DocumentCode
1200834
Title
Magneto-chemical characteristics of copper-cobalt catalysts
Author
Murty, A.N. ; Donatto, U.A. ; Washington, J.W. ; Hoard, T.L. ; Akundi, M.A. ; Harris, C.
Author_Institution
Grambling State Univ., Grambling, LA, USA
Volume
30
Issue
6
fYear
1994
fDate
11/1/1994 12:00:00 AM
Firstpage
4722
Lastpage
4724
Abstract
Transition metals copper and cobalt play vital roles in the conversion of syngas (CO+H2) to liquid fuels. Catalytic studies reveal that product selectivity is governed by intermetallic ratios and method of preparation. Perturbations in metallic charge distribution and morphological changes in metal crystallites could influence both catalytic and magnetic behavior of the catalyst. To examine the correlations between catalytic and magnetic properties, we investigated the zero-field NMR and magnetization character of a series of supported and unsupported Cu-Co catalysts in the range 0.2<Cu/Co<8.0. Significant shifts of NMR lines of cobalt occur in samples for Cu/Co>1, indicating strong interactions between Cu and Co. Chromia serves as a neutral support inhibiting inter-metallic interactions, while titania supported catalysts exhibit strong metal-support interaction (SMSI). Cu-Co-Cr2O3 catalysts show three distinct regions of magnetization character similar to the three regions of selectivity. Magnetic moment of the composite is very low for Cu/Co<1.5 (hydrocarbons), appreciably increases for 1.5<Cu/Co<5.0 (mixed alcohols), and drops again when Cu/Co>5.0 (methanols)
Keywords
catalysts; cobalt alloys; copper alloys; crystallites; magnetic moments; magnetisation; nuclear magnetic resonance; Co-Cu; Cu-Co catalysts; NMR; charge distribution; liquid fuels; magnetic moment; magnetization; magneto-chemical characteristics; metal crystallites; morphological changes; syngas; Cobalt; Copper; Crystallization; Fuels; Hydrocarbons; Intermetallic; Magnetic moments; Magnetic properties; Magnetization; Nuclear magnetic resonance;
fLanguage
English
Journal_Title
Magnetics, IEEE Transactions on
Publisher
ieee
ISSN
0018-9464
Type
jour
DOI
10.1109/20.334201
Filename
334201
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