Premium
Oxidative Dehydrogenation of n‐Butene with V–Mg Complex Oxide with Added Trivalent Metal Oxide
Author(s) -
Kiyokawa Takayasu,
Hagihara Takashi,
Ikenaga Naoki
Publication year - 2019
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201803392
Subject(s) - dehydrogenation , catalysis , oxide , chemistry , calcination , oxygen , mixed oxide , metal , inorganic chemistry , yield (engineering) , nuclear chemistry , materials science , organic chemistry , metallurgy
Oxidative dehydrogenation (ODH) of n‐butene with V−Mg complex oxide catalysts was carried out with a fixed‐bed flow reactor at 480 °C. In order to improve the catalytic performance of V−Mg complex oxide, we examined the effect of added metal oxide on the ODH of n‐butene. When Fe was added to the V−Mg complex oxide, the reactivity of lattice oxygen in the V−Mg complex oxide increased. V−Mg‐Fe(20:30:10) prepared at a molar ratio of V:Mg:Fe=20:30:10 showed high conversion (53.9%) and buta‐1,3‐diene (BD) yield (20.3%) in the ODH with the lattice oxygen. To continuously produce BD, ODH under O 2 flow was also investigated. The V−Mg‐Fe(20:30:10) catalyst exhibited higher BD yield than the V−Mg catalyst, and it was indicated that the high reactivity of the lattice oxygen affected the ODH under O 2 flow. Moreover, the V−Mg‐Fe(20:30:10)‐800 catalyst calcined at 800 °C showed highly stable ODH activity, and the BD yield (11%) was maintained for 420 min. XRD analysis results of the catalyst showed that the maintenance of the ODH activity could be attributed to the maintenance of the crystalline structure of V−Mg‐Fe(20:30:10)‐800 during the reaction.