Direct As(V) Determination Using Screen-Printed Electrodes Modified with Silver Manoparticles

Carbon-nanofiber-based screen-printed electrodes modified with silver nanoparticles (Ag-NP-SPCNFEs) were tested in a pioneering manner for the direct determination of As(V) at low µg L–1 levels by means of differential pulse anodic stripping voltammetry. Screen-printed electrodes were modified with...

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Detalles Bibliográficos
Autores: Torres Rivero Andrade, Karina Victoria Alejandra|||0000-0002-4081-6288, Pérez Ràfols, Clara, Bastos Arrieta, Julio Alonso|||0000-0002-8939-6253, Florido Pérez, Antonio|||0000-0003-4266-7236, Martí Gregorio, Vicenç|||0000-0002-1763-0514, Serrano Plana, Núria
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/332392
Acceso en línea:https://hdl.handle.net/2117/332392
https://dx.doi.org/10.3390/nano10071280
Access Level:acceso abierto
Palabra clave:Nanoparticles
Electrochemistry
Arsenic determination
Silver nanoparticles
Anodic stripping voltammetry
Screen-printed electrodes
Water analysis
Nanopartícules
Arsenic -- AnalisI
Electroquímica
Àrees temàtiques de la UPC::Enginyeria química
Descripción
Sumario:Carbon-nanofiber-based screen-printed electrodes modified with silver nanoparticles (Ag-NP-SPCNFEs) were tested in a pioneering manner for the direct determination of As(V) at low µg L–1 levels by means of differential pulse anodic stripping voltammetry. Screen-printed electrodes were modified with two different types of Ag-NPs, nanoseeds (NS), and nanoprisms (NPr) and characterized both microscopically and electrochemically. Furthermore, after optimizing the direct voltammetric determination of As(V), the analytical performance of considered sensors was compared for the direct determination of As(V). These results suggest that Ag-NS offer a better analytical response compared to Ag-NPr, with a detection and quantification limit of 0.6 and 1.9 µg L–1, respectively. The proposed methodology was validated using a spiked tap water sample with a very high reproducibility and good agreement with inductively coupled plasma - mass spectrometry (ICP-MS) measurements