Investigation of competitive tar reforming using activated char as catalyst

David Buentello-Montoya, Xiaolei Zhang, Simão Marques, Marco Geron

Research output: Contribution to journalConference article

5 Citations (Scopus)
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Abstract

Syngas tar removal is one of the biggest challenges for the gasification of biomass as a clean energy source. Efforts to understand the reforming mechanism of tar compounds have been continuous during the last decades. Kinetic studies often employ a single tar species, neglecting possible interactions between different tar compounds. On the other hand, char, a by-product from biomass gasification, presents opportunities to catalyze tar reforming. In this work, reforming experiments were conducted in a fixed-bed reactor using syngas with a known mixture of benzene (C6H6), toluene (C7H8) and naphthalene (C10H8). Hardwood char and an in-situ CO2-activated hardwood char were used as catalysts. The activated hardwood char exhibited the best reforming capabilities by converting 44% and 90% of the tars at 750 and 850°C, respectively, compared to 24% and 87% tar conversion obtained with the regular hardwood char at 750 and 850°C, respectively. From the experiments, a reduced mechanism model was proposed. This mechanism was used in computational simulations for analysis of the reaction kinetics, including possible catalyst selectivity. It was found that under a range of conditions, the benzene degradation is slower than its formation rate from toluene and naphthalene decomposition. This leads to increases in the benzene fraction at temperatures around 700°C. If the naphthalene and toluene concentrations are sufficient, benzene will accumulate even at high temperatures (around 800°C) regardless of residence times. It can be concluded that when benzene, toluene and naphthalene are present together, char favors the heterogeneous reforming of toluene and naphthalene, with benzene following an homogeneous reforming pathway.
Original languageEnglish
Pages (from-to)828-835
Number of pages8
JournalEnergy Procedia
Volume158
DOIs
Publication statusPublished - 28 Feb 2019
Event10th International Conference on Applied Energy, ICAE 2018 - Hong Kong, China
Duration: 22 Aug 201825 Aug 2018

Fingerprint

Tar
Reforming reactions
Naphthalene
Benzene
Hardwoods
Toluene
Catalysts
Gasification
Biomass
Catalyst selectivity
Reaction kinetics
Byproducts
Experiments
Decomposition
Degradation
Temperature
Kinetics

Keywords

  • tar
  • biomass
  • catalyst
  • char
  • gasification
  • syngas

Cite this

Buentello-Montoya, David ; Zhang, Xiaolei ; Marques, Simão ; Geron, Marco. / Investigation of competitive tar reforming using activated char as catalyst. In: Energy Procedia. 2019 ; Vol. 158. pp. 828-835.
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abstract = "Syngas tar removal is one of the biggest challenges for the gasification of biomass as a clean energy source. Efforts to understand the reforming mechanism of tar compounds have been continuous during the last decades. Kinetic studies often employ a single tar species, neglecting possible interactions between different tar compounds. On the other hand, char, a by-product from biomass gasification, presents opportunities to catalyze tar reforming. In this work, reforming experiments were conducted in a fixed-bed reactor using syngas with a known mixture of benzene (C6H6), toluene (C7H8) and naphthalene (C10H8). Hardwood char and an in-situ CO2-activated hardwood char were used as catalysts. The activated hardwood char exhibited the best reforming capabilities by converting 44{\%} and 90{\%} of the tars at 750 and 850°C, respectively, compared to 24{\%} and 87{\%} tar conversion obtained with the regular hardwood char at 750 and 850°C, respectively. From the experiments, a reduced mechanism model was proposed. This mechanism was used in computational simulations for analysis of the reaction kinetics, including possible catalyst selectivity. It was found that under a range of conditions, the benzene degradation is slower than its formation rate from toluene and naphthalene decomposition. This leads to increases in the benzene fraction at temperatures around 700°C. If the naphthalene and toluene concentrations are sufficient, benzene will accumulate even at high temperatures (around 800°C) regardless of residence times. It can be concluded that when benzene, toluene and naphthalene are present together, char favors the heterogeneous reforming of toluene and naphthalene, with benzene following an homogeneous reforming pathway.",
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Investigation of competitive tar reforming using activated char as catalyst. / Buentello-Montoya, David; Zhang, Xiaolei; Marques, Simão; Geron, Marco.

