TY - JOUR
T1 - Influence of water immersion post-treatment parameters on trivalent chromium conversion coatings formed on AA2024-T351 alloy
AU - Qi, J.
AU - Hashimoto, T.
AU - Thompson, G. E.
AU - Carr, J.
PY - 2016/1/15
Y1 - 2016/1/15
N2 - In thiswork, the influence ofwater immersion post-treatment, with consideration of temperature and pHvalues, on trivalent chromium conversion coating morphologies, compositions and corrosion protection has been investigated, using high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy and electrochemical impedance spectroscopy. Compared to the coating formed without the water immersion post-treatment, the post-treatment in the deionized water bath at 40?C evidently reduced the concentrations of fluorine-containing constituents and increased the extent of oxides/hydroxides across the coating. Consequently, the enhanced corrosion protection property was investigated in the post-treated coatings during full immersion in naturally-Aerated NaCl solution with mass fraction of 3.5%. In terms of water pH effects, the coatings displayed comparable thicknesses after post-treatment in the as-prepared deionized water bath (pH 5) and neutral water bath (pH 7); However, a considerable shrinkage was observed in the caustic water bath (pH 9). It was found that the resultant corrosion resistance of the coatings was greatest after post-coating treatment in the water bath of pH 5 and the least for pH 9. Inductively coupled plasma-Atomic emission spectroscopy was used to trace small amounts of Zr and Cr elements in the used water baths. A robust chemical titration, adding 1, 5-diaminonaphthalene into the used water baths, revealed that Cr species were only in trivalent form.
AB - In thiswork, the influence ofwater immersion post-treatment, with consideration of temperature and pHvalues, on trivalent chromium conversion coating morphologies, compositions and corrosion protection has been investigated, using high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy and electrochemical impedance spectroscopy. Compared to the coating formed without the water immersion post-treatment, the post-treatment in the deionized water bath at 40?C evidently reduced the concentrations of fluorine-containing constituents and increased the extent of oxides/hydroxides across the coating. Consequently, the enhanced corrosion protection property was investigated in the post-treated coatings during full immersion in naturally-Aerated NaCl solution with mass fraction of 3.5%. In terms of water pH effects, the coatings displayed comparable thicknesses after post-treatment in the as-prepared deionized water bath (pH 5) and neutral water bath (pH 7); However, a considerable shrinkage was observed in the caustic water bath (pH 9). It was found that the resultant corrosion resistance of the coatings was greatest after post-coating treatment in the water bath of pH 5 and the least for pH 9. Inductively coupled plasma-Atomic emission spectroscopy was used to trace small amounts of Zr and Cr elements in the used water baths. A robust chemical titration, adding 1, 5-diaminonaphthalene into the used water baths, revealed that Cr species were only in trivalent form.
UR - http://www.scopus.com/inward/record.url?scp=84955462889&partnerID=8YFLogxK
U2 - 10.1149/2.0221605jes
DO - 10.1149/2.0221605jes
M3 - Article
AN - SCOPUS:84955462889
SN - 0013-4651
VL - 163
SP - C131-C138
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 5
ER -