In situ observation of Ni-Mo-S phase formed on NiMo/Al2O3 catalyst sulfided at high pressure by means of Ni and Mo K-edge EXAFS spectroscopy

被引:9
作者
Koizumi, Naoto [1 ]
Hamabe, Yusuke [1 ]
Jung, Sungbong [1 ]
Suzuki, Yasuhiro [1 ]
Yoshida, Shohei [1 ]
Yamada, Muneyoshi [2 ]
机构
[1] Tohoku Univ, Grad Sch Engn, Dept Appl Chem, Aoba Ku, Sendai, Miyagi 9808579, Japan
[2] Akita Natl Coll Technol, Akita 0118511, Japan
来源
JOURNAL OF SYNCHROTRON RADIATION | 2010年 / 17卷
关键词
EXAFS spectroscopy; high-pressure chamber; Ni-Mo-S phase; hydrodesulfurization; NiMo/Al2O3; catalysts; ABSORPTION FINE-STRUCTURE; MOSSBAUER EMISSION-SPECTROSCOPY; HYDRODESULFURIZATION CATALYSTS; LESS-THAN-OR-EQUAL-TO-5.1; MPA; PROBE MOLECULE; CO; CO-MO/AL2O3; SULFIDATION; NI-MO/AL2O3; SAMPLES;
D O I
10.1107/S0909049510004802
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
To obtain direct evidence of the formation of the Ni-Mo-S phase on NiMo/Al2O3 catalysts under high-pressure hydrodesulfurization conditions, a high-pressure EXAFS chamber has been constructed and used to investigate the coordination structure of Ni and Mo species on the catalysts sulfided at high pressure. The high-pressure chamber was designed to have a low dead volume and was equipped with polybenzimidazole X-ray windows. Ni K-edge k(3)chi(k) spectra with high signal-to-noise ratio were obtained using this high-pressure chamber for the NiMo/Al2O3 catalyst sulfided at 613 K and 1.1 MPa over a wide k range (39.5-146 nm(-1)). The formation of Ni-Mo and Mo-Ni coordination shells was successfully proved by Ni and Mo K-edge EXAFS measurement using this chamber. Interatomic distances of these coordination shells were almost identical to those calculated from Ni K-edge EXAFS of NiMo/C catalysts sulfided at atmospheric pressure. These results support the hypothesis that the Ni-Mo-S phase is formed on the Al2O3-supported NiMo catalyst sulfided under high-pressure hydrodesulfurization conditions. (C) 2010 International Union of Crystallography Printed in Singapore - all rights reserved
引用
收藏
页码:414 / 424
页数:11
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