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Temperature Programmed Reduction and Desorption Studies of CO-Precipitated Cobalt-Molybdenum Sulphide Powders

โœ Scribed by R. C. Hoodless; R. B. Moyes; P. B. Wells


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
403 KB
Volume
93
Category
Article
ISSN
0037-9646

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โœฆ Synopsis


red by a variant of the homogeneous sulphide precipitation method. The seriem consimted of nOS2, eight powders with Co/(Co+No) ratios of 0.167 to 0.643, and COgS8. The catalystm were characterised by deuterium adsorption at 673 K, TPR and TPD.

A double maximum was found for the dependence of activity with Co/(Co+PIo) fraction, in a range similar to that found by other workers. Hydrogen retained by the catalyst, and deuterium admorption at 673 K are not related to the hds activity. TPR and TPD measurements, however, show the same two-peak behaviour as the activity across the composition range. The TPR behaviour mhows two peaks of hydrogen uptake at 475 K and 650 K, the relative areas of which depend on the Co/(Co+nO) ratio in a complex way. The high temperature peak is strongly Correlated with hds activity, and thim activity is related both to the formation of defect sites at high temperature and the availability of adsorbed hydrogen. The adsorbed hydrogen measured by desorption between 300 K and 872 K is greatest in the Co/(Co+Mo) range 0.167 to 0.445, the range of highest activity for conventional catalymts, whereas combination of the T P R and TPD results yields the same pattern as is obtained for hds activity.

The results show that the behaviour with rempect to hydrogen im strongly affected by the premence of both cobalt and molybdenum, the synergic effect is much greater than a c o m b i n a t K o f the components.

A seriem of unsupported cobalt molybdenum sulphide powders ham been prepa-

The activity of theme materials was tested using the hds of thiophen.

Recently we have shown that molybdenum disulphide is

We then sought to extend these observations to

EXPERIMENTAL

Static adsorption measurements and activity measurements were made with a conventional high-vacuum gas-handling apparatus. Product analymem were obtained uming a Perkin-Elmer Sigma 1 gam-chromatograph (2). Temperature-programed reduction and dynamic adsorption meaauremantm were made in a flow apparatu8 fitted with precision flow controllers and a thermal conductivity detector linked to a datalogger. The data were analymed using a suite of computer progranu.


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