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Surface structure and mechanisms of gasification catalyst deactivation. Quarterly report, May--July 1977

Technical Report ·
DOI:https://doi.org/10.2172/5232509· OSTI ID:5232509
The ESCA instrument was moved into a new facility and extensive modifications for safety purposes were made. The electron flood gun was tested with mixed results. NiSO/sub 4/ was observed to have a significantly different ESCA spectrum from NiS. It was observed that silica supported NiO was easily reduced by the standard Argon ion etching procedure while alumina supported NiO was much more resistant to reduction. It is suggested that the Argon etching may allow the production of reduced catalysts in situ. Infrared spectra of NiO/MgSiO/sub 3/ catalysts show that CO/sub 3//sup equals/ is adsorbed as was observed for alumina-and-silica-support catalysts. The MgSiO/sub 3/ support produces infrared absorption which is almost identical to NiSiO/sub 3/ except for some doublet structure which can be associated with Ni 3d, 4s electronic levels. Adsorption studies of C/sub 2/H/sub 2/ over NiO/Al/sub 2/O/sub 3/ indicate that CH/sub 2/ and CH/sub 3/ species are formed in the 300/sup 0/C temperature region. Suitable procedures have been developed to stabilize the reduced nickel catalysts and prevent the spontaneous re-oxidation by passivation during examination by x-ray diffraction. X-ray diffraction studies to determine the particle size distribution in reduced and passivated catalysts have been initiated. Several installations for single crystal ribbon preparation and a crystal holder have been made. The chemisorption of air and CO on a sulfided catalyst surface (OCR Test 3) was investigated at room temperature.
Research Organization:
Kentucky Univ., Lexington (USA)
OSTI ID:
5232509
Report Number(s):
FE-2229-6
Country of Publication:
United States
Language:
English

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