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Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition

Ex situ catalytic pyrolysis of biomass using char-supported nanoparticles metals (Fe and Ni) catalyst for syngas production and tar decomposition was investigated. The characterizations of fresh Fe-Ni/char catalysts were determined by TGA, SEM–EDS, Brunauer–Emmett–Teller (BET), and XPS. The results...

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Autores principales: Hu, Mian, Cui, Baihui, Xiao, Bo, Luo, Shiyi, Guo, Dabin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407590/
https://www.ncbi.nlm.nih.gov/pubmed/32708401
http://dx.doi.org/10.3390/nano10071397
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author Hu, Mian
Cui, Baihui
Xiao, Bo
Luo, Shiyi
Guo, Dabin
author_facet Hu, Mian
Cui, Baihui
Xiao, Bo
Luo, Shiyi
Guo, Dabin
author_sort Hu, Mian
collection PubMed
description Ex situ catalytic pyrolysis of biomass using char-supported nanoparticles metals (Fe and Ni) catalyst for syngas production and tar decomposition was investigated. The characterizations of fresh Fe-Ni/char catalysts were determined by TGA, SEM–EDS, Brunauer–Emmett–Teller (BET), and XPS. The results indicated that nanoparticles metal substances (Fe and Ni) successfully impregnated into the char support and increased the thermal stability of Fe-Ni/char. Fe-Ni/char catalyst exhibited relatively superior catalytic performance, where the syngas yield and the molar ratio of H2/CO were 0.91 Nm3/kg biomass and 1.64, respectively. Moreover, the lowest tar yield (43.21 g/kg biomass) and the highest tar catalytic conversion efficiency (84.97 wt.%) were also obtained under the condition of Ni/char. Ultimate analysis and GC–MS were employed to analyze the characterization of tar, and the results indicated that the percentage of aromatic hydrocarbons appreciably increased with the significantly decrease in oxygenated compounds and nitrogenous compounds, especially in Fe-Ni/char catalyst, when compared with no catalyst pyrolysis. After catalytic pyrolysis, XPS was employed to investigate the surface valence states of the characteristic elements in the catalysts. The results indicated that the metallic oxides (Me(x)O(y)) were reduced to metallic Me(0) as active sites for tar catalytic pyrolysis. The main reactions pathway involved during ex situ catalytic pyrolysis of biomass based on char-supported catalyst was proposed. These findings indicate that char has the potential to be used as an efficient and low-cost catalyst toward biomass pyrolysis for syngas production and tar decomposition.
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spelling pubmed-74075902020-08-25 Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition Hu, Mian Cui, Baihui Xiao, Bo Luo, Shiyi Guo, Dabin Nanomaterials (Basel) Article Ex situ catalytic pyrolysis of biomass using char-supported nanoparticles metals (Fe and Ni) catalyst for syngas production and tar decomposition was investigated. The characterizations of fresh Fe-Ni/char catalysts were determined by TGA, SEM–EDS, Brunauer–Emmett–Teller (BET), and XPS. The results indicated that nanoparticles metal substances (Fe and Ni) successfully impregnated into the char support and increased the thermal stability of Fe-Ni/char. Fe-Ni/char catalyst exhibited relatively superior catalytic performance, where the syngas yield and the molar ratio of H2/CO were 0.91 Nm3/kg biomass and 1.64, respectively. Moreover, the lowest tar yield (43.21 g/kg biomass) and the highest tar catalytic conversion efficiency (84.97 wt.%) were also obtained under the condition of Ni/char. Ultimate analysis and GC–MS were employed to analyze the characterization of tar, and the results indicated that the percentage of aromatic hydrocarbons appreciably increased with the significantly decrease in oxygenated compounds and nitrogenous compounds, especially in Fe-Ni/char catalyst, when compared with no catalyst pyrolysis. After catalytic pyrolysis, XPS was employed to investigate the surface valence states of the characteristic elements in the catalysts. The results indicated that the metallic oxides (Me(x)O(y)) were reduced to metallic Me(0) as active sites for tar catalytic pyrolysis. The main reactions pathway involved during ex situ catalytic pyrolysis of biomass based on char-supported catalyst was proposed. These findings indicate that char has the potential to be used as an efficient and low-cost catalyst toward biomass pyrolysis for syngas production and tar decomposition. MDPI 2020-07-18 /pmc/articles/PMC7407590/ /pubmed/32708401 http://dx.doi.org/10.3390/nano10071397 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hu, Mian
Cui, Baihui
Xiao, Bo
Luo, Shiyi
Guo, Dabin
Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition
title Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition
title_full Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition
title_fullStr Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition
title_full_unstemmed Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition
title_short Insight into the Ex Situ Catalytic Pyrolysis of Biomass over Char Supported Metals Catalyst: Syngas Production and Tar Decomposition
title_sort insight into the ex situ catalytic pyrolysis of biomass over char supported metals catalyst: syngas production and tar decomposition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407590/
https://www.ncbi.nlm.nih.gov/pubmed/32708401
http://dx.doi.org/10.3390/nano10071397
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