锌的大气腐蚀。第2部分:海洋大气

E. Almeida, M. Morcillo, B. Rosales
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引用次数: 48

摘要

摘要本文总结了MICAT (Mapa Ibero-Americano de Corrosion s o atmos(拉丁美洲大气腐蚀地图))大气腐蚀项目(一个伊比利亚美洲大气腐蚀项目,涉及14个国家和75个大气试验点)在拉丁美洲地区23个纯海洋和19个混合海洋(即二氧化硫污染)试验点暴露1-4年的锌样品的结果。这些地点的大气具有气候学特征和污染水平特征,因此它们的腐蚀性可以按照ISO标准表示。利用扫描电子显微镜、能谱仪(SEM-EDS)、x射线衍射仪(XRD)、傅里叶变换红外光谱(FTIR)和可溶性盐评价技术对锌腐蚀产物层(zcpl)进行了形态和化学表征。结果表明,锌的腐蚀速率是氯化物污染程度和浸湿时间的函数。虽然也观察到一些特殊类型的行为,但证明了Cl-和SO2的一些协同效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atmospheric corrosion of zinc Part 2: Marine atmospheres
Abstract This paper summarises the results obtained in the MICAT (Mapa Ibero-Americano de Corrosão Atmosférica (Latin American Map of Atmospheric Corrosion)) atmospheric corrosion project (an Iberoamerican project on atmospheric corrosion, involving 14 countries and 75 atmospheric test sites) for zinc specimens exposed in the Latin American region for 1–4 years at 23 pure marine and 19 mixed marine (i.e. SO2 polluted) sites. The atmospheres at these sites were characterised climatologically and in terms of their pollution levels so that their corrosivity could be expressed in accordance with ISO standards. Morphological and chemical characterisation of the zinc corrosion product layers (ZCPLs) was performed using scanning electron microscopy coupled with energy dispersive spectrometry (SEM–EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and soluble salt evaluation techniques. The results obtained show that the corrosion rate of zinc is a function of both the chloride pollution level and the time of wetness. Some synergetic effects of Cl- and SO2 were demonstrated, although some special types of behaviour were also observed.
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