Corrosion product analysis of corrosion resistant ancient Indian iron

被引:50
|
作者
Kumar, AVR
Balasubramaniam, R [1 ]
机构
[1] Indian Inst Technol, Dept Mat & Met Engn, Kanpur 208016, Uttar Pradesh, India
[2] Def Mat & Stores Res Estab, Electrochem & Corros Div, Kanpur 208013, Uttar Pradesh, India
关键词
ancient Indian iron; Delhi iron pillar; rust characterization; mechanism of protection;
D O I
10.1016/S0010-938X(98)00024-9
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The corrosion product formed on an ancient 1500-year old non-corroded iron clamp was studied by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Mossbauer spectroscopy. The iron possessed a non-uniform grain structure with dispersed second phase particles. Microscopy indicated that rust present on the surface was composed of an adherent and compact inner layer and a loose outer layer. Enrichment of P was observed at the metal-scale interface and in the inner rust layer. XRD indicated that the rust was amorphous in nature. The FTIR spectrum provided that the major constituents of the scale were alpha-, gamma-, delta- FeOOH and FePO4.2H(2)O. Mossbauer studies further indicated that these constituents were present in a very fine form, confirming the results obtained by XRD. The presence of ii magnetic oxide with a lower field strength than that of magnetite was also identified. The process of protective rust formation on the ancient Indian iron has been elucidated based on the results of the study. Initially, the corrosion rate of the iron is high due to the presence of the slag particles which results in enhancement of the P content in the surface. In the presence of P, the formation of a protective amorphous compact layer of delta - FeOOH is catalyzed and this confers corrosion resistance. The conversion of FeOOH to magnetite is also indicated and this would further improve the corrosion resistance. Another factor aiding corrosion resistance is the formation of iron phosphates which would lower the rate of corrosion. (C) 1998 Elsevier Science Ltd. All rights reserved
引用
收藏
页码:1169 / 1178
页数:10
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