Abstract
Even though Ni catalysts have shown promising performance in the semi-hydrogenation of ethylene, the selectivity and stability remain to be improved so that they may be used to replace expensive noble metal catalysts. Herein, an aluminate-intercalated NiMgAl-layered double hydroxide (LDH) was prepared through a facile co-precipitation approach, and then a topotactic transformation strategy was employed to convert the tailored LDH precursor to the spinel catalyst. More than 99% of the Ni/MgAl2O4 catalyst's conversion was achieved toward the semi-hydrogenation of acetylene at 140 °C, with a selectivity of more than 80%. Additionally, due to high specific surface area (309 m2/g) with tuned acidity, this catalyst showed outstanding resistance to the deposition of carbonaceous compounds and satisfactory long-term stability during a 28 hr test. It is hoped that this study will inspire the design of supported non-noble metal materials with high activity and efficiency towards organic or organo-thermal reactions, as well as provide a basic understanding of the role and impacts of intercalated aluminates in LDH. © 2022 Elsevier Inc.
| Original language | English |
|---|---|
| Pages (from-to) | 374-384 |
| Journal | Journal of Catalysis |
| Volume | 414 |
| Online published | 8 Sept 2022 |
| DOIs | |
| Publication status | Published - Oct 2022 |
| Externally published | Yes |
Research Keywords
- Coke resistance
- Layered double hydroxide
- Semi-hydrogenation of acetylene
- Spinel-type MII-MIII complex oxide
- Support effect
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