method, the direct combustion method, the catalytic method and the oxidation method, but each of them has its own merit and demerit, hence it is necessary to select the method in accordance with the kind of odor and its generating condition. Mangantid is a compound body of high deodorant material in a honeycomb configuration, and has the features that in comparison with the existing deordorants, its pressure loss is smaller, its deodorizing rate is bigger, and acidic, neutral and basic gaseous components can be removed in a well-balanced manner. Deodorization with mangantid has the mechanism to let the odorous component contact and react with the catalyst and change the component to the non-odorous component in the temperature range from room temperature to the low temperature region. 5 refs., 11 figs., 1 tab.

  5. Studies of structure change of iron sulfates and its catalysis; Ryusantetsukei shokubai no kozo henka to sono shokubai sayo

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    Ogata, E.; Horie, K. [The University of Tokyo, Tokyo (Japan). Faculty of Engineering; Nishijima, A. [National Institute of Materials and Chemical Research, Tsukuba (Japan)

    1996-10-28

    Since a huge amount of coal containing inorganic ash is treated for the commercial hydroliquefaction process, cheap catalysts widely distributing on the earth with large reserves are desired rather than expensive catalysts. This paper describes the effects of addition of sulfur on the catalysis of iron sulfates during the hydroconversion of 1-methylnaphthalene (1-MN). Reactions of 1-MN were conducted at the same charging amount of iron in the reaction system. Sulfur was directly added in the reaction system using ferrous sulfate (FeSO4) as precursor. Consequently, it was found that FeSO4 provides lower but similar catalytic activity to the synthetic pyrite catalyst prepared through the complex processes with the precise control. Thus, it was revealed that high performance pyrrhotite (Fe(1-x)S) catalyst can be prepared for the hydrogenation of aromatic-rings by adding solid sulfur into the reaction system using commercial reagent, FeSO4 as a precursor of the catalyst. 9 figs.

  6. Mesoporous activated carbons with metal-oxide particles prepared from Morwell coal; Morwell tan wo genryo to shita kinzoku sankabutsu tanji kasseitan no saiko kozo

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    Yoshizawa, N.; Yamada, Y.; Shiraishi, M. [National Institute for Resources and Environment, Tsukuba (Japan); Kojima, S.; Tamai, H.; Yasuda, H. [Hiroshima University, Hiroshima (Japan). Faculty of Engineering

    1996-10-28

    The metal dependence of mesoporous activated carbons with various metal acetylacetonate (acac) particles prepared from Morwell coal was studied. In experiment, the mixture of Morwell coal and acac metal complexes were dissipated into tetrahydrofuran, and after agitation in Ar atmosphere, the solvent was removed by vacuum distillation. Coal specimens with Fe(acac)3, Ni(acac)2 and Co(acac)2 as acac complexes were activated by exchanging flow gas with water vapor after heat treatment in N2 gas flow at 900{degree}C. The pore sizes of the specimens were obtained from N2 adsorption isotherms by BET method and BJH method. Conditions of pores and metals in the specimens were examined by XRD measurement and TEM observation. The relation between the above conditions and pore characteristics obtained from adsorption experiment was also examined. As a result, the difference in mesopore ratio between the specimens and blank specimens was larger in the order of Fe, Co and Ni, and the effect of added metal complexes was also larger in this order. 3 refs., 3 figs., 3 tabs.

  7. Change in catalyst properties during coal liquefaction; Kokoritsu sekitan ekika shokubai no kaihatsu (Hanno no shinko ni tomonau shokubai seijo no henka). 1

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    Koyama, T.; Sato, K.; Kaneko, T.; Shimasaki, K. [Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan)

    1996-10-28

    The purpose of this study is to prevent the deactivation of catalysts recycled in the 0.1 t/d bench scale unit (BSU). Catalysts recovered during reactions in the BSU and after reactions in the 5-liter autoclave were analyzed, to investigate the influences of the reaction condition on the property and activity of catalysts. Were used {gamma}-iron oxyhydroxide ({gamma}-FeOOH), {alpha}-iron oxyhydroxide ({alpha}-FeOOH), and natural pyrite (FeS2) as catalysts. At the S/Fe atomic ration of 1.2 under the BSU reaction condition, troilite was more easily formed from {gamma}-FeOOH compared with pyrite and {alpha}-FeOOH. As the reaction proceeded through the first, second, and third reactors, the crystal size increased, the pyrrhotite content decreased, and the troilite content increased. Deactivation due to the formation of troilite was irreversible. At the S/Fe of 3.0, however, both the formation of troilite and the crystal growth of pyrrhotite were not observed. It was found that the deactivation of catalysts can be remarkably suppressed. 5 refs., 6 figs., 1 tab.

  8. Mechanism of pyrrhotite formation from ferric oxyhydroxide catalyst; Kokoritsu sekitan ekika shokubai no kaihatsu (Okishi suisankatetsu shokubai karano pyrrhotite seisei kyodo)

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    Tazawa, K.; Koyama, T.; Kaneko, T.; Shimasaki, K. [Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan)

    1996-10-28

    It is thought that iron-based catalysts for coal liquefaction exercise their catalytic activity by forming pyrrhotite (Fe(1-x)S). However, there are still a lot of unknown problems remained concerning the formation and agglomeration behaviors of pyrrhotite. These make a difficulty for improving the activity of iron-based catalysts. In this study, sulfiding behaviors of {alpha}-iron oxyhydroxide ({alpha}-FeOOH) and {gamma}-iron oxyhydroxide ({gamma}-FeOOH) were investigated to reveal the formation and agglomeration behaviors of pyrrhotite. It was found that pyrrhotite was easily converted from ferric oxyhydroxide catalysts having large specific surface areas at the sulfiding temperature below 250{degree}C, and fine crystallites of pyrrhotite were formed at the initial stage of sulfiding. Crystal growth of pyrrhotite at the sulfiding temperature over 350{degree}C depended on the catalyst forms. It was also found that smaller crystallites of pyrrhotite were formed from {gamma}-FeOOH than from {alpha}-FeOOH and amorphous iron oxyhydroxide. 5 refs., 7 figs., 1 tab.

  9. Air environment purification using photocatalyst. Hikari shokubai ni yoru taiki kankyo joka

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    Takeuchi, K [National Institute for Resources and Environment, Tsukuba (Japan)

    1993-12-02

    Noticing that metal oxides have photocatalysis for reduction in NOx concentration and examining effects of the TiO2 selected on removal of pollutant, the paper proposes a direct purification method for the air environment. Since TiO2 causes electron excitation meeting near ultraviolet irradiation, it manifests a catalytic function for various oxidation/reduction reactions. Details of the reaction mechanism are unknown, various active oxygen species generated on the surface of TiO2 under light irradiation oxidize NOx and acquire it as nitric acid on the surface. It is found that mixture of activated carbon of low hygroscopicity with TiO2 is effective to prevent a tendency of NO to desorb before NO becomes nitric acid. What 40% of the catalyst with fluorine resin is formed into like a sheet shows a high removal rate even in the amount of ultraviolet irradiation in a winter cloudy day in the wide range of 0.5 - 95.0% of NOx and SO2, and if the photocatalyst is applied to the side wall of city buildings, the NOx concentration is estimated to be reduced by as much as 20%. 5 refs., 3 figs.

  10. Catalytic activity of pyrite for coal liquefaction reaction; Tennen pyrite no shokubai seino ni kansuru kento

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    Hirano, K.; Kozu, M.; Okada, T.; Kobayashi, M. [Nippon Coal Oil Co. Ltd., Tokyo (Japan)

    1996-10-28

    Since natural pyrite is easy to obtain and cheap as coal liquefaction catalyst, it is to be used for the 150 t/d scale NEDOL process bituminous coal liquefaction pilot plant. NEDO and NCOL have investigated the improvement of catalytic activity of pulverized natural pyrite for enhancing performance and economy of the NEDOL process. In this study, coal liquefaction tests were conducted using natural pyrite catalyst pulverized by dry-type bowl mill under nitrogen atmosphere. Mechanism of catalytic reaction of the natural pyrite was discussed from relations between properties of the catalyst and liquefaction product. The natural pyrite provided an activity to transfer gaseous hydrogen into the liquefaction product. It was considered that pulverized pyrite promotes the hydrogenation reaction of asphaltene because pulverization increases its contact rate with reactant and the amount of active points on its surface. It was inferred that catalytic activity of pyrite is affected greatly by the chemical state of Fe and S on its surface. 3 refs., 4 figs., 1 tab.

  11. Development of catalyst for diesel engine; Diesel engine yo shokubai no kaihatsu

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    Ueno, H; Furutani, T; Nagami, T [Toyota Motor Corp., Aichi (Japan); Aono, N; Goshima, H; Kasahara, K [Cataler Industrial Co. Ltd., Shizuoka (Japan)

    1997-10-01

    The new concept catalyst for diesel engine has been developed. When the exhaust temperature is low, SOF and HC are temporarily adsorbed by the adsorbent within the catalyst and are oxidized as the temperature rise. The process of this development have manifested as follows. (1) The coating material is important factor to govern the oxidation activity. (2) SOF is reduced by the coating material in low temperature less than 200degC. (3) The coating material, which has low SO2 adsorbing rate suppress the sulfate formation at high temperature. 2 refs., 11 figs., 1 tab.

  12. Development of super thin foil metal supported catalyst; Chousuhaku metal tantai shokubai no kaihatsu

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    Sanji, F; Takada, T [Toyota Motor Corp., Aichi (Japan)

    1997-10-01

    In order to improve warm-up performance, high heat resistance and long life durability of catalysts, the reduction of the metal support heat capacity has been focused. The effects of both reducing foil thickness and lowering cell density on low heat capacity have been investigated. As a result of engine bench and vehicle test, it was apparent that the reduction of foil thickness has greater effects. Newly developed 30 {mu} m foil thickness metal supported catalyst has quicker warm-up performance, and its structural durability up to 950degC is confirmed. 3 refs., 11 figs., 1 tab.

  13. Development of low light-off catalyst; Teion kassei ni sugureta shokubai no kaihatsu

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    Takemoto, T; Ichikawa, S; Koda, Y; Yamamoto, E; Sumida, H; Yamada, H; Shigetsu, M; Komatsu, K [Mazda Motor Corp., Tokyo (Japan)

    1997-10-01

    A new type of three way catalyst was developed in order to reduce HC, CO and NOx in cold exhaust gas. This catalyst consists of double layer, and has a base support material of alumina and oxygen storage components (OSC) loaded with active metals including platinum. palladium and rhodium. It has good light-off performance and high catalytic activity. This catalyst includes two types of OSC. One is CeO2, and the other is CePrO2 that makes possible to improve NOx conversion at high exhaust gas temperature. 8 refs., 13 figs., 2 tabs.

  14. Artificial control of biocatalytic reaction; Seitai shokubai hanno no jin`iteki seigyo

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    Nakamura, K. [Kyoto University, Kyoto (Japan). Institute for Chemical Research

    1997-08-25

    Selective composition of optically active compounds by use of biocatalysts is discussed. No search is made for any particular microbes or enzymes, but predetermined ones are used. For an increase in the selective yield of L-type carnitine by reducing 4-chloroacetoacetic acid ester using baker`s yeast, the ester length should be enlarged to that of octyl ester. Just as in this case, steric control by ground substance modification is often effective. Lipase helps on esterification which is contrary to hydrolysis in an organic solvent and, even in the optical division in this process, steric control by ground substance modification (for example by changing the structure of the acyl section) is effective. Immobilization of biocatalysts for use in reaction occasionally exerts some effect on stereoselectivity. Two types of enzymes may be participating in a reaction and inhibiting selectivity, and then a two-layer system of water and organic solvent may be effective in performing steric control over the situation. Another measure is to inhibit the activity of either of the two enzymes by use of a selective inhibitor utilizing enzyme reaction. The kind of solvent is also an influential factor. 11 refs., 7 figs.

  15. Application of photocatalysts for amenities; Kaiteki kukan no tameno hikari shokubai

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    Sugawara, T. [Akita Univ., Akita (Japan). Mining College

    1996-03-01

    Catalysts with strong decomposing power are necessary in removing the stink of toilets and diapers, the smoke of cigarettes, lampblack in kitchens and mold in bathrooms etc. One of such catalysts attracting attention is titania (Ti02) photocatalyst. Titania has a strong oxidizing force due to its ability to absorb light with a wavelength under 400nm, and meanwhile this substance itself is chemically stable and tender to environment. In this paper, simultaneously with the introduction of the design examples applying the performance and properties of such catalysts, the evaluation on the performance of utility photocatalysts is described. The examples of using tiles with titania coated on ceramic tiles and the photocatalysts obtained by fixing supermicro-particles of titania catalysts with fluorine resin as a binder to decompose the oil vapor near a ventilation fan above a kitchen range and the tobacco tar whose concentration level is as in a living room are introduced as the design examples of utility photocatalysts. 13 refs., 6 figs.

  16. Report of liquefaction catalyst study meeting (March 1996); Ekika shokubai kentokai hokoku

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    NONE

    1996-03-01

    Studied in the research are four iron-based catalysts, which are natural pyrite, synthetic iron sulfide, synthetic iron hydroxide, and catalyst-attached carbon. Tanito Harum coal is treated in a 0.01t/d-capable continuous operation furnace (once-through) under conditions of 450 degrees C and 170kgf/cm{sup 2} with catalyst addition of 1.0, 3.0wt% (catalyst-attached carbon 0.6, 1.0wt%), and a liquid yield of 41.5-48.6wt%-daf coal is achieved. A higher yield results when more catalyst is added. The same yield as achieved by the addition of 3wt% natural pyrite is obtained by the addition of 1.9wt% synthetic iron sulfide, 1.5wt% of synthetic iron hydroxide, or 0.7wt% catalyst-attached coal. The catalyst cost for treating a ton of coal is 4-9 hundred yen, which is far more expensive than the cost set forth as the target. Catalysts whose production process embodiment is now under study are natural pyrite and synthetic iron sulfide, and studies for others are just preliminary. Provided that the practical application of the liquefaction technology realizes in about 2000, then the petroleum price is predicted to be 23 dollars per barrel. Coal liquefaction products will have to be produced at a cost which will enable competition with the said petroleum price. (NEDO)

  17. Catalyst surface characterized by high magnetic field NMR; Kojiba NMR ni yoru shokubai hyomen no kansatsu

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    Sato, S. [Chiba University, Chiba (Japan). Faculty of Engineering

    1997-08-01

    This paper introduces studies performed by the authors on observation of surface of solid catalysts by means of solid NMR measurement using the high-speed MAS technology which uses a high magnetic field device. In the studies, a device with 14.1T (resonant frequency of proton at 600 MHz) was used to conduct CP-MAS NMR measurement on {sup 29}Si to identify bonding of silica carrier in a fixed aluminum chloride catalyst. As a result, it was verified that the surface structure of aluminum chloride species deposited on the silica carrier turns to a structure in which AlCl2 species of a monomeric substance is bonded with a surface hydroxyl group and fixed in four- or five-orientation. When adjusted at low temperatures, an Al2Cl5 structure is formed, which is fixed as a dimeric substance with AlCl3 oriented in the AlCl2 species. It is conceived that the Al2Cl5 species has higher electrophilicity than the AlCl2 species as a result of AlCl3 oriented in AlCl2, whereas the hydroxyl group on the silica surface oriented with the Al2Cl5 species dissociates, discharging protons, thus showing strong acidity. 18 refs., 8 figs., 2 tabs.

  18. Studies on the catalysts for coal liquefaction. ; Specific behaviours of coals of different ranks in their hydrogenolysis reactions catalyzed by various kinds of catalysts. Sekitan ekikayo shokubai ni kansuru kenkyu. ; Suisoka bunkai seiseibutsu sosei ni oyobosu kakushu shokubai no koka

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    Takechi, Y; Ikenaga, N; Oda, H; Yokokawa, C [Kansai University, Osaka (Japan). Faculty of Engineering

    1991-11-07

    Three kinds of coals with different rank of 76, 85 and 87C% were hydrocracked to study the specific reaction behavior of four kinds of 1coal liquefaction catalysts such as CuCrO4, Fe2O3+S, MoO3-TiO2 and MoS3-Al2O3. The reaction was conducted without any solvent to find out the specific phenomenon of each combination of coal and catalyst, and terminated at the point where nearly 30% of an initial amount of coal is converted to benzene-soluble. The products were separated by GPC into four fractions, and their average molecular weights and intrinsic viscosities were measured to study characteristics of each combination. As a result, the molecular weight distribution was obviously dependent on the combination of coal and catalyst, and no specific relation was observed between the molecular weight and intrinsic viscosity. The molecular of each fraction had a bar shape with an elliptic section indicating no apparent correlation with the molecular weight. 3 refs., 1 figs., 2 tabs.

