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Dissolution Behavior of Type Mg-1 mass percent Mn Alloy Anode for Cathodic Protection in Fresh Water

机译:Mg-1质量%Mn合金阳极在淡水中的阴极保护溶液的溶出行为

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The dissolution behavior of Mg-1 mass percent Mn alloy anode for cathodic protection in tap-water was investigated with an electron probe micro analyzer (EPMA), a scanning electron microscope with energy dispersive X-ray spectrometer (SEM-EDX), and a microscope. It was found that the local dissolution of the alloy anode is due to the formation of a local cell within the alloy, and metallic impurities on the alloy surface act as cathode sites of the local cell. When the alloy specimen polished by alpha-Al_2O_3 of the particle size in 0.5 mum was used at current densities of 0.1mA/cm~2 or less, the local dissolution of the alloy was suppressed at least for three months, and the current efficiency was about 80 percent, which is the twice of the usual values. Under this condition, the alloy was dissolved almost uniformly, and amorphous film was formed on the alloy. When the polished alloy specimen was used under the condition exceeding 0.3mA/cm~2, the film was not formed, and the current efficiency was decreased.
机译:采用电子探针微分析仪(EPMA),研究了带有能量分散X射线光谱仪(SEM-EDX)的扫描电子显微镜,研究了用于TAP水中的阴极保护的Mg-1质量%Mn合金阳极的溶出行为。显微镜。结果发现,合金阳极的局部溶解是由于合金内的局部电池,合金表面上的金属杂质用作局部细胞的阴极位点。当在0.5件颗粒尺寸的α-Al_2O_3抛光的合金标本以0.1mA / cm〜2或更低的电流密度下使用时,合金的局部溶解至少为三个月,并且目前的效率是大约80%,这是通常价值的两倍。在这种条件下,合金几乎均匀地溶解,并且在合金上形成非晶膜。当在超过0.3mA / cm〜2的条件下使用抛光合金样品时,未形成薄膜,并且电流效率降低。

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