Highly efficient catalysis of dimethyl terephthalate hydrogenation by Ru catalyst loaded on rod-shaped CeO2

• Excellent hydrogenation catalyst prepared from rod-shaped CeO 2 loaded with Ru. • A strong electronic interaction and special Ru n+ interface between Ru and CeO 2 -NR. • Ru/CeO 2 -NR possesses abundant oxygen vacancies and robust Ru n+ -O V -Ce 3+ interactions. • Oxygen vacancies and Ru n+ enhance hydrogen spillover effects. Hydrogenation of aromatic rings is a promising method for synthesizing fine chemicals and for hydrogen storage. Ruthenium-based catalysts are the most common alternatives for expensive palladium catalysts. However, developing efficient Ru-based catalysts for dimethyl terephthalate (DMT) hydrogenation under mild conditions remains challenging. This study addresses this by synthesizing CeO 2 supports with rod-like (CeO 2 -NR), polyhedral (CeO 2 -NP), and cubic (CeO 2 -NC) morphologies via hydrothermal methods, followed by Ru impregnation. Among these, Ru/CeO 2 -NR demonstrated the optimal catalytic performance owing to its highest oxygen vacancy (O V ) concentration, electron-deficient Ru n+ species, and robust Ru-O-Ce interactions. Under optimized conditions (150°C, 5 MPa H 2 , 1 h), Ru/CeO 2 -NR achieved 99.96% DMT conversion and 98.4% selectivity toward dimethyl 1,4-cyclohexanedicarboxylate (DMCD). Remarkably, the catalyst maintained 99.58% conversion and 98.05% selectivity after ten cycles. Despite its low precious metal loading, its catalytic efficacy exceeded that of the industrially widely used Pd/Al 2 O 3 catalysts and thus exhibited certain industrial potential. Density Functional Theory (DFT) simulations revealed that O V and Ru n+ enhanced the adsorption of DMT and H 2 as well as the desorption of DMCD. Furthermore, the significant hydrogen spillover of ruthenium nanoparticles (NPs) was a crucial element contributing to the great hydrogenation efficacy of Ru/CeO 2 -NR. This work provides a mechanistic understanding of morphology-dependent oxygen vacancy engineering in CeO 2 -supported Ru catalysts, offering a strategic pathway for designing durable and efficient systems for plastic-derived aromatic hydrogenation.

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Journal
Results in Engineering
Published
2026-01-13
DOI
https://doi.org/10.1016/j.rineng.2026.109095
Primary Topic
Catalysis for Biomass Conversion
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article
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article

Highly efficient catalysis of dimethyl terephthalate hydrogenation by Ru catalyst loaded on rod-shaped CeO2

Cai Xu, Quanfu Long, Xiaozhong Wang, Jianhai Yang et al.
Results in Engineering
Catalysis for Biomass Conversion
article

Highly efficient catalysis of dimethyl terephthalate hydrogenation by Ru catalyst loaded on rod-shaped CeO2

Cai Xu, Quanfu Long, Xiaozhong Wang, Jianhai Yang, Liyan Dai, Jun Li, Jia Guo
article en

Abstract

• Excellent hydrogenation catalyst prepared from rod-shaped CeO 2 loaded with Ru. • A strong electronic interaction and special Ru n+ interface between Ru and CeO 2 -NR. • Ru/CeO 2 -NR possesses abundant oxygen vacancies and robust Ru n+ -O V -Ce 3+ interactions. • Oxygen vacancies and Ru n+ enhance hydrogen spillover effects. Hydrogenation of aromatic rings is a promising method for synthesizing fine chemicals and for hydrogen storage. Ruthenium-based catalysts are the most common alternatives for expensive palladium catalysts. However, developing efficient Ru-based catalysts for dimethyl terephthalate (DMT) hydrogenation under mild conditions remains challenging. This study addresses this by synthesizing CeO 2 supports with rod-like (CeO 2 -NR), polyhedral (CeO 2 -NP), and cubic (CeO 2 -NC) morphologies via hydrothermal methods, followed by Ru impregnation. Among these, Ru/CeO 2 -NR demonstrated the optimal catalytic performance owing to its highest oxygen vacancy (O V ) concentration, electron-deficient Ru n+ species, and robust Ru-O-Ce interactions. Under optimized conditions (150°C, 5 MPa H 2 , 1 h), Ru/CeO 2 -NR achieved 99.96% DMT conversion and 98.4% selectivity toward dimethyl 1,4-cyclohexanedicarboxylate (DMCD). Remarkably, the catalyst maintained 99.58% conversion and 98.05% selectivity after ten cycles. Despite its low precious metal loading, its catalytic efficacy exceeded that of the industrially widely used Pd/Al 2 O 3 catalysts and thus exhibited certain industrial potential. Density Functional Theory (DFT) simulations revealed that O V and Ru n+ enhanced the adsorption of DMT and H 2 as well as the desorption of DMCD. Furthermore, the significant hydrogen spillover of ruthenium nanoparticles (NPs) was a crucial element contributing to the great hydrogenation efficacy of Ru/CeO 2 -NR. This work provides a mechanistic understanding of morphology-dependent oxygen vacancy engineering in CeO 2 -supported Ru catalysts, offering a strategic pathway for designing durable and efficient systems for plastic-derived aromatic hydrogenation.

Results in EngineeringVol. 29
Quzhou University (CN), Zhejiang University (CN)
Industry, innovation and infrastructure
Openalex Percentile: Top 90%
Catalysis for Biomass Conversion
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