Hydrogen Peroxide Decomposition on Manganese Oxide Supported Catalyst: From Batch Reactor to Continuous Microreactor
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Russo, V.
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Protasova, L.
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Eindhoven Univ Technol, Micro Flow Chem & Proc Technol Grp, NL-5600 MB Eindhoven, NetherlandsUniv Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, Italy
Protasova, L.
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Turco, R.
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Univ Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, ItalyUniv Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, Italy
Turco, R.
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de Croon, M. H. J. M.
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Eindhoven Univ Technol, Lab Chem Reactor Engn, NL-5600 MB Eindhoven, NetherlandsUniv Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, Italy
de Croon, M. H. J. M.
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Hessel, V.
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Eindhoven Univ Technol, Micro Flow Chem & Proc Technol Grp, NL-5600 MB Eindhoven, NetherlandsUniv Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, Italy
Hessel, V.
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Santacesaria, E.
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Univ Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, ItalyUniv Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, Italy
Santacesaria, E.
[1
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[1] Univ Naples Federico II, Dipartimento Sci Chim, Naples Ind Chem Lab NICL, I-80126 Naples, Italy
The decomposition of hydrogen peroxide, promoted by a manganese oxide catalyst supported on gamma-alumina, has been studied in three different reactors. A batch reactor was used for catalyst screening and for studying the reaction kinetics, whereas a tubular continuous reactor was used for catalyst life testing and manganese loading optimization. In fact, a progressive deactivation was observed passing from 80% to 30% conversion. The final value of conversion remained unchanged for a long time The deactivation was due to partial manganese dissolution. On the contrary, a residual activity was observed, because the undissolved manganese oxide was more strongly bonded to the alumina surface. Therefore, by reducing the amount of loaded manganese from 5 to 2 wt %, a stable catalyst was obtained. Then, catalysts containing different amounts of manganese oxide (up to 2 wt %) were prepared and tested in a kinetic study. The same catalysts were deposited as catalytic coatings on the channels wall of microchanneled stainless steel plates and tested for coating stability. Finally, the best catalyst was also deposited on the walls of a microreactor to verify the possibility of process intensification. The kinetic law derived from the batch runs was successfully used to simulate the performance of the microreactor.
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Univ Yamanashi, Grad Fac Interdisciplinary Res, 4-4-37 Takeda, Kofu, Yamanashi 4008510, JapanUniv Yamanashi, Grad Fac Interdisciplinary Res, 4-4-37 Takeda, Kofu, Yamanashi 4008510, Japan
Omata, Kaori
Nambu, Tomonori
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Natl Inst Technol, Suzuka Coll, Dept Mat Sci & Engn, Shiroko Cho, Suzuka, Mie 5100294, JapanUniv Yamanashi, Grad Fac Interdisciplinary Res, 4-4-37 Takeda, Kofu, Yamanashi 4008510, Japan
Nambu, Tomonori
Yoshinaga, Hideo
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Taiyo Koko Co Ltd, Ako Lab, 1603-1 Higashioki,Nakahiro, Ako, Hyogo 6780232, JapanUniv Yamanashi, Grad Fac Interdisciplinary Res, 4-4-37 Takeda, Kofu, Yamanashi 4008510, Japan