Reactions involved in the electrodeposition of hydrotalcite-type compounds on FeCrAlloy foams and plates

水滑石 电解质 硝酸盐 电化学 化学 无机化学 阴极保护 电流密度 亚硝酸盐 氯化物 电极 化学工程 催化作用 有机化学 物理化学 工程类 物理 量子力学
作者
Phuoc Hoang Ho,Marco Monti,Erika Scavetta,Domenica Tonelli,Elena Bernardi,Lara Nobili,Giuseppe Fornasari,Angelo Vaccari,Patricia Benito
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:222: 1335-1344 被引量:15
标识
DOI:10.1016/j.electacta.2016.11.109
摘要

The cathodic electrodeposition of Mg/Al hydrotalcite-type (HT) compounds on FeCrAlloy plates and foams by the electro-base generation method, using nitrate salts as precursors, was studied. In order to characterize the main mechanisms governing the precipitation of HT compounds, potential sweeps or pulses were applied at both plates and foams dipped in nitrate and chloride baths, with and without Mg2+ and Al3+ precipitating cations. Moreover, nitrate reduction products were analyzed. The features of coatings and pH near foam supports were correlated to electrochemical results. Nitrate and oxygen reduction, as well as H2 evolution, contributed to a pH increase during the electrodeposition of HT compounds, but nitrate reduction was responsible for the highest pH increase at the electrode-electrolyte interface. FeCrAlloy showed a low activity in nitrate reduction to nitrite and ammonia. Mg2+ and Al3+ precipitating cations fostered electrochemical reduction and modified reaction products. The shape of the support, foam or plate, did not significantly alter the electrical conductivity and reduction potentials, but it did affect current density and H2 bubble formation. A higher current density was recorded at the foam, while H2 bubbles were smaller and dissipated rapidly; subsequently, a thicker coating was electrodeposited.

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