In: Energy Procedia, Vol. 158, 28.02.2019, p. 828-835.

Research output: Contribution to journalConference article

TY - JOUR

T1 - Investigation of competitive tar reforming using activated char as catalyst

AU - Buentello-Montoya, David

AU - Zhang, Xiaolei

AU - Marques, Simão

AU - Geron, Marco

PY - 2019/2/28

Y1 - 2019/2/28

N2 - Syngas tar removal is one of the biggest challenges for the gasification of biomass as a clean energy source. Efforts to understand the reforming mechanism of tar compounds have been continuous during the last decades. Kinetic studies often employ a single tar species, neglecting possible interactions between different tar compounds. On the other hand, char, a by-product from biomass gasification, presents opportunities to catalyze tar reforming. In this work, reforming experiments were conducted in a fixed-bed reactor using syngas with a known mixture of benzene (C6H6), toluene (C7H8) and naphthalene (C10H8). Hardwood char and an in-situ CO2-activated hardwood char were used as catalysts. The activated hardwood char exhibited the best reforming capabilities by converting 44% and 90% of the tars at 750 and 850°C, respectively, compared to 24% and 87% tar conversion obtained with the regular hardwood char at 750 and 850°C, respectively. From the experiments, a reduced mechanism model was proposed. This mechanism was used in computational simulations for analysis of the reaction kinetics, including possible catalyst selectivity. It was found that under a range of conditions, the benzene degradation is slower than its formation rate from toluene and naphthalene decomposition. This leads to increases in the benzene fraction at temperatures around 700°C. If the naphthalene and toluene concentrations are sufficient, benzene will accumulate even at high temperatures (around 800°C) regardless of residence times. It can be concluded that when benzene, toluene and naphthalene are present together, char favors the heterogeneous reforming of toluene and naphthalene, with benzene following an homogeneous reforming pathway.

AB - Syngas tar removal is one of the biggest challenges for the gasification of biomass as a clean energy source. Efforts to understand the reforming mechanism of tar compounds have been continuous during the last decades. Kinetic studies often employ a single tar species, neglecting possible interactions between different tar compounds. On the other hand, char, a by-product from biomass gasification, presents opportunities to catalyze tar reforming. In this work, reforming experiments were conducted in a fixed-bed reactor using syngas with a known mixture of benzene (C6H6), toluene (C7H8) and naphthalene (C10H8). Hardwood char and an in-situ CO2-activated hardwood char were used as catalysts. The activated hardwood char exhibited the best reforming capabilities by converting 44% and 90% of the tars at 750 and 850°C, respectively, compared to 24% and 87% tar conversion obtained with the regular hardwood char at 750 and 850°C, respectively. From the experiments, a reduced mechanism model was proposed. This mechanism was used in computational simulations for analysis of the reaction kinetics, including possible catalyst selectivity. It was found that under a range of conditions, the benzene degradation is slower than its formation rate from toluene and naphthalene decomposition. This leads to increases in the benzene fraction at temperatures around 700°C. If the naphthalene and toluene concentrations are sufficient, benzene will accumulate even at high temperatures (around 800°C) regardless of residence times. It can be concluded that when benzene, toluene and naphthalene are present together, char favors the heterogeneous reforming of toluene and naphthalene, with benzene following an homogeneous reforming pathway.

KW - tar

KW - biomass

KW - catalyst

KW - char

KW - gasification

KW - syngas

U2 - 10.1016/j.egypro.2019.01.216

DO - 10.1016/j.egypro.2019.01.216

M3 - Conference article

VL - 158

SP - 828

EP - 835

JO - Energy Procedia

JF - Energy Procedia

SN - 1876-6102

ER -