Temperature dependence of the pseudomorphic transformation of MoO3 to γ-Mo2N

被引:19
作者
Zhang, YJ
Xin, Q
Rodriguez-Ramos, I
Guerrero-Ruiz, A [1 ]
机构
[1] Univ Nacl Educ Distancia, Fac Ciencias, Dept Quim Inorgan, Madrid 28040, Spain
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] CSIC, Inst Catalisis & Petr Quim, Madrid 28049, Spain
基金
中国国家自然科学基金;
关键词
nitrides; crystal growth; X-ray diffraction; X-ray photoelectron spectroscopy; surface properties;
D O I
10.1016/S0025-5408(98)00200-1
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The transformation of MoO3 into gamma-Mo2N during its nitridation by temperature-programmed reaction with NH3/has been investigated. The X-ray diffraction (XRD) results indicate that the conversion of the MoO3 bulk structure was significant at 673 K, although a notable increase in the surface area was observed at higher temperatures such as 773 K. For the sample synthesized at 973 K for 2 h, the achieved surface area was 140 m(2).g(-1) with approximately 60% pore volume within the diameter range of 20-30 Angstrom. The XRD and differential thermal analysis (DTA) results indicate that some intermediates, i.e., H0.3MoO3, MoO2, and gamma-Mo2OxN1-x, were formed during the pseudomorphic transformation of MoO3 to gamma-Mo2N in the temperature range of 673-973 K. Some new information about the transformation reaction was provided by X-ray photoelectron spectroscopy (XPS) and Fourier transformed infrared (FT-IR) spectroscopy. XPS results revealed that Mo2+ species was the main species exposed at the surface of passivated samples. (C) 1999 Elsevier Science Ltd.
引用
收藏
页码:145 / 156
页数:12
相关论文
共 30 条
[1]   CATALYTIC HYDROTREATING OF INDOLE, BENZOTHIOPHENE, AND BENZOFURAN OVER MO2N [J].
ABE, H ;
BELL, AT .
CATALYSIS LETTERS, 1993, 18 (1-2) :1-8
[2]  
BEATHAM N, 1976, ELECT SPECTROSCOPY R, V8, P127
[3]  
BI XX, 1990, MAT RES SOC M BOST M, P167
[4]  
Briggs D., 1990, PRACTICAL SURFACE AN
[5]   SYNTHESIS AND CHARACTERIZATION OF MOLYBDENUM NITRIDE HYDRODENITROGENATION CATALYSTS [J].
CHOI, JG ;
BRENNER, JR ;
COLLING, CW ;
DEMCZYK, BG ;
DUNNING, JL ;
THOMPSON, LT .
CATALYSIS TODAY, 1992, 15 (02) :201-222
[6]   MOLYBDENUM NITRIDE CATALYSTS .1. INFLUENCE OF THE SYNTHESIS FACTORS ON STRUCTURAL-PROPERTIES [J].
CHOI, JG ;
CURL, RL ;
THOMPSON, LT .
JOURNAL OF CATALYSIS, 1994, 146 (01) :218-227
[7]   THE STRUCTURE AND FUNCTION OF SUPPORTED MOLYBDENUM NITRIDE HYDRODENITROGENATION CATALYSTS [J].
COLLING, CW ;
THOMPSON, LT .
JOURNAL OF CATALYSIS, 1994, 146 (01) :193-203
[8]  
DJEAGAMARIADASS.G, 1995, CATAL LETT, V31, P411
[9]   SYNTHESIS OF AMMONIA AND RELATED PROCESSES ON REDUCED MOLYBDENUM DIOXIDE [J].
HILLIS, MR ;
KEMBALL, C ;
ROBERTS, MW .
TRANSACTIONS OF THE FARADAY SOCIETY, 1966, 62 (528P) :3570-&
[10]   GROWTH OF ULTRAFINE PARTICLES OF TRANSITION-METAL NITRIDES BY THE REACTIVE GAS EVAPORATION TECHNIQUE WITH ELECTRON-BEAM HEATING [J].
IWAMA, S ;
HAYAKAWA, K ;
ARIZUMI, T .
JOURNAL OF CRYSTAL GROWTH, 1984, 66 (01) :189-194