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AN INVESTIGATION OF ZINC CORROSION INHIBITION INAQUEOUS SOLUTIONS OF NH4Cl BY ORGANIC COMPOUNDS

机译:有机化合物对锌腐蚀抑制NH4Cl水溶液的研究

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Polarization and impedance measurements were carried out on a zinc electrode in aqueoussolution of NH4Cl containing organic corrosion inhibitors. This measurements have been realised bymeans of analytical and electrochemical methods. The inhibitors investigated were:dodecyltrimethylammonium bromide, tetradecyltrimethylammonium bromide andhexadecyltrimethylammonium bromide. These compounds suppressed both cathodic and anodicprocesses of zinc corrosion in the NH4Cl aqueous solutions. The double layer capacitances obtained fromthe impedance data for the electrode inhibited with organic inhibitors were markedly lower in thepotential region of the cathodic polarization curves than those for the uninhibited electrode.At the cathodic potentials, the calculated impedance values fit the experimental ones only if the Tafelcoefficient for hydrogen discharge is taken to be potential dependent. This fact suggests that the cathodicprocess is multistage with the rate of the overall electrochemical reaction controlled in turn by one of thepartial reactions according to the value of the overpotential. The analysis of the impedance measurementsshowed that the organic inhibitors considered affect both the kinetic coefficients of the anodic process andthe H2 discharge Tafel coefficients.Considering all the results and taking into account the dispersion of the data we came to conclusion thatall the organic inhibitors show a well detectable inhibition of zinc corrosion. A poorly soluble layerconsisting of the inhibitor and zinc corrosion products is proposed to account for protective effect inchloride solutions. On the other hand, pyrrole was successfully electropolymerized at a zinc electrode in anear neutral sodium oxalate solution when a homogenous and adherent polypyrrole film is obtained. Thegrowth of this film was facilitated by the initial pre-treatment of zinc electrode in an aqueous solution of0,2M Na2S to generate a sulphide pseudo-passive layer. This layer was sufficiently protective to inhibitfurther dissolution of zinc electrode and sufficiently conductive to enable the electropolymerization ofpyrrole at the interface and generation of an adherent polypyrrole film. This film remained stable andexhibited significant corrosion protection properties in acidified and neutral chloride solutions even onpolarization to high anodic potentials.
机译:在含有机腐蚀抑制剂的NH4Cl水溶液中,在锌电极上进行极化和阻抗测量。通过分析和电化学方法已经实现了这种测量。研究的抑制剂为:十二烷基三甲基溴化铵,十四烷基三甲基溴化铵和十六烷基三甲基溴化铵。这些化合物抑制了NH4Cl水溶液中锌腐蚀的阴极和阳极过程。从有机抑制剂抑制的电极的阻抗数据获得的双层电容在阴极极化曲线的电势区域明显低于未抑制电极的双层电容。在阴极电势下,仅当Tafelcoefficient氢放电被认为与电位有关。这一事实表明,该阴极过程是多阶段的,整个电化学反应的速率又由部分反应之一根据过电势的值来控制。对阻抗测量结果的分析表明,所考虑的有机抑制剂均会影响阳极过程的动力学系数和H2放电塔菲尔系数。考虑所有结果并考虑数据的分散性,我们得出的结论是所有有机抑制剂均表现良好。可检测到的锌腐蚀抑制作用。提出了由抑制剂和锌腐蚀产物组成的难溶层,以说明氯化物溶液的保护作用。另一方面,当获得均匀且粘附的聚吡咯膜时,吡咯在锌电极中的中性草酸钠溶液中成功地电聚合。通过在0.2M Na 2 S的水溶液中对锌电极进行初始预处理来促进该膜的生长,以生成硫化物假钝化层。该层具有足够的保护性以抑制锌电极的进一步溶解,并且具有足够的导电性以使吡咯在界面处发生电聚合并生成粘附的聚吡咯膜。该膜即使在极化到高阳极电位时,也保持稳定并在酸化和中性氯化物溶液中表现出显着的腐蚀防护性能。

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