大学院工学研究院

佐藤 智司

サトウ サトシ  (Satoshi Sato)

基本情報

所属
千葉大学 大学院工学研究院 教授
学位
博士(工学)(1992年2月 名古屋大学)
工学修士(1985年3月 名古屋大学)

研究者番号
30187190
J-GLOBAL ID
200901062973244110
researchmap会員ID
1000010487

外部リンク

主要な論文

 256
  • Takami Inaba, Enggah Kurniawan, Takayoshi Hara, Yasuhiro Yamada, Satoshi Sato
    Bulletin of the Chemical Society of Japan 97(5) uoae049 2024年5月3日  査読有り最終著者責任著者
  • Yimin Li, Enggah Kurniawan, Fumiya Sato, Takayoshi Hara, Yasuhiro Yamada, Satoshi Sato
    Applied Catalysis A: General 669 119493 2024年1月  査読有り最終著者責任著者
  • TSUKUDA Eriko, SATO Satoshi, TAKAHASHI Ryoji, SODESAWA Toshiaki
    Catal. Commun. 8(9) 1349-1353 2007年9月  査読有り責任著者
  • Satoshi Sato, Ryoji Takahashi, Toshiaki Sodesawa, Nozomi Honda, Hideya Shimizu
    Catalysis Communications 4(2) 77-81 2003年2月  査読有り筆頭著者責任著者
    CeO2 catalyzed the selective dehydration of 1,3-diols into allylic alcohols at temperatures 300-375degreesC. In the dehydration of 1,3-propanediol over pure CeO2, 2-propen-1-ol is produced with the maximum selectivity of 98.9 mol% at 325degreesC. In the dehydration of 1,3-butanediol, 2-buten-1-ol and 3-buten-2-ol were produced with the sum of the selectivity > 99 mol% over CeO2, which showed attractive catalytic performance without decay at temperatures <375degreesC. In the reactions of 2-buten-1-ol, 1,2- and 1,4-butanediol, little dehydrated products were detected over the CeO2. (C) 2002 Elsevier Science B.V. All rights reserved.
  • Satoshi Sato, Ryoji Takahashi, Toshiaki Sodesawa, Ken-ichi Yuma, Yumiko Obata
    Journal of Catalysis 196(1) 195-199 2000年11月  査読有り筆頭著者責任著者
    A Cu metal surface was evaluated by a novel technique combining temperature-programmed reduction (TPR) measurement with N2O oxidation. The technique consists of three steps: the usual TPR measurement, the oxidation of the Cu surface by N2O, and the subsequent TPR measurement. The surface Cu oxidized by N2O was determined as a ratio of the peak area of the second TPR profile to that of the first one. It was found that bulk oxidation gradually proceeds after surface oxidation even at 30 degreesC. After the surface oxidation, the Cu2O produced by N2O oxidation varied with N2O exposure time (t) and had a linear correlation with ta at temperatures below 100 degreesC. The linear correlation in the parabolic plot proves that bulk oxidation proceeds through the diffusion process, and the Y-intercept corresponds to the surface oxidation. Both the dispersion and the Cu metal surface area of the sample were calculated from the intercept in the parabolic plot for the Cu2O produced by N2O oxidation. In addition, we found that a very large Cu metal surface area, as high as 32 m(2) g(cat)(-1), was created on a Cu-MgO catalyst through a citrate process using a molten mixture of copper nitrate, magnesium nitrate, and citric acid. (C) 2000 Academic Press.

