1939
DOI: 10.1007/978-3-662-41802-4
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Diffusion in Metallen

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Cited by 62 publications
(9 citation statements)
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“…7): The diffusional growth kinetics of compound layers are usually treated using parabolic equations of the type x 2 = 2k 1 t, where x is the layer thickness, k 1 the layer growth-rate constant and t the time [9,13,14]. For sufficiently thick layers, such equations produce a quite satisfactory fit to the experimental data ( Fig.…”
Section: Layer-growth Kineticsmentioning
confidence: 98%
“…7): The diffusional growth kinetics of compound layers are usually treated using parabolic equations of the type x 2 = 2k 1 t, where x is the layer thickness, k 1 the layer growth-rate constant and t the time [9,13,14]. For sufficiently thick layers, such equations produce a quite satisfactory fit to the experimental data ( Fig.…”
Section: Layer-growth Kineticsmentioning
confidence: 98%
“…3 -5 In a simplified way, this kind of redistribution, caused by a gradient of the chemical potential across the surface and kinetically controlled by the varying dopant diffusivity, can be traced back to the spinodal decomposition, which is well known as a three-dimensional (3D) effect and explained in terms of an 'up-hill diffusion'. 6,7 Only a few examples of a '2D projection' of this effect, such as concentration patterns of electropositive adsorbates resulting from the up-hill diffusion in two-dimensional firstorder phase transitions under reaction-free conditions, are described in the literature. 8,9 A simple mathematical model, based on the phenomenological consideration of a strong affinity between potassium and oxygen and accounting for Ł Correspondence to: Y. Suchorski, Chemisches Institut, Otto-von-Guericke-Universität Magdeburg, Universitätsplatz 2, D-39106 Magdeburg, Germany.…”
Section: Introductionmentioning
confidence: 99%
“…Conventionally, the intermetallic-layer growth kinetics are treated with the use of parabolic equations following Fick's laws with the assumption of quasi-stationary concentration distribution of any component within the growing layers [13][14][15][16]. However, if the solubility of a solid metal in a liquid soldering alloy is not zero, as is practically always the case, then the growth rate constant found experimentally proves timedependent.…”
Section: Introductionmentioning
confidence: 99%