Deactivation of MoS2/Al2O3 in thiophene hydrodesulfurization: An infrared spectroscopic analysis by adsorbed CO

Citation
Lpaf. Elst et al., Deactivation of MoS2/Al2O3 in thiophene hydrodesulfurization: An infrared spectroscopic analysis by adsorbed CO, J CATALYSIS, 196(1), 2000, pp. 95-103
Citations number
35
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
JOURNAL OF CATALYSIS
ISSN journal
00219517 → ACNP
Volume
196
Issue
1
Year of publication
2000
Pages
95 - 103
Database
ISI
SICI code
0021-9517(20001115)196:1<95:DOMITH>2.0.ZU;2-J
Abstract
Fourier transform infrared spectroscopy on adsorbed carbon monoxide was use d to study the deactivation and rejuvenation of a MoS2/gamma -Al2O3 catalys t during hydrodesulfurization (HDS) of thiophene. The study covered several sample pretreatment steps, each resembling a stage in the catalyst life. T he number of active sites on the sulfided sample was correlated to the inte nsity of CO-stretch absorption bands in the infrared spectrum. It was concl uded that with increasing HDS time on stream the intensity of bands correla ted to CO adsorbed on edge and corner sites decreases, while simultaneously those in the carbon-carbon stretch region (1800-1200 cm(-1)) increase in i ntensity. Rejuvenation of a spent catalyst under H2S/H-2 at 673 K revealed an increase in the number of gas-phase exposed edge and corner sites of the MoS2 slabs, while concurrently the intensities of bands correlated to carb on-carbon stretch vibrations decreased. Thus, it was concluded that catalys t deactivation was caused by preferential coke deposition on the active sit es, which can be removed under H2S/H-2. No differences were found in the co king behavior of edge and corner sites. (C) 2000 Academic Press.