Autocatalyzed and heterogeneously catalyzed esterification kinetics of glycolic acid with ethanol

Literature Information

Publication Date 2021-11-18
DOI 10.1039/D1RE00418B
Impact Factor 4.239
Authors

Laura Reyes, Clémence Nikitine, Léa Vilcocq, Pascal Fongarland


View Original

Abstract

The chemical equilibrium and reaction kinetics in homogeneously and heterogeneously catalyzed systems were investigated for the reversible esterification reaction of glycolic acid with ethanol. In a first approach, the thermodynamic equilibrium of the reaction was established for temperatures between 50 °C and 75 °C. To differentiate catalytic from homogeneous contribution, the esterification was first studied without a catalyst and the data obtained were then used to model the autocatalyzed homogeneous reaction kinetics. The impact of different commercial solid catalysts such as zeolites, oxides and ion exchange resins on the esterification reaction was also investigated. For the latter, the amount of total acid sites was quantified in order to correlate this parameter to the reaction rate and glycolic acid conversion. Finally, the effects of catalyst loading, temperature, presence of water and recyclability were examined for the most efficient catalyst, Amberlyst 70. Moreover, a kinetic adjustment of the experimental results was carried out by fitting the data to a pseudo-homogeneous model and comparing to adsorption-based models.

Related Literature

Copper-catalyzed oxidative multicomponent reaction: synthesis of imidazo fused heterocycles with molecular oxygen

Xianwei Li, Tianzhang Wang, Yu-Jing Lu, Shaomin Ji, Yanping Huo, Bifu Liu

2018-08-02 Paper

DOI: 10.1039/C8OB01532E

Aminative Umpolung cyclization for synthesis of chiral exocyclic vicinal diamines

Feng Liu, Guoqing Zhao, Weiqi Cai, Dongfang Xu, Baoguo Zhao

2018-09-26 Paper

DOI: 10.1039/C8OB02000K

Catalytic properties of 4,5-bridged proline methano- and ethanologues in the Hajos–Parrish intramolecular aldol reaction

Sofiane Hocine, Gilles Berger, K. N. Houk, Stephen Hanessian

2021-12-15 Research Article

DOI: 10.1039/D1QO01688A

Chemoselective synthesis of isolated and fused fluorenones and their photophysical and antiviral properties

Ismail Althagafi, Ranjay Shaw, Rahul Panwar, Shally, Chanda Sinha, Amit Kumar, Yong-Tang Zheng, Ramendra Pratap

2018-09-19 Paper

DOI: 10.1039/C8OB01733F

Total synthesis of (±)-rhazinal, an alkaloidal spindle toxin from Kopsia teoi

Martin G. Banwell, Alison J. Edwards, Jason A. Smith, Ernest Hamel, Pascal Verdier-Pinard

2002-12-19 Paper

DOI: 10.1039/B209992F

Inside front cover

2022-02-01 Cover

DOI: 10.1039/D2QO90009B

Ruthenium-catalyzed enantioselective hydrogenation of quinoxalinones and quinazolinones

Chenghao Li, Shuxin Zhang, Shan Li, Yu Feng, Qing-Hua Fan

2021-12-03 Research Article

DOI: 10.1039/D1QO01598B

Back cover

Cover

DOI: 10.1039/C8OB90144A

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
Self-citation Rate: 8.8%
Articles per Year: 284

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.