  19. Catalytic technology in the energy/environment field. Utilization of catalyst in coal pyrolysis and gasification processes; Energy kankyo bun`ya ni okeru shokubai gijutsu. Sekitan no netsubunkai oyobi gas ka ni okeru shokubai no riyo

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    Otsuka, Y. [Tohoku University, Institute for Chemical Reaction Science (Japan)

    1998-05-20

    This review article focuses on the utilization of several catalysts during coal pyrolysis and gasification. In situ or off line catalytic upgrading of volatile matters during pyrolysis of low rank coals is carried out in pressurized H2 with different reactors to produce BTX (benzene, toluene and xylene). When NiSO4 and Ni(OH)2 are used in the hydropyrolysis of Australian brown coal using an entrained bed reactor with two separated reaction zones, BTX yield reaches 18-23%. MS-13X zeolite and USY zeolite mixed with Al2O3 are effective for producing BTX with powder-particle fluidized bed and two-stage reactors, respectively. Catalytic gasification is described from a standpoint of direct production of SNG(CH4) from coal and steam. When K2CO3 and Ni are compared for this purpose, Ni catalyst is more suitable at low temperatures of 500-600degC, where CH4 formation is thermodynamically favorable. Fe and Ca catalysts can successfully be prepared from inexpensive raw materials and are rather active for steam gasification at {>=}700degC. The use of upgrading and gasification catalysts is discussed in terms of preparation, performance, life and recovery. 27 refs., 6 figs., 2 tabs.

  20. Behavior of catalyst and mineral matter in coal liquefaction; Sekitan ekika hannochu no kobusshitsu to shokubai no kyodo

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    Iwasaki, K.; Wang, J.; Tomita, A. [Tohoku University, Sendai (Japan). Institute for Chemical Reaction Science

    1996-10-28

    Mineral matter in coals is important in various senses for coal liquefaction. It is possible that the catalytic activity is affected by the interaction between catalyst and mineral matter. Iron-based catalyst forms pyrrhotite in the process of liquefaction, but the interaction between it and mineral matter is not known in detail. In this study, the interaction between mineral matter and catalyst and the selective reaction between them were investigated. Tanito Harum coal was used for this study. This coal contains a slight amount of siderite and jarosite besides pyrite as iron compounds. Liquefaction samples were obtained from the 1 t/d NEDOL process PSU. The solid deposits in the reactor mainly contained pyrrhotite and quartz. A slight amount of kaolinite was observed, and pyrite was little remained. It was found that the catalyst (pyrrhotite) often coexisted with quartz, clay and calcite. 8 figs., 2 tabs.

  1. High-speed conversion of carbon dioxide into methanol using catalyst. Shokubai ni yoru nisanka tanso no kosoku methanol ka

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    Inui, T. (Kyoto University, Kyoto (Japan). Faculty of Enineering)

    1993-02-01

    This paper describes high-speed conversion of CO2 into methanol. When a Cu-Zn-Cr-Al oxide-based catalyst (MSCp catalyst) prepared by using a sedimentation process used for synthesizing methanol from CO is applied to converting CO2 into methanol, the methanol yield decreases down to a several fraction of CO to methanol conversion, with a possibility of greater catalytic deactivation. If this catalyst prepared by using a homogeneous gelation process (MSCg catalyst) is used, the yield of methanol from CO2 increases by 240 plus percent over the case of using the MSCp catalyst, and no catalytic deactivation occurs at all during a use for ten and odd hours. Further, when La2O3 is added to the MSCg catalyst at 4% by weight, the methanol yield increases by about two times as much as the case without addition, and the temperature at which the maximum yield is achieved shifts to a lower temperature side by about 20[degree]C. Combining Ag or Pd with the MSCg catalyst provides the same effects. The paper touches on an attempt of high-speed CO2 conversion using this catalyst loaded with ceramic fibers. 15 refs., 5 figs., 2 tabs.

  2. FY 1990 Study Meeting of Catalyst (Iron system). Data; 1990 nendo shokubai kento kai (Tetsu kei) shiryo

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    NONE

    1991-03-01

    The FY 1990 Study Meeting of Iron-system Catalyst was held at NEDO on March 12, 1991, and the data were arranged. In the study meeting, papers titled as follows were made public: About the behavior of H{sub 2}S on iron-system catalyst by Muroran Institute of Technology; Results of the test on iron-system catalyst in the BCL project by Research Institute, Mitsubishi Kasei Corp.; Results of the test on iron-system catalyst by 2.4 t/d PDU by NKK; Results of the test on iron-system catalyst by 0.1 t/d BSU by Mitsui Engineering and Shipbuilding Co.; Results of the test on iron-system catalyst by 1 t/d PSU by Nippon Steel Corp.; Results of the research at Government Industrial Development Laboratory, Hokkaido, and the study; Results of the research at National Chemical Laboratory for Industry and the study; Results of the research at the University of Tokyo and the study; Details of the development of synthetic iron sulfide and the attainment up to now by Asahi Chemical Industry Co. Moreover, the plenary session was held on research items for the development of iron-system catalyst in future. (NEDO)

  3. Evaluating Pt-Ru/C mixtures as ethanol electro-oxidation catalysers

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    Bibian Alonso Hoyos

    2004-09-01

    Full Text Available This work studies ethanol electro-catalytic oxidation by cyclic voltametry in sulphuric acid solutions at different temperatures and concetrations, using platinum.rutenium mixtures supported in vitreous carbon as catalysers. The results indicate that ethanol oxidation in theses electrodes is irreversible, has slow kinetics, is controlled by charge transfer and is brought about by a bi-functional reaction mechanism, this being ethanol adsorption on platinum atoms and additional oxidation of specties adsorbed in the presence of platinum and retenium oxides. Experimental results show increased catalytic activity with electrodes, followed by reduced activity for electrodes having a greater quantity of rutenium.

  4. Evaluation report on the design of solid catalysts for saving energy in petrochemical industry; Sekiyu kagaku no tame no sho energy gata kotai shokubai sekkei hyoka hokokusho

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    NONE

    2001-03-01

    The aim is to improve on hydrocarbon oxidation which is a difficult reaction (analogous to combustion and having potential for heat generation or explosion, with restrictions therefore imposed on reaction conditions) by use of a catalyst supporting porous membrane. The fiscal 1999-2000 results are stated. In this effort, the target reaction is promoted by a catalyst supported by a porous membrane while combustion is controlled by the said porous membrane that separates oxygen and hydrocarbon from each other. Such a design was not available since a catalyst supporting inorganic membrane withstanding so high a temperature was difficult to prepare. Recently, however, a porous membrane with its pores regulated to microstructural dimensions was developed. The activity of a Pd membrane catalyst is evaluated in view of the degree of oxidation of propylene, cyclohexene, and benzene. It is then found that hydrogen that has passed the Pd membrane participates in the reaction. In a propylene oxidation test using a membrane type Ag/Al{sub 2}O{sub 3} catalyst, it is found that acetone is generated and that oxygen after passing through the membrane participates in the reaction. Methods are studied for preparing a metal membrane in which the catalyst system comprises a catalyst supporting porous membrane and a Pd membrane. In the fabrication of metal membranes, a highly selective hydrogen permeable membrane is stably prepared by the thermal CVD (chemical vapor deposition) method. (NEDO)

  5. Recent advances in photoelectrochemistry. Part 1. Preparation and photocatalytic activities of semiconductor microcrystals; Saikin no hikari denki kagaku. 1. Handotai chobiryushi no chosei to hikari shokubai kassei

    Energy Technology Data Exchange (ETDEWEB)

    Yoneyama, H; Torimoto, T [Osaka Univ., Osaka (Japan). Faculty of Engineering

    1995-01-05

    The energy structure of semiconductor microcrystals with less than 10nm particle size is different from that of bulk semiconductor, and the reducing force of electrons and the oxidizing force of holes produced by light in microcrystals are larger than those of bulk semiconductor. Focusing on the application of semiconductor microcrystals to photocatalysis, the effects of the particle size and surface conditions of particles on photocatalytic activity are discussed. It has been shown that the change in the characteristics of semiconductor microcrystals depends on particle size, and microcrystals with narrow distribution of particle sized is necessary for the study of the characteristics of semiconductor microcrystals. An example of high efficient progress of CO2 direct reduction by the use of semiconductor microcrystals is introduced. It has been made clear that the photocatalytic activity of semiconductor is improved when a small amount of electrode catalyst is supported in it. A unique photocatalytic reaction which can not be observed with bulk particles can be progressed by the use of high oxidation and reduction ability caused by quantum size effect of semiconductor microcrystals. 26 refs., 2 figs., 1 tab.

  6. Recent advances in photoelectrochemistry. Part 3. Recent applications of photocatalysis; Saikin no hikari denki kagaku. 3. Hikari shokubai no jitsuyoka kenkyu no genjo

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    Murasawa, S [Ishihara Sangyo Kaisha Ltd., Osaka (Japan)

    1995-01-05

    Titanium oxide has been developed which can be put to practical use in photocatalysis, and trials have been carried out for the application to environmental processing. Some of the cases are quoted to investigate means for the application of the photocatalysis study. During the process of improving the light resistance of titanium oxide pigments, various knowledge on photocatalytic phenomena has been obtained, and titanium oxide having a strong enough activity suitable for practical use is obtained based on the knowledge. There are two methods for the application of photocatalysis to decomposition and deodorization of malodor in living space. Fixation of NOx has been studied to solve the problem of air pollution. A huge reactor is required if photocatalysis is applied to the treatment of a large quantity of water. Various kinds of approach may be needed to structure a compact reactor suitable for practical use. 14 refs., 3 figs., 2 tabs.

  7. Gasification catalysts prepared by the reaction of CaCO3 and coal. Tansan karushiumu to sekitan no ion kokan hanno ni yori choseishita kokassei gas ka shokubai

    Energy Technology Data Exchange (ETDEWEB)

    Otsuka, Y.; Asami, K. (Tohoku University, Sendai (Japan). Institute for Chemical Reaction Science)

    1991-11-07

    Properties of the active gasification catalysts prepared by ion exchange reaction of CaCO3 and coal were studied. Several kinds of Ca-loaded coal specimens were prepared to compare their properties among them by physically mixing coal particles with CaCO3 ones in air, by kneading both materials in pure water while crashing and by impregnating CaCO3 into coal while agitating them in pure water. Although Ca-loading onto the impregnated specimen was nearly one-half that of the kneaded one, its catalysis was equal to the kneaded one. CaCO3 greatly accelerated steam gasification only by mixing it with low rank coal in water, and such a high catalytic activity was caused by ion-exchanged Ca produced by the reaction between CaCO3 and COOH radical in coal. Aragonite of seashells yielded more Ca-loading than calcite of limestone, suggesting one of the useful treatment of seashell waste. 3 refs., 4 figs., 2 tabs.

  8. Trend of research on future development of new biocatalysts. 2; Shinki bio shokubai no sosei ni kansuru kenkyu doko chosa. 2

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-03-01

    Creation of new biocatalysts was surveyed to convert chemical reactions into environment-friendly processes. Biocatalysts are characterized by their high catalytic activity, uniqueness of reactions, and non-pollution under mild conditions. Stability is required for them, such as heat resistance, solvent resistance, acid resistance and alkali resistance, under severe conditions. For the development of new biocatalysts, it is necessary to multiply utilize the techniques containing enzymes, ribozymes, mold synthetic polymers, chemical modification, and non-natural proteins. Natural enzymes have been conventionally improved through the search, imitation and modification. Hereafter, new biocatalysts with functions required for the reactions should be created by integrating information regarding functions, structures and activation of these enzymes. It is indispensable to cooperate closely with supporting techniques, such as gene engineering, organic synthesis, biophysics and computer chemistry. 35 refs., 26 figs., 1 tab.

  9. Effects of solvent and catalysts on the hydrogenolysis of alkylnaphthalenes; Alkylnaphthalene no suisoka bunkai ni okeru yobai to shokubai no koka

    Energy Technology Data Exchange (ETDEWEB)

    Futamura, S. [National Institute for Resources and Environment, Tsukuba (Japan)

    1996-10-28

    Catalytic effects of metal and carbon materials, which promote hydrogen transfer from hydrogen donor solvents, are investigated during hydrogenolysis of benzyl-1-methylnaphthalenes (BMN) selected as a hydrogen acceptor. For the isomer distribution of BMN after the reaction, almost the same molecular ratio before the reaction was obtained independent of the presence of catalysts. Selectivity of position during the addition of hydrogen atoms from tetralin was not found. For the reaction of BMN in tetralin, 1-methylnaphthalene and toluene were obtained as products, but the formation of benzylnaphthalene was not found. As for the nuclear hydride of BMN, the trace amount formation was confirmed by gas chromatography. For the hydrogen transfer from tetralin progressed catalytically, it was found that the nuclear of naphthalene can not be hydrogenated easily. This was considered to be due to the obstruction of hydrogen transfer from tetralin by the strong adsorption of BMN on the Ni surface. 1 ref., 1 fig., 2 tabs.

  10. Influence of catalytic activity and reaction conditions on the product distribution in coal liquefaction; Sekitan ekikayu no seiseibutsu bunpu ni taisuru shokubai kassei oyobi hanno joken no eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Hasuo, H.; Sakanishi, K.; Mochida, I. [Kyushu University, Fukuoka (Japan). Institute of Advanced Material Study

    1996-10-28

    The NiMo sulfide supported on Ketjen Black (KB) was more effective and yielded lighter oil products containing light fractions with their boiling point below 300{degree}C during the two stage liquefaction combining low temperature and high temperature hydrogenation the conventional NiMo/alumina catalyst and FeS2 catalyst. Although the NiMo/alumina yielded increased oil products during the two stage liquefaction, the lighter oil fractions did not increase and the heavier fractions increased mainly. This suggests that the hydrogenation of aromatic rings and successive cleavage of the rings are necessary for producing the light oil, which is derived from the sufficient hydrogenation of aromatic rings using catalysts. For the two stage reaction with NiMo/KB catalyst, it was considered that sufficient hydrogen was directly transferred to coal molecules at the first stage of the low temperature reaction, which promoted the solubilization of coal and the successive hydrogenation at the high temperature reaction. Thus, high activity of the catalyst must be obtained. It is expected that further high quality distillates can be produced through the optimization of catalysts and solvents at the two stage reaction. 1 ref., 4 figs., 1 tab.

  11. Characterization of the various catalyst for solvent hydrogenation at 1t/d PSU; 1t/d PSU ni okeru kakushu yozai suisoka shokubai no seino hyoka

    Energy Technology Data Exchange (ETDEWEB)

    Kakebayashi, H.; Nogami, Y.; Inokuchi, K. [Mitsui SRC Development Co. Ltd., Tokyo (Japan); Aihara, Y.; Imada, K. [Nippon Steel Corp., Tokyo (Japan)

    1996-10-28

    Performance of various catalysts for hydrogenation of recycle solvent was evaluated for the operation of NEDOL process 1 t/d process supporting unit (PSU). Distillate between 220 and 538{degree}C derived from the liquefaction of Tanito Harum coal was used as recycle solvent. Deactivation behaviors of catalysts were compared using a prediction equation of catalyst life, by which aromatic carbon index (fa) after hydrogenation can be determined from the fa of recycle oil before hydrogenation, reaction temperature, and total hydrogenation time. Total hydrogenation time satisfying the {Delta}fa, 0.05 before and after hydrogenation were 8,000, 4,000, and 2,000 hours for NiMo-based catalysts C, A, and B, respectively. Catalyst C showed the longest life. Used catalysts were also characterized. The catalyst C showed larger mean pore size than those of the others, which resulted in the longer life due to the delay of pore blockage. From measurements by XPS and EPMA, relative atomic concentration of carbon increased remarkably after the use for all of catalysts, which was considered to be due to the adhesion of hydrocarbons. Increase of metal atoms, such as Fe and Cr, was also observed due to the contamination of entrainment residues. Deactivation of catalysts was caused by the adhesion of hydrocarbons, and metallic compounds, such as Fe and Cr. 3 refs., 1 fig., 5 tabs.

