碳-沸石复合材料负载双金属CoMo纳米粒子作为二苯并噻吩加氢脱硫催化剂

IF 1.3 Q3 ENGINEERING, CHEMICAL
Z. Mohammadian, M. H. Peyrovi, N. Parsafard
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引用次数: 0

摘要

采用湿浸渍法和CS2预硫化法制备了不同质量比的新型活性炭- hzsm -5复合材料负载型钴钼催化剂。采用x射线粉末衍射、傅里叶变换红外光谱、N2吸附-解吸和扫描电镜分析对催化剂进行了表征。采用固定床反应器,在250 ~ 400℃的常压条件下,每种粉末0.5 g, CS2预硫化,考察了其对二苯并噻吩加氢脱硫反应的活性。CoMo/活性炭- hzsm -5(1:1)催化剂在300 ~ 400℃的温度范围内二苯并噻吩的转化率最高。以CoMo/活性炭- hzsm -5(3:1)为催化剂,在各温度条件下对优势产物环己基苯的选择性最佳。版权所有©2021作者,BCREC集团出版。这是一篇基于CC BY-SA许可(https://creativecommons.org/licenses/by-sa/4.0)的开放获取文章。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bimetallic CoMo Nanoparticles Supported over Carbon-Zeolite Composites as Dibenzothiophene Hydrodesulfurization Catalyst
Cobalt molybdenum catalysts supported on novel activated carbon-HZSM-5 composites with different mass ratios were prepared by wet-impregnation method and pre-sulfided by CS2. Characterization of these catalysts was done using X-ray powder diffraction, Fourier transform infrared spectroscopy, N2 adsorption-desorption, and scanning electron microscope analytics. Their activity for the hydrodesulfurization reaction of dibenzothiophene was investigated at atmospheric pressure in the temperature range of 250–400 °C using the fixed-bed reactor with 0.5 g of each powder and pre-sulfided with CS2. The highest conversion of dibenzothiophene at the temperature range of 300–400 °C was obtained for the CoMo/activated carbon-HZSM-5(1:1) catalyst. The best selectivity for cyclohexylbenzene, which is the dominant product according to gas chromatography results, was obtained at all temperatures using CoMo/activated carbon-HZSM-5(3:1) catalyst. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
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来源期刊
CiteScore
3.20
自引率
6.70%
发文量
52
审稿时长
12 weeks
期刊介绍: Bulletin of Chemical Reaction Engineering & Catalysis, a reputable international journal, provides a forum for publishing the novel technologies related to the catalyst, catalysis, chemical reactor, kinetics, and chemical reaction engineering. Scientific articles dealing with the following topics in chemical reaction engineering, catalysis science and engineering, catalyst preparation method and characterization, novel innovation of chemical reactor, kinetic studies, etc. are particularly welcome. However, articles concerned on general chemical engineering process are not covered and out of scope of this journal
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