Conclusions
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1.
The degree of reduction of nickel on RSG-6Ts cracking catalyst is significantly lower than on SiO2, and the dispersion of the metal on RSG-6Ts is significantly higher, due to the reaction of nickel with the aluminosilicate matrix.
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2.
The antimony is more uniformly distributed on the surface than the nickel, forming a monomolecular layer or small islets of Sb2O5. No reduction of antimony was detected on brief treatment in H2 at 550°C.
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3.
The increase in the “metal stability” of the catalysts in the presence of antimony is due to a decrease in the dispersion of Ni0 and perhaps by modification if its properties caused by the presence of a monolayer of antimony oxide on the Ni/SiO2-Al2O3 interface.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2684–2689, December, 1988.
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Stakheev, A.Y., Grigoryan, A.A., Shpiro, E.S. et al. Study of processes of deactivation of cracking catalysts by heavy metals and the mechanism of their passivation. Russ Chem Bull 37, 2414–2418 (1988). https://doi.org/10.1007/BF00952607
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DOI: https://doi.org/10.1007/BF00952607