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Selective Dissolution and Stress Corrosion Cracking Susceptibility of Austenitic and Duplex Stainless Steels in Sodium Sulfide Containing Alkaline Solutions

机译:奥氏体和双相不锈钢在含碱性硫化钠中的选择性溶解和应力腐蚀开裂敏感性

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The role of de-alloying in stress corrosion cracking (SCC) of the austenitic EN1.4301 (UNS S30400) and duplex stainless steels EN 1.4362 (UNS S32304) and EN 1.4462 (UNS S32205) was evaluated in simulated hot liquor environments. The samples were tested at 190°C using U-bend specimens in 100 g NaOH + 55 g Na_2S and 15 g NaOH + 150 g Na_2S caustic environments simulating hot white (HWL) and hot black (HBL) liquors, respectively. SCC and general corrosion was detected in the steel surface layers. In austenitic stainless steels, severe cracking was observed throughout the samples in both solutions. In duplex stainless steels, cracking was observed only in the affected surface layer in both solutions. In EN 1.4301 steel, selective dissolution of Fe and Cr and enrichment of Cr, Ni, S, O and Na was observed in the affected surface layer and on the wakes of the large SCC cracks depending on the solution. In HWL, Na was clearly enriched and Cr was both selectively dissolved and enriched at different parts of the affected surface layers. In HBL, Na enrichment was lower and Cr was selectively dissolved in the affected surface layers. In the duplex stainless steels EN 1.4362 and EN 1.4462, dissolution of Fe, Cr and Mo and/or enrichment of Ni, Cr, Mo, Na, S and 0 took place depending on the steel and test solution. Cr content of both steels remained unaffected in HBL. In HWL, Cr was enriched in the surface layer in the Mo-alloyed steel (EN1.4462) and remained unaffected in the non-Mo-alloyed steel (EN 1.4362). In HWL, Mo dissolved selectively from the affected surface layer, whereas in HBL Mo enriched in the surface layer in the Mo-alloyed steel. Na was enriched in the affected surface layer of both duplex stainless steels immersed in HWL. Immersion in HBL resulted in a lower Na enrichment in the affected surface layer in the Mo-alloyed steel as compared with that in the non-Mo-alloyed steel. The results suggest that selective dissolution plays an important role in SCC of stainless steels in alkaline environments.
机译:在模拟的热液环境中评估了在模拟的热液环境中评估了奥氏体EN1.4301(UNS S30400)和双相不锈钢EN 1.4362(UNS S32304)和EN 1.4462(UNS S32205)的应力腐蚀裂解(SCC)的作用。在100g NaOH + 55g Na_2s和15g NaOH + 150g Na_2s的U形弯曲标本中使用U形弯曲标本和20g NaOH + 150g Na_2S钝化白色(HWL)和热黑色(HBL)液体,在190℃下测试样品。在钢表面层中检测到SCC和一般腐蚀。在奥氏体不锈钢中,在两种溶液中的整个样品中观察到严重的裂缝。在双相不锈钢中,仅在两种溶液中的受影响的表面层中观察到破裂。在EN 1.4301中,在受影响的表面层中观察到Fe和Cr的选择性溶解和Cr,Ni,S,O和Na的富集,并根据溶液唤醒大的SCC裂缝的唤醒。在HWL中,清楚地富集,Cr均选择性地溶解并富含受影响的表面层的不同部位。在HBL中,Na富集较低,Cr选择性地溶解在受影响的表面层中。在双相不锈钢EN 1.4362和EN 1.4462中,取决于钢和试验溶液,Fe,Cr和Mo的溶解和/或富集Ni,Cr,Mo,Na,S和0。两个钢的Cr含量仍未在HBL中不受影响。在HWL中,CR富集在MO-合金钢(EN1.4462)中的表面层中,并在非MO-合金钢(EN 1.4362)中保持不受影响。在HWL中,Mo从受影响的表面层选择性地溶解,而在富含在Mo合金钢的表面层中的HBLE MO中。 Na富含双链不锈钢的受影响的表面层,浸入HWL中。浸入HBL中,与非Mo合金钢中的浓度在Mo合金钢中的受影响的表面层中导致较低的Na富集。结果表明,选择性溶解在碱环境中不锈钢SCC中发挥着重要作用。

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