Corrosion stability of Zn-Co alloys deposited from baths with high and low Co content - The influence of deposition current density

被引:34
作者
Bajat, J. B. [1 ]
Stankovic, S. [1 ]
Jokic, B. M. [1 ]
Stevanovic, S. I. [2 ]
机构
[1] Univ Belgrade, Fac Technol & Met, Belgrade 11120, Serbia
[2] ICTM IEC, Belgrade 11001, Serbia
关键词
Corrosion; AFM; SEM; X-ray diffraction; Electroplating; Zinc alloy; ELECTRODEPOSITED ZN; ELECTROCHEMICAL DEPOSITION; BINARY-ALLOYS; COATINGS; COBALT; RESISTANCE; BEHAVIOR; MICROSTRUCTURE; MORPHOLOGY; COMPLEXES;
D O I
10.1016/j.surfcoat.2010.02.032
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Electrochemically deposited Zn-Co alloys under various deposition conditions were investigated using atomic absorption spectroscopy (AAS) for determination of chemical composition, anodic linear sweep voltammetry (ALSV) and X-ray diffraction (XRD) for phase structure determination, SEM and AFM for surface morphology analysis, and polarization measurements for determination of corrosion properties. The influence of deposition current density and composition of deposition solution on the phase structure, morphology and corrosion properties of Zn-Co alloys were studied. The plating baths used were with low metal concentration, free of additives and deposition was carried out at room temperature, since the aim of the work was to investigate only the influence of different deposition current densities using economically favorable deposition parameters. It was shown that the ratio of cobalt to zinc ions in the plating bath strongly affects the chemical content and phase structure, as well as the morphology and corrosion stability, of Zn-Co alloys. The single-phased Zn-Co alloys showed the best corrosion stability. The alloys deposited at the highest current density from plating bath with the lower ratio of cobalt to zinc ions, as well as the one deposited at the intermediate current density from bath with higher ratio of cobalt to zinc ions, exhibited the lowest corrosion rates. It was also shown that the deposit having smaller crystallite grains (obtained at higher current density), among two alloy deposits having the same chemical content and phase structure, yielded lower corrosion rate. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2745 / 2753
页数:9
相关论文
共 42 条
[1]
Electrochemical studies on the electrodeposited Zn-Ni-Co ternary alloy in different media [J].
Abou-Krisha, M. M. ;
Rageh, H. M. ;
Matter, E. A. .
SURFACE & COATINGS TECHNOLOGY, 2008, 202 (15) :3739-3746
[2]
Electrodeposition of Zn-Ni alloys from sulfate bath [J].
Abou-Krisha, M. M. ;
Assaf, F. H. ;
Toghan, A. A. .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2007, 11 (02) :244-252
[3]
*AM SOC MET, 1973, MET HDB AM SOC MET, V8, P290
[4]
*AM SOC TEST MAT, 1969, POWD DIFFR FIL IN VO
[5]
Electrochemical deposition and corrosion stability of Zn-Co alloys [J].
Bajat, J. B. ;
Stankovic, S. ;
Jokic, B. M. .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2009, 13 (05) :755-762
[6]
Protective properties of epoxy coatings electrodeposited on steel electrochemically modified by Zn-Ni alloys [J].
Bajat, JB ;
Miskovic-Stankovic, VB .
PROGRESS IN ORGANIC COATINGS, 2004, 49 (03) :183-196
[7]
Electrochemical deposition and characterization of zinc-nickel alloys deposited by direct and pulse current [J].
Bajat, JB ;
Maksimovic, MD ;
Radovic, GR .
JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 2002, 67 (8-9) :625-634
[8]
Electrodeposition and characterization of Zn-Ni alloys as sublayers for epoxy coating deposition [J].
Bajat, JB ;
Maksimovic, MD ;
Miskovic-Stankovic, VB ;
Zec, S .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2001, 31 (03) :355-361
[9]
STUDIES ON COBALT(II) HALIDE COMPLEX-FORMATION .1. SPECTROPHOTOMETRIC STUDY OF CHLORO COBALT(II) COMPLEXES IN STRONG AQUEOUS CHLORIDE SOLUTIONS [J].
BJERRUM, J ;
HALONIN, AS ;
SKIBSTED, LH .
ACTA CHEMICA SCANDINAVICA SERIES A-PHYSICAL AND INORGANIC CHEMISTRY, 1975, 29 (03) :326-332
[10]
Influence of the alloying component on the protective ability of some zinc galvanic coatings [J].
Boshkov, N ;
Petrov, K ;
Kovacheva, D ;
Vitkova, S ;
Nemska, S .
ELECTROCHIMICA ACTA, 2005, 51 (01) :77-84