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Corrosion Behavior of Alloy 625 in Subcritical- and Supercritical Water Containing 0.1 M HCl

机译:625合金在0.1 M HCl的亚临界和超临界水中的腐蚀行为

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摘要

Corrosion tests of alloy 625 in subcritical- and supercritical water containing 0.1 M HCl were performed in the range of temperature of 350 deg C - 450 deg C at 25 MPa. The corrosion rate of alloy 625 was faster in subcritical water than in supercritical water. 0.1 M of hydrogen peroxide seemed critical concentration of oxidizer that accelerated the corrosion rate of alloy 625. Below 0.1 M of hydrogen peroxide, corrosion rate was not influenced, however, over 0.1 M, corrosion rate was increased rapidly with increasing the hydrogen peroxide. Alloy 625 had two corroded layers. Intermediate layer was the porous structure layer in which Ni and/or Fe were dissolved out selectively. The outer layer was a powder-like porous oxide layer mainly composed with chromium oxide. It was found that the main corrosion mechanisms of alloy 625 were selective dissolution of nickel and iron under the subcritical water and selective dissolution of nickel under the highly oxidized supercritical water condition.
机译:在温度为350℃-450℃,压力为25 MPa的条件下,对625合金在亚临界和超临界水中进行了腐蚀试验,该水中含有0.1 M HCl。在亚临界水中,合金625的腐蚀速率比在超临界水中要快。 0.1 M的过氧化氢似乎是氧化剂的临界浓度,可加速合金625的腐蚀速率。低于0.1 M的过氧化氢对腐蚀速率没有影响,但是,超过0.1 M时,腐蚀速率随过氧化氢的增加而迅速增加。合金625具有两个腐蚀层。中间层是其中Ni和/或Fe被选择性地溶解出的多孔结构层。外层是主要由氧化铬组成的粉末状多孔氧化物层。发现625合金的主要腐蚀机理是在亚临界水中选择性溶解镍和铁,以及在高氧化超临界条件下选择性溶解镍。

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