PERFORMANCE OF Ce-INCORPORATED KIT-6 SUPPORTED COBALT CATALYSTS FOR FISCHER–TROPSCH SYNTHESIS

2011 ◽  
Vol 04 (04) ◽  
pp. 369-372 ◽  
Author(s):  
GUODONG TAN ◽  
JINLIN LI ◽  
KONGYONG LIEW

A series of Ce -incorporated structure of cubic large mesoporous molecular sieves, KIT-6, with different Ce contents were synthesized by a direct hydrothermal process. A sample of Ce -loaded KIT-6 material was synthesised by incipent wetness impregnation. Similarly, catalysts with 15 wt.% Co loading on the above supports were also synthesized by incipient wetness impregnation. The supports and catalysts were characterized by X-ray diffraction, diffuse reflectance UV-vis, solid-state 29Si magic-angle spinning nuclear magnetic resonance, H2 -temperature programmed reduction, H2 -temperature programmed desorption and oxygen titration. The structure of the KIT-6 support was well retained after Ce incorporation. Small amounts of Ce in the Co catalyst were found to improve the activity and increase the selectivity to C5+ hydrocarbons for Fischer–Tropsch synthesis, while larger amounts of Ce had the reverse effect. Meanwhile, methane selectivity shows an opposite trend as compared with that of C5+ selectivity. Ce -loaded KIT-6 supported Co catalyst showed lower activity than KIT-6 supported Co catalyst.

2017 ◽  
Vol 2 (1) ◽  
pp. 51-61
Author(s):  
Nima Mohammadi Taher ◽  
Maedeh Mahmoudi ◽  
Seyyede Shahrzad Sajjadivand

Abstract An investigation was done to develop and characterize the alumina supported cobalt catalyst for Fischer-Tropsch Synthesis to produce biodiesel from biomass with the aim to produce alumina-supported cobalt catalysts containing 7 to 19 wt.% cobalt content. By using incipient wetness impregnation of γ-Al2O3 supports with cobalt nitrate hexahydrate with ethanol and distilled water solutions; the 14 wt.% cobalt content in catalyst was achieved. Nitrogen adsorption-desorption, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray fluorescence (XRF), H2temperature programmed reduction (H2-TPR), temperature programmed desorption (TPD), temperature programmed oxidation (TPO) and carbon monoxide chemisorption were used for the characterization of the catalysts to attain an appropriate cobalt catalyst. In order to investigate the effect of the impregnation on the crystalline size, surface area and cobalt content, three different impregnation methods with various durations were investigated. In addition, increasing the impregnation duration increased the cobalt content and its dispersion. Based on results, positive effect of the alumina support and impregnation duration on the crystallite size, surface area, and pore diameter, reducibility of the catalyst and cobalt dispersion were investigated. Thus, cobalt catalyst for using in fixed bed reactor to produce biodiesel from biomass through Fischer-Tropsch Synthesis was prepared and characterized.


ChemCatChem ◽  
2011 ◽  
Vol 3 (8) ◽  
pp. 1342-1347 ◽  
Author(s):  
Jong Wook Bae ◽  
Seon-Ju Park ◽  
Min Hee Woo ◽  
Joo Young Cheon ◽  
Kyoung-Su Ha ◽  
...  

2013 ◽  
Vol 634-638 ◽  
pp. 551-554
Author(s):  
Waritsara Bungmek ◽  
Passakorn Kongkinka ◽  
Siwaruk Chotiwan ◽  
Pinsuda Viravathana

The performance of ZrO2-La promoted silica supported cobalt catalyst (100Co/15ZrO2/ 100Aerosil/0.66La) was compared to the ZrO2-Ru promoted one, 100Co/15ZrO2/100Aerosil/0.66Ru, in Fischer-Tropsch synthesis (FTS). These catalysts were prepared by co-precipitation and incipient wetness impregnation methods. The characterization by XRD confirmed the cobalt phase of Co3O4 in both catalysts. For their catalytic activity on FTS reaction, the results preliminarily showed the higher methane fraction (60-80%) and lower C2-C4(10-20%) and C5+(10-20%) fractions in ZrO2-La promoted catalyst compared to the fractions of methane (20-40%), C2-C4(20-50%), and C5+(10-60%) from the ZrO2-Ru promoted catalyst. During reaction, the maximum n-paraffin selectivity of 40% was at C3and the hydrocarbon chain was up to C6for the ZrO2-La promoted catalyst. For the ZrO2-Ru promoted catalyst, the result showed the maximum n-paraffin of C3at 30 min of reaction time. When the reaction time increased, the maximum n-paraffin selectivity shifted toward higher C number but levelled off (15%) and the hydrocarbon chain was up to C16.