  12. Studies on the catalysts for coal liquefaction. ; Rheological studies of coal liquefaction process. Sekitan ekikayo shokubai ni kansuru kenkyu. ; Sekitan ekika process no rheology teki kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    Muraoka, T; Oda, H; Yokokawa, C [Kansai University, Osaka (Japan). Faculty of Engineering

    1991-11-07

    Hydrogenolysis of different rank coals as Taiheiyo coal (75.7C%) and Pittston coal (85.4C%) were conducted in the presence of four kinds of catalysts (CuCrO4, Fe2O3+S, MoO3-TiO2 and MoS3-Al2O3) with an addition of tetralin as vehicle. The variation in viscosity in every reaction system was traced in the initial stage of the reaction by a torque meter attached to an autoclave. As a result, in every system, the torque decreased in the initial stage of temperature rise because of reduction of a solvent viscosity. The torque subsequently increased with temperature indicating two peaks before the following gradual decrease. In Taiheiyo coal, both peaks were low, and its coal conversion was more than 85%, while in Pittston coal, both peaks were sharp and high, and both subsequent torque reduction and coal conversion were smaller than those of Taiheiyo coal. 5 refs., 10 figs., 2 tabs.

  13. Studies on the catalysts for coal liquefaction. ; Kinetic discussion in initial stage of coal liquefaction. Sekitan ekikayo shokubai ni kansuru kenkyu. ; Sekitan ekika shoki dankai no sokudoronteki kosatsu

    Energy Technology Data Exchange (ETDEWEB)

    Muraoka, T; Ikenaga, N; Oda, H; Yokokawa, C [Kansai University, Osaka (Japan). Faculty of Engineering

    1990-11-29

    Discussions were given on features of various kinds of coal liquefaction catalysts exhibited by them in hydrocracking of coal (Taiheiyo coal), and particularly on selectivity of the reaction in its initial stage. Four kinds of catalysts were tested: Adkins catalyst which is an oxide of copper and chromium, Fe2O3+S, Mo-TiO2 and MoS3-Al2O3. Three grams of coal and 0.3 gram each of the catalysts were charged into an autoclave reactor and experiment was conducted under an initial hydrogen pressure of 10 MPa, temperatures from 653 K to 693 K and for durations of 0 to 120 minutes to derive apparent reaction rate constants. The MoS3-Al2O3 catalyst has promoting the reaction apparently in the primary reaction at any temperature, while the other catalysts had the rate constants varied in the initial and the later stages. It was recognized that the temperature dependence of rate constants varies considerably according to the types of catalyst. Particularly the MoO3-TiO3 catalyst has small temperature dependence in the rate constants, and high molecular weight reducing power. 3 refs., 4 figs., 3 tabs.

  14. Surface wettability control by titanium dioxide photo-induced reaction. Super-hydrophilic properties; Sanka chitan ni yoru hikari reiki shinsuika gijutsu. Hikari shokubai chosinsuisei

    Energy Technology Data Exchange (ETDEWEB)

    Watanabe, T. [The University of Tokyo, Tokyo (Japan). Research Center for Advanced Science and Technology

    1999-05-01

    Hydrophilicity results when the surface of titanium dioxide is reduced for the specified oxygen to be replaced by hydroxyl groups. The ease with which such a structural change occurs is subject to variation between titanium dioxide crystal surfaces, and is dependent greatly on the atmosphere. No hydrophilic trend is observed in an atmosphere of oxygen only without moisture and, in darkness without light, hydrophobicity occurs early. Although the contacta angle titanium dioxide with water with stability is not known, yet it is presumed, on the analogy of the case of strontium titanate, that it is in the range of 20-40 degrees. A hydrophilic trend below the range is attrributed to structural changes. The control of surface wettability is one of the basic tasks to fulfill in various kinds of mechanisms and manufacturing processes. The technology of wettability control using a titanium dioxide coating which is quite durable will be applied not only to functions involving defogging, dripproof, and self-cleaning, but also to the control of heat transmission in the mechanism and to the bonding process. (NEDO)

  15. Surface wettability control by titanium dioxide photo-induced reaction. Super-hydrophilic properties. Sanka chitan ni yoru hikari reiki shinsuika gijutsu. Hikari shokubai chosinsuisei

    Energy Technology Data Exchange (ETDEWEB)

    Watanabe, T. (The University of Tokyo, Tokyo (Japan). Research Center for Advanced Science and Technology)

    1999-05-01

    Hydrophilicity results when the surface of titanium dioxide is reduced for the specified oxygen to be replaced by hydroxyl groups. The ease with which such a structural change occurs is subject to variation between titanium dioxide crystal surfaces, and is dependent greatly on the atmosphere. No hydrophilic trend is observed in an atmosphere of oxygen only without moisture and, in darkness without light, hydrophobicity occurs early. Although the contacta angle titanium dioxide with water with stability is not known, yet it is presumed, on the analogy of the case of strontium titanate, that it is in the range of 20-40 degrees. A hydrophilic trend below the range is attrributed to structural changes. The control of surface wettability is one of the basic tasks to fulfill in various kinds of mechanisms and manufacturing processes. The technology of wettability control using a titanium dioxide coating which is quite durable will be applied not only to functions involving defogging, dripproof, and self-cleaning, but also to the control of heat transmission in the mechanism and to the bonding process. (NEDO)

  16. Report on surveys in fiscal 1999 on research and development of the environment harmonizing catalyst technology; 1999 nendo kankyo chowagata shokubai gijutsu no kenkyu kaihatsu chosa hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-03-01

    This paper reports the surveys in fiscal 1999 on research and development of the environment harmonizing catalyst technology. The discussion subjects taken up included suppression of discharge of carbon dioxide, catalysts used when manufacturing hydrogen and technology thereof, and environment purifying catalysts to decompose harmful substances, and technology thereof. The roles of catalysts and their technologies are expected in reducing the reforming temperatures, achieving energy saving, and reducing decomposition energy. Furthermore, the catalysts are expected of high activity, long life and low cost. Three themes were selected from the emergency and importance points of view. The themes are, in the consumer field, research and development of efficiency improvement in membrane reactors for reforming low-grade hydrocarbons to structure a technology to manufacture hydrogen for small-size portable fuel cells; and in the industrial field, development of hydrogen and carbon product manufacturing technologies with which CO2 generation is suppressed by means of the catalytic decomposition process. In practice, for such discharged harmful substances as dioxins, PCB and volatile organic compounds (VOC), treating them is the urgent environmental problem, and therefore, the fundamental research was taken up for practical application of the second-generation catalysts of the ultra-violet light and visible light responding type. (NEDO)

  17. Study on supported binary sulfide catalysts for secondary hydrogenation of coal-derived liquids; Sekitan ekikayu niji suisoka shokubai no kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    Shimada, H.; Matsubayashi, N.; Sato, T.; Imamura, M.; Yoshimura, Y.; Nishijima, A. [National Institute of Materials and Chemical Research, Tsukuba (Japan)

    1995-07-28

    To utilize the high performance of supported catalysts in coal liquefaction processes, one of the promising ways is to apply hydroprocessing sulfide catalysts to the secondary hydrogenation of coal-derived liquids which have undergone the solid separation unit. However, when the product yield from the first-stage liquefaction is maximized, the feed stocks in the secondary hydrogenation contain large amounts of residual fractions with preasphaltenes and metallic components. In this case, the development of a long-life catalyst is essential to establish the two-stage process as a practical one. From this viewpoint, the authors have investigated the deactivation causes of supported Ni-Mo sulfide catalysts through the analysis of the used catalysts in the secondary hydrogenation of coal-derived liquids for long periods. The major cause of the catalyst deactivation has been found to be metallic and carbonaceous deposition on the catalyst, which results thin layer which covers the catalyst particles. The catalysts located at the reactor inlet are more rapidly deactivated than those at the rector exit because of larger amounts of metallic foul ants and the above described shell-like layer. Hydrocracking active sites are much heavily deactivated compared with hydrogenation active sites. It is inferred that the basic or polar compounds contained in coal liquids are permanency adsorbed on the hydrocracking active sites. Spectroscopic analysis of the used catalysts clarified the destruction of the active phase of the binary sulfides, through the segregation and crystal growth. The structural changes of the catalysts are very likely caused by heteroatom compounds in the preasphaltenes. Thus, the primary cause of the catalyst deactivation is the preasphaltenes in the coal liquids. Hydroaromatic compounds in the coal liquids suppress the change of the deposited carbonaceous materials into inert coke which permanently deactivate the catalyst.

  18. Design of hydroprocessing catalyst for the production of ultra clean fuels. Super clean nenryo wo mezashita jushitsu tanka suiso seisei shokubai no kokinoka

    Energy Technology Data Exchange (ETDEWEB)

    Shimada, Hiromichi (National Chemical Lab. for Industry,Tsukuba, (Japan))

    1990-02-01

    In order to develop high function catalyst for the ultra clean fuel refining and other purposes, the catalyst was studied in correlation between the function and structure. Hydrogenation power of aromatic ring and hydrogenolysis power of carbon-carbon bonding, which are principal functions of catalyst in the hydrogenation refining, were evaluated with model material. 30 kinds of catalyst were figure shown in classification result of evaluation. As for the mutual operation of molybdenum and carrier, it is necessary for molybdenum sulfide to be highly dispersed on carrier in order to heighten the hydrogenation activity. While the hydrogenolysis activity, as necessitating electrically negative molybdenum type to be formed on carrier, is manifested by the formation of Bronsted acidity point with hydrogen sulfide, adhering thereto. As for the molybdenum sulfide catalyst, mainly hydrogenation activity point, in case that structure, similar to molybdenum disulfide, is dispersed as a single layer on carrier, and hydrogenolysis activity point, in case that it forms a multi-layer structure thereon, are formed in edge part of respective crystal. The lowering in activity under a long time sevre condition, which mainly are carbonic material deposition, matallic adhesion, etc., is also influenced by the structural change in catalyst. 10 refs., 5 figs. 2 tabs.

  19. Catalytic effects of various catalysts in hydroprocessing of Cold Lake vacuum bottom. Cold Lake zansayu no hydroprocessing ni okeru kakushu shokubai no koka

    Energy Technology Data Exchange (ETDEWEB)

    Yokoyama, S.; Yamamoto, M.; Maekawa, Y.; Kotanigawa, T. (Government Industrial Development Laboratory, Hokkaido, Sapporo (Japan))

    1991-11-07

    The effects of various types of catalysts were studied on hydroprocessing of Cold Lake vacuum bottom (CLVB). FeS2 [Py] of an analytical reagent grade was used as sulfide catalyst, Fe2O3(SO4)[sup 2[minus

  20. Survey on synthesis and reaction of environmentally benign water-soluble metal complex catalysts; Kankyo chowagata suiyosei sakutai shokubai no gosei hanno no chosa

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-03-01

    This report describes the research trend survey results on the synthesis and reaction of water-soluble metal complexes which are regarded as environmentally benign catalysts. For the synthesis and catalysis of water-soluble complexes, synthetic methods of water-soluble phosphines, such as sulfonated TPPMS and TPPTS, are described in detail. Synthesis and reactivity of hydroxymethylphosphines are introduced, and the application of electrospray mass spectroscopy is elucidated as a tool for the analysis of them. Changes of the application of transition metal complexes with water-soluble phosphines to catalysis are described. Dual catalysts which have both functions of phase transfer catalysts and homogeneous catalysts are introduced. Concept of counter phase transfer catalysts is also introduced, and some catalytic reactions are described. In addition, this report introduces catalysis of water-soluble polymer-supported metal complexes, immobilization of metal colloids with water-soluble ligands and their analysis, and water-soluble complexes as hybrid catalysts. 144 refs., 94 figs., 10 tabs.

  1. Effects of fuel properties and oxidation catalyst on diesel exhaust emissions; Keiyu seijo oyobi sanka shokubai no diesel haishutsu gas eno eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Aihara, S; Morihisa, H; Tamanouchi, M; Araki, H; Yamada, S [Petroleum Energy Center, Advanced Technology and Research Institute, Tokyo (Japan)

    1997-10-01

    Effects of fuel properties (T90 and Poly-Aromatic Hydrocarbons: PAH) and oxidation catalyst on diesel exhaust emissions were studied using three DI diesel engines and two diesel passenger cars. (IDI engine) PM emissions were found to increase as T90 and PAH increased and could be decreased considerably for each fuel if an oxidation catalyst was installed. 5 refs., 9 figs., 3 tabs.

  2. Photocatalytic removal of nitrogen oxides from ambient air using solar energy; Taiyo energy wo riyoshita taikichu no NOx no hikari shokubai jokyo

    Energy Technology Data Exchange (ETDEWEB)

    Fukaya, M; Taoda, H; Watanabe, E; Nonami, T; Iseda, K; Kato, K [National Industrial Research Institute of Nagoya, Nagoya (Japan); Kunieda, S [NGK Insulators, Ltd., Nagoya (Japan); Kato, S

    1997-11-25

    Experiment was made on removal of NOx from ambient air using ceramic blocks coated with a newly developed easy-to- handle TiO2 film photocatalyst. After TiO2 sol was prepared by hydrolyzing titanium tetraisopropoxide, the photocatalytic blocks were prepared through drying and sintering after immersing the blocks in TiO2 sol. The effect of the number of coating on catalytic performance was studied using the single-coated and triple-coated blocks. Artificial solar light of 1mW/cm{sup 2} was used as light source for flowing reaction experiment of air (containing NOx) in a laboratory. NOx concentration rapidly decreased with irradiation, and 94% and 98% of NOx were removed by the single- and triple-coated blocks, respectively. NOx was completely oxidized to HNO3 through NO2 by triple-coated blocks. The demonstration test of removal of NOx from ambient air in Okazaki city showed a removal rate of nearly 90% in noonday and 40% or more in average, while not 0% but 5-20% even in the nighttime. The latter is probably derived from adsorption by the porous photocatalytic blocks. 2 figs., 4 tabs.

  3. Electrostatic settling of catalyst particles in hydrogenation of methyl benzoate. Denkai chinkoho ni yoru ansokukosan mechiru suisoka hannoeki kara no shokubai ryushi bunri

    Energy Technology Data Exchange (ETDEWEB)

    Kato, K. (Japan Energy Corp., Tokyo (Japan). Central Research Lab.)

    1994-03-01

    As benzyl alcohol (BA), which is one of the simplest alcohol having aromatic ring, has been used widely for the fields related to soap, perfume and chemicals industry, its usage has not always been so much because of its expensiveness. Authors developed previously a new process technique to produce cheaper and higher purity BA not through chlorination process using toluene as its raw materials. The BA can be obtained by hydrogenating methyl benzoate (MB) at a dispersion babble tower using cupper-chromium type powder catalyst in mixed solvent of methanol and toluene. The catalyst becomes much fine particles after the reaction. In this study, it is examined to separate MB hydrogenation reaction solution obtained by electrostatic settling into solid and liquid phases as an aim to improve the BA production process. Rate of electrostatic settling does not depend upon solid concentration, slurry forming conditions, electrode materials, specific resistance of slurry layer and others, but is in proportion to electric field intensity. Furthermore, process of the electrostatic settling is expressed by an equation. 9 refs., 9 figs., 3 tabs.

  4. Effects space velocity and gas velocity on DeNOx catalyst with HC reductant; HC tenka NOx kangen shokubai no kukan sokudo oyobi gas ryusoku no eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Niimura, K.; Tsujimura, K.

