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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 6 (1994), S. 469-474 
    ISSN: 1040-0397
    Keywords: Copper ; Triton X-100 ; Adsorption ; Redox processes ; Voltammetry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this work, the redox processes of copper ions were studied by electrochemical methods in NaCl and NaClO4 solutions in the absence or in the presence of nonionic surfactant Triton X-100 (T-X-100). The enhancement of the anodic peak current of copper in the presence of T-X-100 in sodium chloride solutions was observed depending on the Concentrations of T-X-100 and copper (II) ions. This is the consequence of destabilization of the otherwise stabile CuCl2- complex in chloride solutions by the presence of T-X-100. The process involves disproportionation of formed copper (I) species to copper (0) and copper (II).
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 6 (1994), S. 131-137 
    ISSN: 1040-0397
    Keywords: Copper ; Triton X-100 ; Voltammetry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of Triton X-100 (T-X-100) on the redox processes of copper in NaCl solutions and in the presence of oxygen was investigated by anodic stripping alternating current voltammetry (ASacV), anodic stripping direct current voltammetry (ASdcV), and differential pulse anodic stripping voltammetry (DPASV). In the presence of oxygen, copper dissolution from amalgam is characterized by a catalytic process, resulting in a net cathodic current due to the oxidation of Cu(I) to Cu(II) by H2O2 formed on the electrode, and the subsequent reduction of Cu(II) back to Cu (I). Triton X-100 blocks the catalytic process by hindering the formation of H2O2, by competing with CuCl2- and Cl- for the adsorption sites on HMDE surface, and by blocking the formation of Cu(I) and Cu(II) hydroxide deposit on the surface. Its presence also changes the redox processes of copper from reversible to quasireversible. At the same time, T-X-100 increases the oxidation current of copper, probably through disproportionation of Cu(I) to Cu(0) and Cu(II). This last effect was observed regardless of whether oxygen was present in the solutions or not.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 4 (1992), S. 143-150 
    ISSN: 1040-0397
    Keywords: Copper ; redox process ; voltammetry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The redox processes of copper ions were studied by alternating current (ac) voltammetry and cyclic voltammetry in 0.5 M NaCl and NaClO4 solutions. The studies were performed at different pH values in the presence of atmospheric oxygen or by the addition of H2O2 to the process. In the case of copper ions in NaCl solution both in the presence of atmospheric oxygen and added H2O2, a catalytic current was observed. With cyclic voltammetry the current was in the cathodic direction in spite of having an anodic sweep. The key factor is the presence of chloride ions as in the NaClO4 solution; the observed catalytic current peaks are much smaller. The mechanism for the observed redox processes of copper is proposed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2021-05-10
    Description: Melanoidins, condensation products of sugars and amino acids, are thought to represent a key link in the transformation of polysaccharides and proteins to humic material in the marine environment. We investigated adsorption behaviour of melanoidins prepared in equimolar solutions of glucose and amino acids of choice (glutamic acid, valine and lysine) and pseudomelanoidins which were prepared from glucose only. Melanoidins were prepared using different condensation times (2, 4, 16 and 32 days). Synthesized melanoidins were separated into different molecular mass fractions. Fractionation of melanoidins by sorption on the macroreticular resin XAD-8 separated melanoidins into hydrophobic neutral, hydrophobic acid and hydrophilic fractions. Adsorption of melanoidins and their different fractions was studied at a mercury electrode by directly measuring the change of the double layer capacitance caused by the adsorption of organic molecules on the electrode surface through phase sensitive alternating current voltammetry. The hydrophobic acid fraction of melanoidins accounted for most of the adsorption behaviour of melanoidins. Consequently, the higher molecular mass fraction of melanoidins (〉10 kDa) exhibits a stronger adsorption in comparison to the lower molecular mass fraction (〈3 kDa) of the same melanoidin. The good fit of adsorption data of melanoidins and pseudomelanoidins to the same adsorption isotherm supports the idea that melanoidins are comprised of a sugar derived “backbone” that is responsible for the adsorption behaviour of melanoidin, while the presence of nitrogen atoms is responsible for the complexation of copper ions. Adsorption characteristics and complexation ability of melanoidins and natural organic matter were similar. Our results suggest that in the process of humification, selective adsorption of condensation products on aqueous surfaces may lead to a progressive immobilization of certain fractions, i.e., it is probable that higher molecular mass components accumulate at aquatic surfaces, while lower mass components remain in solution.
    Type: Article , PeerReviewed
    Format: text
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