The influence of metalloids on the dissolution of rapidly solidified iron‐metalloid materials has been examined. This paper presents results of a comparative study of the electrochemical behavior of pure polycrystalline iron and of rapidly quenched amorphous in both sulfate and chloride media. In acid sulfate solution, the single phase iron‐boron alloy behaved essentially as an iron electrode. The amorphous state per se was seen to exert little if any influence on the active dissolution kinetics. However, in chloride solutions the boron alloy exhibited characteristics differing from those of crystalline iron. Rapidly quenched and were also examined in sulfate media. These materials containing phosphorus display characteristics differing from iron and . and exhibited faster kinetics for the hydrogen reaction, and the anodic reaction was inhibited.