Effect of synthetic method on CeZr support and catalytic activity of related Rh catalyst in the oxidative reforming reaction
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作者:
Basile, F.
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Univ Bologna, Alma Mater Studiorum, Dipartimento Chim Ind Toso Montanari, Vle Risorgimento 4, I-40136 Bologna, ItalyUniv Bologna, Alma Mater Studiorum, Dipartimento Chim Ind Toso Montanari, Vle Risorgimento 4, I-40136 Bologna, Italy
Basile, F.
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Mafessanti, R.
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Univ Bologna, Alma Mater Studiorum, Dipartimento Chim Ind Toso Montanari, Vle Risorgimento 4, I-40136 Bologna, ItalyUniv Bologna, Alma Mater Studiorum, Dipartimento Chim Ind Toso Montanari, Vle Risorgimento 4, I-40136 Bologna, Italy
Mafessanti, R.
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Fasolini, A.
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Fornasari, G.
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Univ Bologna, Alma Mater Studiorum, Dipartimento Chim Ind Toso Montanari, Vle Risorgimento 4, I-40136 Bologna, ItalyUniv Bologna, Alma Mater Studiorum, Dipartimento Chim Ind Toso Montanari, Vle Risorgimento 4, I-40136 Bologna, Italy
Fornasari, G.
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Lombardi, E.
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Vaccari, A.
[1
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[1] Univ Bologna, Alma Mater Studiorum, Dipartimento Chim Ind Toso Montanari, Vle Risorgimento 4, I-40136 Bologna, Italy
The production of hydrogen by oxy-reforming is a process coupling steam reforming and catalytic partial oxidation allowing a balance of endothermic and exothermic reaction and smoothing the temperature profile. Nevertheless, deactivation of the catalyst by carbon formation is still an issue favored by low O/C and Steam/C ratio used in the process. The development of a catalyst for the oxy-reforming process started with the study of the synthesis by water-in-oil microemulsion of Ce0.5Zr0.5O2, to obtain high oxygen storage capacity, a property that helps the removal of eventually formed carbon. The studied synthesis was able to provide the desired Ce(0.5)Zr(0.5)O(2 )with a good stability with temperature, while classical coprecipitation gives Ce(0.5)Zr(0.5)O(2 )phase. The catalysts were impregnated with 2.7% of Rh and tested in oxy-reforming using low residence time and reaction conditions able to discriminate the differences in catalyst activity. The catalyst prepared using microemulsion CeZr showed higher conversion and stability when compared with the one synthesized by coprecipitation. In particular, differently from the coprecipitated sample, the carbon formation was not present in the one prepared by microemulsion. The activity and stability were linked to the characterization features of the mixed oxides and the impregnated catalysts.
机构:
Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Cao, Lei
Pan, Liwei
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Pan, Liwei
Ni, Changjun
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Ni, Changjun
Yuan, Zhongshan
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Yuan, Zhongshan
Wang, Shudong
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
机构:
Univ Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, SpainUniv Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, Spain
Carrero, A.
Calles, J. A.
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Univ Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, SpainUniv Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, Spain
Calles, J. A.
Vizcaino, A. J.
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Univ Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, SpainUniv Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, Spain
机构:
Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Cao, Lei
Pan, Liwei
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h-index: 0
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Pan, Liwei
Ni, Changjun
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h-index: 0
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Ni, Changjun
Yuan, Zhongshan
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Yuan, Zhongshan
Wang, Shudong
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Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
机构:
Univ Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, SpainUniv Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, Spain
Carrero, A.
Calles, J. A.
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h-index: 0
机构:
Univ Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, SpainUniv Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, Spain
Calles, J. A.
Vizcaino, A. J.
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机构:
Univ Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, SpainUniv Rey Juan Carlos, Dept Chem & Energy Technol, ESCET, Madrid 28933, Spain