Catalytic

A series of dealuminated Y-zeolites impregnated by 0.5 wt% Pt catalysts promoted by different amounts of Ni, Pd or Cr (0.3 and 0.6 wt%) were prepared and characterized as hydrocracking catalysts. The physicochemical and structural characterization of the solid catalysts were investigated and reporte...

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Main Authors: S.A. Hanafi, H.M. Gobara, M.S. Elmelawy, S.A. Abo-El-Enein, A.A. Alkahlawy
Format: Article
Language:English
Published: Egyptian Petroleum Research Institute 2014-03-01
Series:Egyptian Journal of Petroleum
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Online Access:http://www.sciencedirect.com/science/article/pii/S1110062114000178
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author S.A. Hanafi
H.M. Gobara
M.S. Elmelawy
S.A. Abo-El-Enein
A.A. Alkahlawy
author_facet S.A. Hanafi
H.M. Gobara
M.S. Elmelawy
S.A. Abo-El-Enein
A.A. Alkahlawy
author_sort S.A. Hanafi
collection DOAJ
description A series of dealuminated Y-zeolites impregnated by 0.5 wt% Pt catalysts promoted by different amounts of Ni, Pd or Cr (0.3 and 0.6 wt%) were prepared and characterized as hydrocracking catalysts. The physicochemical and structural characterization of the solid catalysts were investigated and reported through N2 physisorption, XRD, TGA-DSC, FT-IR and TEM techniques. Solid catalysts surface acidities were investigated through FT-IR spectroscopy aided by pyridine adsorption. The solid catalytic activities were evaluated through hydroconversion of n-hexane and n-heptane employing micro-catalytic pulse technique directly connected to a gas chromatograph analyzer. The thermal stability of the solids was also investigated up to 800 °C. Crystallinity studies using the XRD technique of all modified samples proved analogous to the parent Y-zeolite, exhibiting nearly an amorphous and microcrystalline character of the second metal oxides. Disclosure of bimetallic catalysts crystalline characterization, through XRD, was not viable. The nitrogen adsorption–desorption isotherms for all samples concluded type I adsorption isotherms, without any hysteresis loop, indicating that the entire pore system is composed of micropores. TEM micrographs of the solid catalysts demonstrate well-dispersed Pt, Ni and Cr nanoparticles having sizes of 2–4 nm and 7–8 nm, respectively. The catalytic activity results indicate that the bimetallic (0.5Pt–0.3Cr)/D18H–Y catalyst is the most active towards n-hexane and n-heptane isomerization while (0.5Pt–0.6Ni)/D18H–Y catalyst can be designed as most suitable as a cracking catalyst.
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spelling doaj-art-cb6a7791a7dc4efabacb3e76cb9346ad2025-08-20T03:04:43ZengEgyptian Petroleum Research InstituteEgyptian Journal of Petroleum1110-06212014-03-0123111913310.1016/j.ejpe.2014.02.015CatalyticS.A. Hanafi0H.M. Gobara1M.S. Elmelawy2S.A. Abo-El-Enein3A.A. Alkahlawy4Catalysis Department, Refining Division, Egyptian Petroleum Research Institute, Nasr City 11727, Cairo, EgyptCatalysis Department, Refining Division, Egyptian Petroleum Research Institute, Nasr City 11727, Cairo, EgyptPhysical Refining Department, Refining Division, Egyptian Petroleum Research Institute, Nasr City 11727, Cairo, EgyptDepartment of Chemistry, Faculty of Science, Ain – Shams University, Cairo, EgyptCatalysis Department, Refining Division, Egyptian Petroleum Research Institute, Nasr City 11727, Cairo, EgyptA series of dealuminated Y-zeolites impregnated by 0.5 wt% Pt catalysts promoted by different amounts of Ni, Pd or Cr (0.3 and 0.6 wt%) were prepared and characterized as hydrocracking catalysts. The physicochemical and structural characterization of the solid catalysts were investigated and reported through N2 physisorption, XRD, TGA-DSC, FT-IR and TEM techniques. Solid catalysts surface acidities were investigated through FT-IR spectroscopy aided by pyridine adsorption. The solid catalytic activities were evaluated through hydroconversion of n-hexane and n-heptane employing micro-catalytic pulse technique directly connected to a gas chromatograph analyzer. The thermal stability of the solids was also investigated up to 800 °C. Crystallinity studies using the XRD technique of all modified samples proved analogous to the parent Y-zeolite, exhibiting nearly an amorphous and microcrystalline character of the second metal oxides. Disclosure of bimetallic catalysts crystalline characterization, through XRD, was not viable. The nitrogen adsorption–desorption isotherms for all samples concluded type I adsorption isotherms, without any hysteresis loop, indicating that the entire pore system is composed of micropores. TEM micrographs of the solid catalysts demonstrate well-dispersed Pt, Ni and Cr nanoparticles having sizes of 2–4 nm and 7–8 nm, respectively. The catalytic activity results indicate that the bimetallic (0.5Pt–0.3Cr)/D18H–Y catalyst is the most active towards n-hexane and n-heptane isomerization while (0.5Pt–0.6Ni)/D18H–Y catalyst can be designed as most suitable as a cracking catalyst.http://www.sciencedirect.com/science/article/pii/S1110062114000178H–Y zeoliteDealuminationBi-metallic catalystsHydroconversion
spellingShingle S.A. Hanafi
H.M. Gobara
M.S. Elmelawy
S.A. Abo-El-Enein
A.A. Alkahlawy
Catalytic
Egyptian Journal of Petroleum
H–Y zeolite
Dealumination
Bi-metallic catalysts
Hydroconversion
title Catalytic
title_full Catalytic
title_fullStr Catalytic
title_full_unstemmed Catalytic
title_short Catalytic
title_sort catalytic
topic H–Y zeolite
Dealumination
Bi-metallic catalysts
Hydroconversion
url http://www.sciencedirect.com/science/article/pii/S1110062114000178
work_keys_str_mv AT sahanafi catalytic
AT hmgobara catalytic
AT mselmelawy catalytic
AT saaboelenein catalytic
AT aaalkahlawy catalytic