Kinetics of Hydrogenation of Dimethyl Oxalate to Methyl Glycolate on an Activated Carbon-Supported Copper Catalyst
A catalyst with the active component Cu loaded onto the carrier activated carbon was prepared, and metal Ca was introduced into the catalyst to modify it. This catalyst was used in the hydrogenation reaction of dimethyl oxalate, and the reaction kinetics was studied. The kinetic experiments were carried out in a fixed bed reactor with a reaction temperature varying from 483 K to 513 K, reaction pressure varying from 1.5 Mpa to 2.5 Mpa, and the weight hourly space velocity of dimethyl oxalate varying from 0.435 h−1 to 0.726 h−1. Eight possible dynamic models were proposed, the optimal model was selected, and the parameters of the optimal model were calculated using MATLAB. The results showed that dimethyl oxalate adsorbed on the active site by dissociation adsorption, and the dissociation adsorption of ester was the rate-controlling step. The parameters of the model were consistent with thermodynamics and statistical analysis, further proving that the model has good forecasting performance.
Authors
- Weihua Shen (ORCID: https://orcid.org/0000-0001-5168-5837)
- Junyou Wang (ORCID: https://orcid.org/0000-0002-4693-850X)
- Yunjin Fang (ORCID: https://orcid.org/0000-0002-7411-3118)
- Pan Shao
Institutions
- East China University of Science and Technology (CN)
- State Key Laboratory of Chemical Engineering (CN)
Publication Details
- Journal
- Catalysts
- Published
- 2025-06-25
- DOI
- https://doi.org/10.3390/catal15070624
- Citations
- 1
- Primary Topic
- Catalysts for Methane Reforming
- Type
- article
- Field-Weighted Citation Impact
- 0.39