4.6 Article

Arsenic(III) detection using electrochemical-chemical-chemical redox cycling at bare indium-tin oxide electrodes

期刊

ANALYST
卷 139, 期 22, 页码 5813-5817

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c4an01174k

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资金

  1. National Research Foundation of Korea [2010-0020780, 2012R1A2A2A06045327, 2012-M3C1A1-048860]
  2. National Research Foundation of Korea [2010-0020780, 2012R1A2A2A06045327] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Sensitive As(III) detection in ground water is of great importance for evaluating the quality of drinking water. We report a sensitive electrochemical method for As(III) detection based on electrochemical-chemical-chemical (ECC) redox cycling involving Ru(IV) [an oxidized species of Ru-III(NH3)(5)NH22+], As(III), and tris(3-carboxyethyl)phosphine (TCEP). Electrochemical oxidation of Ru-III(NH3)(5)NH22+ formed from Ru-III(NH3)(6)(3+) generates Ru(IV), which quickly oxidizes As(III). This electro-mediated oxidation of As(III) produces As(V), which is reduced back to As(III) by TCEP. Electrochemically generated Ru(IV) then reoxidizes As(III), allowing ECC redox cycling to occur at a high rate on bare indium-tin oxide (ITO) electrodes without modifying the surfaces with electrocatalytic materials. Because most interfering metal ions precipitate in a carbonate buffer, water samples are mixed with carbonate buffers prior to electrochemical measurements, rendering the effects of Cu+ Cu2+, Fe2+, Fe3+, and Pb2+ insignificant. The detection limit calculated by ECC redox cycling using a chronocoulogram is 1.2 mu M, much lower than that obtained using only the electro-mediated oxidation of As(III) (90 mu M).

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