Electrochemical identification of corrosion products on historical and archaeological bronzes using the voltammetry of micro-particles attached to a carbon paste electrode

被引:34
|
作者
Satovic, D. [2 ]
Martinez, S. [1 ]
Bobrowski, A. [3 ]
机构
[1] Univ Zagreb, Fac Chem Engn & Technol, Dept Electrochem, HR-10002 Zagreb, Croatia
[2] Acad Fine Arts, Dept Conservat & Restorat, Zagreb 10000, Croatia
[3] Univ Sci & Technol, Fac Mat Sci & Ceram, PL-30059 Krakow, Poland
关键词
Voltammetry of microparticles; Bronze; Patina; Conservation and restoration; ATR-FTIR; NATURAL PATINAS; BEHAVIOR; COPPER; MODEL; IONS;
D O I
10.1016/j.talanta.2010.03.037
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An overview of the electrochemical method for the identification of microsampled corrosion products from historical and archaeological bronzes is reported Two characteristic examples of long-term air and subterranean formed patinas and two artificial patinas formed on Cu-6%Sn bronze in sulphate and chloride solutions, were investigated in 0 1 M HCl(aq) by means of the cyclic voltammetry of microparticles attached to a carbon paste electrode. Patina constituent phases were identified by comparing the electrochemical parameters of the patina samples to those of reference compounds CuO, Cu2O, SnO, SnO2, CuCl, CuCl2 x 2H(2)O and CuSO4 x 5H(2)O. An identification scheme was suggested which may be applied to discern the various corrosion products of bronze based on electrochemical data (voltammetric peak potentials). The presence of two prevalent phases of sulphate and chloride patinas. CuSO4 and CuCl, as well as the presence of Sn compounds was clearly indicated by the cyclic voltammetry of microparticles, in both, naturally and artificially formed samples A comparison to the ATR-FTIR results revealed that the methods are complementary and that their simultaneous application could prove particularly valuable in drawing conclusions about the current shape and prospects of the conservation and restoration of bronze artefacts (C) 2010 Elseviei B.V. All rights reserved
引用
收藏
页码:1760 / 1765
页数:6
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