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首页> 外文期刊>Materials Research >Electrochemical and Quantum Chemical Studies on Corrosion Inhibition Performance of 2,2'-(2-Hydroxyethylimino)bis[N-(alphaalpha-dimethylphenethyl)-N-methylacetamide] on Mild Steel Corrosion in 1M HCl Solution
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Electrochemical and Quantum Chemical Studies on Corrosion Inhibition Performance of 2,2'-(2-Hydroxyethylimino)bis[N-(alphaalpha-dimethylphenethyl)-N-methylacetamide] on Mild Steel Corrosion in 1M HCl Solution

机译:电化学和量子化学研究2,2' - (2-羟乙基氨基氨基)双[N-(αα-二甲基乙基)-N-甲基乙酰胺]对1M HCl溶液温和钢腐蚀的腐蚀抑制性能

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The inhibitory effect of Oxethazaine drug, 2,2'-(2-Hydroxyethylimino)bis[N-(alphaalpha-dimethylphenethyl)-N-methylacetamide] on corrosion of mild steel in 1M HCl solution was studied by weight loss measurements, electrochemical impedance spectroscopy and potentiodynamic polarization methods. The results of gravimetric and electrochemical methods demonstrated that the inhibition efficiency increased with an increase in inhibitor concentration in 1M HCl solution. The results from electrochemical impedance spectroscopy proved that the inhibition action of this drug was due to adsorption on the metal surface. Potentiodynamic polarization studies revealed that the molecule was a mixed type inhibitor. The adsorption of the molecule on the metal surface was found to obey Langmuir Adsorption isotherm. Potential of zero charge at the metal-solution interface was measured to provide the inhibition mechanism. The temperature dependence of the corrosion rate was also studied in the temperature range from 30 to 50 °C. Quantum chemical calculations were applied to correlate electronic structure parameters of the drug with its inhibition performance. The obtained theoretical results have been adapted with the experimental data.
机译:通过减损测量研究了氧乙肽药物,2,2'-(2-羟基乙基咪啶氨基氨基)双[N-(α-(α-二甲基乙基乙基)-N-甲基乙酰胺]对1M HCl溶液中的温和钢腐蚀的抑制作用,电化学阻抗光谱法和电位动力学极化方法。重量和电化学方法的结果表明,抑制效率随1M HCl溶液中的抑制剂浓度的增加而增加。电化学阻抗光谱的结果证明了该药物的抑制作用是由于金属表面的吸附。电位动力学偏振研究表明,分子是混合式抑制剂。发现分子对金属表面上的吸附遵循Langmuir吸附等温线。测量金属溶液界面处的零电荷的电位以提供抑制机制。还在30至50℃的温度范围内研究腐蚀速率的温度依赖性。施用量子化学计算以将药物的电子结构参数与其抑制性能相关联。所获得的理论结果已经适用于实验数据。

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