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Selective Dissolution Characteristics of 26Cr-7Ni-2.5Mo-3W Duplex Stainless Steel in H_2SO_4/HCl Mixed Solution

机译:26Cr-7Ni-2.5Mo-3W双相不锈钢在H_2SO_4 / HCl混合溶液中的选择性溶解特性

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摘要

Selective dissolution of hyper duplex stainless steel was studied by potentiodynamic and potentiostatic test in various concentrations of H2SO_4/HCI solutions at various temperatures. There were two peaks in the active-to-passive transition region in potentiodynamic test in 2M H2SO_4 + 0.5 M HC1 solution at 60 deg C. In potentiostatic tests, the curve at -340mV showed stable current density. As the potential increased, the current density increased and at above -310 mV potential, there was a much longer initial period of nonsteady current value. As the potential reached at -280 mV, the current density started to be stabilized and the current density was completely stabilized at -250 mV. It was found that a preferential dissolution of ferrite phase occurred at -330 mV and with the increase of potential, austenite phase was corroded at a high rate. On the other hand, both two phases were passivated at the potential above - 270 mV, so that selective dissolution was absent.
机译:通过在不同温度下各种浓度的H2SO_4 / HCl溶液中的电位动力学和恒电位测试研究了超双相不锈钢的选择性溶解。在2M H2SO_4 + 0.5 M HCl溶液中于60摄氏度进行的电位动力学测试中,从主动到被动的过渡区域有两个峰。在恒电位测试中,-340mV处的曲线显示出稳定的电流密度。随着电势的增加,电流密度增加,并且在-310 mV以上的电势下,不稳定电流值的初始周期要长得多。当电位达到-280 mV时,电流密度开始稳定,并且电流密度完全稳定在-250 mV。发现在-330mV时优先发生铁素体相的溶解,并且随着电位的增加,奥氏体相被高速腐蚀。另一方面,两相均在高于270 mV的电势下被钝化,因此没有选择性溶解。

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