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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Journal of superconductivity 9 (1996), S. 269-271 
    ISSN: 1572-9605
    Keywords: YBa2Cu3O7 ; pair breaking ; isotope effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: Abstract The effect of pair breaking on the isotope effect coefficientα=−d lnT c/d lnM in La2−x Sr x CuO4 and Pr-, Ca-, and Zn-doped YBa2Cu3O7−x and EuBa2Cu3O7−x is studied using the generalized Abrikosov-Gorkov theory recently employed by Singh and Kishore for superconductivity. It is argued that the isotope effect coefficientα can be further enhanced, in agreement with experimental observations, by considering the dependence of the characteristic scattering timeτ s for Cooper pairs on the concentrationn of impurities (both magnetic and nonmagnetic) and the disorder ignored by them (J. Supercond. 8, 9 (1995).
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 26 (1996), S. 509-514 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract The validity of the chronopotentiometric method, which has been used for studying the kinetics of metal dissolution and cementation (displacement) reactions was examined. Using the dissolution of electrodeposited zinc films as an example, results are presented for the dissolution in a triiodide solution, in an acid solution and in an acidified triiodide solution. The effect of the substrate electrode, on which the zinc film is deposited, was found to be negligible in the case of the triiodide dissolution reaction which is known to be diffusion controlled. However, the substrate electrode can have a profound effect on the dissolution in acid, a reaction which is known to be chemically controlled. In addition, the apparent dissolution rate in acidified triiodide solutions can be greater than the sum of the separate dissolution rates. Explanations for these findings, based on the catalytic effect of the substrate electrodes, are presented. The applicability of the chronopotentiometric method to the cementation of copper (II) on to electrodeposited zinc filsm was also investigated. Similar difficulties to those found with the zinc/acidified triiodide system were encountered. As a result of the understanding of the pit-falls of the chronopotentiometric method developed in this work, it was possible to review critically previous measurements of this type, which have been reported in the literature. It was concluded that, while the majority of previous studies are correct, a serious error has been made in one paper.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 15 (1996), S. 490-493 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1093-1098 
    ISSN: 0009-2940
    Keywords: Indium tris(thiobenzoate) ; Triethylammonium tetrakis(thiobenzoato)indate ; Tin, butyl-, tris(thiobenzoate) ; Tin, dichloro-, bis(thiobenzoate) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indium(III) and tin(IV) thiocarboxylates were prepared and characterized on the basis of their IR, 13C- and 19Sn-NMR data. Indium tris(thiobenzoate) (1) decomposes into a sulfido complex In (S)[S(O)CPh] (2a). The corresponding tris(thioacetate) In[S(O)CMe]3 is thermally too unstable to be isolated. The anionic tetrakis complex [Et3NH]{In[S(O)CPh]4} (3) was characterized by X-ray crystallography which revealed a distorted tetrahedral coordination at the In atom. X-ray diffraction analysis of the complexes BuSn[S(O)CPh]3 (4) and Cl2Sn[S(O)CPh]2 (7) showed distorted tetrahedral and cis-octahedral structures, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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