velvalloy and tytin

Dissolution of mercury from dental amalgam has been shown to be diminished by the formation of a tin oxide film on the surface of the mercury-rich gamma 1 phase (Marek, 1990b). Since tin oxides dissolve at low pH values (Deltombe et al., 1974), acidic conditions in the oral cavity may cause an increase in the mercury release. The purpose of this study was to determine the effect of acidity in the range of pH 1 to pH 8 on the rate of mercury dissolution in synthetic saliva from tin-free and tin-containing gamma 1 phase and two commercial dental amalgams. The tested hypothesis was that pH affects mercury dissolution only when a protective oxide film dissolves in an acidic environment. After exposures of the specimens for 2 hr or 24 hr in sealed glass bottles, the solutions were analyzed by flameless atomic absorption spectrophotometry for mercury and silver. The results have shown pH-independent mercury dissolution in the range of pH 3 to 8, and a much faster dissolution at pH 1. At all pH values, more mercury dissolved from the tin-free phase than from the tin-containing phase, and the rate of dissolution was lowest for the dental amalgams. The results were affected by the length of the test exposure. The pH independence in a wide range of pH values has been attributed to the atomic mechanism of mercury dissolution. The low rate of mercury dissolution from specimens containing tin has been explained by the formation of a barrier tin oxide film, which dissolved only at the lowest pH. Dissolution of silver at low pH values is believed to have accelerated dissolution of mercury from the tin-free gamma 1 phase. Variation of the dissolution rate with concentration of the dissolved species and kinetics of oxide film dissolution caused the effect of the exposure period.

Topics: Analysis of Variance; Corrosion; Dental Alloys; Dental Amalgam; Hydrogen-Ion Concentration; Materials Testing; Mercury; Saliva, Artificial; Solubility; Spectrophotometry, Atomic; Statistics, Nonparametric; Tin Compounds; Volatilization

The release of mercury from two freshly triturated amalgams exposed to a reducing atmosphere, hydrogen, was quantitated at three different temperatures. A low-copper and a high-copper amalgam were placed into a flowing hydrogen gas atmosphere for 60 min after trituration, and then the hydrogen was replaced by compressed air. The results were compared to those obtained in a previous study in which air and argon atmospheres were used under identical conditions. At 37 degrees C, the rate of evaporation of mercury from the amalgams was similar when they were exposed to hydrogen before being exposed to air. During exposure to hydrogen, the evaporation rate appeared to exceed the limit of the gold film mercury analyzer (284 pg/mm2/s), but was rapidly reduced upon exposure to air. The results were identical to those from argon exposure. When the same experiment was performed at 80 degrees C, the evaporation rate after hydrogen exposure was greater than that after exposure to argon, and far greater than that during exposure to air alone. Similar results were achieved at 110 degrees C, but there was less difference between hydrogen and argon exposure. The results support previous studies which show that the evaporation of mercury from amalgam is mainly limited by the formation of an oxide film.

Topics: Air; Air Pollution, Indoor; Argon; Copper; Dental Alloys; Dental Amalgam; Hydrogen; Mercury; Oxidation-Reduction; Oxides; Volatilization

The release of mercury from four freshly-triturated amalgams into air, argon, and moist air environments was quantitated at three different temperatures. Although a measurable amount of mercury was released from dental amalgam, the evaporation rate was immediately reduced by several phenomena, the most important being the formation of an oxide film on the surface. This hypothesis was supported by the fact that release rates were elevated in an inert argon environment, but declined dramatically once air was introduced and oxidation could occur. The further amalgamation of "free" mercury, as well as the presence of water vapor, also contributed to the reduced release rates observed during aging. Mercury release was reduced to a negligible level within three to four hours after trituration. Only one of the amalgams, Tytin, demonstrated a thermal dependence for mercury release in air. The results of this study suggest that the exposure to mercury vapor from a freshly placed amalgam restoration would be negligible in consideration of the normal estimated daily intake from all other sources.

Topics: Air; Argon; Copper; Dental Alloys; Dental Amalgam; Hot Temperature; Humidity; Mercury; Oxidation-Reduction; Oxides; Time Factors; Volatilization; Zinc