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Trace Copper (trace + copper)

Distribution by Scientific Domains

Chemistry	100%

Selected Abstracts

Interference from Trace Copper in Electrochemical Investigations Employing Carboxylic Acid Terminated Thiol Modified Gold Electrodes

ELECTROANALYSIS, Issue 6 2009
Xiaohu Qu
Abstract Unexpectedly, electrochemistry at variable chain length carboxylic acid terminated alkylthiol self-assembled monolayers (SAMs) on gold electrodes gives rise to a Faradaic process in buffered aqueous electrolyte solution. In particular, the three-carbon chain length, 3-mercaptopropionic acid (MPA), exhibits a chemically reversible process with a mid-point potential of 175,mV vs. Ag/AgCl under conditions of cyclic voltammetry. This process is associated with the presence of trace (parts per billion) amounts of copper(II) ions present in the chemical reagents used to prepare the aqueous electrolyte and also from the gold electrode itself. The carboxylic acid moiety on the SAM concentrates Cu2+ ions by coordination and this surface confined layer is then reduced. Methods to minimize the interference of Cu2+ ions at carboxylic acid terminated SAM are discussed and caution with respect to the interpretation of protein electrochemistry is recommended when using carboxylic acid functionalized SAMs to provide biocompatible electrochemical transduction surfaces, unless a metal free environment can be obtained. [source]

Study on Preconcentration of Trace Copper Using Microcrystalline Triphenylmethane Loaded with Malachite Green

CHINESE JOURNAL OF CHEMISTRY, Issue 4 2007
Yong Liang
Abstract The paper describes a novel method for copper preconcentration using microcrystalline triphenylmethane loaded with malachite green prior to the determination by the flame atomic absorption spectrometry (FAAS). Under the optimum conditions, Cu(II) can be totally adsorbed on the surface of microcrystalline triphenylmethane, and completely separated from Pb(II), Cd(II), Co(II), Cr(III), Ni(II), Mn(II), Fe(III) and Al(III) by controlling acidity. The preconcentration factor of this proposed method is 200. The recovery is in a range of 97.5%,105%. The relative standard deviation (RSD) is not beyond 3.0%. The proposed method has been successfully applied to the determination of trace copper in various water samples with satisfactory results. [source]

Selective enrichment of trace copper(II) from biological and natural water samples by SPE using ion-imprinted polymer

JOURNAL OF SEPARATION SCIENCE, JSS, Issue 6-7 2008
Yunhui Zhai
Abstract A novel Cu(II)-imprinted polymer sorbent was prepared by an ion-imprinted polymer (IIP) technique using (2Z)- N,N,-bis(2-aminoethylic)but-2-enediamide as the functional monomer and pentaerythritol triacylate as a crosslinker. IR, XPS, and elemental analysis techniques were used to confirm the obtained product. Subsequently, when this polymer was used as sorbent in SPE, it exhibited excellent selectivity for template ion from an aqueous solution. Quantitative extraction of Cu(II) was achieved in the pH range of 4,7. The time needed to extract each sample was less than 30 min by the batch method. The distribution ratio (D) values of IIP for Cu(II) were greatly larger than that for other ions. At optimal pH value, the maximum extraction capacity of IIP and nonimprinted polymer (NIP) was found to be 29.8 and 7.0 mg/g, respectively. The adsorption behavior of Cu(II) on the sorbents could be described by Langmuir adsorption isotherm equation. The feasible flow rate of Cu(II)-containing solution for quantitative extraction onto the column packed with IIP was 1,4 mL/min, whereas for elution it was less than 1 mL/min. The developed method was successfully applied to the separation and enrichment of trace Cu(II) in biological and natural water samples with satisfactory results. [source]