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Study of the influence of phosphoric acid in steel anaerobic corrosion via the hydrogen evolution reaction.

机译:通过析氢反应研究磷酸对钢厌氧腐蚀的影响。

摘要

Although it is well known that the phosphate species are quiet electrochemically inert when considering their calculated redox potential, few studies since the end of 80’s reported electrochemical phenomenon observed in the reduction domain which were linked to the presence of phosphate species. Some authors proposed that phosphate ions and weak acids in general catalysed the electrochemical reduction of water [1-3] following the kind of reactions written above:ududElectrochemical reactionsudH2PO4- + e-  Had + HPO42-(1)udHad + H2PO4- + e-  H2 + HPO42-(2)udAcido-basic equilibriumudH2PO4- + OH--  H2O + HPO42-(3)ududCombining the reactions, the reduction of water was obtainedud2 H2O + 2e-  H2 + 2OH-(4)ududMarinovic and Despic [1] assumed that the hydrogen evolution was more likely to occur from species other than water, since the bond between the hydrogen atom and the rest of the molecule is weaker in weak acid compared with the hydrogen-oxygen bond in a water molecule. This was shown on silver electrodes [2] and also on platinum ones [1]. In a previous work [3], we showed that phosphate ions exhibited the same electrochemical behaviour on stainless steel. A theoretical model was proposed according to the experimental data the model showed that a significant quantity of molecular hydrogen was produced by the mechanism presented above. udIn the present paper, the influence of phosphoric acid on hydrogen evolution reaction has been studied by voltammetry on platinum and stainless steel rotating disc electrodes. A linear correlation between acid concentration and the absolute value of the current at certain reduction potential has been verified. The effect of the pH value of the solution in the obtained current has demonstrated to be strongly related to the dissociation state of the acid. udIn a second part, as the hydrogen evolution reaction is the principal cathodic reaction of metal corrosion in anaerobic aqueous environments, the role that weak acids can play in this process was studied. Corrosion experiments on carbon steel were carried out in phosphoric acid solution under anaerobic conditions. The influence of hydrogen in the solution was also studied. In the absence of oxygen, a substantial increase of corrosion rate was found when carbon steel samples were submerged in low phosphoric acid concentration solution compared to that obtained in distilled water. ud
机译:尽管众所周知,磷酸盐物质在考虑其氧化还原电势时在电化学上是惰性的,但自80年代末以来报道的在还原域观察到的电化学现象与磷酸盐物质的存在有关,因此很少有研究。一些作者提出,磷酸根离子和弱酸通常会按照上述反应类型催化水的电化学还原[1-3]: ud ud电化学反应 udH2PO4- + e-Had + HPO42-(1) udHad + H2PO4- + e- H2 + HPO42-(2) udAcido碱性平衡 udH2PO4- + OH-- H2O + HPO42-(3) ud ud结合反应,得到水的减少 ud2 H2O + 2e- H2 + 2OH-(4) ud udMarinovic和Despic [1]假设氢的逸出更有可能是由除水以外的其他物种发生的,因为氢原子与其余氢原子之间的键与水分子中的氢-氧键相比,该分子的弱酸弱。银电极[2]和铂电极[1]上都显示了这一点。在以前的工作中[3],我们表明磷酸根离子在不锈钢上表现出相同的电化学行为。根据实验数据提出了一个理论模型,该模型表明通过上述机理产生了大量的分子氢。 ud本文通过伏安法研究了铂和不锈钢旋转圆盘电极上磷酸对氢释放反应的影响。已经证实了酸浓度和一定还原电位下电流绝对值之间的线性关系。已证明溶液的pH值在获得的电流中的作用与酸的解离状态密切相关。第二部分,由于氢的释放反应是厌氧水溶液环境中金属腐蚀的主要阴极反应,因此研究了弱酸在该过程中的作用。碳钢在厌氧条件下在磷酸溶液中进行腐蚀实验。还研究了溶液中氢的影响。在无氧条件下,与蒸馏水相比,将碳钢样品浸入低浓度磷酸溶液中时,腐蚀速率大大提高。 ud

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