The Adsorption of a New Derivative of Mercapthothiazole on Copper Studied by XPS and AES

XPS (X-ray photoemission spectroscopy) and AES (Auger electron spectroscopy) have been used to study the adsorption of a new synthetic flotation collector, a derivative of mercapthothiazole (C sub 6 H sub 6 NS sub 2 K), on a polycrystalline Cu surface in basic solution at various concentrations to c...

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Bibliographic Details
Published inApplications of surface science Vol. 59; no. 1; pp. 1 - 6
Main Authors Contini, G, Turchini, S, Marabini, A M, Di Castro, V, Polzonetti, G
Format Journal Article
LanguageEnglish
Published 09.09.1991
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Summary:XPS (X-ray photoemission spectroscopy) and AES (Auger electron spectroscopy) have been used to study the adsorption of a new synthetic flotation collector, a derivative of mercapthothiazole (C sub 6 H sub 6 NS sub 2 K), on a polycrystalline Cu surface in basic solution at various concentrations to characterize the nature of the surface film. The XPS Cu 2p, S 2p, N 1s edges and Cu L sub 3 M sub 4,5 M sub 4,5 Auger line were detected. On interaction with the ligands, Cu is partially oxidized to Cu(I) indicating that the MT molecules interact directly with the Cu atoms present on the surface. There is no evidence of any complex between Cu and MT formed in the solution and precipitate. The analysis of Cu L sub 3 M sub 4,5 M sub 4,5 Auger spectra suggests that a chemical bond is formed between the collector and Cu. There is a visible interaction between the ligands and the Cu substrate, the effect of which is to prevent the oxidation of the metal even at very low concentration. The 2 x 10 exp --4 M ligand concentration would appear to be the most efficient for ensuring the best corrosion inhibition under the experimental conditions adopted. From 7 x 10 exp --4 -1 x 10 exp --2 M the shape of the Auger line remains stable, showing that the Cu--MT component makes a relevant surface contribution. The chemical bond occurring between Cu and the collectors does not change when the solution concentration is varied; in fact, there is no alteration in either the shape or the binding energy of the XPS signals from the S 2p and N 1s edges.
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ISSN:0378-5963