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Microscopic study of the corrosion behaviour of mild steel in ionic liquids for CO2 capture applications

机译:碳钢捕获离子液体中低碳钢腐蚀行为的微观研究

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Three 1-alkyl-3-methylimidazolium tricyanomethanide (TCM) ionic liquids (ILs) (alkyl = ethyl, butyl and hexyl) and one butyrolactam cation-based IL with a fluorinated anion were synthesised and tested in contact with mild steel (MS) at temperatures up to 80 degrees C. The corrosion behaviour was evaluated by monitoring the morphological changes on the steel surface after testing. Exposure of MS to the IL results in two main types of degradation that depend on the IL type. General etching over the macroscopic surface of the alloy was revealed for the IL with the fluorinated anion. The 1-alkyl-3-methylimidazolium TCM ILs promoted dissolution of MnS inclusions present in the steel. In the ILs with a shorter alkyl chain in the cation (alkyl = ethyl, butyl), the dissolution of MnS was accompanied by generation of corrosion products around the inclusion sites, which are mainly identified as magnetite and maghemite ferrites by micro-Raman spectroscopy. The rest of the macroscopic steel surface remains unaffected. Etching resulted in significant weight loss due to removal of material, whereas no significant weight loss was revealed following MnS dissolution. Butyrolactam cation-based IL severely attacks MS with the formation of a plethora of corrosion products including ferrites (mainly hematite), zinc oxide, sulphates and carbonates. Addition of 500 ppm sodium molybdate to the butyrolactam cation-based IL resulted in efficient inhibition of etching at both room temperature and 60 degrees C due to adsorption of molybdate on the alloy surface. A side effect of MS degradation is that the CO2 absorption capacity of the ILs can be severely reduced through the transfer of metal ions and corrosion products from the metallic surface to the liquid phase. Therefore, gravimetric CO2 absorption capacity and kinetic measurements on the selected 1-alkyl-3-methylimidazolium tricyanomethanide ILs before and after their contact with MS were also conducted with the purpose to unveil and study these side effects. Moreover, CO2 absorption experiments of the butyrolactam cation-based IL before and after contact with MS, as well as in the presence of a sodium molybdate inhibitor, showed that sodium molybdate has the capacity to limit significantly the etching rate without affecting the CO2 capture performance of the IL.
机译:合成了3种1-烷基-3-甲基咪唑三氰基甲磺酸盐(TCM)离子液体(烷基=乙基,丁基和己基)和一种含氟阴离子的丁内酰胺阳离子基IL,并与低碳钢(MS)接触温度高达80摄氏度。通过监测测试后钢表面的形态变化来评估腐蚀行为。 MS暴露于IL会导致两种主要的降解类型,具体取决于IL类型。对于含氟阴离子的离子液体,在合金的宏观表面上进行了一般蚀刻。 1-烷基-3-甲基咪唑鎓TCM ILs促进了钢中存在的MnS夹杂物的溶解。在阳离子中具有较短烷基链的ILs(烷基=乙基,丁基)中,MnS的溶解伴随着包裹体周围腐蚀产物的产生,通过显微拉曼光谱主要鉴定为磁铁矿和磁铁矿铁氧体。其余的宏观钢表面保持不受影响。由于去除了材料,蚀刻导致明显的重量损失,而MnS溶解后未发现明显的重量损失。丁内酰胺阳离子基IL严重腐蚀MS,形成大量腐蚀产物,包括铁素体(主要是赤铁矿),氧化锌,硫酸盐和碳酸盐。在丁内酰胺阳离子基离子液体中加入500 ppm钼酸钠可有效抑制室温和60摄氏度的腐蚀,这是由于钼酸盐在合金表面上的吸附。 MS降解的副作用是,通过金属离子和腐蚀产物从金属表面到液相的转移,IL的CO2吸收能力会大大降低。因此,还进行了与MS接触之前和之后对所选的1-烷基-3-甲基咪唑鎓三氰胺ILs的重量吸收CO2和动力学测量,目的是揭示和研究这些副作用。此外,在与MS接触之前和之后以及存在钼酸钠抑制剂的情况下,丁内酰胺阳离子基IL的CO2吸收实验表明,钼酸钠具有显着限制蚀刻速率的能力,而不会影响CO2捕获性能IL。

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