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There is another problem, which is the structure of the support fund itself.
The conversion behaviour of SLPCs, however, is also influenced by the pore structure of the support.
The results show that preparation method influences porous structure of the support and gold particles size.
Surface chemistry as well as the porous structure of the support, affect the catalyst behaviour.
It was found that while the structure of the support materials remained relatively intact after the incorporation of Ag+ and Fe3+ onto the supports, differences in the structure of the support corresponded with differences in cluster size and composition.
A close examination of product distribution indicated that the major contributing factor was the pore structure of the support.
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After gold deposition the crystalline structure of the supports was not altered.
Catalysts characterization showed that the preparation method did not change the original structure of the supports.
We observed a strong dependence of the immobilized enzyme activities on the chemical nature and physical structure of the supports.
It has also been shown that the pore structure of the supports has a significant effect on the cobalt particles produced [5].
The reactivity and catalytic activity can be very dependent upon geometry arrangement and electronic structure of the supported cluster [2, 6].
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