Finkelstein G F, Greener E H
J Oral Rehabil. 1979 Apr;6(2):189-97. doi: 10.1111/j.1365-2842.1979.tb01280.x.
Polarization of conventional dental amalgam in Ringer's solution produces a dissolution of the gamma 2 phase at--250 mV (SCE) and formation of Sn-Cl and Sn-O-Cl. This study was undertaken to determine the electrochemical nature of these reactions. Potentiostatic polarization scans were run at 4, 37 and 50 degrees C in several dilutions of aerated Ringer's solution. Manipulation of reactant concentrations and electrolyte temperature produced shifts in the potentiostatic profiles. At 50 degrees C, a gamma 2 dissolution peak shift to -300 mV was observed, and at 4 degrees C the peak shifted to -200 mV. Dilution of Ringer's solution with respect to [Cl-] over three orders of magnitude produced a linear shift in the noble direction of 500 mV. Cathodic polarization appears to be limited by the oxygen half cell reaction. Changes of [Cl] affect the shape of the peak, round out its approach to the current maximum. Shifts in peak potential due to temperature and concentration changes agreed with calculations based on critical pitting potential for gamma2 dissolution due to a chloride reaction. Polarization profiles in pooled saliva agreed with calculated potentials based on known saliva [Cl-].
在林格氏溶液中,传统牙科汞合金的极化会导致γ2相在-250 mV(饱和甘汞电极)时溶解,并形成Sn-Cl和Sn-O-Cl。本研究旨在确定这些反应的电化学性质。在4℃、37℃和50℃下,于几种充气林格氏溶液稀释液中进行恒电位极化扫描。对反应物浓度和电解质温度的操控导致了恒电位曲线的偏移。在50℃时,观察到γ2溶解峰移至-300 mV,在4℃时,该峰移至-200 mV。将林格氏溶液相对于[Cl-]稀释三个数量级,会导致在正电位方向上线性偏移500 mV。阴极极化似乎受氧半电池反应限制。[Cl]的变化会影响峰的形状,使其接近电流最大值的过程变平缓。由于温度和浓度变化导致的峰电位偏移与基于氯化物反应引起的γ2溶解临界点蚀电位的计算结果一致。混合唾液中的极化曲线与基于已知唾液[Cl-]计算出的电位相符。