Enhancement of the Corrosion Resistance and Durability of Layered Double Hydroxide Films Through Incorporation of Polyelectrolytes and Dual Corrosion Inhibitors

Yan Wang, Xiang Gao, Wei He, Houyi Ma
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Abstract

ABSTRACT The durability of layered double hydroxide (LDH) films is greatly improved by intercalating organic corrosion inhibitors, modifying the surface with polyelectrolytes, and uniformly doping with inorganic inhibitors. A LDH film was synthesized in situ on the aluminum surface with intercalated sodium polyaspartate (PASP‐Na) as an organic corrosion inhibitor. The film was then modified via a gelation reaction between sodium alginate (SA) and cerium ions (Ce), serving as an inorganic inhibitor, to form a composite coating with improved corrosion resistance and durability. Scanning electron microscopy (SEM) analysis revealed that the composite film had a thickness of approximately 4.9 µm and achieved a corrosion protection efficiency of 99.8%. This efficiency remained as high as 98.8% even after 28 days of immersion in a 3.5 wt% NaCl solution. SEM analysis of scratched samples demonstrated notable self‐healing capability. The self‐healing mechanism is due to PASP‐Na being released and adsorbed onto the scratched areas, along with water absorption by the SA‐Ce gel and Ce ions migrating to the damaged region.
通过加入聚电解质和双重缓蚀剂提高层状双氢氧化物膜的耐蚀性和耐久性
通过嵌入有机缓蚀剂、用聚电解质修饰表面以及均匀掺杂无机缓蚀剂,可以大大提高层状双氢氧化物(LDH)薄膜的耐久性。以嵌层聚天冬氨酸钠(PASP‐Na)为有机缓蚀剂,在铝表面原位合成了LDH膜。然后通过海藻酸钠(SA)和铈离子(Ce)(作为无机抑制剂)之间的凝胶反应对薄膜进行改性,形成具有提高耐腐蚀性和耐久性的复合涂层。扫描电镜(SEM)分析表明,复合膜的厚度约为4.9µm,防腐效率为99.8%。即使在3.5 wt% NaCl溶液中浸泡28天后,这一效率仍高达98.8%。对划伤样品的扫描电镜分析显示出显著的自愈能力。自修复机制是由于PASP - Na被释放并吸附在划伤区域,同时SA - Ce凝胶吸水,Ce离子迁移到受损区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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sodium alginate (SA)
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