Department of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Yokohama 223-8522, Japan.
Talanta. 2013 Jan 15;103:33-7. doi: 10.1016/j.talanta.2012.10.002. Epub 2012 Oct 23.
Individual and simultaneous electrochemical detection of iodide and iodine has been performed via cyclic voltammetry on boron doped diamond (BDD) electrodes in a 1M NaClO(4) (pH 8) solution, representative of typical environmental water conditions. It is feasible to compute accurate calibration curve for both compounds using cyclic voltammetry measurements by determining the peak current intensities as a function of the concentration. A lower detection limit of about 20 μM was obtained for iodide and 10 μM for iodine. Based on the comparison between the peak current intensities reported during the oxidation of KI, it is probable that iodide (I(-)) is first oxidized in a single step to yield iodine (I(2)). The latter is further oxidized to obtain IO(3)(-). This technique, however, did not allow for a reasonably accurate detection of iodate (IO(3)(-)) on a BDD electrode.
通过在 1M NaClO(4) (pH 8)溶液中的循环伏安法,在掺硼金刚石 (BDD)电极上实现了碘离子和碘的单独和同时电化学检测,该溶液代表了典型的环境水样条件。通过确定峰电流强度作为浓度的函数,可以使用循环伏安法测量来计算两种化合物的准确校准曲线。碘离子的检测下限约为 20 μM,碘的检测下限为 10 μM。基于在 KI 氧化过程中报告的峰电流强度的比较,可以认为碘离子 (I(-))首先被单步氧化生成碘 (I(2))。后者进一步被氧化以获得 IO(3)(-)。然而,该技术在 BDD 电极上无法对碘酸盐 (IO(3)(-))进行合理准确的检测。