<p>One of the primary causes of water contamination is heavy metal ions, some of which have been found to have carcinogenic characteristics. Such contamination poses a serious threat to aquatic ecosystems and represents a significant risk to human health. Due to its great sensitivity and efficacy, electrochemical detection is beneficial in light of the growing need for heavy metal detection. Schiff base functionalised magnetic nanoparticles Fe<sub>3</sub>O<sub>4</sub>/SiO<sub>2</sub>/SB were synthesized and applied for the detection of heavy metal ions in water, including Pb<sup>2+</sup>, Hg<sup>2+</sup> and Cd<sup>2+</sup>. Fe<sub>3</sub>O<sub>4</sub>/SiO<sub>2</sub>/SB formation was verified by FT-IR, FESEM, TEM, EDS, TGA, XPS, BET and VSM. Square wave anodic stripping voltammetry (SWASV) was used to determine the analyte cations. The effects of experimental variables on the performance of the modified magnetic electrode were investigated and optimised. The sensor was effectively used to detect Pb<sup>2+</sup>, Hg<sup>2+</sup> and Cd<sup>2+</sup> in the presence of various potentially interfering ions. The detection limits were found to be 0.09&#xa0;µg L<sup>− 1</sup> for Pb<sup>2+</sup>, 0.014&#xa0;µg L<sup>− 1</sup> for Hg<sup>2+</sup> and 0.08&#xa0;µg L<sup>− 1</sup> for Cd<sup>2+</sup> with sensitivities of 1.42, 3.12 and 1.50 µA/µgL<sup>− 1</sup> respectively, when the electrochemical sensor was employed to determine the presence of heavy metal ions in water samples. DFT calculation showed that the detection of Pb<sup>2+</sup>, Hg<sup>2+</sup> and Cd<sup>2+</sup> is dominated by the interaction between the N atom and the metal ion. During complexation, charge is transferred from the Schiff base ligand to Pb<sup>2+</sup>, Hg<sup>2+</sup> and Cd<sup>2+</sup>. Under the optimized SWASV conditions, the Fe<sub>3</sub>O<sub>4</sub>/SiO<sub>2</sub>/SB sensor exhibits a linear response for all three ions in the range 0.2–20 µgL<sup>− 1</sup> and gives recoveries of 96.8–99.6% in spiked tap and river water samples.</p> Graphical abstract <p></p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Modified Fe3O4 nanoparticles for electrochemical sensing of heavy metal ions Hg2+, Pb2+ and Cd2+ in water

  • Megha,
  • Anushka,
  • Giovanni Bella,
  • Alessandro Sinopoli,
  • Diksha,
  • Manish Kumar,
  • Veeranna Yempally,
  • Harminder Kaur

摘要

One of the primary causes of water contamination is heavy metal ions, some of which have been found to have carcinogenic characteristics. Such contamination poses a serious threat to aquatic ecosystems and represents a significant risk to human health. Due to its great sensitivity and efficacy, electrochemical detection is beneficial in light of the growing need for heavy metal detection. Schiff base functionalised magnetic nanoparticles Fe3O4/SiO2/SB were synthesized and applied for the detection of heavy metal ions in water, including Pb2+, Hg2+ and Cd2+. Fe3O4/SiO2/SB formation was verified by FT-IR, FESEM, TEM, EDS, TGA, XPS, BET and VSM. Square wave anodic stripping voltammetry (SWASV) was used to determine the analyte cations. The effects of experimental variables on the performance of the modified magnetic electrode were investigated and optimised. The sensor was effectively used to detect Pb2+, Hg2+ and Cd2+ in the presence of various potentially interfering ions. The detection limits were found to be 0.09 µg L− 1 for Pb2+, 0.014 µg L− 1 for Hg2+ and 0.08 µg L− 1 for Cd2+ with sensitivities of 1.42, 3.12 and 1.50 µA/µgL− 1 respectively, when the electrochemical sensor was employed to determine the presence of heavy metal ions in water samples. DFT calculation showed that the detection of Pb2+, Hg2+ and Cd2+ is dominated by the interaction between the N atom and the metal ion. During complexation, charge is transferred from the Schiff base ligand to Pb2+, Hg2+ and Cd2+. Under the optimized SWASV conditions, the Fe3O4/SiO2/SB sensor exhibits a linear response for all three ions in the range 0.2–20 µgL− 1 and gives recoveries of 96.8–99.6% in spiked tap and river water samples.

Graphical abstract