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6061铝合金上的缓蚀剂改性微弧氧化涂层

Corrosion Inhibitor-Modified Plasma Electrolytic Oxidation Coatings on 6061 Aluminum Alloy.

作者信息

Sowa Maciej, Wala Marta, Blacha-Grzechnik Agata, Maciej Artur, Kazek-Kęsik Alicja, Stolarczyk Agnieszka, Simka Wojciech

机构信息

Faculty of Chemistry, Silesian University of Technology, B. Krzywoustego Street 6, 44-100 Gliwice, Poland.

出版信息

Materials (Basel). 2021 Jan 29;14(3):619. doi: 10.3390/ma14030619.

Abstract

There are many methods for incorporating organic corrosion inhibitors to oxide coatings formed on aluminum alloys. However, typically they require relatively concentrated solutions of inhibitors, possibly generating a problematic waste and/or are time-/energy-consuming (elevated temperature is usually needed). The authors propose a three-step method of oxide layer formation on 6061-T651 aluminum alloy (AAs) via alternating current (AC) plasma electrolytic oxidation (PEO), impregnation with an 8-hydroxyquinoline (8-HQ) solution, and final sealing by an additional direct current (DC) polarization in the original PEO electrolyte. The obtained coatings were characterized by scanning electron microscopy, roughness tests, contact angle measurements, X-ray diffraction, Raman spectroscopy, and X-ray photoelectron spectroscopy. Additionally, corrosion resistance was assessed by potentiodynamic polarization in a NaCl solution. Two types of the coating were formed (A-thicker, more porous at 440 mA cm; B-thinner, more compact at 220 mA cm) on the AA substrate. The 8-HQ impregnation was successful as evidenced by XPS. It increased the contact angle only for the B coatings and improved the corrosion resistance of both coating systems. Additional DC treatment destroyed superficially adsorbed 8-HQ. However, it served to block the coating pores (contact angle ≈ 80°) which improved the corrosion resistance of the coating systems. DC sealing alone did not bring about the same anti-corrosion properties as the combined 8-HQ impregnation and DC treatment which dispels the notion that the provision of the inhibitor was a needless step in the procedure. The proposed method of AA surface treatment suffered from unsatisfactory uniformity of the sealing for the thicker coatings, which needs to be amended in future efforts for optimization of the procedure.

摘要

将有机缓蚀剂掺入铝合金表面形成的氧化膜有多种方法。然而,通常它们需要相对浓缩的缓蚀剂溶液,这可能会产生有问题的废物,并且/或者耗时/耗能(通常需要升高温度)。作者提出了一种在6061-T651铝合金(AA)上形成氧化层的三步法,即通过交流(AC)等离子体电解氧化(PEO)、用8-羟基喹啉(8-HQ)溶液浸渍,以及最后在原始PEO电解液中通过额外的直流(DC)极化进行密封。通过扫描电子显微镜、粗糙度测试、接触角测量、X射线衍射、拉曼光谱和X射线光电子能谱对所得涂层进行了表征。此外,通过在NaCl溶液中进行动电位极化来评估耐腐蚀性。在AA基体上形成了两种类型的涂层(A-较厚,在440 mA/cm时孔隙较多;B-较薄,在220 mA/cm时较致密)。XPS证明8-HQ浸渍是成功的。它仅增加了B涂层的接触角,并提高了两种涂层体系的耐腐蚀性。额外的直流处理破坏了表面吸附的8-HQ。然而,它起到了堵塞涂层孔隙的作用(接触角≈80°),从而提高了涂层体系的耐腐蚀性。单独的直流密封并没有带来与8-HQ浸渍和直流处理相结合相同的防腐性能,这消除了认为在该过程中提供缓蚀剂是不必要步骤的观念。所提出的AA表面处理方法对于较厚涂层的密封均匀性不理想,这需要在未来优化该过程的努力中加以改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ad/7866277/1ad281d62be8/materials-14-00619-g001.jpg

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