1986
DOI: 10.1016/s0009-2614(86)80177-4
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EPR evidence for ruthenium variable valence states in active oxidative catalysts

Abstract: Experimental proof is provided by EPR for the presence of Ru 3+ ions in a RuOJTiO, highly dispersed catalyst. A model is proposed for the mode of intervention of Ru3+/Ru4+ states in oxidative processes.

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Cited by 7 publications
(2 citation statements)
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“…However, in the Ru(OH) x /TiO 2 material with 40 wt% Ru, ruthenium(III) was also identified, thus suggesting that both oxidation states were present in the ruthenium oxide, i.e. RuO 2 ÁRu 2 O 3 , with RuO 2 as the major component and Ru(III) oxide in trace amount [24].…”
Section: Resultsmentioning
confidence: 99%
“…However, in the Ru(OH) x /TiO 2 material with 40 wt% Ru, ruthenium(III) was also identified, thus suggesting that both oxidation states were present in the ruthenium oxide, i.e. RuO 2 ÁRu 2 O 3 , with RuO 2 as the major component and Ru(III) oxide in trace amount [24].…”
Section: Resultsmentioning
confidence: 99%
“…The reasons why no ESR signals of Ru 4+ are observed are explained in terms of a strong zero-field splitting and/or a strong relaxation because of the strong coupling between spin and orbital momentum [19]. The ESR-signals in Fig.…”
Section: Esr Spectra Of Supported Ruo 2 Catalystsmentioning
confidence: 93%