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作 者:刘拥军[1] 王光灿[1] 师真[1] 易汉希[1] 何雯瑾[2] 彭芳芝[1]
机构地区:[1]云南大学现代分析测试中心,昆明650091 [2]昆明物理所,昆明650223
出 处:《理化检验(化学分册)》2012年第9期1058-1062,共5页Physical Testing and Chemical Analysis(Part B:Chemical Analysis)
基 金:国家自然科学基金资助项目(20763009);云南省教育厅科学研究基金资助项目(09Y039)
摘 要:将单壁碳纳米管(SWCNTs)悬浊液和纳米金(nano Au)溶液混匀后滴涂在玻碳电极表面,自然干燥后再将离子液体BMIMPF6的甲醇溶液滴涂在上述电极上,制得单壁碳纳米管-纳米金-离子液体修饰玻碳电极(SWCNTs-nano Au-BMIMPF6/GCE)。用循环伏安方法研究了辛硫磷在pH 4.0的磷酸盐支持电解质中,在电位-1.1~-0.1V(vs.SCE)范围内,在修饰电极上的电化学行为。结果表明:在电位-0.81V处可见明显的还原峰,且其峰电流与辛硫磷的浓度在6.0×10-7~1.2×10-3 mmol.L-1范围内呈线性关系,检出限(3S/N)为3.0×10-7 mmol.L-1。据此提出了用线性伏安法测定辛硫磷的方法,用标准加入法测得其回收率在96.0%~105.5%之间,测定值的相对标准偏差(n=6)在3.3%~3.9%之间。A mixture of dispersion of SWCNTs and nano Au solution was added dropwise onto the surface of glassy carbon electrode (GCE), after air-drying, methanol solution of ionic liquid, BMIMPF6 was added dropwise onto the surface of the above electrode. The modified electrode, designated as SWCNTs-nano Au-BMIMPF6/GCE was thus prepared. Electrochemical behavior of phoxim at the modified electrode was studied by cyclic voltammetry in a phosphate buffer supporting electrolyte of pH 4. 0 in the potential range of --1.1 to --0. 1 V (vs. SCE). As shown by the experimental results, a significant reduction peak was observed at --0. 81 V, and linear relationship between values of reduction peak current and concentration of phoxim was kept in the range of 6.0×10-7 to 1.2×10-3mmol·L-1 , with detection limit (3S/N) of 3. 0×10-7 mmol ·L-1. Based on these findings, a method for determination of phoxim by linear voltammetry was proposed. Recovery was tested by standard addition method, giving values of recovery and RSD's (n=6) in the ranges of 96.0%--105.5% and 3.3%--3.9% respectively.
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