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Deactivation and regeneration of Pt-modified zeolite Beta-Bindzil extrudates in n-hexane hydroisomerization

Hupa Leena; Vajglova Zuzana; Kumar Narendra; Sladkovskiy Dmitry A.; Peurla Markus; Semikin Kirill; Murzin Dmitry Yu

Deactivation and regeneration of Pt-modified zeolite Beta-Bindzil extrudates in n-hexane hydroisomerization

Hupa Leena
Vajglova Zuzana
Kumar Narendra
Sladkovskiy Dmitry A.
Peurla Markus
Semikin Kirill
Murzin Dmitry Yu
Katso/Avaa
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WILEY
doi:10.1002/jctb.6685
URI
https://doi.org/10.1002/jctb.6685
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042821823
Tiivistelmä
BACKGROUND The metal-acid bifunctional catalysts are widely used in many industrially significant chemical processes, including hydroisomerization of n-hexane. Deactivation and regeneration of metal-acid bifunctional extrudates was investigated in continuous n-hexane hydroisomerization in a fixed-bed reactor. Four Pt/H-Beta-25 catalysts containing 30% Bindzil binder were prepared with the same composition and controlled metal deposition.RESULTS Different preparation steps led to differences in the mechanical strength, Pt particle size, acidity and strength, metal-to-acid site (c(Pt)/c(AS)) ratio and proximity between two types of active sites. A very slow deactivation and high selectivity to C-6 isomers was obtained when Pt was deposited on H-Beta-25 zeolite.CONCLUSION Initial selectivity to the desired products was correlated with the physicochemical properties of the catalysts. Location of the metal has a larger influence on catalyst deactivation of the bifunctional catalysts rather than the metal-to-acid site ratio or site proximity. Decline of n-hexane conversion and selectivity to C-6 isomers were correlated with changes in the textural properties and acidity of the deactivated catalyst, respectively. (c) 2021 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
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