罗靖洁

个人信息Personal Information

副教授

博士生导师

硕士生导师

主要任职:Associate professor

性别:女

毕业院校:斯特拉斯堡大学

学位:博士

所在单位:化工海洋与生命学院

学科:化学工程. 化学工艺

办公地点:D01-307

联系方式:jingjie.luo@dlut.edu.cn

电子邮箱:jingjie.luo@dlut.edu.cn

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论文成果

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Metal oxide sub-nanoclusters decorated Ni catalyst for selective hydrogenation of adiponitrile to hexamethylenediamine

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论文类型:期刊论文

发表时间:2020-01-01

发表刊物:JOURNAL OF CATALYSIS

收录刊物:EI、SCIE

卷号:381

页面范围:14-25

ISSN号:0021-9517

关键字:Ni catalyst; Adiponitrile hydrogenation; CeO2 decoration; Electron modification; Synergistic interaction

摘要:Nickel based catalysts were decorated by metal oxide (MOx = CeO2, La2O3 or MgO) and used for the selective hydrogenation of adiponitrile to hexamethylenediamine. Additional MOx sub-nanoclusters were dispersed on surface to manipulate the electron and surface structures of nickel particles. The functional role of, e.g. CeO2 decorator, was to benefit the formation of Ni-CeO2 interfaces and acted as electron donor for the Ni active sites, rather than to change the morphology, crystallization, or the H-2 activation energy barrier. The d-band center calculated by Density Functional Theory was altered and close to the Fermi-level after CeO2 loading, rationally accounting for the accelerated reaction rate. The decorated CeO2 behaved like a double-edge sword. Excessive loading of ceria easily led to the coverage of Ni sites and destroyed the elaborated Ni-CeO2 synergy. By using Ni-Ce-3/Al2O3 with only 3 at% CeO2, adiponitrile can be completely transformed at 90 degrees C in 7 MPa H-2 for 3 h with 90% yield of hexamethylenediamine. The additional CeO2 also resulted in the enhanced stability of Ni catalyst, which maintains its high catalytic stability even after 5 reaction cycles. (C) 2019 Elsevier Inc. All rights reserved.