    1995-04-20

    Discussions were given on the hydrocarbon added reduction catalyst method to reduce NOx in diesel engine exhaust gas. An experiment was carried out with actual exhaust gas from a diesel engine by using a copper ion exchanged zeolite catalyst that has been coated on a honeycomb type substrate, and using propylene as a reductant. When the catalyst volume was changed with the exhaust gas space velocity kept constant, the NOx conversion ratio decreased as the catalyst length is decreased, and the activity shifted to the lower temperature side. The NOx reduction efficiency increased if the faster the gas flow velocity. On the other hand, if the gas flow velocity is slow, the NOx reduction can be carried out with relatively small amount of the reductant. When the catalyst volume was changed with the passing gas amount kept constant, the NOx conversion ratio decreased largely if the catalyst length is decreased. Further, the NOx reduction characteristics shift to the higher temperature side. In the catalyst length direction, the NOx reduction activity shows a relatively uniform action. However, a detailed observation reveals that the reaction heat in the catalyst is transmitted to the wake improving the activity, hence the further down the flow, the NOx conversion ratio gets higher in efficiency. 5 refs., 5 figs., 3 tabs.

  5. Report on the research achievements in the Sunshine Project in fiscal 1992. Studies on a direct gasification catalyst; 1992 nendo chokusetsu ekika shokubai ni kansuru kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1993-10-01

    This paper describes the research achievements in the Sunshine Project in fiscal 1992 in studies on a direct gasification catalyst. The paper summarizes the points where the catalyst research has reached to date. The catalyst surface effective for hydrogenation is the metal surface that can dissociate hydrogen. However, metals having large adsorption heat against hydrogen do not show the activity greatly because these metals are difficult of desorbing hydrogen having high dissociating activity. The coal liquefaction system has the surface oxidized by water content, wherein hydrogen dissociation cannot be expected, and sulfides are suitable. When a sulfide catalyst contacts hydrogen, the catalyst itself is desulfurized, producing H{sub 2}S and becomes a low-order sulfide. When atmospheric H{sub 2}S contacts this sulfide, it dissociates into HS and H, and this H behaves as active hydrogen. However, the liquefaction activity can be recognized even in a sulfuric acid type catalyst containing no sulfide whatsoever, wherein the H{sub 2}S partial pressure in the reaction system becomes extremely low. This fact means that the active hydrogen is not necessarily generated by the dissociation of H{sub 2}S. There is no other way but to think that hydrogen is dissociated directly without going through H{sub 2}S. If this is true, it provides a new guideline in developing and designing the future catalysts. (NEDO)

  6. FY 1998 annual report on the fourth international forum on environmental catalysis (IFEC 99); Dai 4 kai kankyo shokubai kokusai forum (IFEC '99) 1998 nendo hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-03-01

    The 4th international forum on environmental catalysis, held in January 1999 in Chemical Society of Japan's Hall, had a total attendees exceeding 170, including 10 foreign attendees invited. A total of 20 papers (including 10 by foreign attendees) were presented, discussing diversified problems; 3 keynote addresses regarding (to what extent environmental catalyst can contribute); and 5 for the session of catalysts for clean processes, 6 for the session of eco-friendly chemistry, and 8 for the session of environmental catalysts for air pollution. The lectures included (global environmental problems and environmental catalysts) by Prof. Segawa of Sophia University as the opening address; solid base catalysts by Prof. Ono of Tokyo Institute of Technology in the session of (catalysts for clean processes); activation of dioxygen by transition metal complexes-new approach to highly selective catalytic oxidation with molecular oxygen by Prof. Moro-oka of Tokyo Institute of Technology in the session of (Eco-friendly chemistry; and environmental catalysts-present and future as the comprehensive review by Prof. Misono of University of Tokyo in the session of (environmental catalysts for air pollution). (NEDO)

  7. Current status and prospect on photo-catalyst application in environmental problems; Kankyo mondai ni okeru hikari shokubai oyo no ganjo to tenbo

    Energy Technology Data Exchange (ETDEWEB)

    Watanabe, T. [Toto Ltd., Kitakyushu (Japan)

    1995-09-30

    This paper summarizes application of photo-catalysts in environmental problems. The paper lists examples of the application in residential environments. Photo-catalytic decomposition is possible by using ultraviolet rays contained in room illumination if the bacterial presence is sparse. The examples thereof may be cited as follows: if colon bacilli are suspended on a tile with TiO2 photo-catalyst sintered in it and exposed to room illumination, the bacteria are disinfected; using photo-catalysts in a bathroom suppresses deposition of Pseudomonas aeruginosa; a photo-catalyst tile (TiO2 loaded with Cu) and light irradiation reduce intensity of tobacco smoke odor; and adsorbents may be used simultaneously if intermediate products are odor generating substances. The examples of applying photo-catalysts to regional environments may be quoted as follows: growth of algae in a Petri dish is suppressed by presence of Cu loaded TiO2 under room illumination; this leads to an expectation on its effect in a relatively clean water environment; glass beads loaded with a TiO2 photo-catalyst placed in a gold fish breeding tank reduces turbidity, the number of colon bacilluses, and COD value; and the mortality in gold fish shows no change. With an objective of application to exterior building materials, photo-catalyst applied tiles were left outdoors for 160 days. Nitric acid ions were detected that are thought to have been generated by decomposition of microorganisms that have deposited on the tiles. 6 refs., 5 figs., 3 tabs.

  8. Studies on surface structures and mechanism of photocatalytic action of semiconductor oxides; Handotai hikari shokubai no hyomen kozo seigyo to sayo kiko kaimei ni kansuru kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    Takeuchi, H; Sona, S; Koike, H; Hori, H; Negishi, N; Kohara, H; Ibusuki, A [National Institute for Resources and Environment, Tsukuba (Japan); Vakhtin, A; Borovkov, V [New Energy and Industrial Technology Development Organization, Tokyo, (Japan)

    1997-02-01

    Studies are made to define the working mechanism of semiconductor photocatalysts such as TiO2 and to establish designing guidelines for improving on their activity and functions. TiO2 in the air actively produces oxygen seeds for the oxidation and removal of NOx, etc. It is desired that a catalyst have a specific surface area large enough to retain the product of its action. To meet the need, a thin-film photocatalyst which is an aggregate of TiO2 crystals is produced by burning a film of a sol/gel system of reaction doped with macromolecules. This product has a larger specific surface area and is higher in pollutant-removing performance, and may be put into practical use. In another experiment, metal-carrying particles TiO2 suspended in water are employed for the reduction of CO2. Though the main product of catalysts carrying Pt or Pd is methane, a photocatalyst carrying RuO2 produces acetic acid mainly and loses less activity with the passage of time. A hybrid photocatalyst is composed of an organic pigment and inorganic semiconductor, synthesized through a covalent bond between a sililated-surface thin TiO2 film and porphyrin. It is confirmed that the newly developed process brings about an increase in electron migration efficiency. 3 figs.

  9. Optimization of the catalytic converter internal flow by using 3D-CFD; Sanjigen nagare kaiseki ni yoru shokubai converter nai nagare no saitekika

    Energy Technology Data Exchange (ETDEWEB)

    Toi, M; Sugiura, S [Toyota Motor Corp., Tokyo (Japan)

    1997-10-01

    By using computational fluid dynamics and statistical quality control method, we investigated the contribution of front and rear catalytic converter cone shape for the pressure loss and the partial flow, also led the optimal terms and the predictional formulations efficiently. According to this, we can investigate the optimal position of the catalytic converter from the planning. 8 figs., 6 tabs.

  10. Development of metal complexes which has a novel type of dhotocatalysis activity; Shinki hikari shokubai tokusei wo yusuru kinzoku sakutai no sousei

    Energy Technology Data Exchange (ETDEWEB)

    Ishitani, Osamu [Saitama University, Saitama (Japan). Graduate School of Sceince and Engineering

    1999-12-16

    Purpose of this research are (1) development of photocatalysts which selectively drive hydride transfer and (2) their application to the enantioselective reduction of an unsaturated substrate. photocatalysis of [Ru(bpy){sub 2}(py){sub 2}]{sup 2+} (1) and [Ru(tpy)(bpy)(py)]{sup 2+} (2) (bpy=2,2'-bipyridine, tpy=2,2' : 6',2' '-terpyridine, py=pyridine) for reduction of unsaturated compounds was investigated using triethylamine as a reductant. Formation of the hydrogenated compounds was observed but the corresponding one electron reduced compounds were not detected at all. The complex 1 photocatalysed the reduction of trifluoroacetophenone (5) and gave the alcohol in a 67% yield but 2 gave only a 27% yield. The reaction proceeds via the photosubstitution of a py ligand of the ruthenium complex, followed by photochemical formation of the hydride complex. The ruthenium hydride complex reacts with 5 to give [Ru(tpy)(bpy)(OCHPhCF{sub 3})]{sup +} (4). Dissociation of 4 to the alcohol was not efficient and the yield was 10%. (author)

  11. Kinetic analysis of photochemical sterilization of thermoduric bacterial spores in slurry of semiconductor catalyst particles with aeration. Handotai shokubai ryushi no tsuki kendakukei ni okeru tainetsusei saikin hoshi no hikari sakkin to sono sokudoronteki kaiseki

    Energy Technology Data Exchange (ETDEWEB)

    Tone, S; Taya, M; Kato, S; Horie, Y; Ashikaga, Y [Osaka Univ., Osaka (Japan). Faculty of Engineering and Science; Joo, Hyunkyu [Konkuk Univ., Seoul (Korea, Republic of)

    1993-11-10

    To study the utilization of the photochemical sterilization of thermoduric bacterial spores B. stearothermophilus with photocatalysis of TiO2 particles, light irradiation experiments are conducted under various operational conditions. TiO2 particles and dissolved oxygen resulting from aeration must coexist to accelerate the rate of spore sterilization under light irradiation of a high pressure mercury lamp. The sterilization rate increases with larger average light intensity in the reactor, and it is estimated that the dissolved oxygen contributes to the formation of oxidative radicals which become the attacking species. The maximal rate of spore sterilization is obtained under the condition of TiO2 concentration of 5[times]10[sup -2]kg[center dot]m[sup -3]. By combining a second-order rate equation, wherein the spores' death caused by the oxidative radicals formed by TiO2 photocatalysis is taken into consideration, and single-hit multitarget model, wherein the target damaged by the oxidizer in the spores is assumed, the sterilization velocity can be described well, and the effect of light intensity and the obtained rate parameters are correlated well. 13 refs., 7 figs., 3 tabs.

  12. FY1995 studies on surface structures and mechanism of photocatalytic action of semiconductor oxides; 1995 nendo handotai hikari shokubai no hyomen kozo seigyo to sayo kiko kaimei ni kansuru kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-03-01

    Development of the semiconductor photocatalyst such as titanium dioxide is important for photo-energy conversion and purification of the environment. We make clear that the mechanism of the photocatalysis using a spectroscopic or physico-chemical methods, and we developed the new photocatalyst with the control of the surface area, porosity, infinitesimal content, and surface modification of the catalyst surface. Titanium dioxide thin film photocatalysts were prepared by the dip coating method. Surface structure of the thin film was formed by the aggregated TiO{sub 2} anatase particle, its size was around 5 nm. This thin films effectively oxidazed NO, its photocatalytic activity is higher than that of commercial photocatalyst. Metal oxide anchored TiO{sub 2} photocatalysts (RuO{sub 2}/TiO{sub 2}) were prepared by the co-precipitation method. Effective charge separation of the RuO{sub 2}/TiO{sub 2} were confirmed by the measurement of ESR. The RuO{sub 2}/TiO{sub 2} photocatalyst successfully reduced CO{sub 2} and preserved its activity for much longer period than metal loaded catalyst. Hybrid photofunctionalized material was prepared by anchoring porphyrin moieties on the titanium dioxide surface. The relative quantum yield of electron transfer from porphyrin to the titanium dioxide conduction band has been markedly increased by water treatment of quanternized porphyrin-titanium dioxide covalently linked systems owing to removal of adsorbed porphyrin domains. (NEDO)

  13. Fiscal 2000 achievement report. Environment-conscious industrial technology research and development project (Development of environmentally-friendly catalyst technology); 2000 nendo kankyo chowagata shokubai gijutsu kenkyu kaihatsu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    Research and development and basic studies were conducted about novel catalysts which would help reduce impact on global environments. The efforts involved the development of (1) photocatalysts and (2) selective oxidation catalysts. In domain (1), a silicon semiconductor was manufactured for an integrated hydrogen generation catalytic membrane/silicon semiconductor/oxygen generation membrane system as a hybrid multilayer photocatalyst, and a fundamental one-layer type was fabricated. As for a system using a compound semiconductor CIGS (Cu(InGa)Se{sub 2})/CdS membrane, a CIGS membrane was completed, and CdS was deposited in layers to support platinum and it was found that water was decomposed under visible light irradiation although the bias voltage load was slight. In domain (2), the methanol and formaldehyde formation rates greatly increased when some MgO powder was installed in the reaction space in the vapor phase selective oxidation of methane in the presence of a catalyst which was a very small amount of nitrogen dioxide. (NEDO)

  14. Long-term storage and long-distance transportation of hydrogen by use of catalyst-addisted decalin dehydrogenation/naphthalene hydrogenation pair; Dekarin dassuiso/nafutarensuisoka shokubai hannotai wo mochiiru suiso no chokikan chozo/chokyori yuso

    Energy Technology Data Exchange (ETDEWEB)

    Liu, C.; Sakaguchi, M.; Saito, Y. [Scince Univ.of Tokyo, Tokyo (Japan)

    1997-06-01

    To enable taking in and out hydrogen with little energy consumption, it is sufficient if decalin is dehydrogenated to naphthalene under moderate heating condition. It is found that carbon supporting metal catalyst in liquid film state shows extremely high dehydrogeno-aromatization activity of decalin. The result of comparison with liquid hydrogen or metal hydride as media for hydrogen storage and transportation media is reported. The platinum-tungsten composite metal catalyst is prepared from an aqueous solution of K2PtC16 and Li2WO4 in the ratio of 1 to 1 so as to achieve 5wt-metal% carbon supporting. When hydrogen and naphthalene are discharged from the liquid phase reaction medium to the vapor phase and solid phase, respectively, under boiling and refluxing conditions, hydrogen is produced steadily by heating at 200 to 210degC. If economical efficiency is ignored, development of an inter-season energy storage system is desired to be developed which can be used in the season between summertime when sufficient hydrogen is obtained by photovoltaic power generation and electrolysis of water and wintertime when heat source is obtained by catalytic combustion of hydrogen. 11 refs., 4 figs., 4 tabs.

  15. Improvement of liquefaction solvent. Increase of light oil yield with a reduction in catalyst addition; Ekika yozai no kairyo kenkyu. Sekitan ekikayu no keishitsuka to shokubai tenkaryo no teigen

    Energy Technology Data Exchange (ETDEWEB)

    Okuyama, N.; Yasumuro, M.; Sato, K.; Komatsu, N.; Okui, T.; Shimasaki, K. [Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan)

    1996-10-28

    For developing coal liquefaction processes, it is an important problem to improve the light oil yield with increased oil yield. It was previously reported that distillate mainly containing lighter fraction can be produced with high oil yield by reducing the iron/sulfur catalyst addition in slurry, by recycling gas in the process operation, by utilizing these effects, and by using heavy oil as recycling solvent. In this study, the maximum distillate yield of Victorian brown coal was investigated through continuous liquefaction using a bench scale unit. In addition, operation conditions for obtaining sufficient oil yield were investigated under the reduced catalyst addition into one-third. Consequently, it was confirmed that the maximum content of lighter fraction in distillate product was obtained with reduced catalyst addition by using heavy oil as recycling solvent, by adopting new catalyst, and by utilizing effects of CLB recycling and gas recycling in maximum. It was also revealed that lighter distillate can be produced compared with the oil product obtained by recycling conventional solvent. 3 refs., 6 figs., 2 tabs.

