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| 5. |  | FABROWSKI, F. J.; BOLZON de MUÑIZ, G. I.; KLOCK, U. Abordagem botânica das variedades populares da bracatinga (Mimosa scabrella, Bentahm). In: INTERNATIONAL CONGRESS AND EXHIBITION ON FOREST, 5., 1999, Curitiba. Forest 99: [resumos]. Rio de Janeiro: BIOSFERA, 1999. 1 CD-ROM. Autoria bilíngue: CONGRESSO E EXPOSICAO INTERNACIONAL SOBRE FLORESTAS, 5., 1999, Curitiba.| Biblioteca(s): Embrapa Florestas. |
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| 6. | | MARINHO, N. P.; NISGOSKI, S.; BOLZON DE MUÑIZ, G. I. Avaliação das dimensões das fibras de colmos de bambu, Dendrocalamus giganteus (Wall) Munro, em diferentes idades. Ciência Florestal, Santa Maria, v. 24, n. 1, p. 251-256, jan./mar. 2014. Nota Técnica.| Biblioteca(s): Embrapa Florestas. |
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| 11. | | BOLZON de MUNIZ, G. I.; BORSATO, R.; RENNER, R. Caracterização química e físico-mecânica da madeira da espécie miconiacinnamomifolia (de candole) Naudin, Floresta Ombrófila Densa. In: INTERNATIONAL CONGRESS AND EXHIBITION ON FOREST, 5., 1999, Curitiba. Forest 99: [resumos]. Rio de Janeiro: BIOSFERA, 1999. 1 CD-ROM. Autoria bilíngue: CONGRESSO E EXPOSICAO INTERNACIONAL SOBRE FLORESTAS, 5., 1999, Curitiba.| Biblioteca(s): Embrapa Florestas. |
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Registro Completo
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Biblioteca(s): |
Embrapa Florestas. |
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Data corrente: |
06/09/2017 |
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Data da última atualização: |
29/01/2018 |
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Tipo da produção científica: |
Artigo em Anais de Congresso |
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Autoria: |
CADEMARTORI, P. H. G. de; MATTOS, B. D.; LOURENÇON, T. V.; HARRES, A. N.; CAPOBIANCO, G.; MATOS, M. de; BOLZON DE MUNIZ, G. I.; MAGALHAES, W. L. E. |
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Afiliação: |
Pedro Henrique Gonzalez de Cademartori, PHD, UFPR; Bruno Dufau Mattos, Estudante PHD, UFPR; Tainise Vergara Lourençon, Estudanre PHD, UFPR; Andrey Nicolas Harres, Estudante graduada, UFPR; Gino Capobianco, Professor, UNIGUAÇU; Mailson de Matos, Estudante PHD, UFPR; Graciela Ines Bolzon de Muniz, Professora, UFPR; WASHINGTON LUIZ ESTEVES MAGALHAES, CNPF. |
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Título: |
Production of activated carbon from fast-pyrolysis biochar. |
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Ano de publicação: |
2017 |
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Fonte/Imprenta: |
In: INTERNATIONAL SYMPOSIUM ON WOOD, FIBRE AND PULPING CHEMISTRY, 19., 2017, Porto Seguro. Proceedings. Viçosa, MG: UFV, 2017. |
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Páginas: |
p. 229-232. |
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Idioma: |
Inglês |
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Conteúdo: |
Thermochemical conversion of lignocellulosic biomass via fast-pyrolysis technique has become an interesting alternative to produce valuable bio-based products, such as the bio-oil. This alternative, for instance, can increase even more the profitability of such well-consolidated pulp and paper industries by turning it into more energetically self-sufficient processo Besides bio-oil, the fast-pyrolysis process results in many byproducts with high economic and environmental benefits. Biochar is one of these byproducts, and it can be activated by physical and chemical methods to use for water treatment and for environmental remediation. This study investigates the activation of biochar obtained from the fast-pyrolysis of wood biomass. The biochar was collected from a pilot-plant of bio-oil production and then activated via physical route (C02) at 800°C for 30 and 60 minutes; and via chemical route (H3P04) at 450, 550 and 650°C for 60 minutes. The activated carbon was characterized by product yield, proximate analysis, surface area and thermogravimetric analysis. The chemical routes with H3P04 were more efficient than the physical routes with CO2. The chemical activation at 450°C presented the highest product yield (80.47%) followed by a decrease in the yield to 71-75% with the increase of the temperature. The fixed carbon content increased after both physical and chemical activation, remaining around 91%. On the other hand, the volatile matter decreased significantly, especially in the physical routes. The surface area increased from 17.94 (untreated biochar) to 450-655 m2/g, confirming the improvement of the porosity, mainly in the biochar activated by H3P04 at 450°C and by CO2 for 60 minutes. Ali biochar activated by chemical routes presented similar residual mass at 600°C, whereas the material physically activated with CO2 presented lower residual mass, especially the one treated for 30 minutes. Overall, these results provide an alternative to produce a high added-value material from