Smart-Release Inhibition of Corrosion-Driven Organic Coating Delamination on Galvanized Steel Surfaces

被引:3
作者
Williams, G. [1 ]
Geary, S. [1 ]
Loveridge, M. [1 ]
McMurray, H. N. [1 ]
机构
[1] Swansea Univ, Mat Res Ctr, Coll Engn, Swansea SA2 8PP, W Glam, Wales
来源
COATINGS FOR CORROSION PROTECTION | 2012年 / 41卷 / 15期
基金
英国工程与自然科学研究理事会;
关键词
KELVIN PROBE TECHNIQUE; HYDROTALCITE-LIKE PIGMENTS; FILIFORM CORROSION; ALUMINUM-ALLOY; EXCHANGE PIGMENTS; COATED AA2024-T3; PROTECTION; MIXTURE; PAINTS;
D O I
10.1149/1.3696872
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In-coating cation and anion-exchange pigments are studied with respect to their ability to inhibit corrosion-driven organic coating disbondment on the zinc surface of hot-dip galvanized (HDG) steel. The efficiency of inorganic smart-release cation-exchangers, including bentonite and zeolite based pigments containing stored Zn(ii) inhibitor are compared with an organic cation-exchange cross-linked polystyrene based system. In-situ scanning Kelvin probe experiments carried out on HDG samples coated pigment-containing model polymer organic films showed that only the bentonite system was capable of halting delamination over a 24 h holding period, despite having a cation exchange capacity of only one third of the other exchangers. The reasons for this are discussed in terms of the kinetics of underfilm ion-exchange process. A preliminary investigation of anion-exchange hydrotalcite-based pigments is also described. The inhibition efficiency is shown to be highly anion specific, with chromate and phosphate exchanged pigments providing the best protection against organic coating cathodic disbondment.
引用
收藏
页码:93 / 103
页数:11
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