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铌钒氧化物合成方案对二苯并噻吩萃取催化氧化脱硫的影响

The Effect of the NbVO Synthesis Protocol on the Extractive Catalytic Oxidative Desulfurization of Dibenzothiophene.

作者信息

Stawicka Katarzyna, Gajewska Julia, Ziolek Maria, Trejda Maciej

机构信息

Department of Heterogeneous Catalysis, Faculty of Chemistry, Adam Mickiewicz University, Uniwersytetu Poznańskiego 8, 61-614 Poznań, Poland.

出版信息

Molecules. 2025 Jan 25;30(3):551. doi: 10.3390/molecules30030551.

Abstract

NbVO mixed oxides were synthesized, characterized, and evaluated as catalysts for the extractive catalytic oxidative desulfurization (ECODS) of dibenzothiophene (DBT) using acetonitrile as a solvent. The mixed oxides were prepared using two different vanadium precursors: ammonium metavanadate and vanadium(IV)-oxy acetylacetonate. These precursors influenced the acidic/basic properties and the concentration of oxygen vacancies in the resulting catalysts. The texture and surface properties of the synthesized materials were analyzed using nitrogen adsorption/desorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-visible spectroscopy (UV-vis). Their catalytic activity was evaluated through the dehydration and dehydrogenation of 2-propanol and the ECODS of DBT. The mixed oxides synthesized with an excess of ammonium metavanadate (Nb:V = 1:2) demonstrated superior catalytic activity in removing DBT from the oil phase, achieving approximately 90% removal within 90 min at 60 °C. This enhanced activity is attributed to its higher acidity, greater concentration of oxygen vacancies, and the presence of vanadium peroxo ligands on its surface.

摘要

合成了铌钒混合氧化物,对其进行了表征,并评估了其作为以乙腈为溶剂的二苯并噻吩(DBT)萃取催化氧化脱硫(ECODS)催化剂的性能。使用两种不同的钒前驱体:偏钒酸铵和乙酰丙酮氧钒(IV)制备了混合氧化物。这些前驱体影响了所得催化剂的酸/碱性质和氧空位浓度。使用氮气吸附/脱附、X射线衍射(XRD)、X射线光电子能谱(XPS)和紫外可见光谱(UV-vis)分析了合成材料的织构和表面性质。通过2-丙醇的脱水和脱氢以及DBT的ECODS评估了它们的催化活性。用过量偏钒酸铵(Nb:V = 1:2)合成的混合氧化物在从油相中去除DBT方面表现出优异的催化活性,在60℃下90分钟内实现了约90%的去除率。这种增强的活性归因于其较高的酸度、较高的氧空位浓度以及其表面存在的过氧钒配体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb28/11820594/c9d04830726a/molecules-30-00551-g002.jpg

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