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首页> 外文期刊>Journal of the Indian Chemical Society >Influence of pH on hanging mercury drop electrode cyclic voltammetry with aspartic acid in acetate buffers
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Influence of pH on hanging mercury drop electrode cyclic voltammetry with aspartic acid in acetate buffers

机译:pH对乙酸盐缓冲液中天冬氨酸的悬挂式汞滴电极循环伏安法的影响

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As the supporting electrolyte (acetate buffer) itself interacts with mercury, the Hg-acetate current is always superimposed on the Hg-amino acid interaction current. Hence whether ammo acid is present or not there will be the current of Hg-acetate leading to intercept on the current axis of the I_p vs [aspartic acid] plot. There are three processes deduced from Hg-amino acid solution interaction. They are process A, B and G. Process A is due to mercuric mercury complex formation, Hg~o+(asp)<->Hg~(2+) (asp) and process b is due to mercurous mercury complex formation, Hg~o+(asp)<->Hg~(2+) (asp). Process C is the result of mercury-acetate interaction. The peak potentials are shifted to less positive values with increasing pH.
机译:由于支持电解质(乙酸盐缓冲液)本身与汞相互作用,因此,汞乙酸盐电流始终叠加在汞氨基酸相互作用电流上。因此,无论是否存在氨酸,都会存在乙酸汞的电流,导致在I_p对[天冬氨酸]图的电流轴上发生拦截。由Hg-氨基酸溶液相互作用推论出三个过程。它们是过程A,B和G。过程A是由于形成汞汞配合物Hg〜o +(asp)<-> Hg〜(2+)(asp),过程b是由于形成汞汞配合物Hg〜 o +(asp)<-> Hg〜(2+)(asp)。过程C是乙酸汞与乙酸盐相互作用的结果。随着pH值的增加,峰电位移至较小的正值。

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