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首页> 外文期刊>International Journal of Analytical and Bioanalytical Chemistry >Differential pulse anodic stripping voltammetric determination of Ni(II) and Co(II) in water and vegetable samples using analytical reagent 2,2’-{benzene-1,2-diylbis (nitrilomethylylidene]} diphenol
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Differential pulse anodic stripping voltammetric determination of Ni(II) and Co(II) in water and vegetable samples using analytical reagent 2,2’-{benzene-1,2-diylbis (nitrilomethylylidene]} diphenol

机译:使用分析试剂2,2’-{苯-1,2-二基双(亚硝基甲基亚甲基)}二酚的微分脉冲阳极溶出伏安法测定水和蔬菜样品中的Ni(II)和Co(II)

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A highly selective, fairly rapid and economical method for the determination of Ni(II) and Co(II) by differential pulse anodic stripping voltammetric method was developed using 2,2'-{benzene-1,2-diylbis (nitrilomethylylidene]}diphenol as a complexing reagent onto hanging mercury drop electrode(HMDE). The optimum experimental conditions were found to be 2,2'-{benzene-1,2-diylbis(nitrilomethylylidene]}diphenol concentration of 3.0mM, NH4OH-NH4Cl buffer (pH-9.0), scan rate of 12mV/sec, accumulation potential of -300.0 mV versus Ag/AgCl, accumulation time of 110sec, and pulse amplitude of 50mV. The peak currents of Ni(II) and Co(II) were directly proportional to the initial metal concentration in the ranges of 0.01-90|ìg/mL under the optimized conditions. A relative standard deviation of 0.52%(n=5) was obtained, and the limit of detection was found to be 0.0042 and 0.0026 |ìg/mlfor Ni(II) and Co(II) respectively. The method was applied to the determination of Ni(II) and Co(II) ions in water and vegetable samples with satisfactory results.
机译:建立了使用2,2'-{苯-1,2-二基双(亚硝基甲基亚甲基)}二酚的微分脉冲阳极溶出伏安法测定镍(II)和钴(II)的方法作为络合剂在悬挂式汞滴电极(HMDE)上的最佳实验条件为3.0mM的2,2'-{苯-1,2-二基双(亚硝基甲基亚甲基)}二酚浓度为NH4OH-NH4Cl缓冲液(pH -9.0),扫描速度为12mV / sec,相对于Ag / AgCl的累积电势为-300.0 mV,累积时间为110sec,脉冲幅度为50mV.Ni(II)和Co(II)的峰值电流与在最佳条件下,初始金属浓度在0.01-90 |ìg/ mL范围内,相对标准偏差为0.52%(n = 5),检出限为0.0042和0.0026 |ìg/。 ml分别用于测定Ni(II)和Co(II),该方法用于测定水中的Ni(II)和Co(II)离子r和蔬菜样品,结果令人满意。

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