| Literature DB >> 32130789 |
Fuping Li1, Min Ao1, Gia Hung Pham1, Jaka Sunarso2, Yanping Chen3, Jian Liu3,4, Kai Wang1, Shaomin Liu1,5.
Abstract
Direct conversion of syngas to dimethyl ether (DME) through the intermediate of methanol allows more efficient DME production in a simpler reactor design relative to the conventional indirect route. Although Cu/ZnO-based multicomponent catalysts are highly active for methanol synthesis in this process, the sintering issue of Cu during the prolonged reaction generally deteriorates their performance. In this work, Cu/ZnO catalysts in a novel octahedron structure are prepared by a two-step pyrolysis of Zn-doped Cu-BTC metal-organic framework (MOF) in N2 and air. The catalyst CZ-350/A, hybrid of MOF-derived Cu/ZnO sample CZ-350 and γ-Al2 O3 for methanol dehydration, displays the best activity for DME formation (7.74% CO conversion and 70.05% DME selectivity) with the lowest deterioration rate over 40 h continuous reaction. Such performance is superior to its counterpart CZ-CP/A made via the conventional coprecipitation method. This is mainly due to the confinement of Cu nanoparticles within the octahedron matrix hindering their migration and aggregation. Besides, partial reduction of ZnO in the activated CZ-350 prompts the formation of Cu+ -O-Zn, further facilitating the DME production with the highest selectivity compared to literature results. The results clearly indicate that Cu and ZnO distribution in the catalyst architecture plays an important role in DME formation.Entities:
Keywords: Cu/ZnO catalysts; dimethyl ether synthesis; metal-organic framework; multicomponent catalysts; syngas
Year: 2020 PMID: 32130789 DOI: 10.1002/smll.201906276
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281