Abstract
Partial hydrogenolysis of dimethyl oxalate (DMO) to methyl glycolate (MG) is a central step in biodegradable polyglycolic acid (PGA) production. However, it remains a great challenge for efficient and selective DMO hydrogenolysis under mild temperature (<100°C). In this work, we demonstrate an outstanding DMO hydrogenolysis by employing alkaline (Na, K) metal-doped Ru catalysts. Na presents a stronger promotional effect than K. The highest yield of MG is achieved at 90.2% at 85°C in 15 h of reaction on 3Ru-0.4Na/SiO2 and the catalyst can be directly reused more than 10 times without any additional regeneration. The doping of Na effectively enables smaller Ru nanoparticle size, larger capacity of H2 adsorption via a hydrogen pool (includes surface hydride, i.e., Na-Hδ−) on Ru–Na interface, stronger strength of DMO adsorption. It is further revealed that there is a linear relation between the content of surface Ru0 + Ru3+ + Ruδ− and MG yield. Finally, an optimal ratio of Ru3+ + Ruδ−/Ru0 of 1.26 is achieved.
| Original language | English |
|---|---|
| Journal | AIChE Journal |
| DOIs | |
| State | Accepted/In press - 2025 |
Keywords
- alkaline metals
- dimethyl oxalate
- methyl glycolate
- partial hydrogenolysis
- ruthenium
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