TY - JOUR
T1 - Synthesis of Ga-and Zn-H-ZSM-5 zeolite catalysts using Ga-and Zn-impregnated γ-Al2O3 for the transformation of n-butane to aromatic hydrocarbons
AU - Kumar, N.
AU - Lindfors, L. E.
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1995/1/1
Y1 - 1995/1/1
N2 - Ga-and Zn-modified ZSM-5 zeolite catalysts were synthesized by using Ga- and Zn-impregnatedγ-Al2O3. The catalysts were characterized by X-ray powder diffractometry, scanning electron microscopy, X-ray fluorescency, nitrogen adsorption and temperature-programmed desorption of ammonia. The effect of reaction temperatures and space velocities (WHSV) on the conversion of n-butane and selectivity to aromatics were studied by varying the reaction temperatures between 713 K and 803 K and the space velocities between 1.5 h−1 and 5.5 h−1. The catalytic stability test was carried out for 4.5 hours at 803 K. The prepared Ga-H-ZSM-5 and Zn-H-ZSM-5 catalysts exhibited very high n-butane conversion and selectivity to aromatic hydrocarbons.
AB - Ga-and Zn-modified ZSM-5 zeolite catalysts were synthesized by using Ga- and Zn-impregnatedγ-Al2O3. The catalysts were characterized by X-ray powder diffractometry, scanning electron microscopy, X-ray fluorescency, nitrogen adsorption and temperature-programmed desorption of ammonia. The effect of reaction temperatures and space velocities (WHSV) on the conversion of n-butane and selectivity to aromatics were studied by varying the reaction temperatures between 713 K and 803 K and the space velocities between 1.5 h−1 and 5.5 h−1. The catalytic stability test was carried out for 4.5 hours at 803 K. The prepared Ga-H-ZSM-5 and Zn-H-ZSM-5 catalysts exhibited very high n-butane conversion and selectivity to aromatic hydrocarbons.
UR - http://www.scopus.com/inward/record.url?scp=77957297955&partnerID=8YFLogxK
U2 - 10.1016/S0167-2991(06)81239-5
DO - 10.1016/S0167-2991(06)81239-5
M3 - Article
AN - SCOPUS:77957297955
SN - 0167-2991
VL - 94
SP - 325
EP - 332
JO - Studies in Surface Science and Catalysis
JF - Studies in Surface Science and Catalysis
IS - C
ER -