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石墨烯-离子液体修饰玻碳电极同时测定矿石中铅和镉
引用本文:李燕红,陈宗保,董洪霞. 石墨烯-离子液体修饰玻碳电极同时测定矿石中铅和镉[J]. 冶金分析, 2017, 32(2): 25-29. DOI: 10.13228/j.boyuan.issn1000-7571.009953
作者姓名:李燕红  陈宗保  董洪霞
作者单位:上饶师范学院,江西省高等学校应用有机化学重点实验室,江西上饶 334001
基金项目:国家自然基金项目(21465020);江西省教育厅科技项目(151057)
摘    要:将石墨烯(GR)滴涂在玻碳电极(GCE)上制备GR/GCE电极,采用循环伏安法将离子液体(1-辛基-3-甲基咪唑六氟磷酸盐)聚合在GR/GCE电极表面,制得新型OMIMPF_6/GR/GCE修饰电极。以0.1mol/L HAc-NaAc缓冲溶液(pH 4.5)为支持电解液,利用差分脉冲法研究了Pb~(2+)和Cd~(2+)在OMIMPF_6/GR/GCE电极上的电化学行为。结果表明,Pb~(2+)和Cd~(2+)在修饰电极上有较好的电化学行为,Pb~(2+)和Cd~(2+)的浓度分别在1.0×10~(-8)~4.2×10~(-5)mol/L和1.0×10~(-8)~6.0×10~(-5)mol/L范围内与峰电流呈良好的线性关系;Pb~(2+)和Cd~(2+)的检出限分别为1.0×10~(-9) mol/L和5.0×10~(-8)mol/L。实验方法用于矿石中铅和镉的测定,结果的相对标准偏差(RSD,n=6)为2.9%~4.4%;并与原子吸收光谱法对比,测定结果基本一致。

关 键 词:石墨烯-离子液体修饰玻碳电极  差分脉冲伏安法      矿石  
收稿时间:2016-05-30

Simultaneous determination of lead and cadmium in ores by graphene-ionic liquid modified glassy carbon electrode
LI Yan-hong,CHEN Zong-bao,DONG Hong-xia. Simultaneous determination of lead and cadmium in ores by graphene-ionic liquid modified glassy carbon electrode[J]. Metallurgical Analysis, 2017, 32(2): 25-29. DOI: 10.13228/j.boyuan.issn1000-7571.009953
Authors:LI Yan-hong  CHEN Zong-bao  DONG Hong-xia
Affiliation:Key Laboratory of Applied Organic Chemistry,Higher Institutions of Jiangxi Province, Shangrao Normal University, Shangrao 334001,China
Abstract:The graphene (GR) dispersion was coated onto glass carbon electrode (GCE) to prepare GR/GCE electrode. The ionic liquid (1-octyl-3-methylimidazolium hexafluorophosphate, OMIMPF6) was polymerized on the surface of GR/GCE electrode by cyclic voltammetry to prepare the novel OMIMPF6/GR/GCE modified electrode. The electrochemical behaviors of Pb2+ and Cd2+ on OMIMPF6/GR/GCE electrode were studied by differential pulse voltammetry using 0.1 mol/L HAc-NaAc buffer solution (pH 4.5) as supporting electrolyte. The results showed that Pb2+ and Cd2+ had good electrochemical behaviors on the modified electrode. The concentration of Pb2+ and Cd2+ in range of 1.0×10-8-4.2×10-5 mol/L and 1.0×10-8-6.0×10-5 mol/L showed good linear relationship to the peak currents. The detection limit was 1.0×10-9 mol/L and 5.0×10-8 mol/L, respectively. The proposed method was applied to the determination of cadmium and lead in ore samples. The relative standard deviation (RSD,n=6) of determination results were between 2.9% and 4.4%. The found results were consistent with those obtained by atomic absorption spectrometry (AAS).
Keywords:OMIMPF6/GR/GCE modified electrode  differential pulse voltammetry  lead  cadmium  ore  
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