Effect of pore structure on catalytic properties of mesoporous silica supported rhodium catalysts for the hydrogenation of cinnamaldehyde
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Shimizu, Taichi
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Tohoku Univ, Grad Sch Engn, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, JapanTohoku Univ, Grad Sch Engn, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, Japan
Shimizu, Taichi
[1
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Ota, Masaki
[1
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Sato, Yoshiyuki
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Tohoku Univ, Grad Sch Engn, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, JapanTohoku Univ, Grad Sch Engn, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, Japan
Sato, Yoshiyuki
[1
]
Inomata, Hiroshi
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Tohoku Univ, Grad Sch Engn, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, JapanTohoku Univ, Grad Sch Engn, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, Japan
Inomata, Hiroshi
[1
]
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[1] Tohoku Univ, Grad Sch Engn, Res Ctr Supercrit Fluid Technol, Aoba Ku, Sendai, Miyagi 9808579, Japan
Rhodium particles for catalyzing the hydrogenation were effectively confined in the mesopores of MCM-41 and MSU-H silica by using supercritical CO2 as impregnation solvent. It was found that the calcination was an important step to control the size of Rh particles, and its influence was strongly dependent on the pore size distribution of mesoporous silica support. The prepared catalysts were characterized by X-ray diffraction (XRD), nitrogen adsorption, and transmission electron microscopy (TEM). While irregularly big Rh particles were often found on MCM-41 with smaller pore size (2.7 nm) during calcination at 873 K, homogeneous and small Rh particles were maintained inside MSU-H with relatively larger pore size (8.4 nm). The hydrogenation of cinnamaldehyde using the prepared catalysts was carried out in supercritical CO2. Rh/MSU-H which was calcined at 673 K provided the highest catalytic activity among the studied conditions. The results indicated that the catalyst on the support with larger pore size and smaller size of Rh particles might be desirable to attain higher catalytic activity. (C) 2015 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
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DV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, KazakhstanDV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
Talgatov, Eldar
Auyezkhanova, Assemgul
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DV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, KazakhstanDV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
Auyezkhanova, Assemgul
Zharmagambetova, Alima
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DV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, KazakhstanDV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
Zharmagambetova, Alima
Tastanova, Lyazzat
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K Zhubanov Aktobe Reg Univ, Dept Chem & Chem Technol, A Moldagulova Ave 34, Aktobe 030000, KazakhstanDV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
Tastanova, Lyazzat
Bukharbayeva, Farida
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DV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
Abai Kazakh Natl Pedag Univ, Inst Nat Sci & Geog, Kasybek Bi Str 30, Alma Ata 050026, KazakhstanDV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
Bukharbayeva, Farida
Jumekeyeva, Aigul
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DV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, KazakhstanDV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
Jumekeyeva, Aigul
Aubakirov, Talgat
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Pavlodar Pedag Univ, Higher Sch Nat Sci, Mir St 60, Pavlodar 140000, KazakhstanDV Sokolskiy Inst Fuel Catalysis & Electrochem, Lab Organ Catalysis, Kunaev Str 142, Alma Ata 050010, Kazakhstan
机构:
Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R ChinaChinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
Li, Jinjun
Xu, Xiuyan
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Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R ChinaChinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
Xu, Xiuyan
Hao, Zhengping
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Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R ChinaChinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
Hao, Zhengping
Zhao, Wei
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Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R ChinaChinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China