Abstract

The effects of 1% of Cd, In and Sn additives on the physicochemical properties and Fischer-Tropsch synthesis (FTS) performance of a 15% Co/Al2O3 catalyst were investigated. The fresh and spent catalysts were characterized by BET, temperature programmed reduction (TPR), H2-chemisorption, NH3 temperature programmed desorption (TPD), X-ray absorption near edge spectroscopy (XANES), and X ray diffraction (XRD). The catalysts were tested in a 1 L continuously stirred tank reactor (CSTR) at 220 °C, 2.2 MPa, H2/CO = 2.1 and 20–55% CO conversion. Addition of 1% of Cd or In enhanced the reduction degree of 15%Co/Al2O3 by ~20%, while addition of 1% Sn slightly hindered it. All three additives adversely impacted Co dispersion by 22–32% by increasing apparent Co cluster size based on the H2-chemisorption measurements. However, the decreased Co active site density resulting from the additives did not result in a corresponding activity loss; instead, the additives decreased the activity of the Co catalysts to a much greater extent than expected, i.e., 82–93%. The additional detrimental effect on catalyst activity likely indicates that the Cd, In and Sn additives migrated to and covered active sites during reaction and/or provided an electronic effect. XANES results showed that oxides of the additives were present during the reaction, but that a fraction of metal was also likely present based on the TPR and reaction testing results. This is in contrast to typical promoters that become metallic at or below ~350 °C, such as noble metal promoters (e.g., Pt, Ru) and Group 11 promoters (e.g., Ag, Au) on Co catalysts in earlier studies. In the current work, all three additives remarkably increased CH4 and CO2 selectivities and decreased C5+ selectivity, with the Sn and In additives having a greater effect. Interestingly, the Cd, In, or Sn additives were found to influence hydrogenation and isomerization activities. At a similar conversion level (i.e., in the range of 40–50%), the additives significantly increased 2-C4 olefin content from 3.8 to 10.6% and n-C4 paraffin from 50 to 61% accompanied by decreases in 1-C4 olefin content from 48 to 30%. The Sn contributed the greatest impact on the secondary reactions of 1-olefins, followed by the In and Cd. NH3-TPD results suggest enhanced acid sites on cobalt catalysts resulting from the additives, which likely explains the change in selectivities for the different catalysts.

Highlights

  • Supported cobalt catalysts have received renewed attention in converting natural gas to liquid fuels (GTL) due to their high activity, high selectivity toward heavier hydrocarbons and excellent stability in long term operation

  • Further studies by X-ray absorption near edge spectroscopy (XANES)/EXAFS indicated different structures of the noble metal additives. Both Pd-Pd and Pd-Co coordination were found in the spent Pd-Co catalysts, but for the other promoted catalysts (Pt, Re, and Ru-which performed significantly better than the Pd promoted one), only coordination from the additive to Co was detected by EXAFS [6,16]

  • temperature programmed reduction (TPR) and hydrogen chemisorption/pulse reoxidation results showed that only a fraction of Cd, In and Sn was reduced

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Summary

Introduction

Supported cobalt catalysts have received renewed attention in converting natural gas to liquid fuels (GTL) due to their high activity, high selectivity toward heavier hydrocarbons and excellent stability in long term operation. Most of them at low loadings were reported to enhance cobalt reduction and dispersion, and promoted activity and selectivity toward heavier hydrocarbons for cobalt catalysts. According to this large number of additive effect studies, some of them such as Ag and Zr showed great benefits to the performance of the cobalt catalyst and are promising steps toward a potential replacement for Pt. Efforts continue to find potential substitutes for Pt additive and to better understand structure-performance relationships. The effect of these additives on physiochemical properties and FTS performance of 15%Co/Al2 O3 catalysts were carefully studied using various characterization and testing techniques

BET and Porosity Measurements
The cobalt reduction
Catalyst Preparation
BET Surface Area and Porosity Measurements
Temperature Programmed Reduction
NH3 Temperature Programmed Desorption
Catalytic Activity Testing
Conclusions
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