Production of hydrogen from methanol over binary Cu/ZnO catalysts - Part I. Catalyst preparation and characterisation

• Mixed copper-zinc oxide catalysts (Cu/ZnO) were prepared by two different techniques, i.e. from hydroxycarbonate precursors formed in aqueous solution and from oxalate precursors formed in water-in-oil microemulsion. Their physicochemical properties were characterised by nitrogen adsorption-desorption, N2O chemisorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction (TPR) and oxidation (TPO). The BET surface areas ranged from 34 to 87 m(2)/g, depending on the method of preparation. Cu surface areas between 6.6 and 22 m(2)/g were measured. It was a general observation that catalysts prepared by microemulsion technique had lower Cu dispersions than expected (3.4-5.7%), due to a proposed partial embedding of Cu in ZnO. The catalyst prepared by carbonate co-precipitation exhibited a significantly higher Cu dispersion (10.3%). In addition, this catalyst displayed better resistance to successive TPR/TPO than the microemulsion catalysts, which exhibited significant Cu crystallite growth. However, the microemulsion route provided well-mixed materials with a narrow particle size distribution and the possibility to obtain high BET surface areas (up to 87 m(2)/g) by controlling the water/surfactant ratio in the microemulsion. XPS measurements revealed the existence of Cu+ species on the surface of both types of catalysts after exposure to a O-2/CH3OH mixture. The surface composition of the hydroxycarbonate-derived sample was unaffected by reduction in hydrogen and exposure to O-2/CH3OH, while Zn-enrichment on the surface was observed in the microemulsion catalysts after reduction, indicating sintering of the Cu particles. These observations were consistent with the TPR/TPO measurements.

Nyckelord

Cu/ZnO catalyst

hydroxycarbonate precursor

oxalate precursor

microemulsion

characterisation

N2O chemisorption

XPS

TPR/TPO

ray photoelectron-spectroscopy

gel-oxalate coprecipitation

gas shift

reaction

partial oxidation

surface characterization

structural-changes

oxide catalysts

chemical-state

copper surface

zinc-oxide

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