Rong Liu, Pengfei Song*, Mazhar Ahmed Memon, Pengxiang Liu and Yuan Liu*,
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引用次数: 0
摘要
从合成气中合成高级醇类仍然具有挑战性,尤其是在平衡解离吸附和缔合吸附位点方面。在本研究中,我们制备了具有透辉石结构的 CaTi0.7-xCo0.3MnxO3 (x = 0-0.4) 催化剂,以提高醇类产品的选择性。还原后,金属钴和氧化锰均匀地分散在透辉石表面。引入反应气体后,氧化锰部分迁移到 Co 表面,减少了 Co0 位点,促进了电子从 Co 转移到锰,从而减少了碳氢化合物的离解吸附活性位点,促进了 Co2C 活性位点的形成。调整锰的掺杂量可以控制 Co2C 与 Co 的比例,从而调节 CO 的缔合吸附和离解吸附位点。氧化锰层还能防止烧结导致的钴失活。CaTi0.4Co0.3Mn0.3O3 催化剂的性能最佳,在 270 ℃ 时的总醇选择性达到 38.6%,其中高醇占 70.0wt.%。
Manganese Oxide Decorated Co Nanoparticles on CaTiO3 for Higher Alcohols Synthesis from Syngas
Higher alcohols synthesis from syngas remains challenging, especially in balancing dissociative adsorption and associative adsorption sites. In this study, we prepared CaTi0.7-xCo0.3MnxO3 (x = 0–0.4) catalysts with perovskite structure to enhance alcohol products selectivity. After reduction, metallic cobalt and manganese oxide uniformly dispersed on the perovskite’s surface. Upon introducing the reaction gases, MnOx partially migrated onto the surface of the Co, reducing Co0 sites and facilitating electrons transfer from Co to Mn, which decreased the dissociative adsorption active sites for hydrocarbons and promoted the formation of Co2C active sites. Adjusting the Mn doping allowed control over the Co2C to Co ratio, thereby regulating associative adsorption and dissociative adsorption sites for CO. The manganese oxide layer can also prevent cobalt deactivation due to sintering. The CaTi0.4Co0.3Mn0.3O3 catalyst exhibited the best performance, achieving total alcohols selectivity of 38.6% at 270 °C, with higher alcohols constituting 70.0wt.% of them.
期刊介绍:
ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.