Polyphenylenesulphide (PPS) polymer was applied as a sealing material to flame-sprayed nickel–aluminium (Ni–Al) coatings to protect the interior surfaces at the ends where the mild carbon steel (MCS) heat-exchanger tubes are jointed to the tubesheet. The aim of applying PPS is to prevent their corrosion, oxidation and abrasive wear, in a low pH, hypersaline brine geothermal environment at 200°C under a hydrothermal pressure of 1.6 MPa. Although the Ni–Al coatings had an excellent thermal conductivity and a good wear-resistance, the inherent open structure of these coatings allowed the hot brine to permeate them easily under such pressure, causing the development of corrosion-induced stress cracks in the MCS. Furthermore, under these conditions, the coatings underwent oxidation with the formulation of Al2O3 as the major scale compound and NiO as the minor one. PPS sealant was used to solve these problems. However, one major drawback of PPS was its susceptibility to oxidation reaction with hot brine. This reaction not only incorporated more oxygen into the PPS, generating a sulphide → sulphone transformation within PPS, but also it caused the decomposition of PPS, yielding polychloroaryl compound, and sodium sulphate, and also evolving SO2 gases. The SO2 gases had a chemical affinity for oxide scales in Ni–Al, forming water-soluble Al2(SO4)3 and NiSO4 salt reaction products at the PPS/Ni–Al interfaces. Despite the occurrence of such oxidation damage in PPS, an exposure for 14 days showed that there was no development of corrosion-caused cracks at the interfaces between the underlying steel and Ni–Al, nor was a striking oxidation of the sealed coating panels.
