Solketal Production Using Eco-Friendly Reduced Graphene Oxide as the Catalyst

Author:

Rossa Vinicius12ORCID,Vasconcelos Sancler da Costa1ORCID,Díaz Gisel Chenard2,Resende Josué de Almeida2,Mattos João Pedro Reys1ORCID,Madriaga Vinicius Gomes da Costa1,Massante Fernanda Franco3,Cruz Yordanka Reyes2ORCID,Nachez Juan Lucas4ORCID,Xing Yutao5,Ponzio Eduardo Ariel3ORCID,Lima Thiago de Melo1ORCID

Affiliation:

1. Group of Catalysis and Biomass Valorization, Institute of Chemistry, Universidade Federal Fluminense, Niterói 24020-141, RJ, Brazil

2. GreenTec Laboratory, School of Chemistry, Universidade Federal do Rio de Janeiro-EQ-UFRJ, Rio de Janeiro 21941-909, RJ, Brazil

3. Grupo de Eletroquímica e Eletroanalítica, Laboratório de Materiais, Institute of Chemistry, Universidade Federal Fluminense, Niterói 24020-141, RJ, Brazil

4. INFES, Institute of Physics, Universidade Federal Fluminense-IQ-UFF, Niterói 28470-000, RJ, Brazil

5. Laboratório de Microscopia Eletrônica de Alta Resolução, Institute of Physics, Universidade Federal Fluminense-IQ-UFF, Niterói 24210-346, RJ, Brazil

Abstract

In this study, two materials based on reduced graphene oxide (rGOH or rGOE) were synthesized through the Hummers methodology and a more sustainable electrochemical method. These materials were extensively characterized and tested as catalysts in solketal production. Both rGOH and rGOE demonstrated significant catalytic activity, achieving 66.18% and 63.97% conversion rates, respectively. The catalytic activity of the synthesized materials was 30 times more efficient than the homogeneous catalyst p-Toluenesulfonic acid. Pseudo-homogeneous and heterogeneous kinetic models were employed to gain further insights into the glycerol ketalization reaction with acetone. The pseudo-homogeneous model suggested that the direct rate constant was lower than the reverse rate constant. In this sense, a reversible bimolecular reaction was proposed. The heterogeneous kinetic models revealed that in the Langmuir-Hinshelwood-Hougen-Watson mechanism, the controlling step of the reaction was the glycerol-acetone surface reaction on the catalyst. In contrast, in the Eley-Rideal mechanism, the reaction was controlled by the adsorbed glycerol on the reaction surface reacting with the available acetone in the bulk fluid. In the reusability tests, the rGOE catalyst demonstrated superior performance over five consecutive cycles, maintaining the highest activity without needing post-reaction washing or treatment.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior-Brasil (CAPES)—Finance

CNPq and FAPERJ

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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