Rate control for copper tarnishing

被引:13
作者
Cano, E
Polo, JL
La Iglesia, A
Bastidas, JM
机构
[1] CSIC, CENIM, Ctr Nacl Invest Met, E-28040 Madrid, Spain
[2] Univ Castilla La Mancha, Escuela Ingn Tecn Ind, E-45071 Toledo, Spain
[3] Univ Complutense Madrid, Fac Ciencias Geol, Inst Geol Econ, CSIC, E-28040 Madrid, Spain
关键词
copper; copper tarnishing process; potentiodynamic experiments; ohmic resistance;
D O I
10.1016/j.corsci.2004.06.026
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The reduction of copper sulphide and copper oxides originated during artificial tarnishing of copper is studied using potentiodynamic potential/current density experiments. Six copper surface treatments are considered: mechanical polishing; indoor exposure for 7 days; chemical etching in 1.6M nitric acid; chemical etching and heating at 160 degrees C; and chemical etching and dipping in a 9 x 10(-4)M or 0.9M potassium sulphide (K2S) solution at 70 degrees C. Cuprite (Cu2O) and chalcocite (Cu2S) are the main compounds formed. A linear relationship with the square root of the scan rate (v) is obtained by plotting the potentiodynamic potential/current density for the tarnish dissolution processes. A relationship between potential and current density cathodic peaks is not obtained, according to Muller's model, showing a proportionality factor with the dimensions of a resistance. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:977 / 987
页数:11
相关论文
共 23 条
[1]   Characterization of artificially patinated layers on artistic bronze exposed to laboratory SO2 contamination [J].
Bastidas, JM ;
LopezDelgado, A ;
Lopez, FA ;
Alonso, MP .
JOURNAL OF MATERIALS SCIENCE, 1997, 32 (01) :129-133
[2]   Copper corrosion mechanism in the presence of formic acid vapor for short exposure times [J].
Bastidas, JM ;
López-Delgado, A ;
Cano, E ;
Polo, JL ;
López, FA .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (03) :999-1005
[3]   POTENTIODYNAMIC CURRENT/POTENTIAL RELATIONS FOR FILM FORMATION UNDER OHMIC RESISTANCE CONTROL [J].
CALANDRA, AJ ;
DETACCONI, NR ;
PEREIRO, R ;
ARVIA, AJ .
ELECTROCHIMICA ACTA, 1974, 19 (12) :901-905
[4]   THE EARLY STAGE OF ATMOSPHERIC CORROSION OF COPPER BY SULFUR-DIOXIDE [J].
CHAWLA, SK ;
PAYER, JH .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (01) :60-64
[5]  
Davis J.R., 2001, SURFACE ENG CORROSIO
[6]   THE MECHANISM OF OXIDATION OF COPPER IN ALKALINE-SOLUTIONS [J].
DECHIALVO, MRG ;
MARCHIANO, SL ;
ARVIA, AJ .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1984, 14 (02) :165-175
[7]   CHARACTERIZATION OF OXIDE LAYERS ON COPPER BY LINEAR POTENTIAL SWEEP VOLTAMMETRY [J].
DEUTSCHER, RL ;
WOODS, R .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1986, 16 (03) :413-421
[8]   Copper corrosion originated by propionic acid vapors [J].
Echavarría, A ;
Rueda, A ;
Cano, E ;
Echeverría, F ;
Arroyave, C ;
Bastidas, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (04) :B140-B145
[9]  
EVANS UR, 1960, CORROSION OXIDATION, P175
[10]  
Fiaud C., 1989, British Corrosion Journal, V24, P279, DOI 10.1179/000705989798269975