Reactive Distillation of Glycolic Acid Using Heterogeneous Catalysts: Experimental Studies and Process Simulation.

butyl glycolate glycolic acid reaction kinetics reactive distillation vapor–liquid equilibrium

Journal

Frontiers in chemistry
ISSN: 2296-2646
Titre abrégé: Front Chem
Pays: Switzerland
ID NLM: 101627988

Informations de publication

Date de publication:
2022
Historique:
received: 31 03 2022
accepted: 05 05 2022
entrez: 5 7 2022
pubmed: 6 7 2022
medline: 6 7 2022
Statut: epublish

Résumé

The glycerol oxidation reaction was developed leading to selective catalysts and optimum conditions for the production of carboxylic acids such as glycolic acid. However, carboxylic acids are produced in highly diluted mixtures, challenging the recovery and purification, and resulting in high production costs, polymerization, and thermal degradation of some of the products. The protection of the acid function by esterification reaction is one of the most promising alternatives through reactive distillation (RD); this technique allows simultaneously the recovery of carboxylic acids and the elimination of most part of the water. The reactive distillation, experimental and simulation, of glycolic acid was performed, based on kinetic and thermodynamic models developed. For the thermodynamic model, binary parameters of the missing couples were determined experimentally, and the non-random two-liquid (NRTL) model was selected as the most suitable to represent the binary behavior. The kinetic study of the esterification in the presence of homogeneous and heterogeneous catalysis concluded that the heterogeneous reaction can be accurately described either by a pseudo-homogeneous model or the Langmuir-Hinshelwood (L-H) adsorption model. Reactive distillation was conducted in a distillation column filled with random packing sulfonated ion-exchange resin, Nafion NR50

Identifiants

pubmed: 35783208
doi: 10.3389/fchem.2022.909380
pii: 909380
pmc: PMC9240659
doi:

Types de publication

Journal Article

Langues

eng

Pagination

909380

Informations de copyright

Copyright © 2022 Mutschler, Aparicio, Mokbel, Capron, Fongarland, Araque and Nikitine.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Science. 1958 Aug 29;128(3322):480
pubmed: 17834383
Bioresour Technol. 2013 Feb;130:793-7
pubmed: 23380294

Auteurs

Carole Mutschler (C)

CP2M, UMR CNRS 5128, University Lyon 1, CPE Lyon, Villeurbanne, France.

Juliana Aparicio (J)

University Lille, CNRS, Centrale Lille, ENSCL, University Artois, UMR 8181 - UCCS - Unité de Catalyse et Chimie du Solide, Lille, France.

Ilham Mokbel (I)

LMI, UMR CNRS 5615, University Lyon 1, Villeurbanne, France.

Mickaël Capron (M)

University Lille, CNRS, Centrale Lille, ENSCL, University Artois, UMR 8181 - UCCS - Unité de Catalyse et Chimie du Solide, Lille, France.

Pascal Fongarland (P)

CP2M, UMR CNRS 5128, University Lyon 1, CPE Lyon, Villeurbanne, France.

Marcia Araque (M)

University Lille, CNRS, Centrale Lille, ENSCL, University Artois, UMR 8181 - UCCS - Unité de Catalyse et Chimie du Solide, Lille, France.

Clémence Nikitine (C)

CP2M, UMR CNRS 5128, University Lyon 1, CPE Lyon, Villeurbanne, France.

Classifications MeSH