Oxidative dehydrogenation of propane on CeNixOy (0≤x≤1) mixed oxides hydrogen acceptors

被引:0
|
作者
Jalowiecki-Duhamel, L
Ponchel, A
Barbaux, Y
机构
[1] Univ Sci & Tech Lille Flandres Artois, URA CNRS D04020, Catalyse Heterogene & Homogene Lab, F-59655 Villeneuve Dascq, France
[2] Univ Sci & Tech Lille Flandres Artois, F-62307 Lens, France
关键词
D O I
暂无
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The oxidative dehydrogenation of propane has been studied on CeNiXOY (0 less than or equal to x less than or equal to 1) mixed oxides previously reduced under hydrogen. The products obtained are propene and CO2. No CO is obtained, whatever the temperature. An optimum propene yield of 6.9 % is obtained at 648 K on previously, at 473 K under H-2, in-situ reduced CeNi0.5. Whereas without any pretreatment, a propene yield of 5.35 % is obtained. Therefore, a beneficial effect of the pretreatment under H-2 is shown. The reducibility under H-2 of some CeNiXOY mixed oxides has been previously studied and, in particular, it has been reported that these solids are able to store high quantities of hydrogen H* related to the existence of anionic vacancies. These H* species have been proposed to be one half H- species located in the anionic vacancies and the second half H+ species, forming with the O2- species of the solid, OH- groups. As dehydrogenation requires the abstraction of hydrogen from the molecule which could be performed by a lacunar phase, and by analogy to the dissociation of H-2, a mechanism of the dehydrogenation step of the alkane is proposed, involving a heterolytic abstraction of a H- species by an anionic vacancy and of a H+ species by an O2- species of the solid forming an OH group.
引用
收藏
页码:383 / 392
页数:10
相关论文
共 50 条
  • [21] Propane oxidative dehydrogenation over alumina-supported metal oxides
    Al-Zahrani, SM
    Jibril, BY
    Abasaeed, AE
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2000, 39 (11) : 4070 - 4074
  • [22] Low-temperature oxidative dehydrogenation of propane over NiV mixed oxides derived from LDH precursors
    Liu, Zhenxing
    Wang, Jiang
    Wu, Kailu
    Xu, Aiju
    Jia, Meilin
    APL MATERIALS, 2023, 11 (04)
  • [23] Novel mesoporous mixed Nb-M (M = V, Mo, and Sb) oxides for oxidative dehydrogenation of propane
    Li, Y
    Bhatt, S
    Beaucage, G
    Guliants, VV
    Mamedov, S
    Soman, RS
    JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (49): : 23250 - 23254
  • [24] Hydrogen storage in CeNiXOY and CeM0.5NiXOY (M = Zr or Al) mixed oxides
    Jalowiecki-Duhamel, L.
    Debeusscher, S.
    Zarrou, H.
    D'Huysser, A.
    Jobic, H.
    Payen, E.
    CATALYSIS TODAY, 2008, 138 (3-4) : 266 - 271
  • [25] Oxidative dehydrogenation of propane on TiO2-supported chromium and zinc oxides
    Grabowski, R
    Grzybowska, B
    Samson, K
    Sloczynski, J
    Wcislo, K
    REACTION KINETICS AND CATALYSIS LETTERS, 1996, 57 (01): : 127 - 132
  • [26] Catalytic oxidative dehydrogenation of propane over Mg-V/Mo oxides
    Pless, JD
    Bardin, BB
    Kim, HS
    Ko, DG
    Smith, MT
    Hammond, RR
    Stair, PC
    Poeppelmeier, KR
    JOURNAL OF CATALYSIS, 2004, 223 (02) : 419 - 431
  • [27] Oxidative dehydrogenation of propane over supported chromium-molybdenum oxides catalysts
    Jibril, BY
    Al-Zahrani, SM
    Abasaeed, AE
    Hughes, R
    CATALYSIS COMMUNICATIONS, 2003, 4 (11) : 579 - 584
  • [28] Activity of the Ni–Al Mixed Oxides Prepared from Hydrotalcite-Like Precursors in the Oxidative Dehydrogenation of Ethane and Propane
    Lucie Smoláková
    Libor Čapek
    Šárka Botková
    František Kovanda
    Roman Bulánek
    Miloslav Pouzar
    Topics in Catalysis, 2011, 54
  • [29] Oxidative dehydrogenation of propane using mixed phases of magnesium molybdate.
    Jackson, NB
    Miller, JE
    Sault, AG
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 217 : U687 - U687
  • [30] Storage of reactive hydrogen species in CeMxOy (M = Cu, Ni; 0 ≤ x ≤ 1) mixed oxides
    Jalowiecki-Duhamel, L
    Ponchel, A
    Lamonier, C
    INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 1999, 24 (11) : 1083 - 1092