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      Using Electrode Made of Carbon Nanotubes and Bismuth Oxide for the Determination of Metal Concentration by Anodic Stripping Voltammetry

      1 , 2 , 3 , 4
      Journal of Chemistry
      Hindawi Limited

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          Abstract

          We have successfully manufactured a new electrode modified with bismuth oxide (Bi 2O 3) using carbon nanotubes (CNTs). The electrode was fabricated to detect cadmium (Cd), lead (Pb), and indium (In) by differential pulse anodic stripping voltammetry (DP-ASV). The electrode surface was studied by scanning electron microscopy (SEM), and the reduction and oxidation processes were studied by cyclic voltammetry (CV) techniques. Operational parameters such as electrode size, bismuth concentration, and electrolytic background were optimized. The DP-ASV method used fabricated electrodes with a linear response range from 1.5–20 μg·L −1 with Cd(II) and Pb(II) and 2.5–20 μg·L −1 with In(III); low detection limit (LOD) of 0.22 μg·L −1 with Cd(II), 0.65 μg·L −1 with In(III), and 0.26 μg·L −1 with Pb(II); and good repeatability with relative standard deviations (RSD) of 2.65%, 2.51%, and 3.34% with Cd(II), Pb(II), and In(III), respectively ( n = 8). The electrode can be used to test the content of Cd(II), In(III), and Pb(II) in water.

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          Most cited references33

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          Determination of trace metals by anodic stripping voltammetry using a bismuth-modified carbon nanotube electrode.

          A bismuth-modified carbon nanotube electrode (Bi-CNT electrode) was employed for the determination of trace lead, cadmium and zinc. Bismuth film was prepared by in situ plating of bismuth onto the screen-printed CNT electrode. Operational parameters such as preconcentration potential, bismuth concentration, preconcentration time and rotation speed during preconcentration were optimized for the purpose of determining trace metals in 0.1M acetate buffer solution (pH 4.5). The simultaneous determination of lead, cadmium and zinc was performed by square wave anodic stripping voltammetry. The Bi-CNT electrode presented well-defined, reproducible and sharp stripping signals. The peak current response increased linearly with the metal concentration in a range of 2-100 microg/L. The limit of detection was 1.3 microg/L for lead, 0.7 microg/L for cadmium and 12 microg/L for zinc (S/N=3). The Bi-CNT electrode was successfully applicable to analysis of trace metals in real environments.
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            Biomonitoring of 37 trace elements in blood samples from inhabitants of northern Germany by ICP-MS.

            The trace elements Ag, As, Au, B, Ba, Be, Bi, Cd, Ce, Co, Cs, Cu, Ga, Hf, Hg, In, La, Mn, Mo, Ni, Pb, Pd, Rb, Rh, Ru, Sb, Se, Sn, Sr, Te, Th, Tl, U, V, W, Y and Zr were determined in 130 human blood samples from occupationally non-exposed volunteers living in the greater area of Bremen in northern Germany. The blood samples were collected in lithium heparin monovettes developed for trace metal determination and were analysed by inductively coupled plasma mass spectrometry (ICP-MS) with an octopole-based collision/reaction cell. For sample introduction into the ICP, the blood samples were diluted 1/10 (V/V) with a 0.1% Triton-X-100 and 0.5% (V/V) ammonia solution. The method validation of our developed routine method is described for all 37 elements and results about internal and external quality assurance are discussed. Information on exposure conditions of all human subjects were collected by questionnaire-based interviews, including smoking habits, seafood consumption and the type of dental alloys in the teeth. Mean values, geometric mean values, ranges and selected percentiles of all elemental concentrations in human blood are presented, which helps toxicologists and clinical chemists planning research about exposition to metals and health effects caused by exposition to metals.
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              Determination of trace metal ions by AAS in natural water samples after preconcentration of pyrocatechol violet complexes on an activated carbon column.

              I Narin (2000)
              A simple preconcentration method is described for the determination of Cu, Mn, Co, Cd, Pb, Ni and Cr in water samples by flame AAS. Trace metal ions in water were sorbed as pyrocatechol violet complexes on activated carbon column at the pH range of 4-8, then eluted with 1 M HNO(3) in acetone. The effect of major cations and anions of the natural water samples on the sorption of metal ions has been also investigated. The concentration of the metal ions detected after preconcentration was in agreement with the added amount. The present method was found to be applicable to the preconcentration of Cu, Mn, Co, Cd, Pb, Ni and Cr in natural water samples with good results such as R.S.D. from 3 to 8% (N=10) and detection limits under 70 ng l(-1).
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                Author and article information

                Journal
                Journal of Chemistry
                Journal of Chemistry
                Hindawi Limited
                2090-9063
                2090-9071
                September 02 2019
                September 02 2019
                : 2019
                : 1-7
                Affiliations
                [1 ]Faculty of Chemical Technology, Hanoi University of Industry, 298 Cau Dien, Bac Tu Liem, Hanoi, Vietnam
                [2 ]Institute of Chemistry, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Cau Giay, Hanoi, Vietnam
                [3 ]Center of Excellence for Green Energy and Environmental Nanomaterials (CEGrEEN), Nguyen Tat Thanh University, 300A Nguyen Tat Thanh, District 4, Ho Chi Minh City 755414, Vietnam
                [4 ]NTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City 700000, Vietnam
                Article
                10.1155/2019/6170967
                298d3f01-5980-4d93-ab09-665a9026b3b1
                © 2019

                http://creativecommons.org/licenses/by/4.0/

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