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Improving the hydrodesulfurization performance of the sulfur-resistant intermetallic Ni2Si based on a MOF-derived route
Inorganic Chemistry Frontiers ( IF 7 ) Pub Date : 2020-10-22 , DOI: 10.1039/d0qi01018a
Liangliang Zhang 1, 2, 3, 4, 5 , Xiao Chen 5, 6, 7, 8, 9 , Changhai Liang 5, 6, 7, 8, 9
Affiliation  

Carbon-supported intermetallic nickel silicide (Ni2Si/C) as a non-sulfide catalyst derived from Ni-MOF-74 presents high activity and sulphur-resistance in the hydrodesulfurization (HDS) of dibenzothiophene (DBT). The Ni2Si/C catalyst possesses a large specific surface area (168 m2 g−1), small crystallite size (12 nm) and high electronic density of the nickel active sites; thus, they demonstrate HDS properties breaking the metal silicide bottleneck derived from the microelectronic industry during catalysis. Due to the strong electron-donating effect between Ni and Si and the modification effect by a porous carbon matrix, the Ni2Si/C catalyst exhibits an outstanding stability during DBT HDS after 120 h of stability testing.

中文翻译:

基于MOF的路线提高耐硫金属间化合物Ni2Si的加氢脱硫性能

由Ni-MOF-74衍生的碳载金属间金属硅化镍(Ni 2 Si / C)作为非硫化物催化剂在二苯并噻吩(DBT)的加氢脱硫(HDS)中表现出高活性和抗硫性。Ni 2 Si / C催化剂具有比表面积大(168m 2 g -1),微晶尺寸小(12nm)和镍活性部位的高电子密度。因此,他们证明了HDS性能打破了催化过程中源自微电子工业的金属硅化物瓶颈。由于Ni和Si之间的强电子给体作用以及多孔碳基质对Ni 2的改性作用Si / C催化剂在120小时的稳定性测试后显示出出色的DBT HDS稳定性。
更新日期:2020-11-04
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