水中铅、镉含量同时测定的方法学研究:基于还原氧化石墨烯-电沉积汞膜修饰玻碳电极

Methodological study on simultaneous determination of lead and cadmium in water by reduced graphene oxide-electrodeposition mercury film modified glassy carbon electrode

  • 摘要:
    背景 铅、镉等重金属对水的污染日益受到重视。加强对水中重金属的监测和预警是我国环境监测的重要内容,因此有必要建立灵敏、快速的检测方法。
    目的 利用还原氧化石墨烯(rGO)-电沉积汞膜修饰玻碳电极(GCE),建立同时检测水中Pb2+和Cd2+质量浓度的新方法。
    方法 采用线性循环伏安法将氧化石墨烯还原到GCE表面,得到rGO修饰的GCE(rGO/GCE)。然后将rGO/GCE置于10 mg·L-1的Hg2+溶液中,采用电化学沉积法,将Hg2+沉积到rGO/GCE表面,得到rGO-电沉积汞膜修饰的GCE(rGO-Hg/GCE)。采用电化学沉积和差分脉冲伏安相结合的方法同时检测水中Pb2+和Cd2+。优化实验的沉积电位、沉积时间、缓冲液pH。在最佳实验条件下测定Pb2+和Cd2+的线性范围和检出限。评价方法的准确度和精密度,同时进行共存离子干扰试验。将所建立的方法用于水样中铅和镉的同时检测。
    结果 沉积电位为-1.2V、沉积时间为360s、缓冲液pH为4.5时,Pb2+和Cd2+的响应电流最佳。Pb2+质量浓度在1.0~50.0 μg·L-1的范围内,与峰电流呈线性关系,相关系数r=0.997,方法检出限为0.73 μg·L-1,加标回收率为95.8%~105.6%,相对标准偏差为1.98%~5.01%;Cd2+质量浓度在1.0~50.0 μg·L-1范围内,与峰电流呈线性关系,相关系数r=0.998,方法检出限为0.99 μg·L-1,加标回收率为90.9%~100.7%,相对标准偏差为3.33%~5.71%。水中其他常见阳离子对Pb2+和Cd2+溶出峰的峰形和电流值没有干扰。对实际废水样品进行分析,并将检测结果与石墨炉原子吸收分光光度法所测结果进行配对t检验,两种方法测定结果的差异无统计学意义(P>0.05)。
    结论 rGO-Hg/GCE法操作简便,灵敏度高,可用于水样中Pb2+和Cd2+的同时测定。

     

    Abstract:
    Background The pollution of heavy metals such as lead and cadmium in water is receiving increasing attention. Strengthened monitoring and early warning of heavy metals in water is an important part of environmental monitoring in China, so it is necessary to establish a sensitive and rapid detection method.
    Objective This study is conducted to establish a new method for simultaneous determination of Pb2+ and Cd2+ concentrations in water using reduced graphene oxide (rGO)-electrodeposition mercury film modified glassy carbon electrodes (GCE).
    Methods Linear cyclic voltammetry was used to reduce graphene oxide on the surface of glassy carbon electrode (GCE) to obtain rGO modified glassy carbon electrode (rGO/GCE). Then rGO/GCE was placed in a 10 mg·L-1 Hg2+ solution, and Hg2+ was deposited on the surface of rGO/GCE by electrochemical deposition method to obtain rGO-electrodeposition mercury film modified glassy carbon electrode (rGO-Hg/GCE). Pb2+ and Cd2+ were detected by a method combining electrochemical deposition and differential pulse voltammetry. The deposition potential, deposition time, and buffer pH of the proposed method were optimized. The linear range and detection limit of Pb2+ and Cd2+ were determined under the optimal experimental conditions. The accuracy and precision of the method were evaluated, and coexisting ion interference was tested at the same time. The method was applied to the simultaneous detection of lead and cadmium in water samples.
    Results When the deposition potential was -1.2 V, the deposition time was 360 s, and the buffer pH was 4.5, the response currents of Pb2+ and Cd2+ were optimal. The Pb2+ concentration within the range of 1.0-50.0 μg·L-1 showed a good linear relationship with the peak current, the correlation coefficient was 0.997, the detection limit was 0.73 μg·L-1, the standard recovery was 95.8%-105.6%, and the relative standard deviation was 1.98%-5.01%; the Cd2+ concentration within the range of 1.0-50.0 μg·L-1 showed a good linear relationship with the peak current, the correlation coefficient was 0.998, the detection limit was 0.99 μg·L-1, the standard recovery was 90.9%-100.7%, and the relative standard deviation was 3.33%-5.71%. Other common cations in water did not interfere with the peak shape and current value of the Pb2+ and Cd2+ dissolution peaks. In actual waste water samples, the test results by the established method were compared with those by graphite furnace atomic absorption spectrophotometry by paired t test, and there was no significant difference in the results by the two methods (P>0.05).
    Conclusion rGO-Hg/GCE has the advantages of simple operation and high sensitivity, and is suitable for simultaneous determination of Pb2+ and Cd2+ in water samples.

     

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