2013 ◽  
Vol 205 ◽  
pp. 86-93 ◽  
Author(s):  
Nikolaos E. Tsakoumis ◽  
Roya Dehghan ◽  
Rune E. Johnsen ◽  
Alexey Voronov ◽  
Wouter van Beek ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1324
Author(s):  
Byron Bradley Govender ◽  
Samuel Ayodele Iwarere ◽  
Deresh Ramjugernath

The influence of different catalyst cobalt loadings on the C1-C3 hydrocarbon product yields and energy consumption in plasma-catalytic Fischer-Tropsch synthesis (FTS) was investigated from the standpoint of various reactor operating conditions: pressure (0.5 to 10 MPa), current (250 to 450 mA) and inter-electrode gap (0.5 to 2 mm). This was accomplished by introducing a mullite substrate, coated with 2 wt%-Co/5 wt%-Al2O3, 6 wt%-Co/5 wt%-Al2O3 or 0 wt%-Co/5 wt%-Al2O3 (blank catalyst), into a recently developed high pressure arc discharge reactor. The blank catalyst was ineffective in synthesizing hydrocarbons. Between the blank catalyst, 2 wt%, and the 6 wt% Co catalyst, the 6 wt% improved C1-C3 hydrocarbon production at all conditions, with higher yields and relatively lower energy consumption at (i) 10 MPa at 10 s, and 2 MPa at 60 s, for the pressure variation study; (ii) 250 mA for the current variation study; and (iii) 2 mm for the inter-electrode gap variation study. The inter-electrode gap of 2 mm, using the 6 wt% Co catalyst, led to the overall highest methane, ethane, ethylene, propane and propylene yields of 22 424, 517, 101, 79 and 19 ppm, respectively, compared to 40 ppm of methane and < 1 ppm of C1-C3 hydrocarbons for the blank catalyst, while consuming 660 times less energy for the production of a mole of methane. Furthermore, the 6 wt% Co catalyst produced carbon nanotubes (CNTs), detected via transmission electron microscopy (TEM). In addition, scanning electron microscopy (SEM), energy dispersive x-ray spectroscopy (EDX) and x-ray diffraction (XRD) showed that the cobalt catalyst was modified by plasma treatment.


Author(s):  
Reza Roknabadi ◽  
Ali Akbar Mirzaei ◽  
Hossein Atashi

The effects of nanocatalyst composition and calcination parameters on the performance of the Fe–Mn–Ce ternary nanocatalysts supported on alumina granules in a laboratory fixed bed microreactor have been evaluated. Nanocatalysts were synthesized by incipient wetness impregnation under vacuum method (simultaneous impregnation of metal species). The samples used for hydrogenation of carbon monoxide via Fischer-Tropsch synthesis. The optimum nanocatalyst composition for production of light olefins (C=2 – C=4) from synthesis gas is 75 wt%Fe–20 wt%Mn–5 wt%Ce. The calcination parameters (temperature, time and atmosphere) were investigated and their effects on the structure and performance of the nanocatalysts were determined. The maximum ratio of olefins/(methane + paraffin) and the best activity and selectivity belonged to the nanocatalyst which was calcined in static air at 500 °C for 7 h. The nanocatalyst precursors and calcined samples (fresh and used) were characterized by XRD, N2 physisorption, FE‒SEM, EDAX, MAP, TG, DSC, and H2–TPR. The present study results confirm that the structural, morphological and physic-chemical properties of the nanocatalyst have been impressed with metal species and calcination parameters.


Catalysts ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 497 ◽  
Author(s):  
Renata Sadek ◽  
Karolina A. Chalupka ◽  
Pawel Mierczynski ◽  
Jacek Rynkowski ◽  
Jacek Gurgul ◽  
...  

Co-containing Beta zeolite catalysts prepared by a wet impregnation and two-step postsynthesis method were investigated. The activity of the catalysts was examined in Fischer-Tropsch synthesis (FTS), performed at 30 atm and 260 °C. The physicochemical properties of all systems were investigated by means of X-ray diffraction (XRD), in situ XRD, temperature programmed desorption of ammonia (NH3-TPD), X-ray Photoelectron Spectroscopy (XPS), temperature programmed reduction of hydrogen (TPR-H2), and transmission electron microscopy (TEM). Among the studied catalysts, the best results were obtained for the samples prepared by a two-step postsynthesis method, which achieved CO conversion of about 74%, and selectivity to liquid products of about 86%. The distribution of liquid products for Red-Me-Co20Beta was more diversified than for Red-Mi-Co20Beta. It was observed that significant influence of the zeolite dealumination of mesoporous zeolite on the catalytic performance in FTS. In contrast, for microporous catalysts, the dealumination did not play such a significant role and the relatively high activity is observed for both not dealuminated and dealuminated catalysts. The main liquid products of FTS on both mesoporous and microporous catalysts were C10-C14 isoalkanes and n-alkanes. The iso-/n-alkanes ratio for dealuminated zeolite catalysts was three times higher than that for not dealuminated ones, and was related to the presence of different kind of acidic sites in both zeolite catalysts.


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