  16. FY 1998 annual report on the decomposition/removal of harmful compounds in the gaseous phase by porous membrane provided with a catalytic function; 1998 nendo shokubai kinotsuki fuyo takomaku ni yoru kisochu yugai busshitsu no bunkai jokyo chosa hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-03-01

    Harmful compounds, e.g., dioxins and nitrogen oxides, released into the air are causing severer environmental problems on a global scale. In order to solve these problems, it is necessary to efficiently remove the released compounds in the vicinity of the living environments, while preventing, as far as possible, their formation at the sources. An attempt has been made to develop porous membranes impregnated with composites of a variety of metallic oxides showing activities as photocatalysts and for dark reactions by the ion engineering method, in order to drastically solve the above problems. Described herein are the FY 1998 results. Thin films of various titanium oxide crystals (anatase, rutile, and their combinations) are formed on Si substrates by the ion engineering method, as the photocatalysts for decomposition of aldehyde and water (for hydrogen production), to validate the optimum crystalline structures for the photocatalysis. Porous bodies of Ni and carbon are also impregnated with anatase TiO{sub 2} for decomposition of harmful gaseous compounds and water, to validate the effects of the porous membranes provided with catalytic functions. (NEDO)

  17. Fiscal 1998 development report on the high-accuracy quantitative analysis technique of catalyst surfaces by electron spectroscopy; 1998 nendo denshi bunkoho ni yoru shokubai hyomen koseido teiryo bunseki gijutsu no kaihatsu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-03-01

    This project aims at development of the high-accuracy quantitative analysis technique by electron spectroscopy for surface analysis of catalysts and semiconductors. Since conventional analysis technique using an energy-fixed X-ray excitation source is inadequate to obtain satisfactory surface sensitivity and quantitative accuracy for catalysts, for development of the titled technique, this project makes experiment using energy-variable synchrotron radiation to modify the parameter on motion of low-speed electrons in solids which is obtained by Monte Carlo calculation. For establishment of the high-accuracy quantitative analysis technique of surface compositions of materials such as catalyst of which performance is dominated by utmost surface, the project studies the attenuation length of electrons in solids by electron spectroscopy using soft X-rays from synchrotron radiation. In this fiscal year, the project established the equipment and technique for high-accuracy quantitative analysis of the thickness and electron attenuation length of silicon oxide films on silicon wafers by electron spectroscopy. (NEDO)

  18. Fiscal 1999 international cooperation project report. Development of high-precision quantitative analysis technology for catalyst surfaces by electron spectroscopy; 1999 nendo denshi bunkoho ni yoru shokubai hyomen koseido teiryo bunseki bijutsu no kaihatsu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-03-01

    This project targets to make analysis of surface chemical phenomena of solid catalysts possible, and establish the basis of intelligent design for catalytic materials, through development of an advanced electron spectroscopy for surface analysis. In fiscal 1999, the research was promoted by using the diffraction grating and driving mechanism introduced in fiscal 1998, and by developing the measurement result on silicon oxide films by radiation beam photoelectron spectroscopy. The measurement technique was established by the optimized measurement process which can treat variable parameters as constant. The analysis result of measurement data in fiscal 1999 showed the dependence of an electron damping length in silicon oxide films on radiation photon energy. The energy dependence well agreed with a theoretically obtained inelastic mean free path of electrons qualitatively, while was smaller by nearly 30% than the latter quantitatively. Measurement was made on the damping length in oxidation-active Gd and Nd oxide films. In both cases of Si and Si oxide film substrates, oxidation of substrates or formation of silicate was observed. (NEDO)

  19. Research on mechanism of and catalysts for extraction liquefaction of coal using coal-based solvents; Sekitankei yozai ni yoru sekitan no chushutsu ekika kiko to shokubai no kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1981-07-01

    Papers of Professor Yoshio Kamiya of Tokyo University are compiled into this report. The list of the papers includes (1) Synthesis of heavy fuel oils from coal; (2) Research and development of coal liquefaction; (3) Dissolution reaction of coal by hydrogen-donating aromatic solvents (I); (4) Effect of hydrogen-donor solvent on the liquefaction of coal; (5) Recent studies on the chemical structure of solvent refined coal; (6) Dissolution reaction of coal by hydrogen-donating aromatic solvents (II); (7) Future of coal as energy material; (8), (9), (10) same as (6) in the subject discussed; (11) Recent studies on coal liquefaction catalysts; (12) Environmental problems and drain treatment to accompany processes of converting fossil resources into fuels; (13) Chemistry of coal oxidation; (14) Fractionation and analysis of solvent refined coal by gel permeation chromatography; (15) Current state of research and development of coal liquefaction; (16) Properties and components of coal oils from coal liquefaction processes under development; (17) Solvent effect of coal derived aromatic compounds on the liquefaction of Akabira coal; (18) Chemistry of coal liquefaction; (19) Research and development of coal liquefaction in the U.S.; (20) Thermal treatment of coal-related aromatic ethers in tetralin solution; (21) Recent technology of utilizing heavy carbon resources; (22) Chemical properties and reactivity of coal; (23) Current state and future of development of coal liquefaction processes; and (24) Development of overseas coal liquefaction projects. (NEDO)

  20. Studies on the hydroprocessing of deashed oil. 13. ; Characterization of the catalyst used for 7800 hours. De-ashed-oil no suisoka bunkai hanno ni kansuru kenkyu. 13. ; 7800 jikan shiyozumi shokubai no characterization

    Energy Technology Data Exchange (ETDEWEB)

    Kaneko, T. (Mitsubishi Kasei Corp., Tokyo (Japan)); Kimura, T. (Cosmo Research Institute, Tokyo (Japan)); Kageyama, Y. (Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan))

    1992-11-05

    It was intended to darify long-term performance of a secondary hydrogenation catalyst used for about one year in a 50t/d brown coal liquefaction pilot plant built in Australia. A catalyst used for about 3,400 hours in the pilot plant was used to perform a life test of 7,800 hours in total to investigate the catalyst deactivation behavior, ashed metal and carbonaceous material deposition behavior, and changes in catalyst properties. A catalyst is considered to deactivate mainly because of deposition of carbonaceous materials on the catalyst in the initial stage of reaction and accumulation of alkaline metals (Na and K). The catalyst activity is estimated to reduce to about half the initial activity in about 1,000 hours, but it was found that the activity reduces and the properties change very little thereafter. From the fact that changes in selectivity to reaction associated with reduced activity and in product properties are small, and so are in the apparent activation energy, it was made clear that Cu-Ni-Mo/Al2O3 catalyst can be used for about one year. 3 refs., 9 figs., 1 tab.

  1. Studies on the hydroprocessing of deashed oil. 9. ; Characterization of the used catalyst in the pilot plant. Deashed oil no suisoka bunkai hanno ni kansuru kenkyu. 9. ; Pilot plant shiyozumi shokubai no characterization

    Energy Technology Data Exchange (ETDEWEB)

    Kaneko, T.; Hijiriyama, M. (Mitsubishi Kasei Co., Tokyo (Japan)); Kageyama, Y. (Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan))

    1990-11-29

    The secondary hydroprocessing process in the two-stage hydrogenating liquefaction equipment under development at Nippon Brown Coal Liquefaction Company uses a fixed bed system. To elucidate causes of catalyst activity degradation related therewith, catalyst used for about 1000 hours in a S -t/d pilot plant was collected to investigate deposition behavior of cokes and ashed metals and changes in catalyst properties. The catalyst is made of Ca-Ni-Mo/Al2O3, which was recovered from baskets placed in each layer in a reactor, washed in a predetermined manner, dried, and analyzed. In addition, in order to investigate remaining activity, 1-methylnaphthalene was hydrogenated, and deashed oil (DAO) was hydrocracked. The result may be summarized as follows: The major cause for the catalyst activity degradation is deposition of carbonaceous materials and ashed metals on the catalyst; and especially alkali metals (Na and K) were considered to be the major cause for the catalyst deactivation with time. 2 refs., 8 figs.

  2. Studies on the hydroprocessing of deashed Oil. 12. ; Characterization of the used catalyst in the pilot plant (2). Deashed oil no suisoka bunkai hanno ni kansuru kenkyu. 12. ; Pilot shiyozumi shokubai no characterization (2)

    Energy Technology Data Exchange (ETDEWEB)

    Kaneko, T.; Oshima, K. (Mitsubishi Kasei Corp., Tokyo (Japan)); Kageyama, Y. (Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan))

    1991-11-07

    With an objective to clarify causes of deactivation of catalysts used in brown coal liquefaction process, discussions were given on catalysts recovered after use of 3400 hours as to their behavior of accumulating ash metals and carbonaceous substances, changes in the catalyst properties, and remaining activity. The catalysts used were Ca-Ni-Mo/Al2O3. Metals in the catalysts were quantitatively analyzed using ICP emission spectral analysis and atomic absorption analysis, and the C-amount using a CHN coder. The surface area was measured using the BET process and the pore volume using a porosimeter. The remaining activity in the used catalysts was evaluated by modelled hydrogenation of 1-methylnaphthalene. The results may be summarized as follows: Metals deposited on the catalysts are Mg, Ca, Fe, Na, Si and K, identically with the case of 1000-hour used catalysts; carbonaceous mass on the catalysts would range from 10% to 15%; the catalyst surface area and pore volume decrease with increasing carbonaceous matter accumulation; and hydrogenation activity was found decreased in the model hydrogenation, which should be because the activity has correlation with alkaline metal accumulation, and the metals enter fine pores to poison activity points. 3 refs., 6 figs.

  3. Fiscal 2000 achievement report on the development of polymeric material from renewable resource using biocatalyst; 2000 nendo seitai shokubai wo riyoshita saisei kano shigen kara no kobunshi sozai no kaihatsu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    The project aims to develop a biocatalyst-assisted synthesizing method for efficiently manufacturing sugar containing polymers and polylactic acids which generate less environmental impact. The ALP-901 derived from actinomycetes operates best with 5% water content, and remains free of hydrolytic effect even when the rate rises to 20%, and catalyzes transesterification only. The esterification activity of bioprase rose remarkably upon addition of water. A polymer with a molecular weight of scores of thousands was obtained in the polymerization of sugar ester monomers. A sugar undecylenate with a double bond at an end was successfully polymerized. The sugar containing polymer exhibited excellent biodegradability. In a reaction of butanediol and lactide, several types of lactic oligomers different in molecular weight were synthesized. The oligomers were caused to react with divinylcarboxylic acid in the presence of an enzyme, and a polymerizable lactic oligomer was obtained. Furthermore, in a reaction between glucose and lactide, several lactic oligomer derivatives were synthesized, different in molecular weight. In a reaction of the derivatives and divinylcarboxylic acid with an enzyme added thereto, a polymerizable lactic oligomer derivative was obtained, which was brought into polymerization in the presence of a radical polymerization initiator for the production of a high molecular weight gel. (NEDO)

  4. Report on the achievements in the Sunshine Project in fiscal 1988. Coal energy (Studies on coal liquefying catalysts and a method for analyzing liquefied oil); 1988 nendo sekitan ekikayo shokubai oyobi ekikayu binsekiho no kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1989-03-01

    The present study, as part of the studies on coal liquefying technologies, was originally intended to develop optimal catalysts that make it possible to manufacture a liquid fuel from hydrogenation treatment of coal, and establish optimal reaction operation for the liquefaction process. To achieve the intentions, studies were moved forward on the following four sub-themes: (1) fundamentals and developmental research on catalysts for the direct liquefaction, (2) chemical structures of organic constituents in the coal liquefaction process, (3) research on the optimal reaction operation in the direct coal liquefaction process, and (4) studies on nature and behavior of ash constituent in the coal liquefaction process. The current fiscal year has performed the discussions on the following items based on the achievements attained by fiscal 1987: 1. as a study on liquefaction catalysts, (1) a study on properties of liquefaction catalysts, and (2) a study on characteristics of the liquefying reaction; 2. as a study on the analytic method, (1) a study on the liquefying reaction analyzing method, and (2) a study on the liquefied oil property analyzing method. In Item 1-(1), a prototype zeolite-based catalyst having high hydrogenating decomposition activity was used to execute a reaction to lighten the liquefied oil. As a result, it was revealed that the liquefied oil can be lightened efficiently by having the oil go through a two-stage reforming reaction. (NEDO)

  5. BTX production by in-situ contact reforming of low-temperature tar from coal with zeolite-derived catalysts; Zeolite kei shokubai wo mochiita sekitan teion tar no sesshoku kaishitsu ni yoru BTX no seisei

    Energy Technology Data Exchange (ETDEWEB)

    Matsunaga, T.; Fuda, K.; Murakami, K.; Kyo, M.; Hosoya, S.; Kobayashi, S. [Akita University, Akita (Japan). Mining College

    1996-10-28

    On BTX production process from low-temperature tar obtained by pyrolysis of coal, the effect of exchanged metallic species and reaction temperature were studied using metallic ion-exchanged Y-zeolite as catalyst. In experiment, three kinds of coals with different produced tar structures such as Taiheiyo and PSOC-830 sub-bituminous coals and Loy Yang brown coal were used. Y-zeolite ion-exchanged with metal chloride aqueous solution was used as catalyst. Zn{sup 2+}, Ni{sup 2+} and In{sup 3+} were used as metal ions to be exchanged. The experiment was conducted by heating a pyrolysis section up to 600{degree}C for one hour after preheating a contact reforming section up to a certain proper temperature. As a result, the Ni system catalyst was effective for BTX production from aromatic-abundant tar, while the Zn system one from lower aromatic tar. In general, relatively high yields of toluene and xylene were obtained at lower temperature, while those of benzene at higher temperature. 4 figs., 1 tab.

  6. Report on the evaluation of the development of the catalyst surface high accuracy quantitative analysis technology using electron spectroscopy; Denshi bunkoho ni yoru shokubai hyomen koseido teiryo bunseki gijutsu no kaihatsu hyoka hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-03-01

    An objective evaluation from a third party was conducted on the purpose, plan, execution method, achievement, etc. of a project 'The devilment of the catalyst surface high accuracy quantitative analysis technology using electron spectroscopy.' The purpose of the project is to make the relationing possible between the analytical results of the catalyst surface and the catalyst performance which has been so far difficult by heightening the accuracy of the catalyst quantitative surface analytical accuracy using the electron spectroscopy. The purpose and significance are judged to be worth a lot. This project is an industry/university/government joint project between the two countries. The project is excellent both in connection among research institutes and leadership of chief researchers, and it is judged that the joint research system fully functioned. The term of the project was shortened from 3 years in the first plan to 2 years, and therefore, the study was finished only on silicon oxide and organic thin films. However, it was determined that the study results are to be run in the magazine 'Surface and Interface Analysis,' which indicates that the achievement was judged to be very worth in the academic viewpoint. (NEDO)

  7. Report on the FY 1999 international research cooperation project. Development of polymer materials from renewable resources using biocatalyst; 1999 nendo seitai shokubai wo riyoshita saisei kano shigen kara no kobunshi sozai no kaihatsu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-03-01

    The R and D were conducted of saccharide polymer using biocatalyst and polylactic acid using biocatalyst. In the R and D of technology to synthesize polymerizing saccharide ester, the use of ALP901 led to success in acquiring hydrophobic polymerizing saccharide ester and saccharide ester with phenol residue. A study was also made of technology to synthesize polymerizing divinyl ester. In the study of the optimization of enzyme reaction conditions, the optimum temperature of ester exchange was 50 degrees C, and also under much higher temperature, 100 degrees C, the enzyme reaction was found to proceed with. In the study of the synthesis of polylactic acid, it was impossible to obtain polymer in the case of using ester lactate. However, in the case of using lactic acid, polymer was acquired at the numerical average molecular weight of approximately 1,200. In the study of the optimization of enzyme reaction conditions, polymer with high molecular weight was acquired at the enzyme amount of 5-10%. It was found out that the conversion rate exceeds 98% in the case of doing the reaction for more than 3 days at the enzyme amount of 5-10%. (NEDO)

  8. Fiscal 1999 research result report. Research on improvement of boiling heat transfer characteristics by photocatalyst wall; 1999 nendo hikari shokubai hekimen ni yoru futto netsu dentatsu tokusei kaizen ni kansuru kenkyu chosa hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-03-01

    Research was made on improvement of the wettability and boiling heat transfer characteristics of a photocatalyst wall. Measurement experiment of the wettability was made for anatase type titan oxide-coated Al, SUS and Pb plates, rutil type titan oxide-flame coated SUS plate, raw plate, and oxide-plasma coated titan plate. In the ground experiment, the contact angles of distilled water and oil on specimen surfaces were measured. In the microgravity experiment, falling droplet images were recorded by using the facility of Japan Microgravity Center (JAMIC). For obtaining the effect of radioactive emission, UV irradiation, {gamma} ray and neutron beam irradiation by nuclear reactor, and {gamma} ray irradiation by Co-60 were carried out. As the experiment result, the rutil type titan oxide-flame coated SUS plate, nonconductor-coated titan plate, and zircaloy plate showed large improvement of the wettability by {gamma} ray irradiation with Co-60. It was also confirmed that in particular, titan shows the large effect of radioactive emission, and the wettability deteriorates rapidly after {gamma} ray irradiation. (NEDO)

  9. Study on solar chemical heat pump system. Basic experiment on dehydrogenation of 2-propanol using heteropoly-acid photo catalyst; Solar chemical heat pump no kenkyu. Heteropoly sankei hikari shokubai wo mochiita 2-propanol no dassuiso hanno

    Energy Technology Data Exchange (ETDEWEB)

    Doi, T [Electrochemical Laboratory, Tsukuba (Japan); T-Raissi, A; Muradov, N [Florida Solar Energy Center, FL (United States)

    1996-10-27

    With the purpose of converting solar heat energy to an industrial heat energy, an examination was carried out empirically on the case of using a heteropoly-acid photo catalyst for the decomposition reaction process of 2-propanol. The experiment was performed in Florida Solar Energy Center, in the U.S.A.. The device for the experiment was constituted of a reaction part, distribution manifold for feeding from the lower part of the reaction part a 2-propanol solution for which a photo catalyst was suspended, storage tank served also as a gas-liquid separating container, and circulating pump. Silica-tangstic acid was used as the photo catalyst. In an outdoor experiment using solar radiation, the quantity of inclined global solar radiation was 530-950W/m{sup 2} in clear days and 100-600W/m{sup 2} in cloudy days, with temperatures between 17 and 26{degree}C throughout the experiment period. In addition, an indoor experiment was also conducted using an artificial light source (UV light). As a result of the experiment, the energy conversion efficiency was at most about 1% of incident UV light, a low figure compared to a heat utilization ratio of approximately 15% with a thermal catalyst. 6 refs., 8 figs.

