Nickel-substituted silicoaluminophosphate type 41 (NiAPSO-41) molecular sieve has been synthesized hydrothermally using di-n-propylamine as the structure-directing agent. The reducibility of Ni II in NiAPSO-41 by various reduction methods was compared with that of NiH-SAPO-41, where Ni II was introduced into extraframework sites of SAPO-41 by partial ion exchange of H I by Ni II . Dehydration at elevated temperatures or hydrogen treatment at moderate temperatures produces Ni I species in NiH-SAPO-41. Two distinct Ni I species, assigned as isolated Ni I and as a Ni I –(H 2 ) n complex, are observed by electron paramagnetic resonance (EPR) in NiH-SAPO-41 after reduction in hydrogen at 573 K. By contrast, in NiAPSO-41 neither dehydration at high temperatures nor hydrogen reduction was effective in producing Ni I species. Isolated Ni I species could, however, be obtained in NiAPSO-41 by γ-irradiation of the materials at 77 K indicating the more stable nature of the Ni II sites in NiAPSO-41. Both NiAPSO-41 and NiH-SAPO-41 show differences in their EPR characteristics after reduction and adsorption of various adsorbates suggesting that Ni I in these two materials is in different sites. Electron spin echo modulation studies of 31 P modulation of Ni I in NiAPSO-41 and NiH-SAPO-41 also showed significant differences in their modulation patterns. Simulation of the spectrum observed for NiH-SAPO-41 shows two nearest-neighbour phosphorus atoms at a distance of 0.39 nm from Ni I suggesting that the Ni I ions are in the 10-membered ring channel near a 6-ring window. Simulation of the spectrum for NiAPSO-41 gives 12 nearest-neighbour phosphorus atoms at a distance of 0.54 nm and can be rationalized in terms of Ni I ions substituting into a framework phosphorus site.
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Prakash et al. (1997) studied this question.
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