首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >3 in two imidazolium chloride ionic liquids, the 1-butyl-3-methylimidazolium (C 4mimCl) and the 1-ethyl-3-methylimidazolium (C 2mimCl), on a glassy carbon electrode]]>
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3 in two imidazolium chloride ionic liquids, the 1-butyl-3-methylimidazolium (C 4mimCl) and the 1-ethyl-3-methylimidazolium (C 2mimCl), on a glassy carbon electrode]]>

机译:<![CDATA [EUCL的阴极行为的比较研究 3 在两个咪唑氯离子液体中,1-丁基-3-甲基咪唑鎓(C 4 MIMCL)和1-乙基-3-甲基咪唑鎓(C 2 MIMCL), 玻碳电极]]>

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AbstractThis work presents a comparative study of the electrochemical behaviour, on a glassy carbon electrode, of dissolved EuCl3in two chlorobasic ionic liquids, the 1-ethyl-3-methylimidazolium chloride, C2mimCl, and the 1-buthyl-3-methylimidazolium chloride, C4mimCl, over the temperature ranges 363–398K and 343–363K respectively. In both media, the electro-reduction of EuCl63?takes place via only one electrochemical step EuCl63?/EuCl64?. The electrochemical system EuCl64?/Eu(0) has not been observed within the electrochemical window of both ILs, due to the prior reduction of the respective imidazolium cation from the solvents, which inhibits the electro-extraction of Eu(0) from the media on the GC electrode.The paper describes how several electrochemical techniques (e.g. cyclic voltammetry (CV), convolutive potential sweep voltammetry (CPSV), steady state voltammetry (SSV), chronopotentiometry (CP) and chronoamperometry (CA)) have been used experimentally: i) verifying assumptions used in their theoretical analysis, and ii) ensuring reproducible conditions at the electrode/electrolyte interface, with the aim to obtain high-precision measurements of the diffusion coefficient of EuCl63?. In order to know if there are discrepancies between the obtained data, a two
机译:<![cdata [ 抽象 这项工作提出了溶解的EUCL的玻碳电极上的电化学行为的比较研究 3> 3 在两种氯化氯离子液体中,1-乙基-3-甲基咪唑氯化物,C 2 MIMCL,和1-丁基-3-甲基咪唑氯化物,C 4 MIMCL,分别在363-398K和343-363K上。在两个媒体中,EUCL 6 3?通过仅进行一次电化学步骤EUCL 6 3? / EUCL 6 4?。电化学系统EUCL 6 4? / EU(0)尚未观察到ILS的电化学窗口,由于从溶剂的各自的咪唑阳离子的预先降低,这抑制了GC电极上的培养基的EU(0)的电萃取。 纸张描述了几种电化学技术(例如循环伏安法(CV),卷曲电位扫描伏安法(CPSV),稳态伏安法(SSV),计时透术(CP)和计时荧光测量法(CA))已通过实验使用:i)验证其理论分析中使用的假设,II)确保在电极/电解质界面处的可重复条件,目的是获得EUCL 6 3?。为了了解所获得的数据之间存在差异,一两个

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