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1.
Langmuir ; 28(5): 2971-8, 2012 Feb 07.
Artigo em Inglês | MEDLINE | ID: mdl-22200075

RESUMO

A facile and green approach is developed to impart remarkable protection against corrosion to galvanized steel. A protecting multilayer film is formed by alternating the deposition of a polycation bearing catechol groups, used as corrosion inhibitors, with clay that induces barrier properties. This coating does not affect the esthetical aspect of the surface and does not release any toxic molecules in the environment.


Assuntos
Silicatos de Alumínio/química , Di-Hidroxifenilalanina/química , Membranas Artificiais , Polímeros/química , Aço/química , Argila , Corrosão , Técnicas Eletroquímicas , Eletrólitos/química , Estrutura Molecular , Tamanho da Partícula , Propriedades de Superfície
2.
Nitric Oxide ; 12(4): 252-60, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15917218

RESUMO

We report here on the role of copper (II) salts on the acceleration of peroxynitrite (ONOO-) decomposition and ONOO- reaction with the anaesthetic agent propofol (2,6-diisopropylphenol) in alkaline medium. We observed a strong acceleration of the ONOO- decomposition in alkaline medium in the presence of copper (I and II) salts. After 18 h of ONOO- reaction with propofol, we observed nitrosated, nitrated, and oxidized (quinone and diphenylquinone) derivatives of propofol, but in the presence of Cu(II) (20% molar vs ONOO-), the yields of quinone and nitrosopropofol strongly increased. We also observed that the temperature and the atmosphere influenced the effects of Cu(II) on ONOO- reactions with propofol: low temperatures promoted nitrosation and high temperatures promoted oxidation; O2 atmosphere increased the general reactivity and the yield of nitrated and oxidized products. We highlighted the influence of Cu(II) salts on the radical character of the reaction by direct EPR technique. The exact mechanism of the Cu(II) catalysis remains unexplained, but we suggest the formation of a copper complex with propofol or, more probably, the oxidation of ONOO- into ONOO. by copper ions promoting the formation of quinone and nitrosopropofol according to a previously reported mechanism [M. Cudic, C. Ducrocq, Transformations of 2,6-diisopropylphenol by NO-derived nitrogen oxides, particularly peroxynitrite, Nitric Oxide 4 (2000) 147-156].


Assuntos
Álcalis/química , Cobre/química , Ácido Peroxinitroso/química , Propofol/química , Sais/química , Bicarbonatos/química , Dióxido de Carbono/química , Catálise , Espectroscopia de Ressonância de Spin Eletrônica , Concentração de Íons de Hidrogênio , Estrutura Molecular , Nitrogênio/química , Dióxido de Nitrogênio/química , Oxigênio/química , Soluções , Temperatura
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