Selective oxidation of hydrogen sulfide to elemental sulfur with Fe/MgO catalysts in a slurry reactor

Authors
Lee, EKJung, KDJoo, OSShul, YG
Issue Date
2005-02-20
Publisher
WILEY-V C H VERLAG GMBH
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.26, no.2, pp.281 - 284
Abstract
The Fe/MgO catalysts with different Fe loadings (1, 4, 6, 15 and 30 wt% Fe) were prepared by a wet impregnation with iron nitrate as precursor. All of the catalysts were characterized by BET surface analyzer, X-ray diffraction (XRD), temperature-programmed reduction (TPR), and X-ray photoelectron spectroscopy (XPS). The maximum removal capacity of H2S was obtained with 15 wt% Fe/MgO catalyst which had the highest BET surface area among the measured catalysts. XRD of Fe/MgO catalysts showed that well dispersed Fe particles could be present on Fe/MgO with Fe loadings below 15 wt%. The crystallites of bulk alpha-Fe2O3 became evident on 30 wt% Fe/MgO, which were confirmed by XRD. TPR profiles showed that the reducibility of Fe/MgO was strongly related to the loaded amounts of Fe on MgO support. Therefore, the highest removal efficiency of H,S in wet oxidation could be ascribed to a good dispersion and high reducibility of Fe/MgO catalyst. XPS studies indicated that the H,S oxidation with Fe/MgO could proceed via the redox mechanism (Fe3+ <-> Fe2+).
Keywords
H2S; DEHYDROGENATION; PROPANE; XPS; H2S; DEHYDROGENATION; PROPANE; XPS; Fe/MgO catalyst; wet oxidation; H2S; redox mechanism
ISSN
0253-2964
URI
https://pubs.kist.re.kr/handle/201004/136728
Appears in Collections:
KIST Article > 2005
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