Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection

Heavy metal pollution is one of the global issues as the presence of excessive heavy metal in environment threaten both aquatic life and human beings. A selective and fast response sensor with a rapid detection method is urgent needed for the detection of heavy metal ions. Hence, this study used a t...

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Main Author: Chong, Jin Mei
Format: Thesis
Language:English
Published: 2021
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Online Access:http://psasir.upm.edu.my/id/eprint/104287/1/CHONG%20JIN%20MEI%20-%20IR.pdf
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spelling my-upm-ir.1042872023-07-25T02:21:46Z Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection 2021-10 Chong, Jin Mei Heavy metal pollution is one of the global issues as the presence of excessive heavy metal in environment threaten both aquatic life and human beings. A selective and fast response sensor with a rapid detection method is urgent needed for the detection of heavy metal ions. Hence, this study used a thiolated calix[4]arene modified on gold nanoparticles and a screen-printed carbon electrode (TC4/AuNPs/SPCE) for Pb2+and Cu2+ determination. The modified electrodes were characterised via Fourier-transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The modified of thiolated calixarene/gold nanoparticle composite on screen-printed electrode was found enhancing the current response in Pb2+ and Cu2+ determination. Differential pulse anodic stripping voltammetry (DPASV) was used for the detection of Pb2+ and Cu2+ under optimum conditions. The limit of detection (LOD) for detecting Pb2+ and Cu2+ was 0.7982 × 10−2 ppm and 1.3358 × 10−2 ppm, respectively. Except for Zn2+ and Hg2+, the presence of competitive ions caused little effect on the current response when detecting Pb2+. However, all competitive ions caused a significant drop in the current response when detecting Cu2+, except Ca2+ and Mg2+, suggesting the sensing platform is more selective toward Pb2+ rather than Cu2+. The electrochemical sensor demonstrated good reproducibility and excellent repeatability with a low relative standard deviation (RSD) value in detecting Pb2+ and Cu2+. Most importantly, the result obtained in the analysis of Pb2+ and Cu2+ had a good recovery in river water, demonstrating the applicability of the developed sensor for real samples. Electrochemical sensors Calixarenes Nanoparticles 2021-10 Thesis http://psasir.upm.edu.my/id/eprint/104287/ http://psasir.upm.edu.my/id/eprint/104287/1/CHONG%20JIN%20MEI%20-%20IR.pdf text en public masters Universiti Putra Malaysia Electrochemical sensors Calixarenes Nanoparticles Alang Ahmad, Shahrul Ainliah
institution Universiti Putra Malaysia
collection PSAS Institutional Repository
language English
advisor Alang Ahmad, Shahrul Ainliah
topic Electrochemical sensors
Calixarenes
Nanoparticles
spellingShingle Electrochemical sensors
Calixarenes
Nanoparticles
Chong, Jin Mei
Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection
description Heavy metal pollution is one of the global issues as the presence of excessive heavy metal in environment threaten both aquatic life and human beings. A selective and fast response sensor with a rapid detection method is urgent needed for the detection of heavy metal ions. Hence, this study used a thiolated calix[4]arene modified on gold nanoparticles and a screen-printed carbon electrode (TC4/AuNPs/SPCE) for Pb2+and Cu2+ determination. The modified electrodes were characterised via Fourier-transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The modified of thiolated calixarene/gold nanoparticle composite on screen-printed electrode was found enhancing the current response in Pb2+ and Cu2+ determination. Differential pulse anodic stripping voltammetry (DPASV) was used for the detection of Pb2+ and Cu2+ under optimum conditions. The limit of detection (LOD) for detecting Pb2+ and Cu2+ was 0.7982 × 10−2 ppm and 1.3358 × 10−2 ppm, respectively. Except for Zn2+ and Hg2+, the presence of competitive ions caused little effect on the current response when detecting Pb2+. However, all competitive ions caused a significant drop in the current response when detecting Cu2+, except Ca2+ and Mg2+, suggesting the sensing platform is more selective toward Pb2+ rather than Cu2+. The electrochemical sensor demonstrated good reproducibility and excellent repeatability with a low relative standard deviation (RSD) value in detecting Pb2+ and Cu2+. Most importantly, the result obtained in the analysis of Pb2+ and Cu2+ had a good recovery in river water, demonstrating the applicability of the developed sensor for real samples.
format Thesis
qualification_level Master's degree
author Chong, Jin Mei
author_facet Chong, Jin Mei
author_sort Chong, Jin Mei
title Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection
title_short Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection
title_full Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection
title_fullStr Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection
title_full_unstemmed Development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection
title_sort development of electrochemical sensor based on thiolated calixarene/gold nanoparticle composite for lead and copper ions detection
granting_institution Universiti Putra Malaysia
publishDate 2021
url http://psasir.upm.edu.my/id/eprint/104287/1/CHONG%20JIN%20MEI%20-%20IR.pdf
_version_ 1776100427441373184