4.7 Article

Kinetic and thermodynamic studies on direct synthesis of methyl methacrylate from methyl propionate and methanol catalyzed by highly efficient cobalt complex at mild conditions

期刊

CHEMICAL ENGINEERING JOURNAL
卷 468, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.143592

关键词

Methyl methacrylate; Cobalt complex; Aldol condensation; Thermodynamic calculation; Kinetic informatics

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An innovative liquid-phase catalytic system was developed for the direct synthesis of methyl methacrylate (MMA) from methyl propionate and methanol. The new system addressed the issues of poor selectivity, rapid catalyst deactivation, and formaldehyde polymerization that occurred in the traditional one-step aldol reaction. The yield and selectivity of MMA reached up to 50.2% and 81.8% at mild conditions of 60 degrees C and 1 atm.
Methyl methacrylate (MMA) typically produced from the petroleum-based ethylene or isobutene selective oxidation route is a significantly important chemical widely used in industrial manufacture. Herein, an inno-vative and highly efficient liquid-phase catalytic system, cobalt complex catalyzed O2-interrupted hydrogen borrowing pathways, was developed for direct synthesis of MMA from methyl propionate and methanol at mild conditions, considering the problems of poor selectivity, rapid catalyst deactivation, and formaldehyde poly-merization existed in one-step aldol reaction of methyl propionate with formaldehyde at 350-380 degrees C. The yield and selectivity of MMA could reach up to 50.2% and 81.8% at 60 degrees C and 1 atm. Thermodynamic calculations and analysis for this novel transformative process were conducted to confirm the feasibility and reasonability for MMA production at low temperature (below 100 degrees C). On the basis of the reaction networks proposed according to the experimentally detected products, studies on the kinetic informatics of this new process were conducted. The formaldehyde oxidation, aldol condensation of methyl/t-butyl propionate with formaldehyde and trans-esterification of t-butyl propionate/methacrylate with methanol are first-order dependent on their reactant concentrations. While the methanol dehydrogenation and transesterification of methyl propionate/methacrylate with t-BuOK are first-order dependent on the concentration of only methanol and t-BuOK. With the under-standing of kinetic behavior of these reaction steps composed, the global kinetic model was established to describe this catalytic system and the corresponding parameters including pre-exponential factor and activation energy were calculated. The oxidative dehydrogenation of methanol to formaldehyde, with the highest activation energy of 84 kJ/mol, was the kinetic-relevant step, while the aldol condensation of methyl propionate with formaldehyde showed the lowest energy of 36 kJ/mol.

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