Rapid spectrophotometric detection of hydrogen peroxide using (Au)core (Ag)shell nanoparticle
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作者:
Jiang, Zhi-Liang
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机构:Key Laboratory of Environmental Engineering and Protection Evaluation, Department of Environmental Science, Guangxi Normal University, Guilin 541004, China
Jiang, Zhi-Liang
Li, Ji-Shun
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机构:Key Laboratory of Environmental Engineering and Protection Evaluation, Department of Environmental Science, Guangxi Normal University, Guilin 541004, China
Li, Ji-Shun
Zhang, Nan-Nan
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机构:Key Laboratory of Environmental Engineering and Protection Evaluation, Department of Environmental Science, Guangxi Normal University, Guilin 541004, China
Zhang, Nan-Nan
Liang, Ai-Hui
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机构:Key Laboratory of Environmental Engineering and Protection Evaluation, Department of Environmental Science, Guangxi Normal University, Guilin 541004, China
Liang, Ai-Hui
Liu, Qing-Ye
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机构:Key Laboratory of Environmental Engineering and Protection Evaluation, Department of Environmental Science, Guangxi Normal University, Guilin 541004, China
Liu, Qing-Ye
Huang, Zhi
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机构:Key Laboratory of Environmental Engineering and Protection Evaluation, Department of Environmental Science, Guangxi Normal University, Guilin 541004, China
Huang, Zhi
机构:
[1] Key Laboratory of Environmental Engineering and Protection Evaluation, Department of Environmental Science, Guangxi Normal University, Guilin 541004, China
[2] Department of Material and Chemical Engineering, Guilin University of Technology, Guilin 541001, China
来源:
Gaodeng Xuexiao Huaxue Xuebao/Chemical Journal of Chinese Universities
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2008年
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29卷
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10期
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摘要:
Using 10 nm nanogold as seeds, the (Au)core (Ag)shell nanoparticles were prepared in the presence of AgNO3 and trisodium citrate dehydrate, and they were purified by high-speed centrifugation to remove the excess trisodium citrate. The absorption peak of the purified (Au)core (Ag)shell nanoparticles is at 393 nm. In pH = 4.4 HAc-NaAc buffer solution, hydroxyl radical produced from Fenton reaction oxidized the outer silver layer of the nanoparticles to form Ag+, and resulted in decreasing of the absorbance value at 393 nm. The concentration of H2O2 in the range of 6.58-421.1μmol/L was linear to the decreased absorbance at 393 nm (ΔA393nm). Its regression equation was ΔA393nm = 0.00111c + 0.0210, and the correlation coefficient was 0.9908, with a detection limit of 1.73μmol/L. This method was applied to the detection of H2O2 in wastewater, with satisfactory results.
机构:
Univ Strasbourg, Lab ICube, UMR 7357, 23 Rue Loess, F-67037 Strasbourg, FranceUniv Strasbourg, Lab ICube, UMR 7357, 23 Rue Loess, F-67037 Strasbourg, France
Boubiche, Nacer
Cibaka-Ndaya, Cynthia
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Univ Strasbourg, Lab ICube, UMR 7357, 23 Rue Loess, F-67037 Strasbourg, France
Univ Lyon 1, Lab Multimat & Interfaces, Univ Claude Bernard Lyon1, CNRS,UMR 5615, F-69622 Villeurbanne, FranceUniv Strasbourg, Lab ICube, UMR 7357, 23 Rue Loess, F-67037 Strasbourg, France
Cibaka-Ndaya, Cynthia
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Brioude, Arnaud
Javahiraly, Nicolas
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Univ Strasbourg, Lab ICube, UMR 7357, 23 Rue Loess, F-67037 Strasbourg, FranceUniv Strasbourg, Lab ICube, UMR 7357, 23 Rue Loess, F-67037 Strasbourg, France