Abstract

Silica supported cobalt catalysts have been prepared using urea containing cobalt nitrate solution impregnation method, which can give high loading Co3O4 with relatively smaller crystallite size. Compared to the conventional impregnation method, the catalyst prepared with urea added to the cobalt nitrate solution provides higher activity for CO conversion and C5+ selectivity. To optimize the catalyst activation and simulate the industrial activation, TPO–TPR cycle treatment with or without steam has been applied to the prepared catalysts under various conditions. It is shown that reduction of pure hydrogen with high flow rate leads to a sharp temperature rise in the catalyst bed, which results in the sintering of the cobalt particles. A slow temperature rise with dilute hydrogen helps stabilize the cobalt particles, and the cycle treatment of the catalyst using TPO–TPR without steam induction has little effect on the size of cobalt particles. When steam is included in the reduction stream with hydrogen the TPR–TPO cycle treatment can help increase the Co dispersion, which increases the catalyst activity and selectivity to C5+.

Highlights

  • Research on alternative fuels plays an important role in emission reduction and future energy supply

  • Compared to the conventional impregnation method, the catalyst prepared with urea added to the cobalt nitrate solution provides higher activity for CO conversion and C5? selectivity

  • The catalysts prepared with and without urea in the aqueous solution were tested for Fischer–Tropsch synthesis, and the results are shown in Figs. 1 and 2

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Summary

Introduction

Research on alternative fuels plays an important role in emission reduction and future energy supply. It has been demonstrated that metallic Co particles formed on the catalyst surface under FTS conditions are the origin of their catalytic activity for hydrocarbon formation [9, 13,14,15,16,17]. The supports for this process are primarily silica, alumina and titania, over which the active metal particles, e.g., cobalt, are dispersed. The impregnated Co nitrate is decomposed to Co3O4 and these precursor oxides are reduced with H2 to Co0 particles prior to FTS

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