Synthesis of CexZr1‐xO2/SiO2 supports for chromium oxide catalysts of oxidative dehydrogenation of propane with carbon dioxide

脱氢 催化作用 丙烷 选择性 无机化学 化学 氧化物 水解 介孔材料 材料科学 化学工程 冶金 有机化学 工程类
作者
Mikhail Yu. Mashkin,М. А. Тедеева,Anna Fedorova,Evgeniya R. Fatula,А. В. Егоров,S. V. Dvoryak,К. И. Маслаков,A.V. Knotko,А. Е. Баранчиков,Gennadii I. Kapustin,Dmitrii I. Petukhov,Т. Б. Шаталова,И. В. Морозов,Л. М. Кустов,Alexander L. Kustov
出处
期刊:Journal of Chemical Technology & Biotechnology [Wiley]
卷期号:98 (5): 1247-1259 被引量:12
标识
DOI:10.1002/jctb.7339
摘要

Abstract BACKGROUND Propane dehydrogenation is an alternative way both to produce propylene and to utilize CO 2 . Because of the high oxygen mobility in cerium‐zirconium oxide (Ce x Zr 1‐ x O 2 ), it looks promising as a support for the chromium oxide catalysts of propane dehydrogenation with CO 2 . Supports of Ce x Zr 1‐ x O 2 on mesoporous silica were synthesized in this work to combine the high oxygen mobility of the former and the pore structure of the latter. RESULTS Two applied synthetic approaches resulted in materials with different structure and properties. The wet impregnated catalysts demonstrated a higher activity and selectivity to propylene. At the same time, they had larger pore size distribution maxima (~9 nm) than the samples prepared by the introduction of metals simultaneously with Si‐precursor hydrolysis (~2 nm). For the chromium catalysts with the same support, the catalytic activity decreased with varying chromium loading as follows: 5% Cr > 3% Cr ≈ 7% Cr. For the catalysts with different Ce x Zr 1‐ x O 2 supports and equal chromium loading, the activity decreased with x changing as follows: 0.5 > 0.6 > 0.8 for the samples prepared by wet impregnation, and 0.8 ≈ 0.6 > 0.5 for the other synthetic path. CONCLUSIONS Catalysts were tested in oxidative dehydrogenation of propane with CO 2 . The wet impregnation approach turned out to be much more promising in terms of catalytic activity and selectivity to propylene in the reaction of propane dehydrogenation with CO 2 . The selectivity achieved was ≤80% at a 40% conversion. © 2023 Society of Chemical Industry (SCI).
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