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作 者:舒绪刚[1] 吴春丽[1] 陈凤[1] 周萌[1] 李翠金[1] 邱桂雄 吴信[3] 印遇龙[3]
机构地区:[1]仲恺农业工程学院化学化工学院,广州510225 [2]广州天科生物科技有限公司,广州510689 [3]中国科学院亚热带农业生态研究所,长沙410125
出 处:《分析试验室》2015年第9期1058-1061,共4页Chinese Journal of Analysis Laboratory
基 金:广东省科技计划项目(2014A020208131;2013B090900;2013B070704081)资助
摘 要:采用半胱胺锌(C2H7NS)3·Zn SO4·Zn Cl2修饰玻碳电极,以差分脉冲伏安法(DPV)在0.1 mol/L的KCl溶液中对游离Cu2+进行了测定。游离Cu2+浓度与氧化峰电流值在0.01~0.5 mmol/L范围内呈良好线性关系,线性回归方程为I=-0.1005c-1.6×10-5,相关系数为R2=98.63,检出限(S/N=3)为0.1μmol/L。通过加标实验验证修饰电极对Cu2+含量测定,回收率为95.1%~102.6%,RSD(n=5)在3%以内。考察了干扰金属离子(M g2+,Mn2+,Zn2+)对电极检测Cu2+无影响,制备的修饰电极对赖氨酸铜螯合物不响应,直接测定赖氨酸铜螯合物螯合率为91.78%和91.93%。In this study, an electrochemical sensor composed of (C2H7Ns)3 - ZnSO4 · ZnC12 -modified glass carbon electrode was constructed for the determination of copper (Ⅱ) ions with differential pulse voltammetry (DPV) in 0. 1 mol/L KC1 solutions. The proposed electrochemical sensor had a good response towards Cu2+ , and the oxidation peak current exhibited linear relationship with the CuE+ concentration between O. 01 mmol/L and 0.5 mmol/L. The corresponding linear equation was I = - 0. 1005c - 1. 6 × 10-5, with the correlation coefficient of O. 9863 and the detection limit (S/N = 3) of 0. 1 μmol/L. The standard addition test showed that the recoveries were at the range of 95.1% to 102.6% , with the RSD (n = 5) of less than 3 %. Additionally, some common metal ions (Mg2+ , Mn2+ , Zn2+ ) had no interference on the determination of Cu2+ , and the chelating rates of lysine-copper (Ⅱ) were calculated to be 91.78 % and 91.93 % respectively for the two samples.
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