作为硫化物催化剂前体的金属氧化物复合物用于二丁基锡化合物的加氢脱硫反应

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
S. L. Amaya-Bustos, G. Alonso-Núñez, J. N. Díaz De León, S. Fuentes and Adriana Echavarría-Isaza
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引用次数: 0

摘要

通过水热法制备了基于 Ni、Co、Mo 和/或 W 的金属氧化物复合物,并通过 X 射线衍射 (XRD) 鉴定获得了层状结构。随后,用空气和 H2S/H2 对层状材料进行热处理,得到过渡金属硫化物相。此外,还利用原子吸收(AA)化学分析、热重(TGA)和差分(DTA)分析、氢气温度编程还原(H2-TPR)、X 射线光电子能谱(XPS)、氮气物理吸附测量的 BET 表面积、扫描电子显微镜(SEM)和透射电子显微镜(TEM)测定了材料的理化性质。在 593 K 和 5.5 MPa 条件下,对所有催化剂进行了二苯并噻吩(DBT)加氢脱硫(HDS)反应测试。结果表明,催化剂的活性与六价金属(钼和钨)有关。NiCoMoS 催化剂的活性最高,DBT 转化率达到 96%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Metal oxide complexes as precursors of sulfide catalysts for HDS of DBT†

Metal oxide complexes as precursors of sulfide catalysts for HDS of DBT†

Metal oxide complexes based on Ni, Co, Mo, or W were prepared by a hydrothermal method and layered structures, identified by X-ray diffraction (XRD), were obtained. Subsequently, layered materials were thermally treated with air and H2S/H2 to obtain transition metal sulfide phases. The physicochemical properties of the materials were also determined by chemical analysis by atomic absorption (AA), thermogravimetric (TGA) and differential (DTA) analyses, hydrogen temperature-programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS), BET surface area measured by nitrogen physisorption, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). All catalysts were tested in the hydrodesulfurization (HDS) reaction of dibenzothiophene (DBT) at 593 K and 5.5 MPa. The results indicated that the activity of the catalysts is hexavalent metal (Mo and W) dependent. The NiCoMoS catalyst showed the highest activity with a DBT conversion of 96%.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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