4.6 Article

Mechanism and Kinetic Study on Synthesis of Methacrolein Catalyzed by Amine/Acid

Journal

CATALYSTS
Volume 13, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/catal13050799

Keywords

methacrolein; aldol condensation; Mannich reaction; kinetics

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In this study, a series of secondary amines/acids were explored as catalysts for the synthesis of methacrolein (MAL) from formaldehyde and propionaldehyde. The structure of the amines and acids directly affected the yield of MAL. The catalytic performance of the system was systematically studied and optimized.
Methacrolein (MAL) is an important intermediate extensively used in the manufacture of methyl methacrylate and other materials (polymers and resins). In this study, a series of secondary amines/acids were explored as catalysts for the condensation of formaldehyde and propionaldehyde to prepare MAL. It was found that the structure of the amines and acids directly affected the yield of MAL. The effect of the catalyst was closely related to the nucleophilicity of the amines as well as the steric hindrance effect, while acids also played a role as co-catalysts. Dibutylamine acetate was selected as the catalyst after investigation. The catalytic performance of the system was systematically studied by a series of single-factor experiments, including stirring rate, temperature, reaction time, acid/amine ratio, and the solvent, and the optimized reaction conditions were obtained. In the optimum condition, the yield of MAL was up to 97.3%. Kinetic experiments were performed for the condensation of formaldehyde and propionaldehyde to MAL, and the activation energies, reaction orders, and rate-limiting step of the reaction were determined. The results indicate that the decomposition of the Mannich base is a rate-limiting step.

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