Effect of functional groups (methyl, phenyl) on organic–inorganic hybrid sol–gel silica coatings on surface modified SS 316

Abstract Organic–inorganic hybrid sol–gel based silica coatings derived from hydrolysis and condensation of organically modified silane precursors like phenyltrimethoxysilane and methyltriethoxysilane along with tetraethoxysilane were deposited on different surface pre-treated (as-cleaned, plasma-treated, shot-blasted) SS 316 grade stainless steel substrate, using dip coating technique. The coatings were heat treated at 150 °C for 2 h in air. The pre-treated surfaces were characterized using X-ray Photoelectron Spectroscopy and Scanning Electron Microscopy. The water content of the sols was determined by Karl Fischer titration to evaluate the degree of completion of hydrolysis and condensation reactions. Cured coatings were characterized to evaluate thickness, water contact angle, pencil scratch hardness, gloss, and shrinkage in coating thickness. Impact test was carried out on pigmented coatings derived from sols synthesized using the two silane precursors. The corrosion resistance and water durability tests were carried out to compare the coatings derived from using different precursors and different surface pre-treatments. The corrosion tests were carried out for 1 h and 24 h exposure to a 3.5% NaCl solution by electrochemical polarization measurements. It was found that coatings from methyl substituted organically modified alkoxysilane exhibited better hydrophobicity, scratch hardness, impact resistance and barrier properties with respect to corrosion, when compared to those derived from phenyl substituted trialkoxysilane. The difference in performance of coatings was explained on the basis of difference in hydrolysis and condensation rates between the two organically modified silane precursors used for the sol synthesis.