Authors (10): S. A. Kondrat, P. J. Smith, J. H. Carter, J. S. Hayward, G. J. F. .Pudge, G. M. Shaw, M. S. Spencer, J. K. Bartley, S. F. . R. Taylor, G. J. Hutchings
Themes: Environment (2017)
DOI: 10.1039/c6fd00202a
Citations: 31
Pub type: journal-article
Publisher: Royal Society of Chemistry (RSC)
Issue:
License:
Publication date(s): 2017 (online)
Pages: 287-307
Volume: 197 Issue:
Journal: Faraday Discussions
URL: http://dx.doi.org/10.1039/c6fd00202a
The effect of sodium species on the physical and catalytic properties of Cu/ZnO catalysts derived from zincian georgeite has been investigated. Catalysts prepared with <100 ppm to 2.1 wt% Na+, using a supercritical CO2 antisolvent technique, were characterised and tested for the low temperature water–gas shift reaction and also CO2 hydrogenation to methanol. It was found that zincian georgeite catalyst precursor stability was dependent on the Na+ concentration, with the 2.1 wt% Na+-containing sample uncontrollably ageing to malachite and sodium zinc carbonate. Samples with lower Na+ contents (<100–2500 ppm) remained as the amorphous zincian georgeite phase, which on calcination and reduction resulted in similar CuO/Cu particle sizes and Cu surface areas. The aged 2.1 wt% Na+ containing sample, after calcination and reduction, was found to comprise of larger CuO crystallites and a lower Cu surface area. However, calcination of the high Na+ sample immediately after precipitation (before ageing) resulted in a comparable CuO/Cu particle size to the lower (<100–2500 ppm) Na+ containing samples, but with a lower Cu surface area, which indicates that Na+ species block Cu sites. Activity of the catalysts for the water–gas shift reaction and methanol yields in the methanol synthesis reaction correlated with Na+ content, suggesting that Na+ directly poisons the catalyst.
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