Carboxylic acids are surface active agents which adsorb at the water/air interface via their functional groups with hydrocarbon tails extended outward to form a hydrophobic monolayer. When used as corrosion inhibitors, adsorption at the metal/solution interface is by donation of electrons from the oxygen-containing -COOH group to the metal surface. Zisman and coworkers(1-4) have shown that surfaces terminating in fluorocarbon groups are less energetic and are less wettable than are surfaces terminating in hydrocarbon groups. Thus, the idea of using fluorinated molecules as corrosion inhibitors is intriguing because of the possibility of in-situ formation of a low-energy "Teflon-like" surface. Such compounds should be effective corrosion inhibitors if a complete chemisorbed hydrophobic monolayer can be formed by adsorption from the corrosive medium.

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