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  • 1
    Publication Date: 1998-12-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    Publication Date: 2003-09-13
    Print ISSN: 0888-5885
    Electronic ISSN: 1520-5045
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 3
    ISSN: 1572-8838
    Keywords: Organic coatings ; mild steel ; pH
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract Coatings of poly(2-vinylpyridine) have been formed on mild steel substrates in aqueous medium by electrochemical polymerization of the 2-vinylpyridine monomer. The pH of the solution has been found to be critical for this electropolymerization coating process. At low pH (below 3.5), even with an efficient initiation reaction, the propagation process was impeded and no substantial polymer film was formed. At high pH (above 6.0), only a thin and irregular film formed due to the lack of an effective initiation reaction. Only when the solution pH is in the range of 4 to 5.5 can good quality coatings be formed on mild steel substrates. The detailed effects of the pH on the electropolymerization are discussed in terms of a proposed free radical polymerization mechanism. This research has also resolved the issue of some of the non-reproducible experimental results reported in the literature and confirmed the feasibility of forming poly(2-vinylpyridine) coatings on a mild steel substrate by electropolymerization of the monomer.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 18 (1988), S. 323-332 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract The electrochemistry of galena in an acetate solution at pH 4.6 has been studied through the use of linear sweep voltammetry. Analysis of the voltammograms for anodic limits as high as 845 mV indicates that S0 is the sulphur-bearing species generated during the oxidative dissolution of galena. Furthermore, interpretation of the electrochemical data on the basis of thermodynamic considerations indicates that galena interacts with the acetate electrolyte and that Pb(CH3COO)2(aq) is also produced during anodic oxidation. When the scan direction is reversed in the cathodic direction, the oxidation products are removed by two reduction reactions when the solution is quiescent: the recombination of Pb(CH3COO)2 and S0 to form PbS and the reduction of S0 to H2S. In a stirred solution, only the second reaction is possible. Experiments conducted in the presence of 10−3 or 10−2 M lead acetate indicate that the presence of dissolved lead tends to inhibit the dissolution process. Furthermore, metallic lead can begin to deposit on the galena surface when the potential drops below about −330 mV SHE. The data also agree most closely with thermodynamics when Pb(CH3COO)2 is considered to be the aqueous species involved in the deposition and dissolution of metallic lead.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 18 (1988), S. 484-490 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract A systematic electrochemical study of pyrite in H2SO4 solutions containing dissolved silver was undertaken to gain more information about the transfer of silver ions to pyrite and their role in enhancing the direct oxidation of pyrite. The results of cyclic voltammetry experiments provide additional evidence of the formation of metallic silver on the FeS2 surface under open-circuit conditions. A pyrite electrode held at the open-circuit potential for 2 h in the presence of 10−3 m Ag+ exhibits a large and sharp anodic peak at about 0.7V. The current associated with this peak is the result of the dissolution of metallic silver deposited during the initial conditioning period. There is no evidence of silver deposition without preconditioning until the potential drops below about 0.6V for Ag+ concentrations ranging from 10−4 to 10−2 m. However, subsequent silver deposition appears to be very sensitive to the dissolved silver concentration in this range. There is also evidence that the state of the pyrite surface has a pronounced influence on its interaction with silver ions. Agitation has also been found to have a significant effect on the electrochemistry of the Ag−FeS2 system.
    Type of Medium: Electronic Resource
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