Sulfonated Graphene‐Based Materials as Heterogeneous Acid Catalysts for Solketal Synthesis by Acetalization of Glycerol

Author:

Gil‐Gavilán Dolores G.1ORCID,Amaro‐Gahete Juan12ORCID,Rojas‐Luna Raúl1ORCID,Benítez Almudena3ORCID,Estevez Rafael1ORCID,Esquivel Dolores1ORCID,Bautista Felipa M.1ORCID,Romero‐Salguero Francisco J.1ORCID

Affiliation:

1. Departamento de Química Orgánica Instituto Químico para la Energía y el Medioambiente (IQUEMA) Facultad de Ciencias Universidad de Córdoba Campus de Rabanales, Edificio Marie Curie E-14071 Córdoba Spain

2. UGR-Carbon – Materiales Polifuncionales Basados en Carbono Departamento de Química Inorgánica Unidad de Excelencia Química Aplicada a Biomedicina y Medioambiente Universidad de Granada ES18071 Granada Spain

3. Departamento de Química Inorgánica e Ingeniería Química Instituto Químico para la Energía y el Medioambiente (IQUEMA) Facultad de Ciencias Universidad de Córdoba Campus de Rabanales, Edificio Marie Curie E-14071 Córdoba Spain

Abstract

AbstractAcid catalysis plays a pivotal role in the industrial landscape due to its multifaceted contributions to various chemical processes in numerous sectors, including petrochemicals, polymers, food processing, and biodiesel production, among others. Sulfonated graphenes hold notable relevance as heterogeneous acid catalysts due to their unique combination of graphene's structural properties and the introduction of sulfonic groups as catalytic acid sites. Herein, we report the preparation of three sulfonated graphene‐based materials – sulfonated reduced graphene oxide (rGO‐SO3H), chlorosulfonated reduced graphene oxide (rGO‐HSO3Cl) and sulfonated graphene oxide (GO‐SO3H) – by different synthetic approaches. Physicochemical, textural, morphological, and acidic properties of all materials were characterized in detail by different instrumental techniques. Innovatively, these materials have been evaluated as heterogeneous acid catalysts in the solketal synthesis by acetalization of glycerol, which is considered an interesting building block to produce added‐value products. The density of acidic active sites and hydrophobicity were found to be conditioning parameters of the resulting catalytic activity in terms of conversion and selectivity. The best catalytic performance was obtained by rGO‐SO3H, reaching the maximum conversion towards solketal in 15 minutes under mild reaction conditions. The reusability and stability of all materials were also examined after three consecutive acetalization reactions with only a slight loss of catalytic activity.

Funder

Ministerio de Ciencia e Innovación

European Commission

Publisher

Wiley

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