  10. Industrial technology research and development project for global environment in fiscal 1998. Report on achievements in research and development of technologies for environment friendly catalysts; 1998 nendo kankyo chowagata shokubai gijutsu kenkyu kaihatsu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-03-01

    This paper describes the achievements in fiscal 1998 in developing environment friendly catalyst technologies. Development was proceeded in a water decomposing hydrogen production system of double tank system utilizing visible lights. The system connects combination of visible light responding type semiconductor powders with an oxidation and reduction mediator via a membrane (consisting of a hydrogen ion permeating membrane and an electric conductor). Discovery was made on two sets of semiconductor-mediator combinations (to produce hydrogen and oxygen) that meet the requirements. A composite oxide powder catalyst of nano structure was also realized. Verification was made on water decomposing hydrogen production by using multi-layered membranes composed of a hydrogen producing catalytic membrane, a semiconductor membrane, and an oxygen producing catalytic membrane. By using selective oxidation that uses trace amount of nitrogen dioxide as a gaseous phase catalyst, such good results were obtained as conversion rate of 10%, and selection rate of 27% in methanol and 23% in formaldehyde. Selective oxidation mechanisms in iron carried silica and oxidized tin were elucidated theoretically and experimentally. It was elucidated by calculating chemistry that effect of adding nitrogen dioxide lies in draw-out of hydrogen, NO is involved in draw-out of O from CH3OO, and NOx is involved in synthesizing formaldehyde from CH3O. (NEDO)

  11. Survey report for fiscal 2000 on survey of high-efficiency gasification technology of catalyst utilization type; 2000 nendo chosa hokokusho. Shokubai riyo gata kokoritsu gas ka gijutsu chosa

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    Survey and experimental research have been carried out on coal gasification using a pressurized internal circulation fluidized bed, spouted bed hydrogenation pyrolysis, supercritical water gasification, and a possibility of efficiency improvement by utilization of catalyst in chemical raw material production spouted bed gasification system. In the coal gasification using the pressurized internal circulation fluidized bed, an experiment was performed by using active alumina and Ni catalyst, where outstanding effect was identified. In the spouted bed hydrogenation pyrolysis, an experiment was executed by using iron hydroxide catalyst, but no noticeable effect was recognized. In the supercritical water gasification, an experiment was carried out by using Na{sub 2}CO2 and K{sub 2}CO{sub 3} catalysts, where it was found that the effect of the catalysts is little in the supercritical gasification reaction area of 800 degrees C. The power generation system composite with the chemical raw material production spouted bed gasification is a one-path system in which coal is gasified by the spouted bed gasification furnace, catalyst and steam are put into a heat exchanger to perform DME synthesis, and non-reacted gas is supplied as gas turbine fuel. Estimation was made on the possibility by an on-the-desk study, which requires experiments in the future. (NEDO)

  12. Report on the achievements in the Sunshine Project in fiscal 1986. Coal energy (Studies on coal liquefying catalysts and a liquefied oil analyzing method); 1986 nendo sekitan ekikayo shokubai oyobi ekikayu bunsekiho no kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1987-03-01

    The present studies are intended to study catalysts that make manufacture of liquid fuel possible through coal liquefying reactions, and establish a liquefied oil analyzing method. The following items are discussed based on the achievements obtained by fiscal 1985: in the studies on coal liquefying catalysts, (1) a study on selectively liquefying catalysts, in which elucidation is made on effects of catalyst carriers on reaction selectivity and life of coal liquefying catalysts, and fundamental data are accumulated toward designing the catalysts with respect to catalyst carriers capable of selective hydrogenating reactions, and to carrying conditions; and (2) a study on solvent properties and reaction conditions. in which Mo-based catalysts are used to perform kinetic discussions on the relationship between the liquefying reaction conditions and compositions of solvents and produced oil to accumulate data for elucidating the action mechanisms of the Mo-based catalysts. In the study of the liquefied oil analyzing method, discussions are carried out on a measuring technology to expand the conventional method for liquefied oil analysis to hard-to-volatilize components. For the light and medium oils, an analyzing method will be established that utilizes effectively the NMR method and the MS method that have been established to date. (NEDO)

  13. Mesothelioma: Identification of the Key Molecular Events Triggered by BAP1

    Science.gov (United States)

    2016-04-01

    germline BAP1 heterozygous mice is associated with deregulated inflammatory response and increased risk of mesothelioma. Oncogene. 2015 Jun 29. (Epub...Tommaso Campanella Cancer Center. 2015, September. Catanzaro, Italy. 5. 7th International Symposium DAMPS and HMGB. 2015, September. Bonn, Germany . 6...with deregulated inflammatory response and increased risk of mesothelioma A Napolitano1,2, L Pellegrini1, A Dey3, D Larson1, M Tanji1, EG Flores1, B

  14. FY 1998 report on the results of R and D projects by local consortiums for immediate effects. Development of titanium dioxide thin film photocatalysts sensitive to visible light and their applications to cleaning systems; 1998 nendo kashiko kasseina sanka chintan hikari shokubai usumaku no kaihatsu to sono system oyo seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-03-01

    The R and D project has been implemented for developing the thin film-making process techniques which can increase areas of titanium oxide (TiO{sub 2}) photocatalysts sensitive to visible light and their mass production. The fundamental investigations are directed to elucidation of the mechanisms involved in manifestation of activity in visible light of the visible light-sensitive thin film doped with the Cr, V or other ions. The sputtering involving no ion implantation is devised for producing the thin films, to realize the highest visible light sensitivity recorded for the thin TiO{sub 2} film. The sputtering process is investigated in detail for the film-making conditions, e.g., Ar pressure, effects of coexisting O{sub 2} gas, and power gap. The conditions under which the thin film serviceable under commercial conditions can be produced are not established yet, but it is confirmed that the coating film shows superhydrophilicity and photocatalytic activity for, e.g., sterilization, when irradiated with ultraviolet ray. The method has been established for evaluating deodorizing and contamination-preventive functions of the thin films in ultraviolet and visible rays. The project has also confirmed applicability of the techniques to the commercial products, and established the self-cleanable catalyst by combining the oxide catalytic function with the photocatalytic function. (NEDO)

  15. Fe(CO)5-catalyzed coprocessing of coal and heavy oil vacuum residue using syngas-water as a hydrogen source; Fe(CO)5 shokubai ni yoru gosei gas-mizu wo suisogen to suru sekitan-jushitsuyu no coprocessing

    Energy Technology Data Exchange (ETDEWEB)

    Hata, K.; Wada, K.; Mitsudo, T. [Kyoto University, Kyoto (Japan)

    1996-10-28

    Improvement in efficiency and profitability of hydrogenation reaction of heavy hydrocarbon resources is the most important matter to be done. In this study, coprocessing of coal and heavy oil vacuum residue was conducted using syngas-water as a hydrogen source. For the investigation of effect of the reaction temperature during the coprocessing of Wandoan coal and Arabian heavy vacuum residue using Fe(CO)5 as a catalyst, the conversion, 66.0% was obtained at 425{degree}C. For the investigation of effect of reaction time, the yield of light fractions further increased during the two stage reaction at 400{degree}C for 60 minutes and at 425{degree}C for 60 minutes. Finally, almost 100% of THF-soluble matter was obtained through the reaction using 2 mmol of Fe(CO)5 catalyst at 400{degree}C for 60 minutes, and hydrogenation of heavy oil was proceeded simultaneously. When comparing coprocessing reactions using three kinds of hydrogen sources, i.e., hydrogen, CO-water, and syngas-water, the conversion yield and oil yield obtained by using syngas-water were similar to those obtained by using hydrogen, which demonstrated the effectiveness of syngas-water. 2 refs., 2 figs., 2 tabs.

  16. Reaction mechanism of coal liquefaction: hydrogenolysis of model compound using synthetic pyrite as catalysts. 7. Property change of synthetic pyrite catalyst with the time after production; Sekitan ekika hanno kiko (model kagobutsu no hanno). 7. Gosei ryukatetsu shokubai no keiji henka ni tsuite

    Energy Technology Data Exchange (ETDEWEB)

    Ito, H.; Meno, H.; Uemaki, O.; Shibata, T.; Tsuji, T. [Hokkaido University, Sapporo (Japan)

    1996-10-28

    Reactions of various model compounds were investigated using synthetic pyrites for coal liquefaction. In this study, successive changes of the catalysts were investigated from the reactions of model compounds by using three different synthetic pyrites with the lapse of time after production. Benzyl phenyl ether, dibenzyl, and n-octylbenzene were used as model compounds. Reactions were conducted in an autoclave, into which sample, catalyst, decalin as solvent, and initial hydrogen pressure 10 MPa were charged. The autoclave was held at 450 or 475{degree}C of reaction temperature for 1 hour. The catalyst with a shorter lapse of time after production acted to hydrogen transfer, and inhibited the formation of condensation products due to the stabilization of decomposed fragment. It also acted to isomerization of materials by cutting alkyl side chains. When adding sulfur to the catalyst with longer lapse of time after production under these reaction conditions, it inhibited the formation of condensation products for the reaction of benzyl phenyl ether. However, it did not provide the effect for the reaction of n-octylbenzene. 5 refs., 3 figs.

  17. FY 2000 report on the research cooperation project - Research cooperation in developmental support for oil producing countries. Production of catalyst and development of the evaluation technology in Kuwait; 2000 nendo san'yukoku kaihatsu shien kenkyu kyoryoku jigyo seika hokokusho. Kuuweto ni okeru shokubai seizo oyobi hyoka gijutsu no kaihatsu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-09-01

    For the purpose of strengthening the economic infrastructure of Kuwait and also strengthening the relation between Japan and Kuwait by bringing up the catalyst production industry in Kuwait as one of the key industries, the research cooperation was made with Kuwait Catalyst Co. (KCC). In this research cooperation project, the following were conducted: survey of the catalyst production environment in Kuwait, survey of the actual condition of oil factories in Kuwait and the Middle East, trial production of the catalyst to meet the needs of Kuwait, evaluation of the catalyst suitable for oil factories in Kuwait and the Middle East and evaluation of the application conditions, development of technology for production/evaluation/application of the catalyst to meet the needs of Kuwait, etc. As to the trial catalyst production at KCC, the trial products for heavy oil desulfurization and light oil desulfurization stood comparison with the catalysts produced in Japan. KCC started trial operation in fall 2000, and the commercial production is smoothly continuing. In September 2001, the catalyst for heavy oil desulfurizer of KNPC, user, was delivered. The delivery to other users was also planned to be made. (NEDO)

  18. Report on the achievements in the Sunshine Project in fiscal 1991 on research and development of coal energy. Studies on coal liquefying catalysts and a method for analyzing liquefied oil; 1991 nendo sekitan ekikayo shokubai oyobi ekikayu bunseikiho no kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1992-03-01

    This paper describes the achievements in the Sunshine Project in fiscal 1991 on research of coal liquefying catalysts and a method for analyzing liquefied oil. Alkalis and alkali earth metals present during coal liquefied oil hydrogenation treatment deteriorate the activity remarkably as an effect of metal deposition from an Mo-based catalyst on the activity deterioration. Discussions were given on hydrogenating decomposition paths for bi-cyclic compounds by using reaction of model substances. Preliminary discussions were given jointly under the Japanese and Canadian technical cooperation on enhancing the quality of co-treated oil in the coal liquefaction, and on catalysts used therein. A 1-t/d PSU circulating solvent was studied to support the NEDO's bituminous coal liquefaction program. Analyses were carried out on acenaphthenes, biphenyls, phenanthrenes, and anthracenes in the oil liquefied from Wandoan coal. Discussions were given on CoMo/Al{sub 2}O{sub 3} on the effects of catalyst concentrations and particle sizes in the coal liquefying reaction. In order to elucidate different non-covalently bonded high-order structures of coal polymer assemblies, chemical treatment was applied to coals under a relatively mild condition (room temperature to 150 degrees C). Chemical structures as a result of the non-covalent bond in the coals were investigated from change due to the treatment in the pyridine extraction characteristics. (NEDO)

  19. FY 2000 report on the promotion projects by Research Institute of Innovative Technology for the Earth. Proceedings of the international seminar (Reports presented to the international workshop for selective oxidation catalysts); 2000 nendo chikyu kankyo sangyo gijutsu kaihatsu suishin jigyo kokusai seminar jigyo shiryo. Sentaku sanka shokubai kokusai workshop hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    Described herein are the FY 2000 results of the international workshop for selective oxidation catalysts, promoted by RITE. The session of methane activation includes a comprehensive lecture on designs of selective alkane oxidation catalysts developed since the 1980s, describing the simplified catalyst design procedures and, at the same time, pointing out the vapor-phase reactions governing the overall reactions at high temperature. The session of alkane oxidation includes a lecture on oxidation of ethane into acrolein in the presence of a silica catalyst supporting isolated active sites, stressing necessity for controlling the vapor-phase reactions and importance of isolating the active sites. The session of crystalline materials includes a lecture on Ti-siting in Ti-containing molecular sieve and selective oxidation catalyst functions, concentrating discussion on oxidation with H{sub 2}O{sub 2} as the oxidant on TS-1. The session of engineering hybrid includes a lecture on catalytic partial oxidation of alkanes in millisecond reactors, describing that possibility of controlling the vapor-phase reactions in the presence of monolith, porous-plate catalysts in a reactor through which the reactant gases pass in a very short time, of the order of millisecond. (NEDO)

  20. Emission behaviors of nitrous oxide from automobiles. 4th Report. Aging effect of three way catalyst on N2O mass emissions; Jidosha kara haishutsusareru asanka chisso (N2O) no haishutsu kyodo ni kansuru kenkyu. 4. Sangen shokubai no rekka ga N2O haishutsuryo ni oyobosu eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Koike, N; Suzuki, H; Odaka, M [Traffic Safety and Nuisance Research Institute, Tokyo (Japan)

    1997-10-01

    Several kind of three way catalysts with different metal compositions have been developed for trial and their N2O formation behaviors before and after the durability tests have been observed. Then by comparing the N2O formation behavior between new and durability tested catalysts, N2O increase mechanism with aging has been experimentally analyzed. As results, A catalyst temperature at peak N2O formation will sift to higher side by the aging and enters in the range that is the higher percentage in use during test cycle driving. Then this is the main cause of increase in total N2O emission. 4 refs., 10 figs., 2 tabs.

