Ammonia synthesis catalyst 100 years: Practice, enlightenment and challenge

被引:523
作者
Liu, Huazhang [1 ]
机构
[1] Zhejiang Univ Technol, Inst Ind Catalysis, Hangzhou 310014, Zhejiang, Peoples R China
关键词
Ammonia synthesis catalyst; Discovery; Development; Challenge; Practice; Enlightenment; BIOLOGICAL NITROGEN-FIXATION; BIMETALLIC NITRIDE CATALYSTS; FUSED IRON CATALYST; PRECURSOR PHASE-COMPOSITION; TRANSITION-METAL; DESORPTION PERFORMANCE; OXIDE PRECURSOR; SURFACE; TEMPERATURE; POTASSIUM;
D O I
10.1016/S1872-2067(14)60118-2
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ammonia synthesis catalyst found by Haber-Bosch achieves its history of 100 years. The current understanding and enlightenment from foundation and development of ammonia synthesis catalyst are reviewed, and its future and facing new challenge remained today are expected. Catalytic ammonia synthesis technology has played a central role in the development of the chemical industry during the 20th century. During 100 years, ammonia synthesis catalyst has come through diversified seedtime such as Fe3O4-based iron catalysts, Fe1-xO-based iron catalysts, ruthenium-based catalysts, and discovery of a Co-Mo-N system. Often new techniques, methods, and theories of catalysis have initially been developed and applied in connection with studies of this system. Similarly, new discoveries in the field of ammonia synthesis have been extended to other fields of catalysis. There is no other practically relevant reaction that leads to such a close interconnection between theory, model catalysis, and experiment as the high-pressure synthesis of ammonia. Catalytic synthesis ammonia reaction is yet a perfect model system for academic research in the field of heterogeneous catalysis. Understanding the mechanism and the translation of the knowledge into technical perfection has become a fundamental criterion for scientific development in catalysis research. The never-ending story has not ended yet. In addition to questions about the elementary steps of the reaction and the importance of the real structure and subnitrides for the catalyst efficiency, as well as the wide-open question about new catalyst materials, there are also different challenges thrown down by theory for the experimentalist in the prediction of a biomimetic ammonia-synthesis path at room temperature and atmospheric pressure including electrocatalysis, photocatalysis and biomimetic nitrogen fixation. (C) 2014, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1619 / 1640
页数:22
相关论文
共 153 条
[1]   ACTIVATION OF NITROGEN BY ALKALI-METAL PROMOTED TRANSITION-METAL .1. AMMONIA SYNTHESIS OVER RUTHENIUM PROMOTED BY ALKALI-METAL [J].
AIKA, K ;
OZAKI, A ;
HORI, H .
JOURNAL OF CATALYSIS, 1972, 27 (03) :424-&
[2]  
Aika K.-i., 1995, Ammonia: Catalysis and Manufacture
[3]   The interaction of nitrogen with the (111) surface of iron at low and at elevated pressures [J].
Alstrup, I ;
Chorkendorff, I ;
Ullmann, S .
JOURNAL OF CATALYSIS, 1997, 168 (02) :217-234
[4]  
Anderson J.R., 1983, Catalysis: science and technology
[5]   Ammonia synthesis kinetics: surface chemistry, rate expressions, and kinetic analysis [J].
Aparicio, Luis M. ;
Dumesic, James A. .
TOPICS IN CATALYSIS, 1994, 1 (3-4) :233-252
[6]   Influence of potassium oxygen layer on properties of iron surfaces [J].
Arabczyk, W ;
Narkiewicz, U ;
Moszynski, D .
APPLIED CATALYSIS A-GENERAL, 1999, 182 (02) :379-384
[7]   MODEL OF ACTIVE SURFACE OF IRON CATALYST FOR AMMONIA-SYNTHESIS [J].
ARABCZYK, W ;
NARKIEWICZ, U ;
KALUCKI, K .
VACUUM, 1994, 45 (2-3) :267-269
[8]   Double-layer model of the fused iron catalyst for ammonia synthesis [J].
Arabczyk, W ;
Narkiewicz, U ;
Moszynski, D .
LANGMUIR, 1999, 15 (18) :5785-5789
[9]  
Bielawa H, 2001, ANGEW CHEM INT EDIT, V40, P1061, DOI 10.1002/1521-3773(20010316)40:6<1061::AID-ANIE10610>3.3.CO
[10]  
2-2