Salicylic and tartaric ions co-doped polypyrrole to enhance the corrosion protection of polypyrrole/zinc bilayer coating on ZK60 magnesium alloy in Hank's solution

被引:1
|
作者
Luo, Wei [1 ]
Qi, Kai [1 ,2 ,3 ,4 ]
Qiu, Yubing [1 ,2 ,3 ,4 ]
Guo, Xingpeng [2 ,3 ,5 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
[2] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Minist Educ, Wuhan, Peoples R China
[3] Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China
[4] Hubei Engn Res Ctr Biomat & Med Protect Mat, Wuhan 430074, Peoples R China
[5] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Polypyrrole; Zinc coating; Sodium salicylate; ZK60 magnesium alloy; Hank's solution; Protection performance; ULTRA-FAST ELECTROPOLYMERIZATION; CONDUCTIVE POLYPYRROLE; HEAT-TREATMENT; AQUEOUS-MEDIA; SUPERHYDROPHOBIC SURFACE; ELECTROCHEMICAL-BEHAVIOR; SODIUM-SALICYLATE; MG ALLOYS; PPY FILMS; ZINC;
D O I
10.1016/j.porgcoat.2024.108437
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
To enhance the corrosion protection of the polypyrrole/zinc (PPy/Zn) bilayer coating on biodegradable ZK60 magnesium alloy in Hank's solution at 37 degrees C, sodium salicylate (NaSA) in different concentrations ( C NaSA , 0.5-4.0 mM) is selected as a co -doping reagent of tartrate anions (TA - ), and an electropolymerization method that combines potentiostatic and galvanostatic synthesis is developed to prepare PPy(TA + SA)/Zn bilayer coatings. The co -doping of SA - suppresses the growth of PPy and notably increases its synthesis potential ( E poly ) with increasing C NaSA . The co -doped PPy(TA + SA) films have a surface morphology and thickness similar to the PPy(TA) film. However, their chemical composition, structure, and adhesion strength change notably due to their varying growth conditions. In the long-term immersion test of PPy(TA + SA)/Zn/ZK60 samples, the PPy(TA + SA)/Zn coatings exhibit high stability, and the coating prepared with C NaSA = 1.0 mM has the most prolonged protection time (54 +/- 1.5 d). As C NaSA increases, the co -doped PPy(TA + SA) film becomes heavily over -oxidized to produce more defects on PPy chains due to the high E poly , ultimately decreasing the protection time to 40 +/- 1.0 d. The corresponding mechanism involved is thoroughly discussed.
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页数:15
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