  1. FY 1980 Report on results of Sunshine Project. Research and development of coal liquefaction techniques (Development of direct hydrogenation type liquefaction plant and researches on liquefaction reactions in the presence of iron-based catalyst); 1980 nendo sekitan ekika gijutsu no kenkyu kaihatsu, chokusetsu suiten ekika plant no kaihatsu seika hokokusho. Tetsukei shokubai ni yoru ekika hanno no kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1981-03-01

    This program is aimed at development of iron-based catalyst suited for direct hydrogenation type coal liquefaction by elucidating the effects of the catalyst on the liquefaction reactions. The iron-based catalyst seems to act as the radical stabilizer rather than the reaction promoter, because the increased quantity of the catalyst and increased H{sub 2} pressure share the common pattern rather than the catalyst enhances the activity, which is associated with increased reaction temperature or residence time. This is more notably observed when the coal species is changed to brown coal. In other words, recombination of the decomposition products by polycondensation is accelerated in the presence of the catalyst in decomposition of brown coal from bituminous coal, with the result that the catalyst effects are more notably observed. Whether this results from difference in age between brown coal and bituminous coal or content of specific types of ashes should be elucidated, because this point is considered to deeply relate to eventual development of the liquefaction reaction system. The FY 1980 program includes the primary screening of different types of iron compounds and tests of some iron-metal-based catalysts. (NEDO)

  2. Structure and coke preventing characteristics of Ca-Ni-Mo/Al sub 2 O sub 3 catalyst for hydrogenation of brown coal liquid bottoms. Kattan ekikaabura suisokayo Ca-Ni-Mo/Al sub 2 O sub 3 shokubai no kozo to tansoshitsu seisei yokusei sayo

    Energy Technology Data Exchange (ETDEWEB)

    Kimura, T. (Cosmo Oil Co. Ltd., Tokyo (Japan)); Kaneko, T.; Kageyama, Y. (Mitsubishi Kasei Corp., Tokyo (Japan). Research Center); Kawai, S. (Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan))

    1990-09-01

    Operating a 50 t/d fixed bed pilot plant, hydroprocessing of de-ashed coal liquid bottoms (DAO) derived from Victorial Brown coal liquefaction has been carried out in Australia using a newly developed Ca-Ni-Mo/Al {sub 2} O {sub 3} catalyst. This catalyst has a great advantage compared with conventional molybdenum catalysts in that there is less coke formation using this catalyst as indicated by 5,000 h runs in a 0.1 t/d bench scale plant. In this paper, the catalyst active center and the role of Ca in the Ca-Ni-Mo/Al {sub 2} O {sub 3} catalyst were analyzed using Raman, TPS-XPS, EXAFS and AES methods. Molybdenum is loaded as CaMoO {sub 4} and X-ray diffraction data. But the oxide is changed to MoS {sub 2} after sulfiding treatment. Data of the Mo-S bond obtained from EXAFS analysis indicated that MoS {sub 2} has a tendency to pile up on the Ca-Ni-Mo/Al {sub 2} O {sub 3} catalyst. 20 refs., 12 figs., 5 tabs.

  3. Change in concentration distribution and equivalent rate constant with flow velocity in a boundary layer around a catalyst of non-uniform surface activity; Kotai shokubai taihyomen no kassei no fukin`itsusei ni motozuku kankyo sonai nodo bunpu oyobi toka hanno sokudo teisu no ryusoku ni yoru henka

    Energy Technology Data Exchange (ETDEWEB)

    Konno, J [National Institute for Resources and Environment, Tsukuba (Japan)

    1997-09-25

    In a flow system for vapor/solid catalytic reactions, there is a concentration distribution along the external catalyst surface, observed in the vicinity of the surface. Change in the reaction rate constant is followed for the case where the concentration distribution varies by flow. A 2-dimensional numerical model in which flow field and property conditions are simplified is used to analyze the change on the assumption that high-activity and low-activity sites are regularly distributed over the external catalyst surface. The transport equations for the reactants are numerically solved for given flow fields. It is found that the concentration distribution shape and equivalent reaction rate constant are almost the same as those in a stationary system at Pecret number of around 10 or lower, the concentration distribution gradually becomes uniform whereas equivalent rate constant increases as flow rate increases at Pecret number in a range from around 10 to 10{sup 6}, and they are almost constant at Pecret number beyond around 10{sup 6}. 3 refs., 11 figs., 1 tab.

  4. Report on the achievements in the Sunshine Project in fiscal 1992 on research and development of coal energy. Studies on coal liquefying catalysts and a method for analyzing liquefied oil; 1992 nendo sekitan ekikayo shokubai oyobi ekikayu bunsekiho no kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1983-03-01

    This paper describes the achievements in the Sunshine Project in fiscal 1992 on research of coal liquefying catalysts and a method for analyzing liquefied oil. Oxidative regeneration was performed on an Ni-W based waste catalyst used in reforming (hydrogenating) coal liquefied light oil fraction. If the regeneration can be done with low oxygen partial pressure and step-wise temperature rise, the activity after the regeneration can be restored to the level of a new catalyst, with sulfate production being suppressed. Model reaction was discussed by changing the amount of W and Mo carried by alumina. Suppressing the carrying amount can control the hydrogenation activity and the hydrogenating decomposition activity. Comparison was given on compositions of woods and such hydrogenation products as peat and coal. Analysis was performed on composition of the circulating solvent used in the NEDO bituminous coal liquefying PSU. In the initial stage of the operation, the solvent had higher concentrations in the groups of compounds not having alkyl groups, and compounds having the alkyl groups increased in the end of the operation. Discussions were given also on index materials to control the operation of solvent hydrogenating process. Efficient preparation conditions were discussed on an iron sulfide particulate catalyst that utilizes surface reaction of a solid metal while mechanical impact such as vibration is being given. Effects of the catalyst concentration in coal liquefaction were experimented by using oil soluble molybdenum, wherein no change was found in the reaction mechanism. (NEDO)

  5. Report on the achievements in the Sunshine Project in fiscal 1991 on research and development of coal energy. Studies on coal liquefying catalysts and a method for analyzing liquefied oil; 1991 nendo sekitan ekikayo shokubai oyobi ekikayu bunseikiho no kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1992-03-01

    This paper describes the achievements in the Sunshine Project in fiscal 1991 on research of coal liquefying catalysts and a method for analyzing liquefied oil. Alkalis and alkali earth metals present during coal liquefied oil hydrogenation treatment deteriorate the activity remarkably as an effect of metal deposition from an Mo-based catalyst on the activity deterioration. Discussions were given on hydrogenating decomposition paths for bi-cyclic compounds by using reaction of model substances. Preliminary discussions were given jointly under the Japanese and Canadian technical cooperation on enhancing the quality of co-treated oil in the coal liquefaction, and on catalysts used therein. A 1-t/d PSU circulating solvent was studied to support the NEDO's bituminous coal liquefaction program. Analyses were carried out on acenaphthenes, biphenyls, phenanthrenes, and anthracenes in the oil liquefied from Wandoan coal. Discussions were given on CoMo/Al{sub 2}O{sub 3} on the effects of catalyst concentrations and particle sizes in the coal liquefying reaction. In order to elucidate different non-covalently bonded high-order structures of coal polymer assemblies, chemical treatment was applied to coals under a relatively mild condition (room temperature to 150 degrees C). Chemical structures as a result of the non-covalent bond in the coals were investigated from change due to the treatment in the pyridine extraction characteristics. (NEDO)

  6. Research and development of a technology to create original high-function materials in fiscal 1998 (development of precision structure controlling materials by improving petroleum refining). Report on achievements in research and development of precision catalytic polymerization; 1998 nendo dokusoteki kokino zairyo sosei gijutsu no kenkyu kaihatsu seika hokokusho. Sekiyu seisei kodoka seimitsu kozo seigyo zairyo kaihatsu (seimitsu shokubai jugo no kenkyu kaihatsu)

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-03-01

    Research and development on precision catalytic polymerization aims at developing polymerizing catalysts that can control arbitrarily the molecular weight and three-dimensional regularity by which rapid enhancement can be expected in performance of additional polymerization type polymers, and the primary structure of terminal groups. Works are being done on two sub-themes of ultimate additional polymerization and orientation catalyst polymerization. The research and development of the ultimate additional polymerization included structural control in polymerization reaction in vinyl chloride, vinylester and acrylic monomers, radical polymerization with precision orientation control, anionic polymerization with precision structural control, and precision polymerization utilizing asymmetric metal porphyrin complexes. In the research and development of the orientation catalyst polymerization, the orientation catalyst polymerization was researched and developed, elementary reaction of metallocene was elucidated, high-performance carrier catalysts were developed, advanced function polymers were synthesized at high precision based on metathesis, and improvement of functions of polyolefin was researched and developed. Surveys and studies were carried out on fundamental technologies common to the above two themes re-commissioned to five universities. (NEDO)

  7. Fiscal 1999 achievement report on the venture business assisting type regional consortium - Minor business creation base type. Development of hypersensitive photocatalyst using oxide semiconductor thin film having nanostructure; 1999 nendo chiiki consortium kenkyu kaihatsu jigyo seika hokokusho. Nano bisai kozo wo yusuru sankabutsu handotai usumaku ni yoru chokokando hikari shokubai no kaihatsu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    The thin film structure of photocatalytic titanium oxide, capable of efficiently decomposing hazardous pollutants or the like, is refined to have a nanometric scale structure for a larger specific surface for the development of a photocatalytic thin film or powder film and for the development of decomposition capable air cleaner using a thus developed photocatalytic film. Described in this report are the results of a study conducted to elucidate the fabrication conditions, nanostructures, and photocatalytic features of titanium oxide thin films formed by spray thermolysis, RF (radio frequency) sputtering, reactive sputtering, and sol-gel process, a study of hazardous pollutant decomposing capability and nanostructure, the establishment of fabrication technologies, and the construction of a prototype air cleaner with the results of the said studies applied thereto. Among the various fabrication methods, the technology involving a hypersensitive thin film photocatalyst was established by combining the reactive sputtering method and the sol-gel method. It was found that the formation of prismatic crystals in the sol-gel method was the most important in achieving high performance in the hypersensitive thin film photocatalyst. (NEDO)

  8. Report on the achievements in the Sunshine Project in research and development of coal energy in fiscal 1988. Studies on coal liquefying catalysts and a method for analyzing liquefied oil; 1981 nendo sekitan ekikayo shokubai oyobi ekikayu bunsekiho no kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1990-03-01

    This paper describes the achievements in the Sunshine Project in fiscal 1988 in studies on coal liquefying catalysts and a method for analyzing liquefied oil. Acidic nature of the carrier was controlled, and deposition of carbonaceous substance on the catalyst was successfully suppressed while maintaining hydrogenation activity of the catalyst. It was possible to control hydrogenation activity of the liquefying catalyst by controlling the sulfurizing condition and the coalescence condition of Mo. Microscopic structural change in catalytically active metals due to oxygen compounds in the hydrogenation process of the liquefied oil was made clear, and so was the hydrogenation activity declining behavior associated therewith. A method was discovered that can evaluate easily and sensitively the individual functions of hydrogenation activity and hydrogenating decomposition activity of the catalyst. In the study on liquefying reaction characteristics, a fundamental study was performed to analyze the catalyst reaction characteristics in the secondary hydrogenation of liquefied oil. Studies on an analyzing method for the liquefied oil characteristics included those on NRM spectrum database, dynamic behavior of aromatic hydrocarbons in the liquefying solvent during the hydrogenating reaction, analysis of contact hydrogenating reaction using SEC, and stability of the solvent composition in the NEDOL liquefaction process. (NEDO)

  9. Test and survey on a next generation coal liquefying catalyst. Coal molecule scientific test and survey as the base for commercializing the coal liquefying technology; Jisedai sekitan ekika shokubai shiken chosa. Sekitan ekika gijutsu shogyoka kiban to shite no sekitan bunshi kagaku shiken chosa

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-03-01

    The test and survey on a next generation coal liquefying catalyst present a new proposal to raise catalytic activity in coal liquefaction, and perform demonstration experiments in a laboratory scale to search for possibility of developing a new coal liquefying catalyst from various viewpoints. To explain, discussions were given on the catalyst to perform the followings: liquefaction under extremely mild conditions by using ultra strong acids not limited only to metals; ion exchange method and swell carrying method to raise catalyst dispersion very highly, enhance the catalytic activity, and reduce the amount of catalyst to be used; mechanism of producing catalyst activating species to further enhance the activity of iron catalysts; and pursuit of morphological change in the activating species. The coal molecule scientific test and survey as the base for commercializing the coal liquefying technology performed the studies on the following items: pretreatment of coal that can realize reduction of coal liquefaction cost; configuration of the liquefaction reaction, liquefying catalysts, hydrocarbon gas generating mechanism, status of catalysts after liquefaction reaction, and reduction in gas purification cost by using gas separating membranes. Future possibilities were further searched through frank and constructive opinion exchanges among the committee members. (NEDO)

  10. Report on the achievements in the Sunshine Project in fiscal 1990 on research and development of coal energy. Studies on coal liquefying catalysts and a method for analyzing liquefied oil; 1990 nendo sekitan ekikayo shokubai oyobi ekikayu bunsekiho no kenkyu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1991-03-01

    This paper describes the achievements in the Sunshine Project in fiscal 1990 on research of coal liquefying catalysts and a method for analyzing liquefied oil. Regenerating deteriorated hydrogenating catalysts for coal liquefied oil makes the restoration non-reversible because of residual sulfate. Discussions were given on the regenerating mechanisms. It was found that adding Ru enhances activity of an Ni-Mo catalyst for hydrogenating denitrification and hydrogenation. In studying coal liquefying reaction, a basic study was performed to analyze a catalytic mechanism in the hydrogenating decomposition. Sequential lightening reaction process is being analyzed at molecular levels on coal, preasphaltene, asphaltene and oil. Investigations were carried out on hydrogenating denitrification, deoxygenation, ring opening, decomposition mechanism and catalytic action. A study on precision structural analysis has begun on PSU circulating solvent as a NEDO bituminous coal liquefaction supporting technology. In fiscal 1990, a preliminary study was performed to identify the overall image of the composition of the Wandoan coal liquefied oil. Detailed analysis was executed on naphthalenes and their hydrides. This paper also describes composition analysis and reaction analysis by using the GC/MS ion chromatogram method. It also dwells on the study on catalyst utilizing systems. (NEDO)

  11. FY 2000 report on the results of the regional consortium R and D project - Regional consortium energy R and D field. First year report. Commercialization of depth dechlorination/debromination refining catalyst of waste plastic derived oil and the liquefaction process; 2000 nendo chiiki consortium kenkyu kaihatsu jigyo - chiiki consortium kenkyu kaihatsu bun'ya. Hai plastic bunkaiyu no shindo datsuenso dasshuso seisei shokubai oyobi yuka process no jitsuyoka (dai 1 nendo) seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    The development was proceeded with of technology to produce iron oxide/porous carbon composite catalyst which promotes dehalogenation of thermal-degraded oil at low cost and in large quantity. This catalyst enables the improvement in operability and safety in the liquefaction process for mixed plastic and in quality of oil product. The development is also made of a regional distributed small batch liquefaction system with processing ability of 1t/day. Studies were made in the following 6 fields: 1) analysis of the dehalogenation performance of catalyst and the evaluation; 2) development of a method to industrially produce halogen compound refining catalyst; 3) R and D of a method to analyze environmental components; 4) evaluation study of halogen resistant materials and halogen resistant technology; 5) development of a small test device for commercialization of the liquefaction/degradation process; 6) comprehensive investigational study. In 1), the performance of prototype catalyst was confirmed, and the structure was analyzed. Also developed was iron chloride/SiO{sub 2} catalyst which converts organic halogen to inorganic halogen. (NEDO)

  12. Fiscal 1993 international research cooperation project. Feasibility study of finding out the seeds of international joint research (technology for environmental preservation using biotechnology, technology for effective use of unused hydrocarbon resource, technology for development of environmental harmony type catalyst); 1995 nendo kokusai kyoryoku jigyo. Kokusai kyodo kenkyu seeds hakkutsu no tame no FS chosa (biotechnology ni yoru kankyo taisaku gijutsu, miriyo tanka suiso shigen no yuko riyo gijutsu, kankyo chowagata shokubai kaihatsu gijutsu)

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-03-01

    This project is aimed at internationally cooperating in the R and D of industrial technology and improving industrial technology of Japan. For it, the following three technologies were investigated: 1) environmental preservation technology using biotechnology, 2) technology for effective use of unused hydrocarbon resource, 3) technology for development of environmental harmony type catalyst. In 1), a survey was conducted of applicability of biological surfactant to prevention measures of pollution by heavy distillate. It showed that part of the biological surfactants is reaching a stage of its being industrially produced by gene recombination bacteria, but as a whole, biosynthetic genes have hardly been elucidated. In 2), a survey of high-grade treatment technology of petroleum coke was made. It pointed out that it is necessary to develop a technology which makes the most of features of petroleum coke and allows defects. In 3), scientists and engineers of Japan and Europe searched for themes on which they can jointly study in the fields of NOx removal catalyst, up-grading of fuel, and development of catalyst combustion of fuel. 287 refs., 136 figs., 128 tabs.

