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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质量百分比Mn合金阳极在淡水中的溶解行为

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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:用电子探针显微分析仪(EPMA),带能量色散X射线能谱仪的扫描电子显微镜(SEM-EDX)和自来水研究了用于阴极保护的Mg-1质量百分比Mn合金阳极在自来水中的溶解行为。显微镜。已经发现,合金阳极的局部溶解是由于在合金内形成了局部电池,并且合金表面上的金属杂质充当了局部电池的阴极位置。在0.1mA / cm〜2以下的电流密度下使用以0.5μm的粒径的α-Al_2O_3进行了抛光的合金样品时,合金的局部溶解至少被抑制了三个月,电流效率为大约是80%,是通常值的两倍。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,未形成膜,并且电流效率降低。

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