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源自双金属金属有机框架的铜/氧化锌催化剂用于合成气制二甲醚,具有更高的选择性和稳定性

Cu/ZnO Catalysts Derived from Bimetallic Metal-Organic Framework for Dimethyl Ether Synthesis from Syngas with Enhanced Selectivity and Stability.

作者信息

Li Fuping, Ao Min, Pham Gia Hung, Sunarso Jaka, Chen Yanping, Liu Jian, Wang Kai, Liu Shaomin

机构信息

Discipline of Chemical Engineering, WA School of Mines: Minerals, Energy and Chemical Engineering, Curtin University, GPO Box U1987, Perth, Western Australia, 6845, Australia.

Research Centre for Sustainable Technologies, Faculty of Engineering, Computing and Science, Swinburne University of Technology, Jalan Simpang Tiga, Kuching, 93350, Sarawak, Malaysia.

出版信息

Small. 2020 Apr;16(14):e1906276. doi: 10.1002/smll.201906276. Epub 2020 Mar 4.

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 N and air. The catalyst CZ-350/A, hybrid of MOF-derived Cu/ZnO sample CZ-350 and γ-Al O 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.

摘要

通过甲醇中间体将合成气直接转化为二甲醚(DME),相对于传统的间接路线,在更简单的反应器设计中能实现更高效的DME生产。尽管在此过程中,基于Cu/ZnO的多组分催化剂对甲醇合成具有高活性,但长时间反应过程中Cu的烧结问题通常会使其性能下降。在这项工作中,通过在氮气和空气中对锌掺杂的Cu-BTC金属有机框架(MOF)进行两步热解,制备出具有新颖八面体结构的Cu/ZnO催化剂。催化剂CZ-350/A是MOF衍生的Cu/ZnO样品CZ-350与用于甲醇脱水的γ-Al₂O₃的混合物,在40小时连续反应中,其对DME生成表现出最佳活性(CO转化率为7.74%,DME选择性为70.05%)且劣化率最低。这种性能优于通过传统共沉淀法制备的对应物CZ-CP/A。这主要是由于八面体基质内Cu纳米颗粒的受限阻碍了它们的迁移和聚集。此外,活化后的CZ-350中ZnO的部分还原促使形成Cu-O-Zn,与文献结果相比,进一步促进了具有最高选择性的DME生成。结果清楚地表明,催化剂结构中Cu和ZnO的分布在DME形成中起着重要作用。

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