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A regenerable screen-printed voltammetric Hg(II) ion sensor based on tris-thiourea organic chelating ligand grafted graphene nanomaterial
An electrochemical Hg(II) ion sensor has been developed by using a miniaturized carbon paste screen-printed electrode (CSPE) modified with reduced graphene oxide (rGO) sheets and tris-thiourea (TTU) chelating ligand compound, i.e. N,N′,N″-((nitrilotris(ethane-2,1diyl))tris(azanediyl))tris(carbonothi...
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Published in: | Journal of electroanalytical chemistry (Lausanne, Switzerland) Switzerland), 2020-12, Vol.878, p.114670, Article 114670 |
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creator | Sapari, Suhaila Razak, Nurul Hidayah Abdul Hasbullah, Siti Aishah Heng, Lee Yook Chong, Kwok Feng Tan, Ling Ling |
description | An electrochemical Hg(II) ion sensor has been developed by using a miniaturized carbon paste screen-printed electrode (CSPE) modified with reduced graphene oxide (rGO) sheets and tris-thiourea (TTU) chelating ligand compound, i.e. N,N′,N″-((nitrilotris(ethane-2,1diyl))tris(azanediyl))tris(carbonothioyl))tribenz amide. In view of the strong cation-exchange characteristic and adsorption of aromatic TTU tridentate ligand on the graphene nanomaterial surface by non-covalent π–π stacking interaction, the differential pulse voltammetry (DPV) peak current response of the voltammetric sensor was linearly dependent on a broad Hg(II) ion concentration detection range from 0.1–00.0 mg L−1 with a limit of detection (LOD) estimated at 0.02 mg L−1 after accumulation for 10 min. The chemically modified miniaturized SPE showed high stability throughout the course of the sensor lifetime study for the detection of inorganic Hg(II) ion with a relative standard deviation (RSD) of the sensor response obtained at 1.2%. The electrochemical sensor is reusable up to three consecutive Hg(II) ion assays by using 0.05 M acetate buffer (pH 8) as the sensor regeneration solution with a reversibility RSD value of 3.9%. The voltammetric sensor based on TTU derivative element and rGO nanosheets revealed satisfactory selectivity for Hg(II) ion over a large number of potential interfering ions, e.g. Ca(II), Co(II), Cu(II), Fe(II), Ni(II), Na(I) and Zn(II), and demonstrated reliable quantitative results as compared to the results obtained with inductively coupled plasma-mass spectrometer (ICP-MS) standard method for Hg(II) ion detection in river water samples. |
doi_str_mv | 10.1016/j.jelechem.2020.114670 |
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In view of the strong cation-exchange characteristic and adsorption of aromatic TTU tridentate ligand on the graphene nanomaterial surface by non-covalent π–π stacking interaction, the differential pulse voltammetry (DPV) peak current response of the voltammetric sensor was linearly dependent on a broad Hg(II) ion concentration detection range from 0.1–00.0 mg L−1 with a limit of detection (LOD) estimated at 0.02 mg L−1 after accumulation for 10 min. The chemically modified miniaturized SPE showed high stability throughout the course of the sensor lifetime study for the detection of inorganic Hg(II) ion with a relative standard deviation (RSD) of the sensor response obtained at 1.2%. The electrochemical sensor is reusable up to three consecutive Hg(II) ion assays by using 0.05 M acetate buffer (pH 8) as the sensor regeneration solution with a reversibility RSD value of 3.9%. The voltammetric sensor based on TTU derivative element and rGO nanosheets revealed satisfactory selectivity for Hg(II) ion over a large number of potential interfering ions, e.g. Ca(II), Co(II), Cu(II), Fe(II), Ni(II), Na(I) and Zn(II), and demonstrated reliable quantitative results as compared to the results obtained with inductively coupled plasma-mass spectrometer (ICP-MS) standard method for Hg(II) ion detection in river water samples.