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Formation and Structure of Alkyl-Phosphonic Acid Layers on Passive Iron

机译:无源铁上烷基 - 膦酸层的形成与结构

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Phosphonate layer formation on passive iron surface has been investigated by electrochemical and atomic force microscopy techniques. It was found that phosphonate groups bond more strongly to oxide surface, while metallic iron surface is disadvantageous for phosphonate layer formation in aqueous solutions. The rate of anodic dissolution is continually decreasing due to the time-dependent formation of protective phosphonate layer. The kinetics of phosphonate layer formation on passive iron is determined by the potential applied for preceding passive film formation. The size and shape of iron oxide grains depends slightly on the potential of passivation. Changes in morphology due to the phosphonate layer formation have been recorded by AFM.
机译:通过电化学和原子力显微镜技术研究了无源铁表面上的膦酸盐层形成。发现膦酸酯基团对氧化物表面更强烈键,而金属铁表面对水溶液中的膦酸盐层形成不利。由于保护膦酸盐层的时间依赖性形成,阳极溶解速率连续降低。通过施加在前面的被动膜形成的可能性来确定无源铁上膦酸盐层形成的动力学。氧化铁晶粒的尺寸和形状略微呈钝化的潜力。由于AFM记录了由于膦酸盐层形成引起的形态的变化。

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