The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.
Characterization of Molybdenum Carbides for Methane Reforming by TPR, XRD, and XPS
Abstract
The relationship between various unsupported molybdenum carbides and their activity toward methane reforming at 973 K and 1 atm was studied. Unsupported molybdenum carbides catalyzed the formation of hydrogen in high selectivity, forming ethylene and ethane rather than benzene as the carbon-containing products. η-Mo 3 C 2, which was nitrided at 973 K and subsequently carbided at 1173 K, was more active than both α-MoC 1 - x and β-Mo 2 C in methane decomposition, forming hydrogen in high selectivity. α-MoC 1 - x and γ-Mo 2 N were transformed to η-Mo 3 C 2 in the bulk structure during methane reforming at 973 K. This transformation caused a significant increase in the turnover frequency of methane reforming. η-molybdenum carbide was also formed during CH 4 -TPR of γ-Mo 2 N at 788 K. The linear relationship between the amount of η-carbide determined through H 2 -TPR of the catalysts and the methane disappearance rate revealed that η-Mo 3 C 2 is the active species for methane reforming. From the XPS analysis, Mo 0 was the dominant molybdenum species for the η-Mo 3 C 2 catalysts.
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Cites
The Chemistry of Transition Metal Carbides and Nitrides
(1996) · Springer eBooks · doi:10.1007/978-94-009-1565-7 · Cited by 1,144
Dehydrogenation and aromatization of methane under non-oxidizing conditions
Wang, L., Tao, L., Xie, M., Xu, G., Huang, J., & Xu, Y. (1993) · Catalysis Letters · doi:10.1007/bf00767368 · Cited by 841
Chen, J. G. (1996) · Chemical Reviews · doi:10.1021/cr950232u · Cited by 773
Compounds of molybdenum and tungsten with high specific surface area
Volpe, L., & Boudart, M. (1985) · Journal of Solid State Chemistry · doi:10.1016/0022-4596(85)90302-0 · Cited by 508
Lee, J. S., Oyama, S. T., & Boudart, M. (1987) · Journal of Catalysis · doi:10.1016/0021-9517(87)90218-1 · Cited by 431
Aromatization of Methane over Supported and Unsupported Mo-Based Catalysts
Solymosi, F., Cserényi, J., Szöke, A., Bánsági, T., & Oszkó, A. (1997) · Journal of Catalysis · doi:10.1006/jcat.1997.1478 · Cited by 396
Borry, R. W., Kim, Y. H., Huffsmith, A., Reimer, J. A., & Iglesia, E. (1999) · The Journal of Physical Chemistry B · doi:10.1021/jp990866v · Cited by 342
Lee, J. S., Volpe, L., Ribeiro, F. H., & Boudart, M. (1988) · Journal of Catalysis · doi:10.1016/0021-9517(88)90119-4 · Cited by 222
Aegerter, P. A., Quigley, W. W. C., Simpson, G. J., Ziegler, D. D., Logan, J. W., McCrea, K. R., Glazier, S., & Bussell, M. E. (1996) · Journal of Catalysis · doi:10.1006/jcat.1996.0367 · Cited by 201
Catalysis over molybdenum carbides and nitrides I. Catalyst characterization
RANHOTRA, G. (1987) · Journal of Catalysis · doi:10.1016/0021-9517(87)90152-7 · Cited by 134
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Vrubel, H., & Hu, X. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201207111 · Cited by 1,302
Wang, S., Wang, J., Zhu, M., Bao, X., Xiao, B., Su, D., Li, H., & Wang, Y. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b07924 · Cited by 435
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Metadata
- Authors
- Oshikawa, K., Nagai, M., & Omi, S.
- Venue
- The Journal of Physical Chemistry B
- Publisher
- American Chemical Society (ACS)
- Published
- 2001-08-23
- Volume
- 105
- Issue
- 38
- Pages
- 9124-9131
- ISSN
- 1520-5207 (ISSN-L)
- 1520-6106
- OpenAlex
- W2003708160
- Cited by
- 279
- References
- 13
- FWCI
- 2.35
- Type
- journal article
- Language
- en
- Open access
- closed
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