</description><identifier>ISSN: 1572-6657</identifier><identifier>EISSN: 1873-2569</identifier><identifier>DOI: 10.1016/j.jelechem.2020.114670</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Cation exchanging ; Chelate ; Chelation ; Chemical sensors ; Copper ; Electrochemical sensor ; Ethane ; Graphene ; Hg(II) ion ; Inductively coupled plasma mass spectrometry ; Ion concentration ; Ion detectors ; Ligands ; Mercury compounds ; Nanomaterials ; Nickel ; Reduced graphene oxide ; Regeneration ; Selectivity ; Sensors ; Thioureas ; Tris-thiourea ; Voltammetry ; Water sampling</subject><ispartof>Journal of electroanalytical chemistry (Lausanne, Switzerland), 2020-12, Vol.878, p.114670, Article 114670</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. Dec 1, 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-17ab7e58e498d3f8340f0c2e75c2c168527ca5eef44a1db8812e3467895bf2a93</citedby><cites>FETCH-LOGICAL-c340t-17ab7e58e498d3f8340f0c2e75c2c168527ca5eef44a1db8812e3467895bf2a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sapari, Suhaila</creatorcontrib><creatorcontrib>Razak, Nurul Hidayah Abdul</creatorcontrib><creatorcontrib>Hasbullah, Siti Aishah</creatorcontrib><creatorcontrib>Heng, Lee Yook</creatorcontrib><creatorcontrib>Chong, Kwok Feng</creatorcontrib><creatorcontrib>Tan, Ling Ling</creatorcontrib><title>A regenerable screen-printed voltammetric Hg(II) ion sensor based on tris-thiourea organic chelating ligand grafted graphene nanomaterial</title><title>Journal of electroanalytical chemistry (Lausanne, Switzerland)</title><description>An electrochemical Hg(II) ion sensor has been developed by using a miniaturized carbon paste screen-printed electrode (CSPE) modified with reduced graphene oxide (rGO) sheets and tris-thiourea (TTU) chelating ligand compound, i.e. N,N′,N″-((nitrilotris(ethane-2,1diyl))tris(azanediyl))tris(carbonothioyl))tribenz amide. In view of the strong cation-exchange characteristic and adsorption of aromatic TTU tridentate ligand on the graphene nanomaterial surface by non-covalent π–π stacking interaction, the differential pulse voltammetry (DPV) peak current response of the voltammetric sensor was linearly dependent on a broad Hg(II) ion concentration detection range from 0.1–00.0 mg L−1 with a limit of detection (LOD) estimated at 0.02 mg L−1 after accumulation for 10 min. The chemically modified miniaturized SPE showed high stability throughout the course of the sensor lifetime study for the detection of inorganic Hg(II) ion with a relative standard deviation (RSD) of the sensor response obtained at 1.2%. The electrochemical sensor is reusable up to three consecutive Hg(II) ion assays by using 0.05 M acetate buffer (pH 8) as the sensor regeneration solution with a reversibility RSD value of 3.9%. The voltammetric sensor based on TTU derivative element and rGO nanosheets revealed satisfactory selectivity for Hg(II) ion over a large number of potential interfering ions, e.g. Ca(II), Co(II), Cu(II), Fe(II), Ni(II), Na(I) and Zn(II), and demonstrated reliable quantitative results as compared to the results obtained with inductively coupled plasma-mass spectrometer (ICP-MS) standard method for Hg(II) ion detection in river water samples.