## Abstract The anodic behaviour of massive and dental amalgam alloys in artificial saliva containing different concentrations of Cl^−^ or F^−^ ions has been studied. Quantitative relations could be established between concentrations of these ions and the height of the peaks corresponding to anodic
Dental amalgam – the effect of the technology of alloy powder preparation on the corrosion behaviour and the release of mercury
✍ Scribed by L. Joska; J. Bystrianský; P. Novák
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- German
- Weight
- 357 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0947-5117
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✦ Synopsis
Abstract
Dental amalgams are based on a broad spectrum of materials differing in their chemical composition, metallurgical treatment, and in the way the initial alloys powders are prepared. In addition to their chemical composition, amalgams based on various powders differ in both their microstructure and the amount of mercury needed for preparation. All these facts may affect electrochemical processes occurring during their interaction with oral fluids, and also mercury release. While verifying the effect of the technology used for the preparation of the high‐copper ternary alloy powder on the properties of resulting amalgams, this study aimed at the mechanism of their interaction with a model saliva solution as well as mercury release was included. Measurements were done in a model saliva solution using standard electrochemical methods and exposition measurements. The interaction of individual types of amalgams with artificial saliva did not reveal any significant differences. The free corrosion potential of all these amalgams in an aerated solution settled in the range of values in which tin oxidation, resulting in a layer of insoluble corrosion producsts, turned out to be the dominant anodic process. The rate of mercury release was the lowest for amalgams based on a gas‐atomized alloy. The highest rate of mercury release, and also its dependence on time, was exhibited by lathe‐cut powder based amalgam. In addition to different volume fraction of the Ag‐Hg phase and the level of its tin alloying, this different behaviour may be explained by differences in the rate at which a layer of tin corrosion products acting as a barrier to mercury release is formed.
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