Studies of Ni/Kaolinite Catalysts for the Hydrogenation of Toluene

No mention appears to have been made in the literature to the use of kaolinite as a support for nickel catalysts in the hydrogenation of toluene. In this study, kaolinite-supported Ni catalysts (1–7 wt%) were prepared and characterized, and their activity in the catalytic hydrogenation of toluene at...

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Main Authors: G.M.S. ElShafei, T. Zaki, Gh. Eshaq, M. Riad
Format: Article
Language:English
Published: SAGE Publishing 2006-12-01
Series:Adsorption Science & Technology
Online Access:https://doi.org/10.1260/026361707781422031
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author G.M.S. ElShafei
T. Zaki
Gh. Eshaq
M. Riad
author_facet G.M.S. ElShafei
T. Zaki
Gh. Eshaq
M. Riad
author_sort G.M.S. ElShafei
collection DOAJ
description No mention appears to have been made in the literature to the use of kaolinite as a support for nickel catalysts in the hydrogenation of toluene. In this study, kaolinite-supported Ni catalysts (1–7 wt%) were prepared and characterized, and their activity in the catalytic hydrogenation of toluene at atmospheric pressure established. XRD, DSC, N 2 adsorption and TPR methods were used as characterization techniques. XRD revealed that interaction occurs between the Ni species and the support at low Ni content (up to 3 wt%) but decreases as the Ni loading increases. This results in an increase in the number of Ni active sites with increased Ni loading and is reflected in the catalytic activity towards toluene conversion into methylcyclohexane, which increased as the Ni content of the catalyst increased. Modification by post-impregnation with KNO 3 or Zn(NO 3 ) 2 (2–6 wt% K or Zn) affected the extent of interaction between the Ni species and the support. Thus, the catalytic activity increased in the presence of 2 wt% modifier (K or Zn). However, at higher levels of modification (4 and 6 wt%), the catalytic activity decreased relative to that for the unmodified sample containing the same Ni loading. This loss in catalytic activity increased as the modifier content increased. Furthermore, in the presence of K as a modifier, the decrease in toluene conversion was accompanied by a shift in the temperature of maximum conversion from 200°C for the unmodified sample to a value of 250°C. This was attributed to the covering of the Ni active sites by some incompletely decomposed KNO 3 .
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spelling doaj-art-3c78bbed716d4d4cab8b9727a5fef19d2025-01-02T22:37:59ZengSAGE PublishingAdsorption Science & Technology0263-61742048-40382006-12-012410.1260/026361707781422031Studies of Ni/Kaolinite Catalysts for the Hydrogenation of TolueneG.M.S. ElShafei0T. Zaki1Gh. Eshaq2M. Riad3 Chemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, Egypt Egyptian Petroleum Research Institute, Nasr City, P.O. 11727, Cairo, Egypt Egyptian Petroleum Research Institute, Nasr City, P.O. 11727, Cairo, Egypt Egyptian Petroleum Research Institute, Nasr City, P.O. 11727, Cairo, EgyptNo mention appears to have been made in the literature to the use of kaolinite as a support for nickel catalysts in the hydrogenation of toluene. In this study, kaolinite-supported Ni catalysts (1–7 wt%) were prepared and characterized, and their activity in the catalytic hydrogenation of toluene at atmospheric pressure established. XRD, DSC, N 2 adsorption and TPR methods were used as characterization techniques. XRD revealed that interaction occurs between the Ni species and the support at low Ni content (up to 3 wt%) but decreases as the Ni loading increases. This results in an increase in the number of Ni active sites with increased Ni loading and is reflected in the catalytic activity towards toluene conversion into methylcyclohexane, which increased as the Ni content of the catalyst increased. Modification by post-impregnation with KNO 3 or Zn(NO 3 ) 2 (2–6 wt% K or Zn) affected the extent of interaction between the Ni species and the support. Thus, the catalytic activity increased in the presence of 2 wt% modifier (K or Zn). However, at higher levels of modification (4 and 6 wt%), the catalytic activity decreased relative to that for the unmodified sample containing the same Ni loading. This loss in catalytic activity increased as the modifier content increased. Furthermore, in the presence of K as a modifier, the decrease in toluene conversion was accompanied by a shift in the temperature of maximum conversion from 200°C for the unmodified sample to a value of 250°C. This was attributed to the covering of the Ni active sites by some incompletely decomposed KNO 3 .https://doi.org/10.1260/026361707781422031
spellingShingle G.M.S. ElShafei
T. Zaki
Gh. Eshaq
M. Riad
Studies of Ni/Kaolinite Catalysts for the Hydrogenation of Toluene
Adsorption Science & Technology
title Studies of Ni/Kaolinite Catalysts for the Hydrogenation of Toluene
title_full Studies of Ni/Kaolinite Catalysts for the Hydrogenation of Toluene
title_fullStr Studies of Ni/Kaolinite Catalysts for the Hydrogenation of Toluene
title_full_unstemmed Studies of Ni/Kaolinite Catalysts for the Hydrogenation of Toluene
title_short Studies of Ni/Kaolinite Catalysts for the Hydrogenation of Toluene
title_sort studies of ni kaolinite catalysts for the hydrogenation of toluene
url https://doi.org/10.1260/026361707781422031
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