</description><subject>Cation exchanging</subject><subject>Chelate</subject><subject>Chelation</subject><subject>Chemical sensors</subject><subject>Copper</subject><subject>Electrochemical sensor</subject><subject>Ethane</subject><subject>Graphene</subject><subject>Hg(II) ion</subject><subject>Inductively coupled plasma mass spectrometry</subject><subject>Ion concentration</subject><subject>Ion detectors</subject><subject>Ligands</subject><subject>Mercury compounds</subject><subject>Nanomaterials</subject><subject>Nickel</subject><subject>Reduced graphene oxide</subject><subject>Regeneration</subject><subject>Selectivity</subject><subject>Sensors</subject><subject>Thioureas</subject><subject>Tris-thiourea</subject><subject>Voltammetry</subject><subject>Water sampling</subject><issn>1572-6657</issn><issn>1873-2569</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFUMtOwzAQjBBIlMIvIEtc4JBiOw8nN1AFtFIlLnC2HGeTOkrsYrtIfAJ_zVaFM6e1Z2dmdydJrhldMMrK-2ExwAh6C9OCU44gy0tBT5IZq0SW8qKsT_FdCJ6WZSHOk4sQBkp5VTE-S74fiYceLHjVjECC9gA23XljI7Tk041RTRNEbzRZ9bfr9R0xzpIANjhPGhWQhH_shzRujdt7UMT5XlkU4Eqjisb2ZDSItKT3qjvYYt1tcSaxyrpJRfBGjZfJWafGAFe_dZ68Pz-9LVfp5vVlvXzcpDrLaUyZUI2AooK8rtqsqxDsqOYgCs01K6uCC60KgC7PFWubw5WQYSBVXTQdV3U2T26OvjvvPvYQohxwbYsjJc9rxmkmyhxZ5ZGlvQvBQycxk0n5L8moPMQuB_kXuzzELo-xo_DhKAS84dOAl0EbsBpa40FH2Trzn8UPsgKQ1w</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Sapari, Suhaila</creator><creator>Razak, Nurul Hidayah Abdul</creator><creator>Hasbullah, Siti Aishah</creator><creator>Heng, Lee Yook</creator><creator>Chong, Kwok Feng</creator><creator>Tan, Ling Ling</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20201201</creationdate><title>A regenerable screen-printed voltammetric Hg(II) ion sensor based on tris-thiourea organic chelating ligand grafted graphene nanomaterial</title><author>Sapari, Suhaila ; 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In view of the strong cation-exchange characteristic and adsorption of aromatic TTU tridentate ligand on the graphene nanomaterial surface by non-covalent π–π stacking interaction, the differential pulse voltammetry (DPV) peak current response of the voltammetric sensor was linearly dependent on a broad Hg(II) ion concentration detection range from 0.1–00.0 mg L−1 with a limit of detection (LOD) estimated at 0.02 mg L−1 after accumulation for 10 min. The chemically modified miniaturized SPE showed high stability throughout the course of the sensor lifetime study for the detection of inorganic Hg(II) ion with a relative standard deviation (RSD) of the sensor response obtained at 1.2%. The electrochemical sensor is reusable up to three consecutive Hg(II) ion assays by using 0.05 M acetate buffer (pH 8) as the sensor regeneration solution with a reversibility RSD value of 3.9%. The voltammetric sensor based on TTU derivative element and rGO nanosheets revealed satisfactory selectivity for Hg(II) ion over a large number of potential interfering ions, e.g. Ca(II), Co(II), Cu(II), Fe(II), Ni(II), Na(I) and Zn(II), and demonstrated reliable quantitative results as compared to the results obtained with inductively coupled plasma-mass spectrometer (ICP-MS) standard method for Hg(II) ion detection in river water samples.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jelechem.2020.114670</doi></addata></record> |
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subjects | Cation exchanging Chelate Chelation Chemical sensors Copper Electrochemical sensor Ethane Graphene Hg(II) ion Inductively coupled plasma mass spectrometry Ion concentration Ion detectors Ligands Mercury compounds Nanomaterials Nickel Reduced graphene oxide Regeneration Selectivity Sensors Thioureas Tris-thiourea Voltammetry Water sampling |
title | A regenerable screen-printed voltammetric Hg(II) ion sensor based on tris-thiourea organic chelating ligand grafted graphene nanomaterial |
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