Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol

Autores
Chiosso, María Eugenia; Lick, Ileana Daniela; Casella, Mónica Laura; Merlo, Andrea Beatriz
Año de publicación
2020
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
In this paper, the catalytic behaviour of two different carbonaceous systems, commercial carbon (Cc) and synthetic carbon (Cs) functionalized with concentrated sulfuric acid (–SO₃H) and with reduced aryl diazonium salt (–PhSO₃H), was studied in the etherification of glycerol (Gly) with benzyl alcohol (BA). The catalytic activity and selectivity were studied varying the catalyst percentage (5, 10 and 15 wt%) and the initial reactant mass ratio. Taking into account the results obtained, the experimental conditions selected to continue with the catalytic studies were: temperature 393 K, Gly:BA molar ratio 3:1 and a catalyst loading of 10 wt%. Mono- and diethers were the main products. For the Cc-based catalysts, higher conversion (66%) and selectivity (90%) were obtained with the most acidic system, Cc–PhSO₃H. Changing the carbon functionalization method (–PhSO₃H for –SO₃H groups) produced a considerable increase in glycerol conversion (from 23 to 66%) and in selectivity to ME + DE (from 62 to 90%). On the other hand, for both Cs-based systems a great increase in performance was obtained, about 95% conversion after 360 min of reaction. Monoether was the major product of the reaction with a selectivity of 79% for Cs–SO₃H and 87% for Cs–PhSO₃H, which was maintained with reuse. Etherification of glycerol (Gly) with benzyl alcohol (BA) with two carbonaceous systems synthesized in the laboratory and functionalized with –SO₃H and –PhSO₃H.
Facultad de Ciencias Exactas
Centro de Investigación y Desarrollo en Ciencias Aplicadas
Materia
Ciencias Exactas
Química
Glycerol
Etherifcation
Acid catalysts
Sulfonated carbon
Benzyl alcohol
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/128455

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oai_identifier_str oai:sedici.unlp.edu.ar:10915/128455
network_acronym_str SEDICI
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network_name_str SEDICI (UNLP)
spelling Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcoholChiosso, María EugeniaLick, Ileana DanielaCasella, Mónica LauraMerlo, Andrea BeatrizCiencias ExactasQuímicaGlycerolEtherifcationAcid catalystsSulfonated carbonBenzyl alcoholIn this paper, the catalytic behaviour of two different carbonaceous systems, commercial carbon (Cc) and synthetic carbon (Cs) functionalized with concentrated sulfuric acid (–SO₃H) and with reduced aryl diazonium salt (–PhSO₃H), was studied in the etherification of glycerol (Gly) with benzyl alcohol (BA). The catalytic activity and selectivity were studied varying the catalyst percentage (5, 10 and 15 wt%) and the initial reactant mass ratio. Taking into account the results obtained, the experimental conditions selected to continue with the catalytic studies were: temperature 393 K, Gly:BA molar ratio 3:1 and a catalyst loading of 10 wt%. Mono- and diethers were the main products. For the Cc-based catalysts, higher conversion (66%) and selectivity (90%) were obtained with the most acidic system, Cc–PhSO₃H. Changing the carbon functionalization method (–PhSO₃H for –SO₃H groups) produced a considerable increase in glycerol conversion (from 23 to 66%) and in selectivity to ME + DE (from 62 to 90%). On the other hand, for both Cs-based systems a great increase in performance was obtained, about 95% conversion after 360 min of reaction. Monoether was the major product of the reaction with a selectivity of 79% for Cs–SO₃H and 87% for Cs–PhSO₃H, which was maintained with reuse. Etherification of glycerol (Gly) with benzyl alcohol (BA) with two carbonaceous systems synthesized in the laboratory and functionalized with –SO₃H and –PhSO₃H.Facultad de Ciencias ExactasCentro de Investigación y Desarrollo en Ciencias Aplicadas2020-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf129-137http://sedici.unlp.edu.ar/handle/10915/128455enginfo:eu-repo/semantics/altIdentifier/issn/0104-6632info:eu-repo/semantics/altIdentifier/issn/1678-4383info:eu-repo/semantics/altIdentifier/doi/10.1007/s43153-019-00002-zinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:30:58Zoai:sedici.unlp.edu.ar:10915/128455Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:30:58.919SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
title Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
spellingShingle Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
Chiosso, María Eugenia
Ciencias Exactas
Química
