Abstract
A moderate rate of oxidation of the sulphide groups in polyphenylenesulphide (PPS) played a key role in ensuring that PPS coatings adequately protect aluminium (Al) alloys from corrosion in wet, harsh environments. There are three major reasons for a good protective performance: 1) the superior hydrothermal stability of PPS itself, 2) the limited amount of sulphonic acid formed by the oxidation of sulphide, and 3) the formation of a discontinuous, intermediate layer of Al2(SO4)3 as the interfacial reaction product between A12O3 at the top surface of Al, and oxidized PPS. Widespread oxidation of PPS led to an increase in the rate of the interfacial interaction, forming sulphonic acid-enriched A12(SO4)3 intermediate layers, thereby improving the bond strength at Al-to-PPS adhesive joints. However, an overabundance of these reaction products resulted in an inadequate coating that failed to protect the Al during a long-term exposure in a harsh, corrosive environment because of the susceptibility of these salt products to dissolution in water.
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