首页> 外文期刊>Central European Journal of Chemistry >Interfacial transfer of Cd~(2+) assisted by 4'- morpholino-acetophenone-4-phenyl-3- thiosemicarbazone across the water/1,2- dichloroethane interface
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Interfacial transfer of Cd~(2+) assisted by 4'- morpholino-acetophenone-4-phenyl-3- thiosemicarbazone across the water/1,2- dichloroethane interface

机译:4'-吗啉代-苯乙酮-4-苯基-3-硫代半脲协助水/ 1,2-二氯乙烷界面的Cd〜(2+)界面转移

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摘要

The assisted transfer of heavy metal ions by interfacial complexation with 4'-morpholinoacetophenone-4-phenyl-3-thiosemicarbazone (MAPPT) at the interface between two immiscible electrolyte solutions (ITIES) was studied by cyclic voltammetry. The voltammograms obtained across the water/1,2-dichloroethane interface using the MAPPT ligand in the organic phase shows that the assisted metal ion transfers have different nature for different ions. The quasi-reversible voltammetric peak of the Cd~(2+) ion was obtained and is discussed in detail. The dependence of the half-wave transfer potential on MAPPT concentration showed that the equilibrium is effectively displaced towards a 1:3 (metal:ligand) stoichiometry with an association constant of logβ~0 =15.46 (±0.11) for the Cd~(2+) ion, corresponding to the TIC/TID mechanism.
机译:通过循环伏安法研究了在两种不混溶的电解质溶液(ITIES)之间的界面上与4'-吗啉代乙酰苯-4-苯基-3-硫代半脲(MAPPT)的界面络合辅助重金属离子的转移。在有机相中使用MAPPT配体在水/ 1,2-二氯乙烷界面上获得的伏安图表明,辅助金属离子转移对于不同离子具有不同的性质。得到了Cd〜(2+)离子的准可逆伏安峰,并进行了详细讨论。半波传输电势对MAPPT浓度的依赖性表明,Cd〜(2)的平衡有效地朝着化学计量比为1:3(金属:配体)移动,缔合常数为logβ〜0 = 15.46(±0.11)。 +)离子,对应于TIC / TID机制。

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