首页> 外文期刊>RSC Advances >Coordination matrix/signal amplifier strategy for simultaneous electrochemical determination of cadmium(II), lead(II), copper(II), and mercury(II) ions based on polyfurfural film/multi-walled carbon nanotube modified electrode
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Coordination matrix/signal amplifier strategy for simultaneous electrochemical determination of cadmium(II), lead(II), copper(II), and mercury(II) ions based on polyfurfural film/multi-walled carbon nanotube modified electrode

机译:聚糠醛膜/多壁碳纳米管修饰电极同时电化学测定镉(II),铅(II),铜(II)和汞(II)离子的配位矩阵/信号放大器策略

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In this work, we firstly propose and confirm a novel coordination matrix/signal amplifier strategy to construct a highly sensitive lead(II) electrochemical sensor. Lead(II) ions can be efficiently accumulated and deposited on the electrode surface by strong coordination bonds between the unoccupied d-orbital of lead(II) ions and conjugated π-electron backbones of polyfurfural film (coordination matrix), and then the anodic stripping current can be significantly enhanced by multi-walled carbon nanotubes (MWCNTs, signal amplifier), finally realizing the highly sensitive determination of lead(II). The polyfurfural film/MWCNT modified glassy carbon electrode (GCE) sensor provided a wide linear detection range from 0.05 to 10 μg L?1 and a low detection limit of 0.01 μg L?1 (S/N = 3) for lead(II). Compared with a classical mercury film sensor (a classical and effective method for determining heavy metal ions), our proposed sensor was more sensitive and achieved better results. Moreover, based on the coordination matrix/signal amplifier strategy, the polyfurfural film/MWCNTs/GCE sensor was further successfully utilized for the simultaneous determination of Cd2+, Pb2+, Cu2+, and Hg2+, demonstrating a wide linear detection range for Cd2+ (0.5–15 μg L?1), Pb2+ (0.1–15 μg L?1), Cu2+ (0.1–12 μg L?1), and Hg2+ (1.5–12 μg L?1) and a low detection limit for Cd2+ (0.03 μg L?1, S/N = 3), Pb2+ (0.01 μg L?1, S/N = 3), Cu2+ (0.06 μg L?1, S/N = 3), and Hg2+ (0.1 μg L?1, S/N = 3). Finally, the proposed sensor was successfully applied to simultaneously determine Cd2+, Pb2+, Cu2+, and Hg2+ in real tap water samples. This work provides a novel and effective analytical strategy for constructing novel electrochemical sensors and shows broad application prospects in heavy metal ion determination for the future.
机译:在这项工作中,我们首先提出并确认一种新颖的配位矩阵/信号放大器策略,以构建高灵敏度的铅( II )电化学传感器。铅( II )离子的未占据d轨道与共轭π电子之间的强配位键可有效地将铅( II )离子累积并沉积在电极表面上多壁碳纳米管(配位矩阵)的骨架,然后通过多壁碳纳米管(MWCNT,信号放大器)显着增强阳极剥离电流,最终实现了对铅( II )的高灵敏度测定。聚糠醛膜/ MWCNT修饰的玻碳电极(GCE)传感器提供从0.05到10μgL ?1 的宽线性检测范围和低至0.01μgL的检测限铅( II )的 ?1 (S / N = 3)。与传统的汞膜传感器(一种用于测定重金属离子的经典有效方法)相比,我们提出的传感器更加灵敏并获得了更好的结果。此外,基于配位矩阵/信号放大器策略,将糠醛薄膜/ MWCNTs / GCE传感器进一步成功地用于同时测定Cd 2 + ,Pb 2 + ,Cu 2 + 和Hg 2 + ,证明了Cd 2 + (0.5–15μgL ?1 )的宽线性检测范围, Pb 2 + (0.1–15μgL ?1 ),Cu 2+ (0.1–12μgL ?1 )和Hg 2 + (1.5–12μgL ?1 )和Cd 2 + 的低检测限(0.03μgL ?1 ,S / N = 3),Pb 2 + (0.01μgL ?1 ,S / N = 3),Cu 2 + (0.06μgL ?1 ,S / N = 3)和Hg 2 + (0.1μgL ?1 ,S / N = 3)。最后,该传感器成功应用于同时测定Cd 2 + ,Pb 2 + ,Cu 2 + 和Hg 2 + 。这项工作为构建新型电化学传感器提供了一种新颖而有效的分析策略,并为将来在重金属离子测定中显示了广阔的应用前景。

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