Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
692972 | Progress in Organic Coatings | 2011 | 8 Pages |
Epoxy-amine adduct was prepared by reaction between DGEBA and 1,1-iminodi-2-propanol. The kinetic of the reaction was investigated by differential scanning calorimetry (DSC) and a model-free approach. The epoxy-amine adducts were prepared with various molar ratios of amine functionalities. Waterborne dispersions of these resins have been prepared by neutralization of amine functionalities in the epoxy-amine adducts. Fourier Transform Infrared Spectroscopy (FTIR) and DSC were also used to characterize the prepared epoxy-amine adducts. The stability behavior of the neutralized epoxy-amine adducts has been studied at 25 °C in aqueous solution of acetic acid. In each case, the experimental stability ratios (W) versus electrolyte concentration plots were fitted using the Derjaguin–Landau–Verwey–Overbeek (DLVO) theory and modified Fuch's model. The resulted values of diffuse potentials and Hamaker constants were obtained for the aqueous dispersions of the epoxy-amine adducts. According to the resulted Hamaker values, the applicability of the DLVO theory to the colloidal particles of epoxy amine adducts was investigated. The cathodic electrodeposition behavior of the prepared dispersions were also investigated. It was found that the samples with lower degree of neutralization result in a more efficient film deposition followed by higher dry film thickness although they show lower stability in the electrodeposition bath.
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