期刊
ANALYTICAL CHEMISTRY
卷 82, 期 5, 页码 1727-1732出版社
AMER CHEMICAL SOC
DOI: 10.1021/ac9022555
关键词
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资金
- Thailand Research Fund [PHD/0256/2549]
- Ratchadphiseksomphot Endowment Fund, Chulalongkorn University [PCU136.2009]
- Thailand-United States Education Foundation
A novel lab-on-paper device combining electrochemical and colorimetric detection for the rapid screening of Au(III) in the presence of it common interference, Fe(III), in industrial waste solutions is presented here. With dilute aqua regia (0.1 M HCl + 0.05 M HNO3) as the supporting electrolyte, square wave voltammetry on paper provided it well-defined reduction peak for Au(III) at similar to 287 +/- 12 mV vs Ag/AgCl. Under the optimized working conditions, the calibration curve showed good linearity in the concentration range of 1-200 ppm of Au(III) with a correlation coefficient of 0.997. The limit of detection (LOD) of the proposed method is 1 ppm. Interferences from various cations were also studied. Fe(III) is the only metal that affects the electrochemical determination of Au(III) when present above it 2.5-fold excess concentration of that of the Au(III). To overcome this limitation, a colorimetric method was used to simultaneously detect Fe(III) its it screening tool. The procedure was then successfully applied to determine Au(III) in gold-refining waste solutions. The results are in agreement with those obtained from inductively coupled plasma-atomic emission spectrometry (ICP-AES).
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