  13. Fiscal 1998 achievement report on regional consortium research and development project. Venture business fostering regional consortium research and development in its 2nd year--Creation of key industries (Development of energy-efficient catalytic decomposition device for persistent halogen compounds for environmental conservation); 1998 nendo kankyo hozen no tame no nanbunkaisei halogen kagobutsu no sho energy shokubai bunkai sochi no kaihatsu seika hokokusho. 2

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-03-01

    Devices that decompose halogen compounds by use of AlPO{sub 4} are built, and studies are made concerning the collection of basic knowledge and findings, the settlement of problems that accompany scaleup, and the elucidation of mechanism of catalytic function occurrence. Tests are conducted at an intermediate plant, when catalytic performance is observed using a unit accommodating 1 liter of catalyst and chlorofluorocarbon (CFC) 12 is subjected to decomposition for the selection of proper operating conditions. Results similar to those from micro-reactor operation are attained when the reaction tube temperature is controlled. On the basis of the results, a real reactor and reaction system are designed and constructed, and CFC12 containing some CFC115 and CFC22 is made to undergo a decomposition reaction in this real reactor. It is then clarified that CFC catalytic decomposition proceeds at a low cost without generating dioxins and that therefore the process is commercially viable. In the study of catalytic adjustment, it is found that adjustment may be sufficiently effected when baking is conducted at 1,000 degrees C even when the extrusion process which demands low manufacturing cost is employed. Studies are also conducted about the mechanism of co-catalytic function occurrence. (NEDO)

  14. Predictors of antipsychotic monotherapy with olanzapine during a 1-year naturalistic study of schizophrenia patients in Japan

    Directory of Open Access Journals (Sweden)

    Ye W

    2012-01-01

    Full Text Available Wenyu Ye1, Haya Ascher-Svanum2, Jennifer A Flynn3, Yuka Tanji3, Michihiro Takahashi3,41Lilly Suzhou Pharmaceutical Co, Shanghai, People's Republic of China; 2Eli Lilly and Company, Indianapolis, IN, USA; 3Lilly Research Laboratories Japan, Eli Lilly Japan K.K., Kobe, 4Terauchi-Takahashi Psychiatric Clinic, Ashiya, JapanPurpose: Although expert guidelines for the treatment of schizophrenia recommend antipsychotic monotherapy, the use of antipsychotic polypharmacy is common. This study identified characteristics that differentiate patients with schizophrenia who are treated with olanzapine monotherapy versus polypharmacy in usual care in Japan.Patients and methods: In a large (N = 1850 prospective, observational study, Japanese patients with schizophrenia who initiated treatment with olanzapine were followed for 1 year. Consistent with past research, antipsychotic polypharmacy was defined as the concurrent use of olanzapine and another antipsychotic for at least 60 days. Switching was defined as discontinuing a prior antipsychotic therapy rather than augmenting the medication regimen. Predictors of antipsychotic monotherapy were based on information available at the time of olanzapine initiation. Baseline characteristics were compared using t-tests and Χ2 tests. Stepwise logistic regression was used to identify independent predictors of monotherapy.Results: Patients treated with olanzapine monotherapy (43.2% differed from those treated with antipsychotic polypharmacy (56.8% on demographics, treatment history, baseline symptom levels, functional levels, and treatment-emergent adverse events. Stepwise logistic regression identified multiple variables that significantly predicted monotherapy: older age, shorter duration of schizophrenia, outpatient status, comorbid medical conditions, lower body mass index, no prior anticholinergic use, no prior mood stabilizer use, and switching from a previous antipsychotic (typical or atypical

  15. Parent-child relationships and self‑control in male university students' desire to play video games.

    Science.gov (United States)

    Karbasizadeh, Sina; Jani, Masih; Keshvari, Mahtab

    2018-06-12

    To determine the relationship between the parent-child relationship, self-control and demographic characteristics and the desire to play video games among male university students at one university in Iran. This was a correlational, descriptive, applied study. A total of 103 male students were selected randomly as a study sample from the population of male students at Isfahan University in Iran. Data collection tools used were the Video Games Questionnaire, Tanji's Self-Control Scale, Parent-Child Relationship Questionnaire, and Demographic Questionnaire. Data were analysed using stepwise regression analysis. This study found several factors increased male students' desire to play video games. Demographic characteristics associated with increased tendency to play video games among male students in Iran are older age, larger number of family members, lower parental level of education and higher socio-economic class, while other significant factors are a lower level of self‑control and a poorer parent-child relationship. PARTICIPANTS': higher socio-economic class, lower level of self-control and older age explained 8.2%, 5.2% and 5.9% of their desire to play video games, respectively. These three variables together accounted for significantly 16.9% of a male student's desire to play video games in this study ( P video games in Iran. Moreover, lower levels of self-control and a poorer parent-child relationship were found to be accompanied by a greater desire to play video games among male university students. © 2018 RCN Publishing Company Ltd. All rights reserved. Not to be copied, transmitted or recorded in any way, in whole or part, without prior permission of the publishers.

  16. Restoration of Degraded Salt Affected Lands to Productive Forest Ecosystem

    Science.gov (United States)

    Singh, Yash; Singh, Gurbachan; Singh, Bajrang; Cerdà, Artemi

    2017-04-01

    Soil system determines the fluxes of energy and matter in the Earth and is the source of goods, services and resources to the humankind (Keesstra et al., 2012; Brevik et al., 2015; Keesstra et al., 2016). To restore and rehabilitate the soil system is a key strategy to recover the services the soils offers (Celentano et al., 2016; Galati et al., 2016; Parras-Alcantara et al., 2016). Transformation of degraded sodic lands in biodiversity rich productive forest ecosystem is a challenging task before the researchers all over the world. The soils of the degraded sites remain almost unfavorable for the normal growth, development and multiplication of organisms; all our attempts tend to alleviate the soil constraints. Land degradation due to presence of salts in the soil is an alarming threat to agricultural productivity and sustainability, particularly in arid and semiarid regions of the world (Tanji, 1990; Qadir et al., 2006). According to the FAO Land and Nutrition Management Service (2008), over 6% of the world's lands are affected by salinity, which accounts for more than 800 million ha in 100 countries. This is due to natural causes, extensive utilization of land (Egamberdieva et al., 2008), poor drainage systems and limited availability of irrigation water which causes salinization in many irrigated soils (Town et al., 2008).In India, about 6.73 million ha are salt affected which spread in 194 districts out of 584 districts in India and represents 2.1% of the geographical area of the country (Mandal et al., 2009).Out of these, 2.8 million ha are sodic in nature and primarily occurring in the Indo-Gangetic alluvial plains. These lands are degraded in structural, chemical, nutritional, hydrological and microbiological characteristics. The reclamation of salt affected soils with chemical amendments like gypsum and phospho-gypsum are in practice for the cultivation field crops under agricultural production. Forest development on such lands although takes considerable

  17. Safety and effectiveness of rapid-acting intramuscular olanzapine for agitation associated with schizophrenia – Japan postmarketing surveillance study

    Directory of Open Access Journals (Sweden)

    Katagiri H

    2018-01-01

    Full Text Available Hideaki Katagiri,1 Masanori Taketsuna,2 Shinpei Kondo,3 Kenta Kajimoto,4 Etsuko Aoi,5 Yuka Tanji1 1Bio Medicine, 2Statistical Sciences, 3Post Marketing Study Management, 4Scientific Communications, Medicines Development Unit Japan, 5Global Patient Safety Japan, Quality and Patient Safety, Eli Lilly Japan K.K., Kobe, Japan Objective: The objective of this study was to evaluate the safety and effectiveness of rapid-acting intramuscular (IM olanzapine in the treatment of acute agitation associated with schizophrenia in real-world clinical settings in Japan.Methods: In this multicenter, postmarketing surveillance (PMS study, patients with acute agitation associated with schizophrenia were treated with IM olanzapine daily in a daily clinical setting. The observational period ranged from 1 to 7 days, including the day of initial administration. Safety was assessed by reporting treatment-emergent adverse events (TEAEs and adverse drug reactions (ADRs. The Positive and Negative Syndrome Scale – Excited Component (PANSS-EC score was used to evaluate effectiveness at baseline and at 2 hours (after each administration, 2 days, and 3 days (end of the observational period from the last administration of the IM olanzapine injection.Results: The safety analysis set included 999 patients, and the initial dose of 10 mg was administered to 955 patients. TEAEs were reported in 28 patients (36 events, the most common of which were dyslalia (5 patients, akathisia and somno­lence (4 patients each, hepatic function abnormal (3 patients, and constipation and dehydration (2 patients each. One serious adverse event of akathisia occurred during the observation period. The PANSS-EC score (mean ± standard deviation was 23.3±6.4 (n=625 at baseline, 16.9±7.0 (n=522 at 2 hours after initial injection, and 14.9±6.5 (n=650 at the last observation carried forward.Conclusion: The results of this Japanese PMS study demonstrated that IM olanzapine is safe and has a

  18. Perceptions and impact of bipolar disorder in Japan: results of an Internet survey

    Directory of Open Access Journals (Sweden)

    Watanabe K

    2016-11-01

    Full Text Available Koichiro Watanabe,1 Eiji Harada,2 Takeshi Inoue,3 Yuka Tanji,2 Toshiaki Kikuchi1 1Department of Neuropsychiatry, Kyorin University, School of Medicine, Tokyo, 2Medical Science, Medicines Development Unit-Japan, Eli Lilly Japan KK, Hyogo, 3Department of Psychiatry, Tokyo Medical University, Tokyo, Japan Abstract: Bipolar disorder is a recurrent and episodic illness. This survey study assessed experiences and identified clinical insights of individuals with bipolar disorder. An Internet-based monitor system database was screened for patients with bipolar disorder in Japan (February and March 2013. Of 1,050 patients, 457 completed surveys, and results were analyzed with descriptive statistics. Approximately one-fourth of respondents were diagnosed with bipolar disorder on their first visit to medical institutions, although the most common initial diagnosis was depression/depressive state (65%. Mean time lag between first-time visit to a medical institution and receipt of correct diagnosis of bipolar disorder was 4 years; one-third of patients experienced more than 5 years of lag time. Three perceived reasons for lapsed time before correct diagnosis were “(patients Did not consider manic symptoms as illness, and did not tell the doctor about them,” “I (patient did not know of bipolar disorder,” and “Lack of communication between my doctor and myself (patient.” Among participants who believed that they were initially incorrectly diagnosed and improperly treated, most experienced socioeconomic problems, such as having long-term inability to work or to study (65%. Sources of encouragement for participants included “To have someone to consult with” (41% followed by having “People around me treat me the same as before” (40%. Individuals with bipolar disorder reported a time lag of many years before accurate diagnosis, and substantial burden imposed by the illness. Encouragement should be provided for individuals to live positively

  19. Predictors of continuation with olanzapine during the 1-year naturalistic treatment of patients with schizophrenia in Japan

    Directory of Open Access Journals (Sweden)

    Ye W

    2011-12-01

    Full Text Available Wenyu Ye1, Haya Ascher-Svanum2, Yuka Tanji3, Jennifer A Flynn3, Michihiro Takahashi3,41Lilly Suzhou Pharmaceutical Co, Shanghai, People’s Republic of China; 2Eli Lilly and Company, Indianapolis, IN, USA; 3Lilly Research Laboratories Japan, Eli Lilly Japan KK, Kobe, 4Terauchi-Takahashi Psychiatric Clinic, Ashiya, JapanPurpose: Treatment continuation is considered an important measure of antipsychotic effectiveness in schizophrenia, reflecting the medication’s efficacy, safety, and tolerability from both patients’ and clinicians’ perspectives. This study identified characteristics of patients with schizophrenia who continue olanzapine therapy for a 1-year period in Japan.Methods: In a large (N = 1850, prospective, observational study, Japanese patients with schizophrenia who initiated treatment with olanzapine were followed for 1 year. Baseline characteristics were compared using t-tests and chi-square tests. Stepwise logistic regression was used to identify independent baseline predictors of treatment continuation.Results: Most patients (68.2% continued with olanzapine therapy for the full 1-year study period, with an average duration of 265.5 ± 119.4 days. At baseline, patients who continued were significantly more likely to be male, older, and inpatients; have longer illness duration, higher negative and cognitive symptoms, better health-related quality of life, and prior anticholinergic use. Continuers were significantly less likely to engage in social activities, live independently, work for pay, or have prior antidepressant use. Continuers showed significantly greater early (3-month improvement in global symptom severity. Logistic regression found that continuation was significantly predicted by longer illness duration, lower positive symptoms, higher negative symptoms, and better health-related quality of life.Conclusions: In this large naturalistic study in Japan, most patients with schizophrenia stayed on olanzapine therapy for

  20. Effectiveness and safety of oral olanzapine treatment transitioned from rapid-acting intramuscular olanzapine for agitation associated with schizophrenia

    Directory of Open Access Journals (Sweden)

    Katagiri H

    2018-04-01

    Full Text Available Hideaki Katagiri,1 Masanori Taketsuna,2 Shinpei Kondo,3 Kenta Kajimoto,4 Etsuko Aoi,5 Yuka Tanji1 1Bio-Medicines, Medicines Development Unit Japan, Eli Lilly Japan K.K., Kobe, Japan; 2Statistical Sciences, Medicines Development Unit Japan, Eli Lilly Japan K.K., Kobe, Japan; 3Post Marketing Study Management, Medicines Development Unit Japan, Eli Lilly Japan K.K., Kobe, Japan; 4Scientific Communications, Medicines Development Unit Japan, Eli Lilly Japan K.K., Kobe, Japan; 5Global Patient Safety Japan, Quality and Patient Safety, Eli Lilly Japan K.K., Kobe, Japan Objective: To assess the effectiveness and safety of oral olanzapine treatment transitioned from rapid-acting intramuscular olanzapine (RAIM in patients with acute agitation associated with schizophrenia in a real-world clinical setting. Methods: The postmarketing surveillance study with a 3-day observational period after the last RAIM administration was conducted (original study. Following this, an extended study was added for patients who received oral olanzapine after RAIM administration during the original study period, in order to additionally observe them for 7 days after initial RAIM administration. Effectiveness and safety from initial RAIM administration were evaluated using the Positive and Negative Syndrome Scale-Excited Component score and treatment-emergent adverse events (TEAEs, respectively. Results: The effectiveness and safety analysis set included a total of 521 and 522 patients, respectively. A majority of patients received 10 mg of RAIM (475/522 patients, 91.0%. The mean ± SD total Positive and Negative Syndrome Scale-Excited Component score was 23.6±6.2 (n=318 at baseline (before initial RAIM administration, 17.4±6.8 (n=280 at 2 hours after initial administration, 16.2±6.8 (n=246 2 days after final administration, 14.9±6.2 (n=248 3 days after final administration, 13.8±5.9 (n=242 4 days after final administration, 13.2±5.8 (n=221 7 days after initial