CO-hydrogenation over silica supported iron based catalysts: Influence of potassium loading
Description
Graphical abstract: Five different Fe–Cu/SiO2 catalysts were prepared by a combination of co-precipitation and wet impregnation technique at different K-loading ranging from 0 to 5 wt.% for the conversion of syngas to liquid fuel. Detailed Catalyst characterization was done by BET, TPR, TGA, XRD and TEM techniques. Maximum CO-hydrogenation obtained near to 1% K-loading and catalytic activity decreased at 3% and 5% K loading. Display Omitted - Highlights: • CO-hydrogenation was performed with K promoted Fe–Cu/SiO2 catalysts at different K-loading from 0.0 to 5.0 wt%. • Catalyst characterization was done by BET, TPR, TPD, TG-DTA, XRD, SEM–EDX and TEM techniques. • Maximum CO-hydrogenation obtained with 1% K-loading, further activity decreased with 3% and 5% K-loading. • Effect of K-promoter towards conversion, selectivity and deactivation of catalysts was studied for FT-process. - Abstract: Five different Fe–Cu/SiO2 catalysts were prepared by a combination of co-precipitation and wet impregnation technique at different K-loading ranging from 0 to 5 wt.% for the conversion of syngas to liquid fuel. The physiochemical characterization of these catalysts was performed by using N2 adsorption, X-ray diffraction (XRD), H2-TPR, NH3-TPD, TEM, Inductive Couple Plasma Mass Spectroscopy (ICP-MS), and SEM–EDX to study the effect of potassium on the textural properties, structural change, reduction behavior, acidity and morphological change to the above K-loading catalysts. The effect of addition of potassium promoter was studied for CO-Hydrogenation in a fixed bed reactor simultaneously with the effect of promoter on the CO-conversion, selectivity and deactivation. The maximum catalytic activity was obtained from 1% K-loading and the catalytic activity decreased thereafter. The activity for water–gas shift (WGS) also enhanced with increasing K loading. The results revealed that increasing K loading decreases gaseous hydrocarbon formation and shifts selectivity to higher molecular weight hydrocarbons. Incorporation of potassium suppresses the hydrogenation activity of the Fe–Cu/SiO2 catalyst, leading to higher olefin yield in the products
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apenergy.2013.04.070Additional details
Identifiers
- DOI
- 10.1016/j.apenergy.2013.04.070;
- PII
- S0306-2619(13)00366-8;
Publishing Information
- Journal Title
- Applied Energy
- Journal Volume
- 111
- Journal Page Range
- p. 267-276
- ISSN
- 0306-2619
- CODEN
- APENDX
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46000896
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- AMMONIA; CARBON MONOXIDE; CATALYSTS; COPRECIPITATION; DEACTIVATION; DIFFERENTIAL THERMAL ANALYSIS; HYDROCARBONS; HYDROGEN; HYDROGENATION; ICP MASS SPECTROSCOPY; IRON; LIQUID FUELS; MORPHOLOGICAL CHANGES; POTASSIUM; SCANNING ELECTRON MICROSCOPY; SILICA; THERMAL GRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; WATER GAS; X-RAY DIFFRACTION
- Descriptors DEC
- ALKALI METALS; CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; CHEMICAL ANALYSIS; CHEMICAL REACTIONS; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; ELEMENTS; ENERGY SOURCES; FLUIDS; FUEL GAS; FUELS; GAS FUELS; GASES; GRAVIMETRIC ANALYSIS; HYDRIDES; HYDROGEN COMPOUNDS; INTERMEDIATE BTU GAS; MASS SPECTROSCOPY; METALS; MICROSCOPY; MINERALS; NITROGEN COMPOUNDS; NITROGEN HYDRIDES; NONMETALS; ORGANIC COMPOUNDS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PRECIPITATION; QUANTITATIVE CHEMICAL ANALYSIS; SCATTERING; SEPARATION PROCESSES; SPECTROSCOPY; THERMAL ANALYSIS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.