Enhancing the catalytic properties of a biochar-supported copper oxide in nitric oxide selective reduction with hydrogen
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作者:
Yakub, Ibrahim
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Univ Sheffield, Dept Chem & Biol Engn, Mappin St, Sheffield S1 4LZ, England
Univ Malaysia Sarawak, Dept Chem Engn & Energy Sustainabil, Jalan Dato Mohd Musa, Kota Samarahan 94300, Sarawak, MalaysiaUniv Sheffield, Dept Chem & Biol Engn, Mappin St, Sheffield S1 4LZ, England
Yakub, Ibrahim
[1
,2
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Said, Khairul Anwar Mohamad
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Univ Malaysia Sarawak, Dept Chem Engn & Energy Sustainabil, Jalan Dato Mohd Musa, Kota Samarahan 94300, Sarawak, MalaysiaUniv Sheffield, Dept Chem & Biol Engn, Mappin St, Sheffield S1 4LZ, England
Said, Khairul Anwar Mohamad
[2
]
Baini, Rubiyah
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Univ Malaysia Sarawak, Dept Chem Engn & Energy Sustainabil, Jalan Dato Mohd Musa, Kota Samarahan 94300, Sarawak, MalaysiaUniv Sheffield, Dept Chem & Biol Engn, Mappin St, Sheffield S1 4LZ, England
Baini, Rubiyah
[2
]
Amin, Mohamed Afizal Mohamed
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Univ Malaysia Sarawak, Dept Chem Engn & Energy Sustainabil, Jalan Dato Mohd Musa, Kota Samarahan 94300, Sarawak, MalaysiaUniv Sheffield, Dept Chem & Biol Engn, Mappin St, Sheffield S1 4LZ, England
Copper oxide supported on a biochar could suffer from a low nitrogen-selectivity and carbon combustion, despite the sustainability prospect it provides in replacing the utilization of non-renewable materials as the catalyst support to reduce nitric oxide. Bimetallic catalysis is a means to improve catalytic properties including conversion and selectivity. Therefore, this work investigates the enhancement of carbon-supported copper oxides in nitric oxide selective reduction using hydrogen by co-impregnating iron or manganese with copper. The bimetallic catalysts were prepared via sequential incipient wetness method where copper oxide was impregnated and calcined prior to the impregnation and calcination of the co-catalyst. As iron was paired with copper, the nitrogen selectivity was enhanced by 20% (almost 100% selective) at 200 degrees C while reducing the carbon combustion rate by 20% at a higher temperature (300 degrees C). This improvement was regarded as the synergistic effects obtained by the bimetallic oxide catalysts as a result of the altered elemental composition (from 60% carbon content to 50%), catalyst acidity (from 12 mmol NH3 desorbed/g to 16 mmol NH(3)d/g) and redox properties (from 5 mmol H-2 consumed/g to 3 mmol H-2/g). Flash elemental analyser showed that this catalyst has lower carbon content but higher oxygen amount (30% compared to 19%) which is correlated to the higher acidic sites, as confirmed via temperature-programmed desorption analysis and Fourier-Transform infra-red spectroscopy. Varying the ratio between the two catalysts revealed that different mechanisms govern the reaction that could be the key to understanding the enhancement of the nitrogen-selectivity. Nevertheless, further studies are required to ensure the applicability of this catalytic system in the industry.
机构:
State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
Zhichen Duan
Jian Liu
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State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
Jian Liu
Juan Shi
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State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
Juan Shi
Zhen Zhao
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State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
Zhen Zhao
Yuechang Wei
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State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
Yuechang Wei
Xiao Zhang
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机构:
State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
Xiao Zhang
Guiyuan Jiang
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State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
Guiyuan Jiang
Aijun Duan
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State Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of PetroleumState Key Laboratory of Heavy Oil Processing, Beijing Key Lab of Oil & Gas Pollution Control, China University of Petroleum
机构:Nankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Li, LD
Chen, JX
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机构:Nankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Chen, JX
Zhang, SJ
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机构:Nankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Zhang, SJ
Guan, NJ
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Nankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R ChinaNankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Guan, NJ
Richter, M
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机构:Nankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Richter, M
Eckelt, R
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机构:Nankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Eckelt, R
Fricke, R
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机构:Nankai Univ, Cooperat Inst Nankai, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
机构:
Korea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South Korea
Sungkyunkwan Univ, Dept Energy Sci, Suwon 16419, South KoreaKorea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South Korea
Zhang, Zhenru
Park, Cheolwoo
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Korea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South KoreaKorea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South Korea
Park, Cheolwoo
Noh, Sunghyun
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Korea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South KoreaKorea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South Korea
Noh, Sunghyun
Kim, Hyo Won
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Korea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South KoreaKorea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South Korea
Kim, Hyo Won
Ahn, Tae Kyu
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Sungkyunkwan Univ, Dept Energy Sci, Suwon 16419, South KoreaKorea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South Korea
Ahn, Tae Kyu
Kim, Wooyul
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Korea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South KoreaKorea Inst Energy Technol KENTECH, KENTECH Inst Environm & Climate Technol, Dept Energy Engn, Naju 58330, South Korea