Catalytic decomposition of biomass tars: The impact of wood char surface characteristics on the catalytic performance for naphthalene removal
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作者:
Nestler, Florian
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Fraunhofer Inst Solar Energy Syst ISE, Heidenhofstr 2, D-79110 Freiburg, GermanyFraunhofer Inst Solar Energy Syst ISE, Heidenhofstr 2, D-79110 Freiburg, Germany
Nestler, Florian
[1
]
Burhenne, Luisa
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Univ British Columbia, 2360 East Mall, Vancouver, BC V6T 1Z3, CanadaFraunhofer Inst Solar Energy Syst ISE, Heidenhofstr 2, D-79110 Freiburg, Germany
Burhenne, Luisa
[2
]
Amtenbrink, Meike Juliane
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Fraunhofer Inst Solar Energy Syst ISE, Heidenhofstr 2, D-79110 Freiburg, GermanyFraunhofer Inst Solar Energy Syst ISE, Heidenhofstr 2, D-79110 Freiburg, Germany
Amtenbrink, Meike Juliane
[1
]
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Aicher, Thomas
[1
]
机构:
[1] Fraunhofer Inst Solar Energy Syst ISE, Heidenhofstr 2, D-79110 Freiburg, Germany
[2] Univ British Columbia, 2360 East Mall, Vancouver, BC V6T 1Z3, Canada
Catalytic decomposition of naphthalene over four different wood chars has been investigated. The effect of the pyrolysis temperature and activation with CO2 on the char structure and catalytic activity of the wood char has been studied in order to elucidate the tar decomposition rate and char stability towards deactivation. The wood char catalysts were produced by pyrolyzing spruce wood chips in a tubular batch reactor at 500 and 800 degrees C. Part of both char samples was further activated by purging CO2 through a bed of the pyrolysis char at 800 degrees C. The wood char reactivity for naphthalene cracking was investigated using a fixed bed quartz reactor in a heated furnace with a constant inlet gas flow of naphthalene. Thermal decomposition was evaluated at temperatures between 700 and 1050 degrees C and taken into account when assessing the catalytic activity of each wood char at 850 and 1050 degrees C. The structural features of the char catalyst were examined before and after the tar cracking experiment by CO2 and N-2 adsorption technique as well as scanning electron microscopy (SEM). Catalytic deactivation was studied by analyzing the surface structure of the char samples over exposure time to naphthalene. The self produced wood char samples were compared to a commercial activated carbon to classify their structural and catalytic properties. Catalytic tar cracking tests with all wood char catalysts confirmed that the activated char samples showed a high catalytic activity for naphthalene decomposition into carbon and hydrogen, whereas the non-activated char samples did not enhance the tar cracking reaction at 850 degrees C significantly. N-2 adsorption revealed that deactivation of the char catalyst happens mainly due to coke deposition blocking the char active sites. The time evolution of the wood char's tar cracking activity was found to be proportional to the amount of micropores with a pore diameter smaller than 0.7 nm. SEM measurements visualized structural changes on the macroscopic char surface caused by naphthalene decomposition under an inert nitrogen atmosphere. (C) 2016 Elsevier B.V. All rights reserved.
机构:
Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Gai, Chao
Jia, Hongxia
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Minist Ecol & Environm, Informat Ctr, Beijing 100029, Peoples R ChinaChinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Jia, Hongxia
Liu, Zhengang
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Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Liu, Zhengang
Luo, Lei
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Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Luo, Lei
Li, Dong
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Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
机构:
Pall Filtersyst GmbH Werk Schumacher Crailsheim, D-74564 Crailsheim, GermanyPall Filtersyst GmbH Werk Schumacher Crailsheim, D-74564 Crailsheim, Germany
Nacken, Manfred
Ma, Lina
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Vrije Univ Brussels, Dept Chem Engn CHIS, B-1050 Brussels, BelgiumPall Filtersyst GmbH Werk Schumacher Crailsheim, D-74564 Crailsheim, Germany
Ma, Lina
Heidenreich, Steffen
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Pall Filtersyst GmbH Werk Schumacher Crailsheim, D-74564 Crailsheim, GermanyPall Filtersyst GmbH Werk Schumacher Crailsheim, D-74564 Crailsheim, Germany
Heidenreich, Steffen
Baron, Gino V.
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Vrije Univ Brussels, Dept Chem Engn CHIS, B-1050 Brussels, BelgiumPall Filtersyst GmbH Werk Schumacher Crailsheim, D-74564 Crailsheim, Germany
机构:
China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R ChinaChina Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
Du, Shilin
Dong, Yichen
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China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R ChinaChina Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
Dong, Yichen
Guo, Feiqiang
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China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R ChinaChina Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
Guo, Feiqiang
Tian, Beile
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China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R ChinaChina Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
Tian, Beile
Mao, Songbo
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China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R ChinaChina Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
Mao, Songbo
Qian, Lin
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China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R ChinaChina Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
Qian, Lin
Xin, Chengyun
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China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R ChinaChina Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
机构:
Kyonggi Univ, Grad Sch, Dept Environm Energy Syst Engn, Suwon 443760, Gyeonggi Do, South KoreaKyonggi Univ, Grad Sch, Dept Environm Energy Syst Engn, Suwon 443760, Gyeonggi Do, South Korea
Kim, Sung Su
Hong, Sung Chang
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Kyonggi Univ, Grad Sch, Dept Environm Energy Syst Engn, Suwon 443760, Gyeonggi Do, South KoreaKyonggi Univ, Grad Sch, Dept Environm Energy Syst Engn, Suwon 443760, Gyeonggi Do, South Korea
机构:
Nanjing Inst Technol, Sch Energy & Power Engn, Nanjing 211167, Peoples R China
Shanghai Jiao Tong Univ, 1 Dongchuan Rd, Shanghai 200240, Peoples R ChinaNanjing Inst Technol, Sch Energy & Power Engn, Nanjing 211167, Peoples R China
Zhao, Shanhui
Xun, Chao
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Nanjing Inst Technol, Sch Energy & Power Engn, Nanjing 211167, Peoples R ChinaNanjing Inst Technol, Sch Energy & Power Engn, Nanjing 211167, Peoples R China
Xun, Chao
Xu, Wanjun
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Nanjing Inst Technol, Sch Energy & Power Engn, Nanjing 211167, Peoples R ChinaNanjing Inst Technol, Sch Energy & Power Engn, Nanjing 211167, Peoples R China