The acid site distribution and the catalytic activity of SAPO5, MgAPO5
and CoAPO5 samples for cracking of light alkanes was studied. The aci
d strength of all samples was found to be similar to that of faujasite
s, that of CoAPO5 being somewhat weaker than that of the other samples
. The catalytic activity for cracking of n-hexane and n-butane was nea
rly identical for most of the SAPO5 samples investigated. For n-hexane
cracking, one of the SAPO5 samples also showed a significantly higher
activity than the other SAPO5 samples. The catalytic activity was thr
ee times higher for CoAPO5 and MgAPO5. Their higher activity is not du
e to a higher strength of the acid sites, but was concluded to be caus
ed by a higher contribution of the bimolecular cracking mechanism.