Mechanism of coke formation and corresponding gas fraction characteristics in biochar-catalyzed tar reforming during Corn Straw Pyrolysis

Formation of coke deposition is the main problem that restricts the development of tar reforming and even biomass thermal conversion. Biochar, prepared from gasification at 800 °C, was used for the catalytic reforming of biomass pyrolysis tar at 650 °C, monitoring the syngas formation during coke de...

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Veröffentlicht in:Fuel processing technology 2021-10, Vol.221, p.106903, Article 106903
Hauptverfasser: Sun, Hongliang, Sun, Shaozeng, Feng, Dongdong, Zhao, Yijun, Zhang, Yu, Zhang, Linyao, Wu, Jiangquan, Qin, Yukun
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container_issue
container_start_page 106903
container_title Fuel processing technology
container_volume 221
creator Sun, Hongliang
Sun, Shaozeng
Feng, Dongdong
Zhao, Yijun
Zhang, Yu
Zhang, Linyao
Wu, Jiangquan
Qin, Yukun
description Formation of coke deposition is the main problem that restricts the development of tar reforming and even biomass thermal conversion. Biochar, prepared from gasification at 800 °C, was used for the catalytic reforming of biomass pyrolysis tar at 650 °C, monitoring the syngas formation during coke deposition. The principal consequences and conclusions are as follows: the coke yield increases from 10.9% to 18.9%, and the tar removal efficiency decreases from 89.0% to 56.7% when the feeding time of biomass is extended (10–50 min). The number of O-containing groups on the biochar surface decreases, and the proportion of minor aromatic rings increases. Biochar is more efficient in the catalytic removal of aliphatic components from tar than aromatic components. Catalytic reforming leads to the development of tar in the direction of increased aromatization. The addition of biochar has essentially no effect on CO yield and CO2 yield, while the CH4 yield decreases and the H2 yield increases. In addition to tar reforming, CH4 cracking is one of the pathways for coke generation on the biochar surface. The number of physical adsorption sites (nN2) and adsorption equilibrium constant (b) of biochar are obtained based on the N2 adsorption test. [Display omitted] •During feeding (0–50 min), the coke yield on biochar increases without saturation.•Evaluating tar conversion rate over biochar based on N2 adsorption was developed.•Coke deposition leads to reduced surface reactivity of biochar catalyst.•Addition of biochar increases H2 yield but decreases CH4 yield in the gas.•Coke deposition comes from aromatics, long-chain alkanes and CH4 in pyrolysis gas.
doi_str_mv 10.1016/j.fuproc.2021.106903
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Biochar, prepared from gasification at 800 °C, was used for the catalytic reforming of biomass pyrolysis tar at 650 °C, monitoring the syngas formation during coke deposition. The principal consequences and conclusions are as follows: the coke yield increases from 10.9% to 18.9%, and the tar removal efficiency decreases from 89.0% to 56.7% when the feeding time of biomass is extended (10–50 min). The number of O-containing groups on the biochar surface decreases, and the proportion of minor aromatic rings increases. Biochar is more efficient in the catalytic removal of aliphatic components from tar than aromatic components. Catalytic reforming leads to the development of tar in the direction of increased aromatization. The addition of biochar has essentially no effect on CO yield and CO2 yield, while the CH4 yield decreases and the H2 yield increases. In addition to tar reforming, CH4 cracking is one of the pathways for coke generation on the biochar surface. The number of physical adsorption sites (nN2) and adsorption equilibrium constant (b) of biochar are obtained based on the N2 adsorption test. [Display omitted] •During feeding (0–50 min), the coke yield on biochar increases without saturation.•Evaluating tar conversion rate over biochar based on N2 adsorption was developed.•Coke deposition leads to reduced surface reactivity of biochar catalyst.•Addition of biochar increases H2 yield but decreases CH4 yield in the gas.•Coke deposition comes from aromatics, long-chain alkanes and CH4 in pyrolysis gas.</description><identifier>ISSN: 0378-3820</identifier><identifier>EISSN: 1873-7188</identifier><identifier>DOI: 10.1016/j.fuproc.2021.106903</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adsorption ; Aromatic compounds ; aromatization ; Biochar ; Biomass ; carbon dioxide ; Coke deposition ; Coke oven gas ; corn straw ; Deposition ; Gasification ; Methane ; Methane cracking ; N2 adsorption ; Pyrolysis ; Reforming ; Surface chemistry ; Synthesis gas ; Tar reforming</subject><ispartof>Fuel processing technology, 2021-10, Vol.221, p.106903, Article 106903</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. 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Biochar, prepared from gasification at 800 °C, was used for the catalytic reforming of biomass pyrolysis tar at 650 °C, monitoring the syngas formation during coke deposition. The principal consequences and conclusions are as follows: the coke yield increases from 10.9% to 18.9%, and the tar removal efficiency decreases from 89.0% to 56.7% when the feeding time of biomass is extended (10–50 min). The number of O-containing groups on the biochar surface decreases, and the proportion of minor aromatic rings increases. Biochar is more efficient in the catalytic removal of aliphatic components from tar than aromatic components. Catalytic reforming leads to the development of tar in the direction of increased aromatization. The addition of biochar has essentially no effect on CO yield and CO2 yield, while the CH4 yield decreases and the H2 yield increases. In addition to tar reforming, CH4 cracking is one of the pathways for coke generation on the biochar surface. The number of physical adsorption sites (nN2) and adsorption equilibrium constant (b) of biochar are obtained based on the N2 adsorption test. 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Biochar, prepared from gasification at 800 °C, was used for the catalytic reforming of biomass pyrolysis tar at 650 °C, monitoring the syngas formation during coke deposition. The principal consequences and conclusions are as follows: the coke yield increases from 10.9% to 18.9%, and the tar removal efficiency decreases from 89.0% to 56.7% when the feeding time of biomass is extended (10–50 min). The number of O-containing groups on the biochar surface decreases, and the proportion of minor aromatic rings increases. Biochar is more efficient in the catalytic removal of aliphatic components from tar than aromatic components. Catalytic reforming leads to the development of tar in the direction of increased aromatization. The addition of biochar has essentially no effect on CO yield and CO2 yield, while the CH4 yield decreases and the H2 yield increases. In addition to tar reforming, CH4 cracking is one of the pathways for coke generation on the biochar surface. 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subjects Adsorption
Aromatic compounds
aromatization
Biochar
Biomass
carbon dioxide
Coke deposition
Coke oven gas
corn straw
Deposition
Gasification
Methane
Methane cracking
N2 adsorption
Pyrolysis
Reforming
Surface chemistry
Synthesis gas
Tar reforming
title Mechanism of coke formation and corresponding gas fraction characteristics in biochar-catalyzed tar reforming during Corn Straw Pyrolysis
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