Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires

Autores
Correa Muriel, Daniela; Valencia Sánchez, Hoover; Cortes Hernández, Héctor; González Vera, Daniela; Herrera, Javiera; Campos, Cristian H.; Casella, Mónica Laura; Arteaga Perez, Luis E.; Osorio Vargas, Paula
Año de publicación
2022
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Pyrolysis as a waste treatment method has gained relevance because it can generate higher value-added products in addition to reducing the environment’s secondary pollution. In this study, the catalytic pyrolysis of waste tires was evaluated using NiTiO3 and CoTiO3 ilmenites as catalysts and precursors of metal catalysts with the aim to produce an oil enriched in high-value hydrocarbons, such as benzene, toluene, a xylenes mixture, and products less-reported, such as p-cymene and p-cymenene. The experiments were performed in an analytical pyrolyzer coupled to GC/MS. The effect of the nature of the catalysts on the product distribution was compared with the uncatalyzed reaction. The main products of uncatalyzed pyrolysis were D, L-limonene (~60%), and isoprene (~25%) due to the depolymerization of natural rubber. Meanwhile, Ni-ilmenites-based catalysts favored the formation of target compounds to expense D, L-limonene. Moreover, the presence of metal in reduced-ilmenite sharply enhanced the selectivity by ~50% concerning oxidized ilmenite and above 80% compared to the uncatalyzed reaction for p-cymene and p-cymenene. By contrast, the Co-ilmenites-based catalysts showed a marginal effect on secondary reactions. Finally, the feasibility of forming the aromatic terpenes, p-cymene, and p-cymenene from limonene in the non-catalytic pyrolysis was evaluated.
Centro de Investigación y Desarrollo en Ciencias Aplicadas
Materia
Química
Metal catalysts
Ilmenites
Waste tire pyrolysis
Aromatics production
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/152913

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network_name_str SEDICI (UNLP)
spelling Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tiresCorrea Muriel, DanielaValencia Sánchez, HooverCortes Hernández, HéctorGonzález Vera, DanielaHerrera, JavieraCampos, Cristian H.Casella, Mónica LauraArteaga Perez, Luis E.Osorio Vargas, PaulaQuímicaMetal catalystsIlmenitesWaste tire pyrolysisAromatics productionPyrolysis as a waste treatment method has gained relevance because it can generate higher value-added products in addition to reducing the environment’s secondary pollution. In this study, the catalytic pyrolysis of waste tires was evaluated using NiTiO3 and CoTiO3 ilmenites as catalysts and precursors of metal catalysts with the aim to produce an oil enriched in high-value hydrocarbons, such as benzene, toluene, a xylenes mixture, and products less-reported, such as p-cymene and p-cymenene. The experiments were performed in an analytical pyrolyzer coupled to GC/MS. The effect of the nature of the catalysts on the product distribution was compared with the uncatalyzed reaction. The main products of uncatalyzed pyrolysis were D, L-limonene (~60%), and isoprene (~25%) due to the depolymerization of natural rubber. Meanwhile, Ni-ilmenites-based catalysts favored the formation of target compounds to expense D, L-limonene. Moreover, the presence of metal in reduced-ilmenite sharply enhanced the selectivity by ~50% concerning oxidized ilmenite and above 80% compared to the uncatalyzed reaction for p-cymene and p-cymenene. By contrast, the Co-ilmenites-based catalysts showed a marginal effect on secondary reactions. Finally, the feasibility of forming the aromatic terpenes, p-cymene, and p-cymenene from limonene in the non-catalytic pyrolysis was evaluated.Centro de Investigación y Desarrollo en Ciencias Aplicadas2022info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/152913enginfo:eu-repo/semantics/altIdentifier/issn/2073-4344info:eu-repo/semantics/altIdentifier/doi/10.3390/catal12111437info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:39:33Zoai:sedici.unlp.edu.ar:10915/152913Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:39:33.542SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
title Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
spellingShingle Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
Correa Muriel, Daniela
Química
Metal catalysts
Ilmenites
Waste tire pyrolysis
Aromatics production
title_short Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
title_full Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
title_fullStr Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
title_full_unstemmed Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
title_sort Nickel and cobalt ilmenites-based catalysts for upgrading pyrolytic oil during pyrolysis ofwaste tires
dc.creator.none.fl_str_mv Correa Muriel, Daniela
Valencia Sánchez, Hoover
Cortes Hernández, Héctor
González Vera, Daniela
Herrera, Javiera
Campos, Cristian H.