Glycerol
Etherifcation
Acid catalysts
Sulfonated carbon
Benzyl alcohol
title_short Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
title_full Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
title_fullStr Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
title_full_unstemmed Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
title_sort Acid functionalized carbons as catalyst for glycerol etherification with benzyl alcohol
dc.creator.none.fl_str_mv Chiosso, María Eugenia
Lick, Ileana Daniela
Casella, Mónica Laura
Merlo, Andrea Beatriz
author Chiosso, María Eugenia
author_facet Chiosso, María Eugenia
Lick, Ileana Daniela
Casella, Mónica Laura
Merlo, Andrea Beatriz
author_role author
author2 Lick, Ileana Daniela
Casella, Mónica Laura
Merlo, Andrea Beatriz
author2_role author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Química
Glycerol
Etherifcation
Acid catalysts
Sulfonated carbon
Benzyl alcohol
topic Ciencias Exactas
Química
Glycerol
Etherifcation
Acid catalysts
Sulfonated carbon
Benzyl alcohol
dc.description.none.fl_txt_mv In this paper, the catalytic behaviour of two different carbonaceous systems, commercial carbon (Cc) and synthetic carbon (Cs) functionalized with concentrated sulfuric acid (–SO₃H) and with reduced aryl diazonium salt (–PhSO₃H), was studied in the etherification of glycerol (Gly) with benzyl alcohol (BA). The catalytic activity and selectivity were studied varying the catalyst percentage (5, 10 and 15 wt%) and the initial reactant mass ratio. Taking into account the results obtained, the experimental conditions selected to continue with the catalytic studies were: temperature 393 K, Gly:BA molar ratio 3:1 and a catalyst loading of 10 wt%. Mono- and diethers were the main products. For the Cc-based catalysts, higher conversion (66%) and selectivity (90%) were obtained with the most acidic system, Cc–PhSO₃H. Changing the carbon functionalization method (–PhSO₃H for –SO₃H groups) produced a considerable increase in glycerol conversion (from 23 to 66%) and in selectivity to ME + DE (from 62 to 90%). On the other hand, for both Cs-based systems a great increase in performance was obtained, about 95% conversion after 360 min of reaction. Monoether was the major product of the reaction with a selectivity of 79% for Cs–SO₃H and 87% for Cs–PhSO₃H, which was maintained with reuse. Etherification of glycerol (Gly) with benzyl alcohol (BA) with two carbonaceous systems synthesized in the laboratory and functionalized with –SO₃H and –PhSO₃H.
Facultad de Ciencias Exactas
Centro de Investigación y Desarrollo en Ciencias Aplicadas
description In this paper, the catalytic behaviour of two different carbonaceous systems, commercial carbon (Cc) and synthetic carbon (Cs) functionalized with concentrated sulfuric acid (–SO₃H) and with reduced aryl diazonium salt (–PhSO₃H), was studied in the etherification of glycerol (Gly) with benzyl alcohol (BA). The catalytic activity and selectivity were studied varying the catalyst percentage (5, 10 and 15 wt%) and the initial reactant mass ratio. Taking into account the results obtained, the experimental conditions selected to continue with the catalytic studies were: temperature 393 K, Gly:BA molar ratio 3:1 and a catalyst loading of 10 wt%. Mono- and diethers were the main products. For the Cc-based catalysts, higher conversion (66%) and selectivity (90%) were obtained with the most acidic system, Cc–PhSO₃H. Changing the carbon functionalization method (–PhSO₃H for –SO₃H groups) produced a considerable increase in glycerol conversion (from 23 to 66%) and in selectivity to ME + DE (from 62 to 90%). On the other hand, for both Cs-based systems a great increase in performance was obtained, about 95% conversion after 360 min of reaction. Monoether was the major product of the reaction with a selectivity of 79% for Cs–SO₃H and 87% for Cs–PhSO₃H, which was maintained with reuse. Etherification of glycerol (Gly) with benzyl alcohol (BA) with two carbonaceous systems synthesized in the laboratory and functionalized with –SO₃H and –PhSO₃H.
publishDate 2020
dc.date.none.fl_str_mv 2020-03
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/128455
url http://sedici.unlp.edu.ar/handle/10915/128455
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0104-6632
info:eu-repo/semantics/altIdentifier/issn/1678-4383
info:eu-repo/semantics/altIdentifier/doi/10.1007/s43153-019-00002-z
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
129-137
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instname:Universidad Nacional de La Plata
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