• Title of article

    Adsorption behavior of caffeine as a green corrosion inhibitor for copper

  • Author/Authors

    de Souza، نويسنده , , Fernando Sيlvio and Giacomelli، نويسنده , , Cristiano Nunes Gonçalves، نويسنده , , Reinaldo Simُes and Spinelli، نويسنده , , Almir، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2012
  • Pages
    9
  • From page
    2436
  • To page
    2444
  • Abstract
    Electrochemical and impedance experiments were carried out to evaluate the corrosion behavior of copper in aerated 0.1 mol L− 1 H2SO4 solutions in the presence of three xanthine derivatives with similar chemical structures. The corrosion rate of copper was found to increase in the presence of theophylline and theobromine and decrease in the presence of caffeine. The adsorption and inhibitory effect of caffeine on copper surfaces in aerated 0.1 mol L− 1 H2SO4 solutions were then investigated in detail by potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), contact angle measurements, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and fluorescence experiments. The data obtained indicate that caffeine behaves as a cathodic-type inhibitor adsorbing onto the copper surface according to the Temkin isotherm, with the negative ∆G°ads value of − 31.1 kJ mol− 1 signifying a spontaneous adsorption process. The corrosion inhibition efficiency increased with caffeine concentration in the range of 1.0–10.0 mmol L− 1. Furthermore, the EIS results obtained at the open-circuit potential and surface analysis (SEM, EDS and fluorescence) clearly demonstrated the adsorption of the organic compound onto the copper electrode. The contact angle measurements revealed the formation of a hydrophobic protective film. This film covers up to 72% of the total active surface, acts as a protective barrier and prevents interaction between the metal, water and oxygen molecules.
  • Keywords
    caffeine , Adsorption , Surface Analysis , electrochemical techniques , Copper
  • Journal title
    Materials Science and Engineering C
  • Serial Year
    2012
  • Journal title
    Materials Science and Engineering C
  • Record number

    2102305