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Application of Scanning Kelvin Probe for Studying Corrosion under the Polymeric Coatings

机译:开尔文扫描探针在聚合物涂层下腐蚀研究中的应用

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In this research, corrosion protection of different polymeric nanocomposites coated on mild steel was investigated by the application of scanning Kelvin probe (SKP). The samples were mild steel coated with a neat epoxy, polyanilne embedded epoxy and clay embedded epoxy respectively. The potential difference between the tip and sample which was defined as Volta potential was measured by SKP. Potential decrease is an apparent phenomenon caused by corrosion induced Fermi level misalignment at the interface between the tip and the Iron substrate. Contact potential difference between the conducting tip and sample, is called 61ta potential difference. Promoting corrosion in presence of electrolyte leads to metal surface potential drop that can be measured by means of Kelvin probe. Although the corrosion potential calculation is not easy, the relation between the Volta potential difference measured by the Kelvin probe and the electrode potential at the buried interface is straightforward, Volta potential differences between the probe and the sample were measured by means of scanning Kelvin probe. SKP plots were obtained at different exposure times with 121 points for each measurement. The average Volta potential difference of each sample was also calculated and plotted versus exposure time. At initial times, Volta potential difference for all the samples were about -200 mVvs. SCE. It means that before water diffusion and corrosion initiation, samples surfaces were in similar conditions. But 61ta potentials were different in samples due to their composition and corrosion role after exposure for long hours. Different capacitors between the probe and conductive substrate may form in the case of the coated steel exposed to aqueous corrosive media. Coating capacitance vary as a consequence of water diffusion. Initial drop in surface 61ta potential differences of all the coated steels were due to diffusion of electrolyte and corrosive ions through the coating defects. CV was introduced as an index in order to compare the deviations of Volta potential differences from their mean values for the coated steels with or without PANs. Results are plotted in.CV defines deviation of Volta potential differences from the mean value in each sample for different exposure times in humidity chamber. If CV equals 1, there is no deviation from average, which means a completely uniform corrosion. On the other hand, if CV=0, a complete localized corrosion is anticipated. These two ideal situations would never take place but this could be a good method for comparing corrosion uniformity or localization in different conditions beneath the coatings by the application of SKP.
机译:在这项研究中,通过扫描开尔文探针(SKP)的应用研究了低碳钢上涂覆的不同聚合物纳米复合材料的腐蚀防护。样品是软钢,分别涂有纯净的环氧树脂,聚对苯二甲酸乙二酯和黏土。通过SKP测量尖端和样品之间的电位差,其被定义为伏特电位。电位下降是一种明显的现象,该现象是由腐蚀引起的尖端和铁基材之间的界面处的费米能级未对准所引起的。导电尖端与样品之间的接触电势差称为\ 61ta电势差。在电解质存在下促进腐蚀会导致金属表面电势下降,可以通过开尔文探针进行测量。尽管计算腐蚀电位并不容易,但通过开尔文探针测得的伏特电势差与埋入界面处的电极电势之间的关系很简单,通过扫描开尔文探针测得探针与样品之间的伏特电势差。在不同的曝光时间获得SKP图,每次测量得到121个点。还计算了每个样品的平均伏特电势差,并将其与暴露时间作图。在初始时间,所有样品的伏特电势差约为-200 mVvs。 SCE。这意味着在水扩散和腐蚀开始之前,样品表面处于相似的条件下。但是,由于长时间暴露后样品的成分和腐蚀作用,样品中的\ 61ta电位是不同的。在涂层钢暴露于水性腐蚀性介质的情况下,探针和导电基材之间可能会形成不同的电容器。涂层电容因水扩散而变化。所有涂层钢的表面\ 61ta电位差的初始下降是由于电解质和腐蚀性离子通过涂层缺陷的扩散所致。引入CV作为指标是为了比较带或不带PAN的涂层钢的Volta电位差与其平均值之间的偏差。结果以图表示。CV定义了在潮湿箱中不同暴露时间下,每个样品的伏特电位差与平均值的偏差。如果CV等于1,则不会偏离平均值,这意味着完全均匀的腐蚀。另一方面,如果CV = 0,则预期会发生完全的局部腐蚀。这两个理想的情况将永远不会发生,但是这可能是通过使用SKP来比较涂层下不同条件下腐蚀均匀性或局部性的好方法。

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