Molybdenum nitrides from structures to industrial applications

被引:17
作者
Jaf, Zainab N. [1 ]
Miran, Hussein A. [1 ]
Jiang, Zhong-Tao [3 ]
Altarawneh, Mohammednoor [2 ]
机构
[1] Univ Baghdad, Dept Phys, Coll Educ Pure Sci Ibn Al Haitham, Baghdad 10071, Iraq
[2] United Arab Emirates Univ, Dept Chem & Petr Engn, Sheikh Khalifa bin Zayed St, Al Ain 15551, U Arab Emirates
[3] Murdoch Univ, Surface Anal & Mat Engn Res Grp, Coll Sci Hlth Engn & Educ, Murdoch, WA 6150, Australia
关键词
binary nitrides; catalysts; density functional theory; hydrodesulfurization; hydrogenation; TRANSITION-METAL NITRIDES; HIGH-PRESSURE SYNTHESIS; SURFACE-AREA; HYDROGEN-EVOLUTION; SELECTIVE HYDROGENATION; ELECTRONIC-PROPERTIES; P-CHLORONITROBENZENE; CRYSTAL-STRUCTURE; AMMONIA-SYNTHESIS; THIOPHENE HYDRODESULFURIZATION;
D O I
10.1515/revce-2021-0002
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Owing to their remarkable characteristics, refractory molybdenum nitride (MoNx)-based compounds have been deployed in a wide range of strategic industrial applications. This review reports the electronic and structural properties that render MoNx materials as potent catalytic surfaces for numerous chemical reactions and surveys the syntheses, procedures, and catalytic applications in pertinent industries such as the petroleum industry. In particular, hydrogenation, hydrodesulfurization, and hydrodeoxygenation are essential processes in the refinement of oil segments and their conversions into commodity fuels and platform chemicals. N-vacant sites over a catalyst's surface are a significant driver of diverse chemical phenomena. Studies on various reaction routes have emphasized that the transfer of adsorbed hydrogen atoms from the N-vacant sites reduces the activation barriers for bond breaking at key structural linkages. Density functional theory has recently provided an atomic-level understanding of Mo-N systems as active ingredients in hydrotreating processes. These Mo-N systems are potentially extendible to the hydrogenation of more complex molecules, most notably, oxygenated aromatic compounds.
引用
收藏
页码:329 / 361
页数:33
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