主要なMISC

 37
  • Yue Li, Daolai Sun, Xinqiang Zhao, Yasuhiro Yamada, Satoshi Sato
    Applied Catalysis A: General 626 118340 2021年9月25日  査読有り最終著者責任著者
    Long-term stability of catalysts is one of important factors in heterogeneous catalysis. Solid acid catalysts are widely used in various reactions in the chemical industry, whereas they readily deactivate in most cases because of coke deposition on the acid sites. Therefore, efficient methods for controlling deactivation of solid acid catalysts are highly required. A method including both the doping of transition metals and the reaction operation in H2 flow (named as Metal-H2 method) is effective for suppressing coke deposition on solid acids in various cases. Although the Metal-H2 methodology has been utilized in some processes by different research groups, it has not been systematically summarized. In this review, we originally define the Metal-H2 method, and summarize the specific applications of the Metal-H2 method for controlling deactivation in cracking, reforming, dehydration, aldol condensation, and other processes.
  • Daolai Sun, Yue Li, Chenhui Yang, Yijie Su, Yasuhiro Yamada, Satoshi Sato
    Fuel Processing Technology 197 106193 2020年1月  査読有り招待有り最終著者責任著者
    Global supply of 1,3-butadiene (abbreviated as BD) is faced with a problem such as variation in chemical feedstock in recent years. Many research efforts have been made to produce BD from some renewable resources to replace petroleum. Biomass-derived C4 alcohols such as 2,3-, 1,3-, and 1,4-butanediol (BDO) can be regarded as alternative resources to manufacture BD. Direct dehydration of BDOs into BD as well as two-step dehydration through the corresponding unsaturated alcohols such as 3-buten-2-ol, 2-buten-1-ol, and 3-buten-1-ol has been proposed as an alternative BD production process. 2,3-BDO and 1,4-BDO can be directly dehydrated to produce BD over Sc2O3 and Yb2O3, respectively, whereas stepwise dehydration is necessary for other BDOs. In the two-step dehydration, efficient production of unsaturated alcohols from BDOs is a key technology to form BD with high selectivity. CeO2 with a cubic fluorite phase is extremely effective for the conversion of 1,3-BDO to form 3-buten-2-ol and 2-buten-1-ol, while heavy rare earth oxides are effective for the dehydration of 1,4-BDO to produce 3-buten-1-ol. We reviewed the BD production from C4 alcohols through not only direct dehydration but also stepwise dehydration in addition to the BD production through dehydrogenation of butenes which could be produced from 1- and 2-butanol.
  • Daolai Sun, Yasuhiro Yamada, Satoshi Sato, Wataru Ueda
    GREEN CHEMISTRY 19(14) 3186-3213 2017年7月  査読有り責任著者
    Production of fuels and chemicals from renewable biomass resources is an attractive way to alleviate the shortage of fossil fuels and reduce CO2 emission. Glycerol is an important biomass derivative currently produced as a by-product in the manufacture of biodiesel in a huge amount close to 10 wt% of the overall biodiesel production. The application of glycerol as a renewable raw material has attracted much attention in the last decade, and some catalytic technologies for the conversion of glycerol into useful chemicals such as methanol, epichlorohydrin, and 1,2-propanediol have been established. Acrylic acid is an important bulk chemical widely used in the manufacture of polymeric products and is currently produced in the petrochemical industry via two-step gas-phase oxidation of propylene. The depletion of fossil resources motivates developments in the production of acrylic acid from renewable raw materials. Glycerol has potential for use as a raw material for the production of acrylic acid, and the variety of glycerol derivatives provides opportunities for producing acrylic acid from glycerol through different ways. In this review, possible routes and the corresponding catalytic technologies for the conversion of glycerol to acrylic acid are primarily summarized, and the advantages as well as the challenges in each route are discussed.
  • Daolai Sun, Yasuhiro Yamada, Satoshi Sato, Wataru Ueda
    APPLIED CATALYSIS B-ENVIRONMENTAL 193 75-92 2016年9月  査読有り責任著者
    Applications of renewable biomass provide facile routes to alleviate the shortage of fossil fuels as well as to reduce the emission of CO2. Glycerol, which is currently produced as a waste in the biodiesel production, is one of the most attractive biomass resources. In the past decade, the conversion of glycerol into useful chemicals has attracted much attention, and glycerol is mainly converted by steam reforming, hydrogenolysis, oxidation, dehydration, esterification, carboxylation, acetalization, and chlorination. In this review, we focused on the catalytic hydrogenolysis of glycerol into C3 chemicals, which contain many industrially important products such as 1,2-propanediol, 1,3-propanediol, allyl alcohol, 1-propanol and propylene. In the hydrogenolysis of glycerol into propanediols, advantages and disadvantages of liquid and vapor-phase reactions are compared. In addition, recent studies on catalysts, reaction conditions, and proposed pathways are primarily summarized and discussed. Furthermore, new research trends are introduced in connection with the hydrogenolysis of glycerol into allyl alcohol, propanols and propylene. (C) 2016 Elsevier B.V. All rights reserved.

共同研究・競争的資金等の研究課題

 11