摘要
基于I-能与Ag+生成难溶化合物特性,在银微盘电极上研究了I-的示差脉冲溶出伏安法(DPSV)。该法不需镀汞,不要搅拌,可在较稀的支持电解质溶液中实施。于0.08 mol/L HAc-NaAc及 0.01 mol/L EDTA介质中,能检出 1.00×10-8mol/L的I,I-的浓度为5.00 × 10-8~1.20×10-6mol/L范围与峰电流有良好的线性关系。该法用于自来水中I-的测定,相对偏差为4.3%;标准加入回收率为94%,用于加碘食盐中I-的测定,与标准分析法比较,相对误差为-4.0%。
I- may combine with Ag+ to form insoluble AgI. On this basis the cathodic strip- ping voltammetry(CSV) of iodine at silver microdisk electrode was investigated. CSV for the determination of I- was carried out in very diluted media under no stirring. The optimal ex- perimental conditions were discussed. The detection limit is about 1 × 10-8 mol/L I- with differential pulse cathodic stripping voltammetry (DPSV). A good proportionality between the peak current of DPSV and iodide concentration in the range of 5. 0 × 10-8 - 1. 2 × 10-6 mol/L has been observed. This method was successfully applied to the direct determination of trace iodine in tap water and iodized edible salt. For tap water a mean value of 1. 46 × 10-7 mol/L I- was found, while for iodized edible salt the value was 28. 7 μg/g I-. The relative standard deviation for iodine is 4. 3% and 4. 0% respectively.
出处
《分析化学》
SCIE
EI
CAS
CSCD
北大核心
1997年第1期59-62,共4页
Chinese Journal of Analytical Chemistry
关键词
银微盘电极
溶出伏安法
DPSV
碘离子
Silver micro-disk electrode, differential pulse stripping voltammetry, iodide, tap water, added iodine salt