Synthesis and characterization of new hydrodesulphurization Co-Mo catalysts supported on calcined and pyrolyzed bone

A series of cobalt-molybdenum catalysts supported on calcined bone (hydroxyapatite, HAP) and pyrolyzed bone (hydroxyapatite-carbon, HAP-C) have been prepared by an impregnation method. The catalysts were characterized by XRD, FT-IR spectroscopy, UV-Vis spectroscopy, TPR, TPD of CO 2 , BET, FE-SEM, E...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:RSC advances 2015-01, Vol.5 (51), p.4647-4656
Hauptverfasser: Yazdani, M. Emami, Monjezi, B. H, Mokfi, M, Bozorgzadeh, H, Gil, A, Ghiaci, M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:A series of cobalt-molybdenum catalysts supported on calcined bone (hydroxyapatite, HAP) and pyrolyzed bone (hydroxyapatite-carbon, HAP-C) have been prepared by an impregnation method. The catalysts were characterized by XRD, FT-IR spectroscopy, UV-Vis spectroscopy, TPR, TPD of CO 2 , BET, FE-SEM, EDX and TEM techniques. Hydrodesulphurization (HDS) experiments were carried out in a fixed-bed reactor at 15 bar hydrogen pressure, liquid hourly space velocity (LHSV) of 4.5 h −1 , a volumetric hydrogen/feed ratio of 175 NL L −1 and 310 °C. HDS reactions of dibenzothiophene (DBT), dimethyl disulfide (DMDS) and industrial naphtha over the synthesized catalysts were investigated. The Co-Mo/HAP-C and Co-Mo/HAP catalysts displayed a satisfactory performance comparable with the commercial catalyst. Co-Mo/Al 2 O 3 and Co-Mo/HAP catalysts were tested for hydrodesulphurization of DMDS, and Co-Mo/HAP showed a higher activity than the commercial catalyst (Co-Mo/Al 2 O 3 ) and lowered the sulfur content of the feedstock from 2500 ppm to 9 ppm. A series of cobalt-molybdenum catalysts supported on calcined bone (hydroxyapatite, HAP) and pyrolyzed bone (hydroxyapatite-carbon, HAP-C) have been prepared by an impregnation method.
ISSN:2046-2069
2046-2069
DOI:10.1039/c5ra00828j