Casella, Mónica Laura
Arteaga Perez, Luis E.
Osorio Vargas, Paula
author Correa Muriel, Daniela
author_facet Correa Muriel, Daniela
Valencia Sánchez, Hoover
Cortes Hernández, Héctor
González Vera, Daniela
Herrera, Javiera
Campos, Cristian H.
Casella, Mónica Laura
Arteaga Perez, Luis E.
Osorio Vargas, Paula
author_role author
author2 Valencia Sánchez, Hoover
Cortes Hernández, Héctor
González Vera, Daniela
Herrera, Javiera
Campos, Cristian H.
Casella, Mónica Laura
Arteaga Perez, Luis E.
Osorio Vargas, Paula
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Química
Metal catalysts
Ilmenites
Waste tire pyrolysis
Aromatics production
topic Química
Metal catalysts
Ilmenites
Waste tire pyrolysis
Aromatics production
dc.description.none.fl_txt_mv Pyrolysis as a waste treatment method has gained relevance because it can generate higher value-added products in addition to reducing the environment’s secondary pollution. In this study, the catalytic pyrolysis of waste tires was evaluated using NiTiO3 and CoTiO3 ilmenites as catalysts and precursors of metal catalysts with the aim to produce an oil enriched in high-value hydrocarbons, such as benzene, toluene, a xylenes mixture, and products less-reported, such as p-cymene and p-cymenene. The experiments were performed in an analytical pyrolyzer coupled to GC/MS. The effect of the nature of the catalysts on the product distribution was compared with the uncatalyzed reaction. The main products of uncatalyzed pyrolysis were D, L-limonene (~60%), and isoprene (~25%) due to the depolymerization of natural rubber. Meanwhile, Ni-ilmenites-based catalysts favored the formation of target compounds to expense D, L-limonene. Moreover, the presence of metal in reduced-ilmenite sharply enhanced the selectivity by ~50% concerning oxidized ilmenite and above 80% compared to the uncatalyzed reaction for p-cymene and p-cymenene. By contrast, the Co-ilmenites-based catalysts showed a marginal effect on secondary reactions. Finally, the feasibility of forming the aromatic terpenes, p-cymene, and p-cymenene from limonene in the non-catalytic pyrolysis was evaluated.
Centro de Investigación y Desarrollo en Ciencias Aplicadas
description Pyrolysis as a waste treatment method has gained relevance because it can generate higher value-added products in addition to reducing the environment’s secondary pollution. In this study, the catalytic pyrolysis of waste tires was evaluated using NiTiO3 and CoTiO3 ilmenites as catalysts and precursors of metal catalysts with the aim to produce an oil enriched in high-value hydrocarbons, such as benzene, toluene, a xylenes mixture, and products less-reported, such as p-cymene and p-cymenene. The experiments were performed in an analytical pyrolyzer coupled to GC/MS. The effect of the nature of the catalysts on the product distribution was compared with the uncatalyzed reaction. The main products of uncatalyzed pyrolysis were D, L-limonene (~60%), and isoprene (~25%) due to the depolymerization of natural rubber. Meanwhile, Ni-ilmenites-based catalysts favored the formation of target compounds to expense D, L-limonene. Moreover, the presence of metal in reduced-ilmenite sharply enhanced the selectivity by ~50% concerning oxidized ilmenite and above 80% compared to the uncatalyzed reaction for p-cymene and p-cymenene. By contrast, the Co-ilmenites-based catalysts showed a marginal effect on secondary reactions. Finally, the feasibility of forming the aromatic terpenes, p-cymene, and p-cymenene from limonene in the non-catalytic pyrolysis was evaluated.
publishDate 2022
dc.date.none.fl_str_mv 2022
dc.type.none.fl_str_mv info:eu-repo/semantics/article
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dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/2073-4344
info:eu-repo/semantics/altIdentifier/doi/10.3390/catal12111437
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
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