费托合成中铁基催化剂性能的研究:温度和促进剂效应

IF 0.7 Q4 ENGINEERING, CHEMICAL
Mahin Jabalameli, Yahya Zamani, Sahar Baniyaghoob, Laleh Shirazi
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引用次数: 0

摘要

采用湿浸渍法制备了铁基催化剂。最终铁催化剂的组成,关于重量比如下%Fe/γ-Al2O3, 14%Fe/3%Cu/γ-Al2O3, 14%Fe/3%Sn/γ-Al2O3 and 14%Fe/3%Cu/1%Sn/γ-Al2O3. The catalysts were characterized using XRD, ICP, BET, H2-TPR, FE-SEM and EDX techniques. The catalytic activity was evaluated in a fixed bed reactor under 2.0 MPa of pressure, H2 : CO = 1 : 1, GHSV = 2 L h–1 \({\text{g}}_{{{\text{cat}}}}^{{-1}}\), in the temperature range of 270–300°C. Then, the effect of temperature and promoters (Cu and Sn) on the catalyst performance was investigated. CO conversion and product selectivity were also calculated using the results of GC. The results showed that the Cu and Sn promoters increased the reduction rate of Fe2O3 by providing H2 dissociation sites. Higher temperatures were also shown to change the CO conversion and product selectivity. The selectivity of both methane and C2–C4 hydrocarbons decreased while the selectivity of C5+ increased because of simultaneous use of Cu and Sn for promoting iron catalyst. Sn promoter increased FT and WGS activities.
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Study of Iron-Based Catalysts Performance in Fischer–Tropsch Synthesis: Temperature and Promoter Effect

Study of Iron-Based Catalysts Performance in Fischer–Tropsch Synthesis: Temperature and Promoter Effect

The iron-based catalysts were prepared via wet-impregnation method. The composition of the final iron catalysts, regarding to the weight ratio is as follow 14%Fe/γ-Al2O3, 14%Fe/3%Cu/γ-Al2O3, 14%Fe/3%Sn/γ-Al2O3 and 14%Fe/3%Cu/1%Sn/γ-Al2O3. The catalysts were characterized using XRD, ICP, BET, H2-TPR, FE-SEM and EDX techniques. The catalytic activity was evaluated in a fixed bed reactor under 2.0 MPa of pressure, H2 : CO = 1 : 1, GHSV = 2 L h–1 \({\text{g}}_{{{\text{cat}}}}^{{-1}}\), in the temperature range of 270–300°C. Then, the effect of temperature and promoters (Cu and Sn) on the catalyst performance was investigated. CO conversion and product selectivity were also calculated using the results of GC. The results showed that the Cu and Sn promoters increased the reduction rate of Fe2O3 by providing H2 dissociation sites. Higher temperatures were also shown to change the CO conversion and product selectivity. The selectivity of both methane and C2–C4 hydrocarbons decreased while the selectivity of C5+ increased because of simultaneous use of Cu and Sn for promoting iron catalyst. Sn promoter increased FT and WGS activities.

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来源期刊
Catalysis in Industry
Catalysis in Industry ENGINEERING, CHEMICAL-
CiteScore
1.30
自引率
14.30%
发文量
21
期刊介绍: The journal covers the following topical areas: Analysis of specific industrial catalytic processes: Production and use of catalysts in branches of industry: chemical, petrochemical, oil-refining, pharmaceutical, organic synthesis, fuel-energetic industries, environment protection, biocatalysis; technology of industrial catalytic processes (generalization of practical experience, improvements, and modernization); technology of catalysts production, raw materials and equipment; control of catalysts quality; starting, reduction, passivation, discharge, storage of catalysts; catalytic reactors.Theoretical foundations of industrial catalysis and technologies: Research, studies, and concepts : search for and development of new catalysts and new types of supports, formation of active components, and mechanochemistry in catalysis; comprehensive studies of work-out catalysts and analysis of deactivation mechanisms; studies of the catalytic process at different scale levels (laboratory, pilot plant, industrial); kinetics of industrial and newly developed catalytic processes and development of kinetic models; nonlinear dynamics and nonlinear phenomena in catalysis: multiplicity of stationary states, stepwise changes in regimes, etc. Advances in catalysis: Catalysis and gas chemistry; catalysis and new energy technologies; biocatalysis; nanocatalysis; catalysis and new construction materials.History of the development of industrial catalysis.
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