Abstract

Samples of well-controlled nanoparticles consisting of alloys of cobalt and nickel of different atomic ratios were synthesized using wet chemical methods with oleylamine as the solvent and the reducing agent. These materials were characterized by a variety of techniques, including high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), X-ray energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD). Small amounts of heterogenized catalysts were prepared using alumina as the support. However, the potential for use of Co–Ni catalysts in CO hydrogenation was explored using a larger amount of Co–Ni/alumina catalyst prepared from standard aqueous impregnation methods and tested in a continuously stirred tank reactor (CSTR) for Fischer–Tropsch synthesis (FTS). Results are compared to a reference catalyst containing only cobalt. The heterogenized catalysts were characterized using synchrotron methods, including temperature programmed reduction with extended X-ray absorption fine structure spectroscopy and X-ray absorption near edge spectroscopy (TPR-EXAFS/XANES). The characterization results support intimate contact between Co and Ni, strongly suggesting alloy formation. In FTS testing, drawbacks of Ni addition included decreased CO conversion on a per gram catalyst basis, although Ni did not significantly impact the turnover number of cobalt, and produced slightly higher light gas selectivity. Benefits of Ni addition included an inverted induction period relative to undoped Co/Al2O3, where CO conversion increased with time on-stream in the initial period, and the stabilization of cobalt nanoparticles at a lower weight % of Co.

Highlights

  • Cobalt catalysts are important for the Fischer–Tropsch synthesis (FTS) reaction, which is at the heart of the gas-to-liquids (GTL) process [1]

  • This restricted oxidation was confirmed by the structural characterization through high-angle annular dark-field (HAADF)-Scanning transmission electron microscopy (STEM) and X-ray diffraction (XRD), and by the TPR-XANES profiles of Co and Ni, where the heterogenized unconventional catalysts exhibited high initial Co0 and Ni0 content (Samples #1 and 2) or high CoO/NiO content (Sample #3) in comparison with the catalyst prepared by traditional aqueous impregnation of nitrates; the conventional catalyst started in a higher oxidation state, with Co3 O4 and Ni2+ associated with Co3 O4

  • The TPR-XANES results at the Ni edge show that this Ni2+ undergoes a shift to lower energy when Co3 O4 reduces to CoO in the case of the conventional catalyst prepared by aqueous impregnation

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Summary

Introduction

Cobalt catalysts are important for the Fischer–Tropsch synthesis (FTS) reaction, which is at the heart of the gas-to-liquids (GTL) process [1]. Do they offer good activity and stability, as well as high selectivity toward heavier hydrocarbons, but they possess low water–gas shift (WGS). Cobalt is an expensive metal, with a price that has ranged from $22 to $100 per kg within the past five years [3]. In order to maximize its surface area, cobalt is typically supported on a metal oxide carrier such as γ-Al2 O3 or TiO2. There are three major problems with heterogenized cobalt catalysts that are of interest to commercial developers

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