Issue 66, 2017, Issue in Progress

Promotion of hydrogenation activity and sulfur resistance over Ni/ASA catalyst by support modification simultaneously with P and USY

Abstract

Individual and simultaneous P and USY promoted amorphous SiO2–Al2O3 (ASA) supported Ni catalysts were prepared using the hydrothermal synthesis method with the assistance of cis-9-octadecenylamine. The catalysts were characterized by X-ray diffraction (XRD), N2-adsorption and desorption, UV-vis diffuse reflectance spectroscopy, FTIR spectroscopy of adsorbed pyridine (Py-IR), transmission electron microscopy (TEM), temperature-programmed hydrogen reduction (H2-TPR) and X-ray photoelectron spectroscopy (XPS). The effects of P and USY loading on the activity of naphthalene hydrogenation were evaluated in a fixed bed reactor under the following reaction conditions: P = 4 MPa, GHSV = 16 h−1, H2/oil = 600 volume ratio, T = 200, 240, 280 and 320 °C. Experimental results verified that all individual P and USY modified catalysts displayed higher hydrogenation activity than the freely P and USY decorated catalyst at 200–280 °C. Furthermore, the catalyst simultaneously modified with 1.0 wt% P and 10 wt% USY had the highest hydrogenation activity and sulfur tolerance. Multiple effects, such as metal dispersion, acid amount, surface exposure of the active Ni° species and the [NiOh2+]/[NiTd2+] ratio were responsible for the high hydrogenation activity of P and USY-promoted catalysts.

Graphical abstract: Promotion of hydrogenation activity and sulfur resistance over Ni/ASA catalyst by support modification simultaneously with P and USY

Supplementary files

Article information

Article type
Paper
Submitted
13 May 2017
Accepted
27 Jul 2017
First published
25 Aug 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 41460-41470

Promotion of hydrogenation activity and sulfur resistance over Ni/ASA catalyst by support modification simultaneously with P and USY

S. Cui, J. Ge, G. Wang, Y. Yang and B. Liu, RSC Adv., 2017, 7, 41460 DOI: 10.1039/C7RA05413K

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