a fast-pyrolysis byproduct, encouraging the exploration of thermochemical conversion of lignocellulosic biomass. MenosThermochemical conversion of lignocellulosic biomass via fast-pyrolysis technique has become an interesting alternative to produce valuable bio-based products, such as the bio-oil. This alternative, for instance, can increase even more the profitability of such well-consolidated pulp and paper industries by turning it into more energetically self-sufficient processo Besides bio-oil, the fast-pyrolysis process results in many byproducts with high economic and environmental benefits. Biochar is one of these byproducts, and it can be activated by physical and chemical methods to use for water treatment and for environmental remediation. This study investigates the activation of biochar obtained from the fast-pyrolysis of wood biomass. The biochar was collected from a pilot-plant of bio-oil production and then activated via physical route (C02) at 800°C for 30 and 60 minutes; and via chemical route (H3P04) at 450, 550 and 650°C for 60 minutes. The activated carbon was characterized by product yield, proximate analysis, surface area and thermogravimetric analysis. The chemical routes with H3P04 were more efficient than the physical routes with CO2. The chemical activation at 450°C presented the highest product yield (80.47%) followed by a decrease in the yield to 71-75% with the increase of the temperature. The fixed carbon content increased after both physical and chemical activation, remaining around 91%. On the other hand, the volatile matter decreased significantly, especiall... Mostrar Tudo |
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Palavras-Chave: |
Bio óleo; Bio-oil; Biochar activation; Biorefinaria; Conversão termoquímica; Thermochemical conversion. |
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Thesaurus NAL: |
Activated carbon; Biorefining; surface area. |
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Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/163591/1/2017-Washington-ISWFPC-Production.pdf
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Marc: |
LEADER 03102nam a2200313 a 4500
001 2075214
005 2018-01-29
008 2017 bl uuuu u00u1 u #d
100 1 $aCADEMARTORI, P. H. G. de
245 $aProduction of activated carbon from fast-pyrolysis biochar.$h[electronic resource]
260 $aIn: INTERNATIONAL SYMPOSIUM ON WOOD, FIBRE AND PULPING CHEMISTRY, 19., 2017, Porto Seguro. Proceedings. Viçosa, MG: UFV$c2017
300 $ap. 229-232.
520 $aThermochemical conversion of lignocellulosic biomass via fast-pyrolysis technique has become an interesting alternative to produce valuable bio-based products, such as the bio-oil. This alternative, for instance, can increase even more the profitability of such well-consolidated pulp and paper industries by turning it into more energetically self-sufficient processo Besides bio-oil, the fast-pyrolysis process results in many byproducts with high economic and environmental benefits. Biochar is one of these byproducts, and it can be activated by physical and chemical methods to use for water treatment and for environmental remediation. This study investigates the activation of biochar obtained from the fast-pyrolysis of wood biomass. The biochar was collected from a pilot-plant of bio-oil production and then activated via physical route (C02) at 800°C for 30 and 60 minutes; and via chemical route (H3P04) at 450, 550 and 650°C for 60 minutes. The activated carbon was characterized by product yield, proximate analysis, surface area and thermogravimetric analysis. The chemical routes with H3P04 were more efficient than the physical routes with CO2. The chemical activation at 450°C presented the highest product yield (80.47%) followed by a decrease in the yield to 71-75% with the increase of the temperature. The fixed carbon content increased after both physical and chemical activation, remaining around 91%. On the other hand, the volatile matter decreased significantly, especially in the physical routes. The surface area increased from 17.94 (untreated biochar) to 450-655 m2/g, confirming the improvement of the porosity, mainly in the biochar activated by H3P04 at 450°C and by CO2 for 60 minutes. Ali biochar activated by chemical routes presented similar residual mass at 600°C, whereas the material physically activated with CO2 presented lower residual mass, especially the one treated for 30 minutes. Overall, these results provide an alternative to produce a high added-value material from a fast-pyrolysis byproduct, encouraging the exploration of thermochemical conversion of lignocellulosic biomass.
650 $aActivated carbon
650 $aBiorefining
650 $asurface area
653 $aBio óleo
653 $aBio-oil
653 $aBiochar activation
653 $aBiorefinaria
653 $aConversão termoquímica
653 $aThermochemical conversion
700 1 $aMATTOS, B. D.
700 1 $aLOURENÇON, T. V.
700 1 $aHARRES, A. N.
700 1 $aCAPOBIANCO, G.
700 1 $aMATOS, M. de
700 1 $aBOLZON DE MUNIZ, G. I.
700 1 $aMAGALHAES, W. L. E.
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